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  • Carbon Practice Questions

    Carbon and Its Compounds

    CLASS X  ·  STRUCTURAL FORMULAE & NOMENCLATURE  ·  PRACTICE SHEET
    Section A — Drawing Structural Formulae
    Q1. Draw the electron dot structure and structural formula of methane (CH₄).
    Show Answer
    Methane has one carbon atom forming four single covalent bonds with four hydrogen atoms. \[ \text{H} – \underset{\displaystyle \big| }{\overset{\displaystyle \text{H}}{\text{C}}} – \text{H} \quad \text{with a fourth H below the C} \] Structural formula: CH₄, with C at the centre bonded to 4 H atoms by 4 single bonds (tetrahedral arrangement)
    Q2. Write the structural formula of ethane (C₂H₆) and identify the number of covalent bonds present.
    Show Answer
    \[ \text{H}_3\text{C} – \text{CH}_3 \] Ethane contains 1 C–C bond and 6 C–H bonds, making a total of 7 covalent bonds.
    Q3. Draw the structural formula of ethene (C₂H₄) and ethyne (C₂H₂). State the type of bond between the two carbon atoms in each.
    Show Answer
    Ethene: \[ \text{H}_2\text{C} = \text{CH}_2 \] — carbon atoms joined by a double bond.

    Ethyne: \[ \text{HC} \equiv \text{CH} \] — carbon atoms joined by a triple bond.
    Q4. Draw the structural formula of propane, and show all the possible structural isomers of butane (C₄H₁₀).
    Show Answer
    Propane: \[ \text{CH}_3 – \text{CH}_2 – \text{CH}_3 \] Butane has two structural isomers:

    n-butane (straight chain): \[ \text{CH}_3 – \text{CH}_2 – \text{CH}_2 – \text{CH}_3 \] 2-methylpropane / isobutane (branched chain): \[ \text{CH}_3 – \underset{\displaystyle \text{CH}_3}{\text{CH}} – \text{CH}_3 \] (the central carbon bears a methyl branch)
    Q5. Draw the structural formulae of ethanol (C₂H₅OH) and ethanoic acid (CH₃COOH), clearly showing the functional group in each.
    Show Answer
    Ethanol (functional group: –OH, alcohol): \[ \text{CH}_3 – \text{CH}_2 – \text{OH} \] Ethanoic acid (functional group: –COOH, carboxylic acid): \[ \text{CH}_3 – \text{C}(=\text{O}) – \text{OH} \]
    Section B — IUPAC Nomenclature
    Q6. Write the IUPAC names of the following compounds: (a) CH₃–CH₂–CH₂–CH₃ (b) CH₃–CH₂–OH (c) CH₃–CHO (d) CH₃–CO–CH₃
    Show Answer
    (a) Butane
    (b) Ethanol
    (c) Ethanal
    (d) Propanone
    Q7. Name the functional groups present in the following compounds and give the general formula of each homologous series: (a) alcohols (b) aldehydes (c) ketones (d) carboxylic acids
    Show Answer
    (a) Alcohol — functional group –OH; general formula \( \text{C}_n\text{H}_{2n+1}\text{OH} \)
    (b) Aldehyde — functional group –CHO; general formula \( \text{C}_n\text{H}_{2n+1}\text{CHO} \)
    (c) Ketone — functional group \(>\!\text{C}=\text{O}\); general formula \( \text{C}_n\text{H}_{2n+1}\text{CO}\text{C}_m\text{H}_{2m+1} \)
    (d) Carboxylic acid — functional group –COOH; general formula \( \text{C}_n\text{H}_{2n+1}\text{COOH} \)
    Q8. Write the structural formula for: (a) propanal (b) pentan-1-ol (c) but-2-ene (d) propyne
    Show Answer
    (a) Propanal: \( \text{CH}_3 – \text{CH}_2 – \text{CHO} \)
    (b) Pentan-1-ol: \( \text{CH}_3 – \text{CH}_2 – \text{CH}_2 – \text{CH}_2 – \text{CH}_2\text{OH} \)
    (c) But-2-ene: \( \text{CH}_3 – \text{CH} = \text{CH} – \text{CH}_3 \)
    (d) Propyne: \( \text{CH}_3 – \text{C} \equiv \text{CH} \)
    Q9. Differentiate between saturated and unsaturated hydrocarbons with one structural example each, and state the general formula for each class (alkanes, alkenes, alkynes).
    Show Answer
    Saturated hydrocarbons (alkanes) contain only single bonds between carbon atoms.
    General formula: \( \text{C}_n\text{H}_{2n+2} \)   e.g. ethane, \( \text{CH}_3-\text{CH}_3 \)

    Unsaturated hydrocarbons contain at least one double or triple bond.
    Alkenes: \( \text{C}_n\text{H}_{2n} \)   e.g. ethene, \( \text{H}_2\text{C}=\text{CH}_2 \)
    Alkynes: \( \text{C}_n\text{H}_{2n-2} \)   e.g. ethyne, \( \text{HC}\equiv\text{CH} \)
    Q10. Draw all possible isomers of pentane (C₅H₁₂) and give their IUPAC names.
    Show Answer
    n-pentane: \[ \text{CH}_3 – \text{CH}_2 – \text{CH}_2 – \text{CH}_2 – \text{CH}_3 \] 2-methylbutane: \[ \text{CH}_3 – \underset{\displaystyle \text{CH}_3}{\text{CH}} – \text{CH}_2 – \text{CH}_3 \] 2,2-dimethylpropane (neopentane): \[ \text{CH}_3 – \underset{\displaystyle \text{CH}_3}{\underset{\displaystyle |}{\text{C}}} – \text{CH}_3, \text{ with a second } \text{CH}_3 \text{ also on the central C} \]

  • Functional Groups – BSEB PYQ Based Practice

    Functional Groups – BSEB PYQ Based Practice

    Instruction: Identify the functional group present in each compound. Write the name of the functional group.

    1. \(\mathrm{CH_3-CH_2-OH}\)
    2. \(\mathrm{CH_3-CHO}\)
    3. \(\mathrm{CH_3-CO-CH_3}\)
    4. \(\mathrm{CH_3-COOH}\)
    5. \(\mathrm{CH_3-CH_2-CH_2-OH}\)
    6. \(\mathrm{CH_3-CH_2-CHO}\)
    7. \(\mathrm{CH_3-CH_2-CO-CH_3}\)
    8. \(\mathrm{CH_3-CH_2-COOH}\)
    9. \(\mathrm{CH_3-OH}\)
    10. \(\mathrm{H-CHO}\)
    11. \(\mathrm{H-COOH}\)
    12. \(\mathrm{CH_3-CH(OH)-CH_3}\)
    13. \(\mathrm{CH_3-CH_2-CH_2-CHO}\)
    14. \(\mathrm{CH_3-CH_2-CO-CH_2-CH_3}\)
    15. \(\mathrm{CH_3-CH_2-CH_2-COOH}\)
    16. \(\mathrm{CH_3-CH_2-CH_2-CH_2-OH}\)
    17. \(\mathrm{CH_3-CH(CH_3)-CHO}\)
    18. \(\mathrm{CH_3-CH(CH_3)-COOH}\)
    19. \(\mathrm{CH_3-CO-CH(CH_3)-CH_3}\)
    20. \(\mathrm{CH_3-CH(OH)-CH_2-CH_3}\)
    1. Alcohol / Hydroxyl group (–OH)
    2. Aldehyde / Aldehydic group (–CHO)
    3. Ketone / Ketonic carbonyl group (>C=O)
    4. Carboxylic acid / Carboxyl group (–COOH)
    5. Alcohol / Hydroxyl group (–OH)
    6. Aldehyde / Aldehydic group (–CHO)
    7. Ketone / Ketonic carbonyl group (>C=O)
    8. Carboxylic acid / Carboxyl group (–COOH)
    9. Alcohol / Hydroxyl group (–OH)
    10. Aldehyde / Aldehydic group (–CHO)
    11. Carboxylic acid / Carboxyl group (–COOH)
    12. Alcohol / Hydroxyl group (–OH)
    13. Aldehyde / Aldehydic group (–CHO)
    14. Ketone / Ketonic carbonyl group (>C=O)
    15. Carboxylic acid / Carboxyl group (–COOH)
    16. Alcohol / Hydroxyl group (–OH)
    17. Aldehyde / Aldehydic group (–CHO)
    18. Carboxylic acid / Carboxyl group (–COOH)
    19. Ketone / Ketonic carbonyl group (>C=O)
    20. Alcohol / Hydroxyl group (–OH)

    Functional Group – PYQ Style Questions

    1. The functional group present in ethanol is:
      \[ \mathrm{CH_3-CH_2-OH} \]
    2. The functional group present in propanal is:
      \[ \mathrm{CH_3-CH_2-CHO} \]
    3. The functional group present in butanone is:
      \[ \mathrm{CH_3-CO-CH_2-CH_3} \]
    4. The functional group present in ethanoic acid is:
      \[ \mathrm{CH_3-COOH} \]
    5. Identify the functional group: \[ \mathrm{-OH} \]
    6. Identify the functional group: \[ \mathrm{-CHO} \]
    7. Identify the functional group: \[ \mathrm{>C=O} \]
    8. Identify the functional group: \[ \mathrm{-COOH} \]
    9. Which functional group is present in methanal? \[ \mathrm{HCHO} \]
    10. Which functional group is present in propanone? \[ \mathrm{CH_3COCH_3} \]
    11. Which functional group is present in propanol? \[ \mathrm{C_3H_7OH} \]
    12. Which functional group is present in propanoic acid? \[ \mathrm{CH_3CH_2COOH} \]
    1. Hydroxyl / Alcohol (–OH)
    2. Aldehyde (–CHO)
    3. Ketone (>C=O)
    4. Carboxylic acid (–COOH)
    5. Hydroxyl / Alcohol
    6. Aldehyde
    7. Ketone / Carbonyl
    8. Carboxyl / Carboxylic acid
    9. Aldehyde
    10. Ketone
    11. Alcohol
    12. Carboxylic acid

    Write the Functional Group Formula

    Instruction: Write the structural formula of the functional group asked in each question.

    1. Write the functional group of alcohols.
    2. Write the functional group of aldehydes.
    3. Write the functional group of ketones.
    4. Write the functional group of carboxylic acids.
    5. Write the structural formula of the hydroxyl group.
    6. Write the structural formula of the aldehydic group.
    7. Write the structural formula of the ketonic group.
    8. Write the structural formula of the carboxyl group.
    1. \(\mathrm{-OH}\)
    2. \(\mathrm{-CHO}\)
    3. \(\mathrm{>C=O}\)
    4. \(\mathrm{-COOH}\)
    5. \(\mathrm{-OH}\)
    6. \(\mathrm{-CHO}\)
    7. \(\mathrm{>C=O}\)
    8. \(\mathrm{-COOH}\)
  • Carbon and Its CompoundsIUPAC Nomenclature Practice

    Class 10 BSEB Science
    Carbon and Its Compounds
    IUPAC Nomenclature Practice

    Instruction: Name each compound using its correct IUPAC name.

    Set 1 – Basic Carbon Chains

    1. \(\mathrm{CH_4}\)
    2. \(\mathrm{CH_3-CH_3}\)
    3. \(\mathrm{CH_3-CH_2-CH_3}\)
    4. \(\mathrm{CH_3-CH_2-CH_2-CH_3}\)
    5. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_3}\)
    6. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_2-CH_3}\)
    7. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_2-CH_2-CH_3}\)
    8. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_2-CH_2-CH_2-CH_3}\)
    9. \(\mathrm{CH_2=CH_2}\)
    10. \(\mathrm{CH_2=CH-CH_3}\)
    11. \(\mathrm{CH_2=CH-CH_2-CH_3}\)
    12. \(\mathrm{CH_3-CH=CH-CH_3}\)
    13. \(\mathrm{CH\equiv CH}\)
    14. \(\mathrm{CH\equiv C-CH_3}\)
    15. \(\mathrm{CH\equiv C-CH_2-CH_3}\)
    16. \(\mathrm{CH_3-C\equiv C-CH_3}\)
    17. \(\mathrm{CH_3-OH}\)
    18. \(\mathrm{CH_3-CH_2-OH}\)
    19. \(\mathrm{CH_3-CHO}\)
    20. \(\mathrm{CH_3-COOH}\)
    Answers:
    1. Methane
    2. Ethane
    3. Propane
    4. Butane
    5. Pentane
    6. Hexane
    7. Heptane
    8. Octane
    9. Ethene
    10. Propene
    11. But-1-ene
    12. But-2-ene
    13. Ethyne
    14. Propyne
    15. But-1-yne
    16. But-2-yne
    17. Methanol
    18. Ethanol
    19. Ethanal
    20. Ethanoic acid

    Set 2 – Alkanes, Alkenes and Alkynes

    1. \(\mathrm{CH_3-CH_2-CH_2-CH_3}\)
    2. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_3}\)
    3. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_2-CH_3}\)
    4. \(\mathrm{CH_2=CH-CH_2-CH_2-CH_3}\)
    5. \(\mathrm{CH_3-CH=CH-CH_2-CH_3}\)
    6. \(\mathrm{CH_3-CH_2-CH=CH-CH_2-CH_3}\)
    7. \(\mathrm{CH_2=CH-CH_2-CH_2-CH_2-CH_3}\)
    8. \(\mathrm{CH_3-CH=CH-CH_2-CH_2-CH_3}\)
    9. \(\mathrm{CH\equiv C-CH_2-CH_2-CH_3}\)
    10. \(\mathrm{CH_3-C\equiv C-CH_2-CH_3}\)
    11. \(\mathrm{CH_3-CH_2-C\equiv C-CH_2-CH_3}\)
    12. \(\mathrm{CH\equiv C-CH_2-CH_2-CH_2-CH_3}\)
    13. \(\mathrm{CH_3-CH_2-CH_2-C\equiv CH}\)
    14. \(\mathrm{CH_3-CH_2-CH=CH_2}\)
    15. \(\mathrm{CH_3-CH=CH-CH_2-CH_2-CH_3}\)
    16. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_3}\)
    17. \(\mathrm{CH_2=CH-CH_2-CH_2-CH_2-CH_2-CH_3}\)
    18. \(\mathrm{CH_3-CH_2-CH_2-CH=CH-CH_3}\)
    19. \(\mathrm{CH\equiv C-CH_2-CH_2-CH_2-CH_3}\)
    20. \(\mathrm{CH_3-CH_2-CH_2-CH_2-C\equiv CH}\)
    Answers:
    1. Butane
    2. Pentane
    3. Hexane
    4. Pent-1-ene
    5. Pent-2-ene
    6. Hex-3-ene
    7. Hex-1-ene
    8. Hex-2-ene
    9. Pent-1-yne
    10. Pent-2-yne
    11. Hex-3-yne
    12. Hex-1-yne
    13. Pent-1-yne
    14. But-1-ene
    15. Hex-2-ene
    16. Pentane
    17. Hept-1-ene
    18. Hex-2-ene
    19. Hex-1-yne
    20. Hex-1-yne

    Set 3 – Alcohols

    1. \(\mathrm{CH_3-OH}\)
    2. \(\mathrm{CH_3-CH_2-OH}\)
    3. \(\mathrm{CH_3-CH_2-CH_2-OH}\)
    4. \(\mathrm{CH_3-CH(OH)-CH_3}\)
    5. \(\mathrm{CH_3-CH_2-CH_2-CH_2-OH}\)
    6. \(\mathrm{CH_3-CH(OH)-CH_2-CH_3}\)
    7. \(\mathrm{CH_3-CH_2-CH(OH)-CH_3}\)
    8. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_2-OH}\)
    9. \(\mathrm{CH_3-CH(OH)-CH_2-CH_2-CH_3}\)
    10. \(\mathrm{CH_3-CH_2-CH(OH)-CH_2-CH_3}\)
    11. \(\mathrm{CH_3-CH_2-CH_2-CH(OH)-CH_2-CH_3}\)
    12. \[ \begin{array}{c} \mathrm{\ \ CH_3}\\[-4pt] \mathrm{\ \ |}\\[-4pt] \mathrm{CH_3-CH-OH} \end{array} \]
    13. \[ \begin{array}{c} \mathrm{\ \ CH_3}\\[-4pt] \mathrm{\ \ |}\\[-4pt] \mathrm{CH_3-CH-CH_2-OH} \end{array} \]
    14. \[ \begin{array}{c} \mathrm{\ \ CH_3}\\[-4pt] \mathrm{\ \ |}\\[-4pt] \mathrm{CH_3-CH-CH_2-CH_3}\\[-4pt] \end{array} \]
    15. \(\mathrm{CH_3-CH(CH_3)-CH_2-OH}\)
    16. \(\mathrm{CH_3-C(OH)(CH_3)-CH_2-CH_3}\)
    17. \(\mathrm{CH_3-CH_2-C(OH)(CH_3)-CH_3}\)
    18. \(\mathrm{CH_3-CH(OH)-CH_2-CH_2-CH_2-CH_3}\)
    19. \(\mathrm{CH_3-CH_2-CH(OH)-CH_2-CH_2-CH_3}\)
    20. \(\mathrm{CH_3-CH_2-CH_2-CH(OH)-CH_2-CH_3}\)
    Answers:
    1. Methanol
    2. Ethanol
    3. Propan-1-ol
    4. Propan-2-ol
    5. Butan-1-ol
    6. Butan-2-ol
    7. Butan-2-ol
    8. Pentan-1-ol
    9. Pentan-2-ol
    10. Pentan-3-ol
    11. Hexan-3-ol
    12. Propan-2-ol
    13. 2-Methylpropan-1-ol
    14. 2-Methylbutane
    15. 2-Methylpropan-1-ol
    16. 2-Methylbutan-2-ol
    17. 2-Methylbutan-2-ol
    18. Hexan-2-ol
    19. Hexan-3-ol
    20. Hexan-3-ol

    Set 4 – Aldehydes

    1. \(\mathrm{H-CHO}\)
    2. \(\mathrm{CH_3-CHO}\)
    3. \(\mathrm{CH_3-CH_2-CHO}\)
    4. \(\mathrm{CH_3-CH_2-CH_2-CHO}\)
    5. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CHO}\)
    6. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_2-CHO}\)
    7. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_2-CH_2-CHO}\)
    8. \(\mathrm{CH_3-CH(CH_3)-CHO}\)
    9. \(\mathrm{CH_3-CH(CH_3)-CH_2-CHO}\)
    10. \(\mathrm{CH_3-CH_2-CH(CH_3)-CHO}\)
    11. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH_2-CHO}\)
    12. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH_2-CHO}\)
    13. \(\mathrm{CH_3-CH(CH_3)-CH(CH_3)-CHO}\)
    14. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH(CH_3)-CHO}\)
    15. \(\mathrm{CH_3-CH_2-CH_2-CH(CH_3)-CHO}\)
    16. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH(CH_3)-CHO}\)
    17. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH_2-CH_2-CHO}\)
    18. \(\mathrm{CH_3-CH(CH_3)-CH(CH_3)-CH_2-CHO}\)
    19. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH(CH_3)-CH_2-CHO}\)
    20. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH_2-CH(CH_3)-CHO}\)
    Answers:
    1. Methanal
    2. Ethanal
    3. Propanal
    4. Butanal
    5. Pentanal
    6. Hexanal
    7. Heptanal
    8. 2-Methylpropanal
    9. 3-Methylbutanal
    10. 2-Methylbutanal
    11. 4-Methylpentanal
    12. 3-Methylpentanal
    13. 2,3-Dimethylbutanal
    14. 2,3-Dimethylpentanal
    15. 2-Methylpentanal
    16. 2,4-Dimethylpentanal
    17. 3-Methylhexanal
    18. 2,3-Dimethylpentanal
    19. 2,3-Dimethylhexanal
    20. 2,5-Dimethylhexanal

    Set 5 – Ketones

    1. \(\mathrm{CH_3-CO-CH_3}\)
    2. \(\mathrm{CH_3-CO-CH_2-CH_3}\)
    3. \(\mathrm{CH_3-CH_2-CO-CH_2-CH_3}\)
    4. \(\mathrm{CH_3-CO-CH_2-CH_2-CH_3}\)
    5. \(\mathrm{CH_3-CH_2-CO-CH_2-CH_2-CH_3}\)
    6. \(\mathrm{CH_3-CO-CH_2-CH_2-CH_2-CH_3}\)
    7. \(\mathrm{CH_3-CH_2-CO-CH_2-CH_2-CH_3}\)
    8. \(\mathrm{CH_3-CO-CH_2-CH(CH_3)-CH_3}\)
    9. \(\mathrm{CH_3-CO-CH(CH_3)-CH_2-CH_3}\)
    10. \(\mathrm{CH_3-CH(CH_3)-CO-CH_2-CH_3}\)
    11. \(\mathrm{CH_3-CO-CH_2-CH_2-CH(CH_3)-CH_3}\)
    12. \(\mathrm{CH_3-CH(CH_3)-CO-CH_2-CH_2-CH_3}\)
    13. \(\mathrm{CH_3-CH_2-CO-CH(CH_3)-CH_3}\)
    14. \(\mathrm{CH_3-CO-CH(CH_3)-CH(CH_3)-CH_3}\)
    15. \(\mathrm{CH_3-CH(CH_3)-CO-CH(CH_3)-CH_3}\)
    16. \(\mathrm{CH_3-CO-CH_2-CH_2-CH_2-CH_2-CH_3}\)
    17. \(\mathrm{CH_3-CH_2-CO-CH_2-CH_2-CH_2-CH_3}\)
    18. \(\mathrm{CH_3-CH_2-CH_2-CO-CH_2-CH_2-CH_3}\)
    19. \(\mathrm{CH_3-CO-CH_2-CH(CH_3)-CH_2-CH_3}\)
    20. \(\mathrm{CH_3-CH(CH_3)-CO-CH_2-CH(CH_3)-CH_3}\)
    Answers:
    1. Propanone
    2. Butan-2-one
    3. Pentan-3-one
    4. Pentan-2-one
    5. Hexan-3-one
    6. Hexan-2-one
    7. Hexan-3-one
    8. 4-Methylpentan-2-one
    9. 3-Methylpentan-2-one
    10. 3-Methylpentan-2-one
    11. 5-Methylhexan-2-one
    12. 2-Methylhexan-3-one
    13. 2-Methylpentan-3-one
    14. 3,4-Dimethylpentan-2-one
    15. 2,4-Dimethylpentan-3-one
    16. Heptan-2-one
    17. Heptan-3-one
    18. Heptan-4-one
    19. 4-Methylhexan-2-one
    20. 2,5-Dimethylhexan-3-one

    Set 6 – Carboxylic Acids

    1. \(\mathrm{H-COOH}\)
    2. \(\mathrm{CH_3-COOH}\)
    3. \(\mathrm{CH_3-CH_2-COOH}\)
    4. \(\mathrm{CH_3-CH_2-CH_2-COOH}\)
    5. \(\mathrm{CH_3-CH_2-CH_2-CH_2-COOH}\)
    6. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_2-COOH}\)
    7. \(\mathrm{CH_3-CH_2-CH_2-CH_2-CH_2-CH_2-COOH}\)
    8. \(\mathrm{CH_3-CH(CH_3)-COOH}\)
    9. \(\mathrm{CH_3-CH_2-CH(CH_3)-COOH}\)
    10. \(\mathrm{CH_3-CH(CH_3)-CH_2-COOH}\)
    11. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH_2-COOH}\)
    12. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH_2-COOH}\)
    13. \(\mathrm{CH_3-CH(CH_3)-CH(CH_3)-COOH}\)
    14. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH(CH_3)-COOH}\)
    15. \(\mathrm{CH_3-CH_2-CH_2-CH(CH_3)-COOH}\)
    16. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH(CH_3)-COOH}\)
    17. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH_2-CH_2-COOH}\)
    18. \(\mathrm{CH_3-CH(CH_3)-CH(CH_3)-CH_2-COOH}\)
    19. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH(CH_3)-CH_2-COOH}\)
    20. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH_2-CH(CH_3)-COOH}\)
    Answers:
    1. Methanoic acid
    2. Ethanoic acid
    3. Propanoic acid
    4. Butanoic acid
    5. Pentanoic acid
    6. Hexanoic acid
    7. Heptanoic acid
    8. 2-Methylpropanoic acid
    9. 2-Methylbutanoic acid
    10. 3-Methylbutanoic acid
    11. 2-Methylpentanoic acid
    12. 4-Methylpentanoic acid
    13. 2,3-Dimethylbutanoic acid
    14. 2,3-Dimethylpentanoic acid
    15. 2-Methylpentanoic acid
    16. 2,4-Dimethylpentanoic acid
    17. 3-Methylhexanoic acid
    18. 2,3-Dimethylpentanoic acid
    19. 2,3-Dimethylhexanoic acid
    20. 2,5-Dimethylhexanoic acid

    Set 7 – Branched Hydrocarbons

    1. \(\mathrm{CH_3-CH(CH_3)-CH_3}\)
    2. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH_3}\)
    3. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH_2-CH_3}\)
    4. \(\mathrm{CH_3-C(CH_3)_2-CH_3}\)
    5. \(\mathrm{CH_3-CH(CH_3)-CH(CH_3)-CH_3}\)
    6. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH_2-CH_2-CH_3}\)
    7. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH_2-CH_3}\)
    8. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH(CH_3)-CH_3}\)
    9. \(\mathrm{CH_3-C(CH_3)_2-CH_2-CH_3}\)
    10. \(\mathrm{CH_3-CH(CH_3)-CH(CH_3)-CH_2-CH_3}\)
    11. \(\mathrm{CH_3-CH_2-C(CH_3)_2-CH_2-CH_3}\)
    12. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH(CH_3)-CH_3}\)
    13. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH_2-CH(CH_3)-CH_3}\)
    14. \(\mathrm{CH_3-C(CH_3)_2-CH_2-CH(CH_3)-CH_3}\)
    15. \(\mathrm{CH_3-CH(CH_3)-C(CH_3)_2-CH_3}\)
    16. \(\mathrm{CH_3-CH_2-CH(CH_3)-CH(CH_3)-CH_2-CH_3}\)
    17. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH(CH_3)-CH_2-CH_3}\)
    18. \(\mathrm{CH_3-CH_2-C(CH_3)_2-CH_2-CH_3}\)
    19. \(\mathrm{CH_3-CH(CH_3)-CH(CH_3)-CH(CH_3)-CH_3}\)
    20. \(\mathrm{CH_3-C(CH_3)_2-CH_2-C(CH_3)_2-CH_3}\)
    Answers:
    1. 2-Methylpropane
    2. 2-Methylbutane
    3. 3-Methylpentane
    4. 2,2-Dimethylpropane
    5. 2,3-Dimethylbutane
    6. 3-Methylhexane
    7. 2-Methylpentane
    8. 2,3-Dimethylpentane
    9. 2,2-Dimethylbutane
    10. 2,3-Dimethylpentane
    11. 3,3-Dimethylpentane
    12. 2,4-Dimethylpentane
    13. 2,4-Dimethylhexane
    14. 2,2,4-Trimethylpentane
    15. 2,2,3-Trimethylbutane
    16. 3,4-Dimethylhexane
    17. 2,4-Dimethylhexane
    18. 3,3-Dimethylpentane
    19. 2,3,4-Trimethylpentane
    20. 2,2,4,4-Tetramethylpentane

    Set 8 – Mixed Compounds

    1. \(\mathrm{CH_3-CH_2-OH}\)
    2. \(\mathrm{CH_3-CH(OH)-CH_3}\)
    3. \(\mathrm{CH_3-CHO}\)
    4. \(\mathrm{CH_3-CH_2-CHO}\)
    5. \(\mathrm{CH_3-CO-CH_3}\)
    6. \(\mathrm{CH_3-CO-CH_2-CH_3}\)
    7. \(\mathrm{CH_3-COOH}\)
    8. \(\mathrm{CH_3-CH_2-COOH}\)
    9. \(\mathrm{CH_2=CH-CH_3}\)
    10. \(\mathrm{CH_3-CH=CH-CH_3}\)
    11. \(\mathrm{CH\equiv C-CH_3}\)
    12. \(\mathrm{CH_3-C\equiv C-CH_3}\)
    13. \(\mathrm{CH_3-CH(CH_3)-CH_3}\)
    14. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH_3}\)
    15. \(\mathrm{CH_3-CH(OH)-CH_2-CH_3}\)
    16. \(\mathrm{CH_3-CH_2-CH(CH_3)-OH}\)
    17. \(\mathrm{CH_3-CH(CH_3)-CHO}\)
    18. \(\mathrm{CH_3-CH(CH_3)-COOH}\)
    19. \(\mathrm{CH_3-CH(CH_3)-CH_2-OH}\)
    20. \(\mathrm{CH_3-CH_2-CO-CH_2-CH_3}\)
    Answers:
    1. Ethanol
    2. Propan-2-ol
    3. Ethanal
    4. Propanal
    5. Propanone
    6. Butan-2-one
    7. Ethanoic acid
    8. Propanoic acid
    9. Propene
    10. But-2-ene
    11. Propyne
    12. But-2-yne
    13. 2-Methylpropane
    14. 2-Methylbutane
    15. Butan-2-ol
    16. Butan-2-ol
    17. 2-Methylpropanal
    18. 2-Methylpropanoic acid
    19. 2-Methylpropan-1-ol
    20. Pentan-3-one

    Set 9 – Higher Practice

    1. \(\mathrm{CH_2=CH-CH(CH_3)-CH_3}\)
    2. \(\mathrm{CH_3-CH=CH-CH(CH_3)-CH_3}\)
    3. \(\mathrm{CH\equiv C-CH(CH_3)-CH_3}\)
    4. \(\mathrm{CH_3-C\equiv C-CH(CH_3)-CH_3}\)
    5. \(\mathrm{CH_3-CH(OH)-CH(CH_3)-CH_3}\)
    6. \(\mathrm{CH_3-CH_2-CH(OH)-CH(CH_3)-CH_3}\)
    7. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH_2-OH}\)
    8. \(\mathrm{CH_3-CH(OH)-CH_2-CH(CH_3)-CH_3}\)
    9. \(\mathrm{CH_3-CH(CH_3)-CHO}\)
    10. \(\mathrm{CH_3-CH_2-CH(CH_3)-CHO}\)
    11. \(\mathrm{CH_3-CH(CH_3)-CO-CH_3}\)
    12. \(\mathrm{CH_3-CO-CH_2-CH(CH_3)-CH_3}\)
    13. \(\mathrm{CH_3-CH(CH_3)-CO-CH_2-CH_3}\)
    14. \(\mathrm{CH_3-CH(CH_3)-COOH}\)
    15. \(\mathrm{CH_3-CH_2-CH(CH_3)-COOH}\)
    16. \(\mathrm{CH_3-CH(CH_3)-CH(CH_3)-CH_3}\)
    17. \(\mathrm{CH_3-C(CH_3)_2-CH_2-CH_3}\)
    18. \(\mathrm{CH_3-CH(CH_3)-CH_2-CH(CH_3)-CH_3}\)
    19. \(\mathrm{CH_3-CH=CH-CH(CH_3)-CH_3}\)
    20. \(\mathrm{CH_3-CH(OH)-CH(CH_3)-CH_2-CH_3}\)
    Answers:
    1. 3-Methylbut-1-ene
    2. 4-Methylpent-2-ene
    3. 3-Methylbut-1-yne
    4. 4-Methylpent-2-yne
    5. 3-Methylbutan-2-ol
    6. 2-Methylpentan-3-ol
    7. 3-Methylbutan-1-ol
    8. 4-Methylpentan-2-ol
    9. 2-Methylpropanal
    10. 2-Methylbutanal
    11. 3-Methylbutan-2-one
    12. 4-Methylpentan-2-one
    13. 2-Methylpentan-3-one
    14. 2-Methylpropanoic acid
    15. 2-Methylbutanoic acid
    16. 2,3-Dimethylbutane
    17. 2,2-Dimethylbutane
    18. 2,4-Dimethylpentane
    19. 4-Methylpent-2-ene
    20. 3-Methylpentan-2-ol

    Set 10 – Board-Level Challenge

    1. \[ \mathrm{CH_3-CH_2-CH(CH_3)-CH_2-CH_3} \]
    2. \[ \mathrm{CH_3-CH(CH_3)-CH_2-CH(CH_3)-CH_3} \]
    3. \[ \mathrm{CH_2=CH-CH(CH_3)-CH_2-CH_3} \]
    4. \[ \mathrm{CH_3-CH=CH-CH(CH_3)-CH_3} \]
    5. \[ \mathrm{CH\equiv C-CH(CH_3)-CH_2-CH_3} \]
    6. \[ \mathrm{CH_3-C\equiv C-CH(CH_3)-CH_3} \]
    7. \[ \mathrm{CH_3-CH(OH)-CH_2-CH(CH_3)-CH_3} \]
    8. \[ \mathrm{CH_3-CH(CH_3)-CH_2-CH_2-OH} \]
    9. \[ \mathrm{CH_3-CH_2-CH(OH)-CH(CH_3)-CH_3} \]
    10. \[ \mathrm{CH_3-CH(CH_3)-CHO} \]
    11. \[ \mathrm{CH_3-CH_2-CH(CH_3)-CHO} \]
    12. \[ \mathrm{CH_3-CO-CH(CH_3)-CH_3} \]
    13. \[ \mathrm{CH_3-CO-CH_2-CH(CH_3)-CH_3} \]
    14. \[ \mathrm{CH_3-CH(CH_3)-COOH} \]
    15. \[ \mathrm{CH_3-CH_2-CH(CH_3)-COOH} \]
    16. \[ \mathrm{CH_3-CH(CH_3)-CH(CH_3)-CH_3} \]
    17. \[ \mathrm{CH_3-C(CH_3)_2-CH_2-CH_3} \]
    18. \[ \mathrm{CH_3-CH=CH-CH(CH_3)-CH_3} \]
    19. \[ \mathrm{CH_3-CH_2-CO-CH(CH_3)-CH_2-CH_3} \]
    20. \[ \mathrm{CH_3-CH(OH)-CH(CH_3)-CH_2-CH_3} \]
    Answers:
    1. 3-Methylpentane
    2. 2,4-Dimethylpentane
    3. 3-Methylpent-1-ene
    4. 4-Methylpent-2-ene
    5. 3-Methylpent-1-yne
    6. 4-Methylpent-2-yne
    7. 4-Methylpentan-2-ol
    8. 3-Methylbutan-1-ol
    9. 2-Methylpentan-3-ol
    10. 2-Methylpropanal
    11. 2-Methylbutanal
    12. 3-Methylbutan-2-one
    13. 4-Methylpentan-2-one
    14. 2-Methylpropanoic acid
    15. 2-Methylbutanoic acid
    16. 2,3-Dimethylbutane
    17. 2,2-Dimethylbutane
    18. 4-Methylpent-2-ene
    19. 4-Methylhexan-3-one
    20. 3-Methylpentan-2-ol
  • Carbon and Its CompoundsIUPAC Nomenclature – Structure Based Practice

    Class 10 BSEB Science

    Carbon and Its Compounds

    IUPAC Nomenclature – Structure Based Practice

    10 Sets × 20 Questions = 200 Questions

    Instructions: Name each of the following carbon compounds using the correct IUPAC nomenclature.
    Important: Students must write the names themselves. The answer key is hidden below each set.
    Set 1 – Straight-Chain Alkanes
    1. CH4
    2. CH3–CH3
    3. CH3–CH2–CH3
    4. CH3–CH2–CH2–CH3
    5. CH3–CH2–CH2–CH2–CH3
    6. CH3–(CH2)4–CH3
    7. CH3–(CH2)5–CH3
    8. CH3–(CH2)6–CH3
    9. CH3–(CH2)7–CH3
    10. CH3–(CH2)8–CH3
    11. CH3–CH2–CH2–CH2–CH2–CH3
    12. CH3–CH2–CH2–CH2–CH2–CH2–CH3
    13. CH3–CH2–CH2–CH2–CH2–CH2–CH2–CH3
    14. CH3–(CH2)9–CH3
    15. CH3–(CH2)10–CH3
    16. CH3–CH2–CH2–CH2–CH2–CH2–CH2–CH2–CH3
    17. CH3–(CH2)11–CH3
    18. CH3–(CH2)12–CH3
    19. CH3–(CH2)13–CH3
    20. CH3–(CH2)14–CH3
    1. Methane
    2. Ethane
    3. Propane
    4. Butane
    5. Pentane
    6. Hexane
    7. Heptane
    8. Octane
    9. Nonane
    10. Decane
    11. Hexane
    12. Heptane
    13. Octane
    14. Undecane
    15. Dodecane
    16. Nonane
    17. Tetradecane
    18. Pentadecane
    19. Hexadecane
    20. Heptadecane
    Set 2 – Alkenes
    1. CH2=CH2
    2. CH2=CH–CH3
    3. CH2=CH–CH2–CH3
    4. CH3–CH=CH–CH3
    5. CH2=CH–CH2–CH2–CH3
    6. CH3–CH=CH–CH2–CH3
    7. CH3–CH2–CH=CH–CH2–CH3
    8. CH2=CH–CH2–CH2–CH2–CH3
    9. CH3–CH=CH–CH2–CH2–CH3
    10. CH3–CH2–CH=CH–CH2–CH2–CH3
    11. CH2=CH–CH2–CH2–CH2–CH2–CH3
    12. CH3–CH=CH–CH2–CH2–CH2–CH3
    13. CH2=CH–CH2–CH2–CH2–CH2–CH2–CH3
    14. CH3–CH2–CH=CH–CH2–CH2–CH2–CH3
    15. CH2=CH–CH2–CH2–CH2–CH2–CH2–CH2–CH3
    16. CH3–CH=CH–CH2–CH2–CH2–CH2–CH2–CH3
    17. CH2=CH–CH2–CH2–CH2–CH2–CH2–CH2–CH2–CH3
    18. CH3–CH2–CH=CH–CH2–CH2–CH2–CH2–CH2–CH3
    19. CH2=CH–CH2–CH2–CH2–CH2–CH2–CH2–CH2–CH2–CH3
    20. CH3–CH=CH–CH2–CH2–CH2–CH2–CH2–CH2–CH3
    1. Ethene
    2. Propene
    3. But-1-ene
    4. But-2-ene
    5. Pent-1-ene
    6. Pent-2-ene
    7. Hex-3-ene
    8. Hex-1-ene
    9. Hex-2-ene
    10. Hept-3-ene
    11. Hept-1-ene
    12. Hept-2-ene
    13. Oct-1-ene
    14. Oct-3-ene
    15. Non-1-ene
    16. Non-2-ene
    17. Dec-1-ene
    18. Dec-4-ene
    19. Undec-1-ene
    20. Undec-2-ene
    Set 3 – Alkynes
    1. CH≡CH
    2. CH≡C–CH3
    3. CH≡C–CH2–CH3
    4. CH3–C≡C–CH3
    5. CH≡C–CH2–CH2–CH3
    6. CH3–C≡C–CH2–CH3
    7. CH3–CH2–C≡C–CH2–CH3
    8. CH≡C–CH2–CH2–CH2–CH3
    9. CH3–C≡C–CH2–CH2–CH3
    10. CH3–CH2–C≡C–CH2–CH2–CH3
    11. CH≡C–CH2–CH2–CH2–CH2–CH3
    12. CH3–C≡C–CH2–CH2–CH2–CH3
    13. CH3–CH2–C≡C–CH2–CH2–CH3
    14. CH≡C–CH2–CH2–CH2–CH2–CH2–CH3
    15. CH3–C≡C–CH2–CH2–CH2–CH2–CH3
    16. CH3–CH2–C≡C–CH2–CH2–CH2–CH3
    17. CH≡C–CH2–CH2–CH2–CH2–CH2–CH2–CH3
    18. CH3–C≡C–CH2–CH2–CH2–CH2–CH2–CH3
    19. CH3–CH2–C≡C–CH2–CH2–CH2–CH2–CH3
    20. CH≡C–CH2–CH2–CH2–CH2–CH2–CH2–CH2–CH3
    1. Ethyne
    2. Propyne
    3. But-1-yne
    4. But-2-yne
    5. Pent-1-yne
    6. Pent-2-yne
    7. Hex-3-yne
    8. Hex-1-yne
    9. Hex-2-yne
    10. Hept-3-yne
    11. Hept-1-yne
    12. Hept-2-yne
    13. Hept-3-yne
    14. Oct-1-yne
    15. Oct-2-yne
    16. Oct-3-yne
    17. Non-1-yne
    18. Non-2-yne
    19. Non-3-yne
    20. Dec-1-yne
    Set 4 – Alcohols
    1. CH3–OH
    2. CH3–CH2–OH
    3. CH3–CH2–CH2–OH
    4. CH3–CH(OH)–CH3
    5. CH3–CH2–CH2–CH2–OH
    6. CH3–CH(OH)–CH2–CH3
    7. CH3–CH2–CH(OH)–CH3
    8. CH3–CH2–CH2–CH2–CH2–OH
    9. CH3–CH(OH)–CH2–CH2–CH3
    10. CH3–CH2–CH(OH)–CH2–CH3
    11. CH3–CH2–CH2–CH(OH)–CH2–CH3
    12. (CH3)2CH–OH
    13. CH3–CH(CH3)–CH2–OH
    14. CH3–CH(OH)–CH(CH3)–CH3
    15. CH3–CH2–CH(CH3)–CH2–OH
    16. CH3–C(OH)(CH3)–CH2–CH3
    17. CH3–CH2–C(OH)(CH3)–CH3
    18. CH3–CH2–CH2–CH(OH)–CH2–CH3
    19. CH3–CH(OH)–CH2–CH2–CH2–CH3
    20. CH3–CH2–CH(OH)–CH2–CH2–CH3
    1. Methanol
    2. Ethanol
    3. Propan-1-ol
    4. Propan-2-ol
    5. Butan-1-ol
    6. Butan-2-ol
    7. Butan-2-ol
    8. Pentan-1-ol
    9. Pentan-2-ol
    10. Pentan-3-ol
    11. Hexan-3-ol
    12. Propan-2-ol
    13. 2-Methylpropan-1-ol
    14. 3-Methylbutan-2-ol
    15. 2-Methylbutan-1-ol
    16. 2-Methylbutan-2-ol
    17. 2-Methylbutan-2-ol
    18. Hexan-3-ol
    19. Hexan-2-ol
    20. Hexan-3-ol
    Set 5 – Aldehydes
    1. H–CHO
    2. CH3–CHO
    3. CH3–CH2–CHO
    4. CH3–CH2–CH2–CHO
    5. CH3–CH2–CH2–CH2–CHO
    6. CH3–CH2–CH2–CH2–CH2–CHO
    7. CH3–CH2–CH2–CH2–CH2–CH2–CHO
    8. CH3–CH2–CH2–CH2–CH2–CH2–CH2–CHO
    9. CH3–CH2–CH2–CH2–CH2–CH2–CH2–CH2–CHO
    10. CH3–CH2–CH2–CH2–CH2–CH2–CH2–CH2–CH2–CHO
    11. CH3–CH(CH3)–CHO
    12. CH3–CH(CH3)–CH2–CHO
    13. CH3–CH2–CH(CH3)–CHO
    14. CH3–CH(CH3)–CH2–CH2–CHO
    15. CH3–CH2–CH(CH3)–CH2–CHO
    16. CH3–CH(CH3)–CH(CH3)–CHO
    17. CH3–CH2–CH(CH3)–CH(CH3)–CHO
    18. CH3–CH2–CH2–CH(CH3)–CHO
    19. CH3–CH(CH3)–CH2–CH(CH3)–CHO
    20. CH3–CH2–CH(CH3)–CH2–CH2–CHO
    1. Methanal
    2. Ethanal
    3. Propanal
    4. Butanal
    5. Pentanal
    6. Hexanal
    7. Heptanal
    8. Octanal
    9. Nonanal
    10. Decanal
    11. 2-Methylpropanal
    12. 3-Methylbutanal
    13. 2-Methylbutanal
    14. 4-Methylpentanal
    15. 3-Methylpentanal
    16. 2,3-Dimethylbutanal
    17. 2,3-Dimethylpentanal
    18. 2-Methylpentanal
    19. 2,4-Dimethylpentanal
    20. 3-Methylhexanal
    Set 6 – Ketones
    1. CH3–CO–CH3
    2. CH3–CO–CH2–CH3
    3. CH3–CH2–CO–CH2–CH3
    4. CH3–CO–CH2–CH2–CH3
    5. CH3–CH2–CO–CH2–CH2–CH3
    6. CH3–CO–CH2–CH2–CH2–CH3
    7. CH3–CH2–CO–CH2–CH2–CH3
    8. CH3–CO–CH2–CH2–CH2–CH2–CH3
    9. CH3–CH2–CO–CH2–CH2–CH2–CH3
    10. CH3–CH2–CH2–CO–CH2–CH2–CH3
    11. CH3–CO–CH(CH3)–CH3
    12. CH3–CO–CH2–CH(CH3)–CH3
    13. CH3–CH(CH3)–CO–CH2–CH3
    14. CH3–CO–CH(CH3)–CH2–CH3
    15. CH3–CH2–CO–CH(CH3)–CH3
    16. CH3–CO–CH2–CH2–CH(CH3)–CH3
    17. CH3–CH(CH3)–CO–CH2–CH2–CH3
    18. CH3–CH2–CO–CH2–CH(CH3)–CH3
    19. CH3–CO–CH(CH3)–CH(CH3)–CH3
    20. CH3–CH(CH3)–CO–CH(CH3)–CH3
    1. Propanone
    2. Butan-2-one
    3. Pentan-3-one
    4. Pentan-2-one
    5. Hexan-3-one
    6. Hexan-2-one
    7. Hexan-3-one
    8. Heptan-2-one
    9. Heptan-3-one
    10. Heptan-4-one
    11. 3-Methylbutan-2-one
    12. 4-Methylpentan-2-one
    13. 2-Methylpentan-3-one
    14. 3-Methylpentan-2-one
    15. 2-Methylpentan-3-one
    16. 5-Methylhexan-2-one
    17. 2-Methylhexan-3-one
    18. 5-Methylhexan-3-one
    19. 3,4-Dimethylpentan-2-one
    20. 2,4-Dimethylpentan-3-one
    Set 7 – Carboxylic Acids
    1. H–COOH
    2. CH3–COOH
    3. CH3–CH2–COOH
    4. CH3–CH2–CH2–COOH
    5. CH3–CH2–CH2–CH2–COOH
    6. CH3–CH2–CH2–CH2–CH2–COOH
    7. CH3–CH2–CH2–CH2–CH2–CH2–COOH
    8. CH3–CH2–CH2–CH2–CH2–CH2–CH2–COOH
    9. CH3–CH2–CH2–CH2–CH2–CH2–CH2–CH2–COOH
    10. CH3–CH2–CH2–CH2–CH2–CH2–CH2–CH2–CH2–COOH
    11. CH3–CH(CH3)–COOH
    12. CH3–CH2–CH(CH3)–COOH
    13. CH3–CH(CH3)–CH2–COOH
    14. CH3–CH2–CH(CH3)–CH2–COOH
    15. CH3–CH(CH3)–CH2–CH2–COOH
    16. CH3–CH(CH3)–CH(CH3)–COOH
    17. CH3–CH2–CH(CH3)–CH(CH3)–COOH
    18. CH3–CH2–CH2–CH(CH3)–COOH
    19. CH3–CH(CH3)–CH2–CH(CH3)–COOH
    20. CH3–CH2–CH(CH3)–CH2–CH2–COOH
    1. Methanoic acid
    2. Ethanoic acid
    3. Propanoic acid
    4. Butanoic acid
    5. Pentanoic acid
    6. Hexanoic acid
    7. Heptanoic acid
    8. Octanoic acid
    9. Nonanoic acid
    10. Decanoic acid
    11. 2-Methylpropanoic acid
    12. 2-Methylbutanoic acid
    13. 3-Methylbutanoic acid
    14. 2-Methylpentanoic acid
    15. 4-Methylpentanoic acid
    16. 2,3-Dimethylbutanoic acid
    17. 2,3-Dimethylpentanoic acid
    18. 2-Methylpentanoic acid
    19. 2,4-Dimethylpentanoic acid
    20. 3-Methylhexanoic acid
    Set 8 – Branched-Chain Alkanes
    1. CH3–CH(CH3)–CH3
    2. CH3–CH(CH3)–CH2–CH3
    3. CH3–CH2–CH(CH3)–CH2–CH3
    4. CH3–C(CH3)2–CH3
    5. CH3–CH(CH3)–CH(CH3)–CH3
    6. CH3–CH2–CH(CH3)–CH2–CH2–CH3
    7. CH3–CH(CH3)–CH2–CH2–CH3
    8. CH3–CH2–CH(CH3)–CH(CH3)–CH3
    9. CH3–C(CH3)2–CH2–CH3
    10. CH3–CH(CH3)–CH(CH3)–CH2–CH3
    11. CH3–CH2–C(CH3)2–CH2–CH3
    12. CH3–CH(CH3)–CH2–CH(CH3)–CH3
    13. CH3–CH2–CH(CH3)–CH2–CH(CH3)–CH3
    14. CH3–C(CH3)2–CH2–CH(CH3)–CH3
    15. CH3–CH(CH3)–C(CH3)2–CH3
    16. CH3–CH2–CH(CH3)–CH(CH3)–CH2–CH3
    17. CH3–CH(CH3)–CH2–CH(CH3)–CH2–CH3
    18. CH3–CH2–C(CH3)2–CH2–CH3
    19. CH3–CH(CH3)–CH(CH3)–CH(CH3)–CH3
    20. CH3–C(CH3)2–CH2–C(CH3)2–CH3
    1. 2-Methylpropane
    2. 2-Methylbutane
    3. 3-Methylpentane
    4. 2,2-Dimethylpropane
    5. 2,3-Dimethylbutane
    6. 3-Methylhexane
    7. 2-Methylpentane
    8. 2,3-Dimethylpentane
    9. 2,2-Dimethylbutane
    10. 2,3-Dimethylpentane
    11. 3,3-Dimethylpentane
    12. 2,4-Dimethylpentane
    13. 2,4-Dimethylhexane
    14. 2,2,4-Trimethylpentane
    15. 2,2,3-Trimethylbutane
    16. 3,4-Dimethylhexane
    17. 2,4-Dimethylhexane
    18. 3,3-Dimethylpentane
    19. 2,3,4-Trimethylpentane
    20. 2,2,4,4-Tetramethylpentane
    Set 9 – Mixed Functional Groups
    1. CH3–CH2–OH
    2. CH3–CH(OH)–CH3
    3. CH3–CH2–CH2–OH
    4. CH3–CHO
    5. CH3–CH2–CHO
    6. CH3–CO–CH3
    7. CH3–CO–CH2–CH3
    8. CH3–COOH
    9. CH3–CH2–COOH
    10. CH3–CH2–CH2–COOH
    11. CH2=CH–CH3
    12. CH3–CH=CH–CH3
    13. CH≡C–CH3
    14. CH3–C≡C–CH3
    15. CH3–CH(CH3)–CH3
    16. CH3–CH(CH3)–CH2–CH3
    17. CH3–CH(OH)–CH2–CH3
    18. CH3–CH2–CO–CH2–CH3
    19. CH3–CH(CH3)–COOH
    20. CH3–CH(CH3)–CH2–OH
    1. Ethanol
    2. Propan-2-ol
    3. Propan-1-ol
    4. Ethanal
    5. Propanal
    6. Propanone
    7. Butan-2-one
    8. Ethanoic acid
    9. Propanoic acid
    10. Butanoic acid
    11. Propene
    12. But-2-ene
    13. Propyne
    14. But-2-yne
    15. 2-Methylpropane
    16. 2-Methylbutane
    17. Butan-2-ol
    18. Pentan-3-one
    19. 2-Methylpropanoic acid
    20. 2-Methylpropan-1-ol
    Set 10 – Board-Level Challenge
    1. CH3–CH2–CH(CH3)–CH2–CH3
    2. CH3–CH(CH3)–CH2–CH(CH3)–CH3
    3. CH3–CH=CH–CH2–CH3
    4. CH2=CH–CH(CH3)–CH3
    5. CH≡C–CH(CH3)–CH3
    6. CH3–C≡C–CH(CH3)–CH3
    7. CH3–CH(OH)–CH2–CH(CH3)–CH3
    8. CH3–CH(CH3)–CH2–CH2–OH
    9. CH3–CH2–CH(OH)–CH2–CH3
    10. CH3–CH(CH3)–CHO
    11. CH3–CH2–CH(CH3)–CHO
    12. CH3–CH(CH3)–CO–CH3
    13. CH3–CO–CH2–CH(CH3)–CH3
    14. CH3–CH(CH3)–COOH
    15. CH3–CH2–CH(CH3)–COOH
    16. CH3–CH(CH3)–CH(CH3)–CH3
    17. CH3–C(CH3)2–CH2–CH3
    18. CH3–CH=CH–CH(CH3)–CH3
    19. CH3–CH2–CO–CH(CH3)–CH2–CH3
    20. CH3–CH(OH)–CH(CH3)–CH2–CH3
    1. 3-Methylpentane
    2. 2,4-Dimethylpentane
    3. Pent-2-ene
    4. 3-Methylbut-1-ene
    5. 3-Methylbut-1-yne
    6. 4-Methylpent-2-yne
    7. 4-Methylpentan-2-ol
    8. 2-Methylbutan-1-ol
    9. Pentan-3-ol
    10. 2-Methylpropanal
    11. 2-Methylbutanal
    12. 3-Methylbutan-2-one
    13. 4-Methylpentan-2-one
    14. 2-Methylpropanoic acid
    15. 2-Methylbutanoic acid
    16. 2,3-Dimethylbutane
    17. 2,2-Dimethylbutane
    18. 4-Methylpent-2-ene
    19. 4-Methylhexan-3-one
    20. 3-Methylpentan-2-ol
  • Carbon and Its Compounds – Nomenclature Practice

    Class 10 BSEB Science

    Carbon and Its Compounds – Nomenclature Practice

    10 Sets × 20 Questions = 200 Questions

    Instructions: Write the correct IUPAC name of each compound. In questions asking for a formula, write the correct structural/condensed formula.
    Set 1 – Basic Nomenclature
    1. CH4
    2. C2H6
    3. C3H8
    4. C4H10
    5. C5H12
    6. C2H4
    7. C3H6
    8. C4H8
    9. C2H2
    10. C3H4
    11. Write the formula of methane.
    12. Write the formula of ethane.
    13. Write the formula of propane.
    14. Write the formula of butane.
    15. Write the formula of ethene.
    16. Write the formula of propene.
    17. Write the formula of ethyne.
    18. Write the formula of propyne.
    19. Write the formula of methanol.
    20. Write the formula of ethanol.
    1. Methane
    2. Ethane
    3. Propane
    4. Butane
    5. Pentane
    6. Ethene
    7. Propene
    8. Butene
    9. Ethyne
    10. Propyne
    11. CH4
    12. C2H6
    13. C3H8
    14. C4H10
    15. C2H4
    16. C3H6
    17. C2H2
    18. C3H4
    19. CH3OH
    20. C2H5OH
    Set 2 – Hydrocarbons
    1. CH3CH2CH2CH3
    2. CH3CH2CH2CH2CH3
    3. CH3CH2CH2CH2CH2CH3
    4. CH3CH(CH3)CH3
    5. CH3CH(CH3)CH2CH3
    6. CH2=CHCH3
    7. CH2=CHCH2CH3
    8. CH3CH=CHCH3
    9. CH2=CHCH2CH2CH3
    10. CH3CH2CH=CHCH3
    11. CH≡CH
    12. CH≡CCH3
    13. CH≡CCH2CH3
    14. CH3C≡CCH3
    15. Write the formula of pentane.
    16. Write the formula of hexane.
    17. Write the formula of but-1-ene.
    18. Write the formula of but-2-ene.
    19. Write the formula of pent-1-yne.
    20. Write the formula of pent-2-yne.
    1. Butane
    2. Pentane
    3. Hexane
    4. 2-Methylpropane
    5. 2-Methylbutane
    6. Propene
    7. But-1-ene
    8. But-2-ene
    9. Pent-1-ene
    10. Pent-2-ene
    11. Ethyne
    12. Propyne
    13. But-1-yne
    14. But-2-yne
    15. CH3CH2CH2CH2CH3
    16. CH3CH2CH2CH2CH2CH3
    17. CH2=CHCH2CH3
    18. CH3CH=CHCH3
    19. CH≡CCH2CH2CH3
    20. CH3C≡CCH2CH3
    Set 3 – Alcohols
    1. CH3OH
    2. CH3CH2OH
    3. CH3CH2CH2OH
    4. CH3CH(OH)CH3
    5. CH3CH2CH2CH2OH
    6. CH3CH(OH)CH2CH3
    7. (CH3)2CHOH
    8. Write the formula of methanol.
    9. Write the formula of ethanol.
    10. Write the formula of propan-1-ol.
    11. Write the formula of propan-2-ol.
    12. Write the formula of butan-1-ol.
    13. Write the formula of butan-2-ol.
    14. What is the functional group of alcohols?
    15. What suffix is used for alcohols?
    16. Name the compound C5H11OH.
    17. Name CH3CH2OH.
    18. Write the condensed formula of propan-1-ol.
    19. Write the condensed formula of propan-2-ol.
    20. Write the condensed formula of butan-1-ol.
    1. Methanol
    2. Ethanol
    3. Propan-1-ol
    4. Propan-2-ol
    5. Butan-1-ol
    6. Butan-2-ol
    7. Propan-2-ol
    8. CH3OH
    9. CH3CH2OH
    10. CH3CH2CH2OH
    11. CH3CH(OH)CH3
    12. CH3CH2CH2CH2OH
    13. CH3CH(OH)CH2CH3
    14. –OH
    15. –ol
    16. Pentanol
    17. Ethanol
    18. CH3CH2CH2OH
    19. CH3CH(OH)CH3
    20. CH3CH2CH2CH2OH
    Set 4 – Aldehydes and Ketones
    1. HCHO
    2. CH3CHO
    3. CH3CH2CHO
    4. CH3CH2CH2CHO
    5. CH3COCH3
    6. CH3COCH2CH3
    7. CH3CH2COCH2CH3
    8. What is the functional group of aldehydes?
    9. What is the functional group of ketones?
    10. What suffix is used for aldehydes?
    11. What suffix is used for ketones?
    12. Write the formula of methanal.
    13. Write the formula of ethanal.
    14. Write the formula of propanal.
    15. Write the formula of propanone.
    16. Write the formula of butanone.
    17. Name CH3CHO.
    18. Name CH3COCH3.
    19. Name CH3CH2CHO.
    20. Name CH3COCH2CH3.
    1. Methanal
    2. Ethanal
    3. Propanal
    4. Butanal
    5. Propanone
    6. Butan-2-one
    7. Pentan-3-one
    8. –CHO
    9. >C=O
    10. –al
    11. –one
    12. HCHO
    13. CH3CHO
    14. CH3CH2CHO
    15. CH3COCH3
    16. CH3COCH2CH3
    17. Ethanal
    18. Propanone
    19. Propanal
    20. Butan-2-one
    Set 5 – Carboxylic Acids
    1. HCOOH
    2. CH3COOH
    3. CH3CH2COOH
    4. CH3CH2CH2COOH
    5. CH3CH2CH2CH2COOH
    6. What is the functional group of carboxylic acids?
    7. What suffix is used for carboxylic acids?
    8. Write the formula of methanoic acid.
    9. Write the formula of ethanoic acid.
    10. Write the formula of propanoic acid.
    11. Write the formula of butanoic acid.
    12. Write the formula of pentanoic acid.
    13. Name CH3COOH.
    14. Name HCOOH.
    15. Name CH3CH2COOH.
    16. Name CH3CH2CH2COOH.
    17. How many carbon atoms are present in ethanoic acid?
    18. How many carbon atoms are present in propanoic acid?
    19. Write the condensed formula of ethanoic acid.
    20. Write the condensed formula of butanoic acid.
    1. Methanoic acid
    2. Ethanoic acid
    3. Propanoic acid
    4. Butanoic acid
    5. Pentanoic acid
    6. –COOH
    7. –oic acid
    8. HCOOH
    9. CH3COOH
    10. CH3CH2COOH
    11. CH3CH2CH2COOH
    12. CH3CH2CH2CH2COOH
    13. Ethanoic acid
    14. Methanoic acid
    15. Propanoic acid
    16. Butanoic acid
    17. 2
    18. 3
    19. CH3COOH
    20. CH3CH2CH2COOH
    Set 6 – Mixed Functional Groups
    1. CH3OH
    2. CH3CHO
    3. CH3COOH
    4. CH3COCH3
    5. CH3CH2OH
    6. CH3CH2CHO
    7. CH3CH2COOH
    8. CH3CH2COCH3
    9. CH3CH2CH2OH
    10. CH3CH2CH2CHO
    11. CH3CH2CH2COOH
    12. CH3CH(OH)CH3
    13. CH3CH=CHCH3
    14. CH≡CCH3
    15. Write the formula of propanone.
    16. Write the formula of propanal.
    17. Write the formula of propanoic acid.
    18. Write the formula of propan-2-ol.
    19. Write the formula of but-2-ene.
    20. Write the formula of but-1-yne.
    1. Methanol
    2. Ethanal
    3. Ethanoic acid
    4. Propanone
    5. Ethanol
    6. Propanal
    7. Propanoic acid
    8. Butan-2-one
    9. Propan-1-ol
    10. Butanal
    11. Butanoic acid
    12. Propan-2-ol
    13. But-2-ene
    14. Propyne
    15. CH3COCH3
    16. CH3CH2CHO
    17. CH3CH2COOH
    18. CH3CH(OH)CH3
    19. CH3CH=CHCH3
    20. CH≡CCH2CH3
    Set 7 – Branched-Chain Compounds
    1. CH3CH(CH3)CH3
    2. CH3CH(CH3)CH2CH3
    3. CH3CH2CH(CH3)CH2CH3
    4. (CH3)3CH
    5. CH3C(CH3)2CH3
    6. CH3CH(CH3)CH(CH3)CH3
    7. CH3CH2CH(CH3)CH2CH2CH3
    8. Write the formula of 2-methylpropane.
    9. Write the formula of 2-methylbutane.
    10. Write the formula of 3-methylpentane.
    11. Write the formula of 2,2-dimethylpropane.
    12. Write the formula of 2,3-dimethylbutane.
    13. How many carbon atoms are in 2-methylpropane?
    14. How many carbon atoms are in 2-methylbutane?
    15. What is the parent chain in 2-methylpropane?
    16. What is the parent chain in 2-methylbutane?
    17. Name CH3CH(CH3)CH3.
    18. Name CH3CH(CH3)CH2CH3.
    19. Name CH3CH(CH3)CH(CH3)CH3.
    20. Name CH3C(CH3)2CH3.
    1. 2-Methylpropane
    2. 2-Methylbutane
    3. 3-Methylpentane
    4. 2-Methylpropane
    5. 2,2-Dimethylpropane
    6. 2,3-Dimethylbutane
    7. 3-Methylhexane
    8. CH3CH(CH3)CH3
    9. CH3CH(CH3)CH2CH3
    10. CH3CH2CH(CH3)CH2CH3
    11. CH3C(CH3)2CH3
    12. CH3CH(CH3)CH(CH3)CH3
    13. 4
    14. 5
    15. Propane
    16. Butane
    17. 2-Methylpropane
    18. 2-Methylbutane
    19. 2,3-Dimethylbutane
    20. 2,2-Dimethylpropane
    Set 8 – Naming from Structural Formula
    1. CH3–CH2–CH3
    2. CH3–CH=CH2
    3. CH3–CH2–CH=CH2
    4. CH3–C≡CH
    5. CH3–CH2–C≡CH
    6. CH3–OH
    7. CH3–CH2–OH
    8. CH3–CHO
    9. CH3–CH2–CHO
    10. CH3–CO–CH3
    11. CH3–CO–CH2–CH3
    12. H–COOH
    13. CH3–COOH
    14. CH3–CH2–COOH
    15. CH3–CH(OH)–CH3
    16. CH3–CH2–CH2–OH
    17. CH3–CH=CH–CH3
    18. CH3–C≡C–CH3
    19. CH3–CH(CH3)–CH3
    20. CH3–CH(CH3)–CH2–CH3
    1. Propane
    2. Propene
    3. But-1-ene
    4. Propyne
    5. But-1-yne
    6. Methanol
    7. Ethanol
    8. Ethanal
    9. Propanal
    10. Propanone
    11. Butan-2-one
    12. Methanoic acid
    13. Ethanoic acid
    14. Propanoic acid
    15. Propan-2-ol
    16. Propan-1-ol
    17. But-2-ene
    18. But-2-yne
    19. 2-Methylpropane
    20. 2-Methylbutane
    Set 9 – Formula from IUPAC Name
    1. Methane
    2. Ethane
    3. Propane
    4. Butane
    5. Pentane
    6. Propene
    7. But-1-ene
    8. But-2-ene
    9. Propyne
    10. But-1-yne
    11. Methanol
    12. Ethanol
    13. Propan-1-ol
    14. Propan-2-ol
    15. Ethanal
    16. Propanal
    17. Propanone
    18. Methanoic acid
    19. Ethanoic acid
    20. Propanoic acid
    1. CH4
    2. CH3CH3
    3. CH3CH2CH3
    4. CH3CH2CH2CH3
    5. CH3CH2CH2CH2CH3
    6. CH2=CHCH3
    7. CH2=CHCH2CH3
    8. CH3CH=CHCH3
    9. CH≡CCH3
    10. CH≡CCH2CH3
    11. CH3OH
    12. CH3CH2OH
    13. CH3CH2CH2OH
    14. CH3CH(OH)CH3
    15. CH3CHO
    16. CH3CH2CHO
    17. CH3COCH3
    18. HCOOH
    19. CH3COOH
    20. CH3CH2COOH
    Set 10 – Board-Level Mixed Practice
    1. Name CH3CH2CH2CH3.
    2. Name CH3CH(CH3)CH3.
    3. Name CH2=CHCH2CH3.
    4. Name CH3CH=CHCH3.
    5. Name CH≡CCH2CH3.
    6. Name CH3OH.
    7. Name CH3CH(OH)CH3.
    8. Name CH3CHO.
    9. Name CH3CH2CHO.
    10. Name CH3COCH3.
    11. Name CH3COCH2CH3.
    12. Name HCOOH.
    13. Name CH3COOH.
    14. Name CH3CH2COOH.
    15. Write the formula of 2-methylpropane.
    16. Write the formula of but-2-ene.
    17. Write the formula of propan-2-ol.
    18. Write the formula of butan-2-one.
    19. Write the formula of propanoic acid.
    20. Write the formula of butanal.
    1. Butane
    2. 2-Methylpropane
    3. But-1-ene
    4. But-2-ene
    5. But-1-yne
    6. Methanol
    7. Propan-2-ol
    8. Ethanal
    9. Propanal
    10. Propanone
    11. Butan-2-one
    12. Methanoic acid
    13. Ethanoic acid
    14. Propanoic acid
    15. CH3CH(CH3)CH3
    16. CH3CH=CHCH3
    17. CH3CH(OH)CH3
    18. CH3COCH2CH3
    19. CH3CH2COOH
    20. CH3CH2CH2CHO
  • Class-11 Ch.1 Physics

    अध्याय 1: मात्रक और मापन — सरल नोट्स
    कक्षा 11 · भौतिक विज्ञान · अध्याय 1

    मात्रक और मापन

    सरल भाषा में व्याख्या — दैनिक जीवन के उदाहरणों के साथ

    1.1हमें मात्रकों की आवश्यकता क्यों है?

    कल्पना कीजिए कि आप किसी से कहते हैं, “मेज 5 लंबी है।” पाँच क्या? पाँच इंच? पाँच फीट? या पाँच मीटर? बिना किसी मात्रक के, संख्या “5” का कोई अर्थ नहीं रह जाता। एक मात्रक (Unit) सर्वसम्मत अंतरराष्ट्रीय मानक होता है, जिसके साथ हम भौतिक राशियों की तुलना करते हैं, ताकि हर व्यक्ति एक ही माप को एक ही अर्थ में समझ सके।

    इसे ऐसे समझें यदि आप कहें “मैं 5 दौड़ा” और यह न बताएं कि किलोमीटर या मील, तो कोई नहीं समझ पाएगा कि आप वास्तव में कितनी दूर दौड़े। मात्रक ही वह साधन है जो संख्या को वास्तविक अर्थ प्रदान करता है।

    भौतिकी में केवल कुछ ही मूल राशियां (Fundamental/Base Quantities) होती हैं — जैसे लंबाई, द्रव्यमान और समय — जिन्हें और छोटे घटकों में नहीं तोड़ा जा सकता। शेष सभी भौतिक राशियां (जैसे चाल, बल, ऊर्जा, दाब) इन्हीं मूल राशियों के संयोजन से बनती हैं। संयुक्त राशियों के मात्रकों को व्युत्पन्न मात्रक (Derived Units) कहा जाता है।


    1.2मात्रकों की अंतर्राष्ट्रीय प्रणाली (SI)

    प्राचीन समय में, अलग-अलग देश अलग-अलग प्रणालियों का उपयोग करते थे — जैसे CGS (सेन्टीमीटर-ग्राम-सेकंड), FPS (फुट-पाउंड-सेकंड, ब्रिटेन व अमरीका में प्रचलित), तथा MKS (मीटर-किलोग्राम-सेकंड)। इससे विभिन्न देशों के वैज्ञानिकों के बीच शोध साझा करते समय भ्रम पैदा होता था।

    इसलिए, संपूर्ण विश्व ने एक सर्वमान्य प्रणाली अपनाई: SI प्रणाली (Système International d’Unités — फ्रांसीसी भाषा में “मात्रकों की अंतर्राष्ट्रीय प्रणाली”)। यह 7 मूल मात्रकों पर आधारित है, जिनमें से प्रत्येक को एक स्थिर नियतांक (Physical Constant) से परिभाषित किया गया है ताकि दुनिया में कहीं भी कोई भी वैज्ञानिक इन्हें पूरी शुद्धता से पुनरुत्पादित कर सके।

    7 मूल मात्रक (Base Units)

    मूल राशिमात्रक का नामप्रतीकपरिभाषा का आधार
    लंबाई (Length)मीटर (metre)mनिर्वात में प्रकाश की चाल
    द्रव्यमान (Mass)किलोग्राम (kilogram)kgप्लांक नियतांक (Planck constant)
    समय (Time)सेकंड (second)sसीज़ियम परमाणु की विकिरण आवृत्ति
    विद्युत धारा (Electric Current)एम्पियर (ampere)Aमूल विद्युत आवेश (e)
    तापमान (Temperature)केल्विन (kelvin)Kबोल्ट्ज़मान नियतांक (Boltzmann constant)
    पदार्थ की मात्रा (Amount of Substance)मोल (mole)molआवोगाद्रो नियतांक (Avogadro constant)
    ज्योति तीव्रता (Luminous Intensity)कैंडेला (candela)cdप्रकाश की दीप्त दक्षता
    केवल धातु की छड़ को “1 मीटर” का मानक क्यों नहीं माना गया? क्योंकि धातु की छड़ें समय के साथ घिस सकती हैं, उनमें ज़ंग लग सकता है या तापमान से उनकी लंबाई बदल सकती है। प्रकृति के मूलभूत नियतांकों (जैसे प्रकाश की चाल) पर आधारित परिभाषाएं कभी नहीं बदलतीं — ब्रह्मांड में कहीं भी सही उपकरणों के साथ इन्हें सटीक रूप से पुनः मापा जा सकता है।

    इन 7 मूल मात्रकों के अतिरिक्त कोण मापने के लिए दो पूरक मात्रक भी हैं: समतल कोण के लिए रेडियन (radian – rad) और घन कोण के लिए स्टेरेडियन (steradian – sr)। ये दोनों “विमाहीन” (Dimensionless) राशियां हैं — अर्थात ये केवल दो समान राशियों के अनुपात हैं (जैसे चाप की लंबाई / त्रिज्या), इसलिए इनकी कोई भौतिक विमा नहीं होती।

    प्रश्न: “घन कोण” (Solid Angle) क्या होता है?

    उत्तर: एक साधारण समतल कोण यह मापता है कि कागज पर दो रेखाओं के बीच का क्षेत्र कितना चौड़ा है। घन कोण 3D (त्रिविम) स्थान में यह मापता है कि कोई शंकु (cone) कितना फैला हुआ है — जैसे आपकी दृष्टि सीमा में कोई वस्तु कितना स्थान घेरती है। इसे स्टेरेडियन में मापा जाता है।


    1.3सार्थक अंक (Significant Figures)

    प्रत्येक मापन में कुछ न कुछ अनिश्चितता होती है — कोई भी मापक यंत्र शत-प्रतिशत परिशुद्ध नहीं होता। सार्थक अंक हमें यह बताते हैं कि किसी मान को कितनी यथार्थता के साथ मापा गया है, ताकि हम उपकरण की क्षमता से अधिक यथार्थता का दावा न करें।

    दैनिक जीवन का उदाहरण यदि आपकी रसोई का तराजू केवल निकटतम ग्राम तक ही माप सकता है, तो यह कहना कि “मैंने 250.437 ग्राम चीनी मापी है” गलत और भ्रामक है। सार्थक अंक हमें मापन की वास्तविक परिशुद्धता के प्रति ईमानदार रखते हैं।

    सार्थक अंक गिनने के सरल नियम

    • सभी गैर-शून्य (Non-zero) अंक सार्थक होते हैं। 247 में 3 सार्थक अंक हैं।
    • दो गैर-शून्य अंकों के बीच आने वाले सभी शून्य सार्थक होते हैं। 1005 में 4 सार्थक अंक हैं।
    • प्रथम गैर-शून्य अंक से पहले आने वाले प्रारंभिक शून्य सार्थक नहीं होते। 0.0025 में केवल 2 सार्थक अंक हैं (2 और 5)।
    • दशमलव बिंदु के बिना अंत में आने वाले शून्य सार्थक नहीं होते। 1200 में केवल 2 सार्थक अंक हैं (जब तक कि इसे वैज्ञानिक संकेतन में न लिखा जाए)।
    • दशमलव बिंदु के बाद अंत में आने वाले शून्य हमेशा सार्थक होते हैं। 3.500 में 4 सार्थक अंक हैं — क्योंकि इन शून्यों को जानबूझकर मापा और दर्ज किया गया है।
    वैज्ञानिक संकेतन (Scientific Notation) भ्रम को कैसे दूर करता है? 1200 लिखना अस्पष्ट है — क्या इसमें 2, 3 या 4 सार्थक अंक हैं? परंतु 1.200 × 10³ लिखने से यह पूरी तरह स्पष्ट हो जाता है कि इसमें ठीक 4 सार्थक अंक हैं।

    गणितीय गणनाओं के नियम

    गुणा/भाग: अंतिम उत्तर में केवल उतने ही सार्थक अंक होने चाहिए जितने कि सबसे कम सार्थक अंक वाली दी गई राशि में हैं।

    योग/घटाव: अंतिम उत्तर में दशमलव के बाद केवल उतने ही स्थान होने चाहिए जितने कि सबसे कम दशमलव स्थान वाली दी गई राशि में हैं।

    हल किया गया उदाहरण

    द्रव्यमान = 4.237 g, आयतन = 2.51 cm³। कैलकुलेटर से भाग देने पर घनत्व 1.68804780876 g/cm³ प्राप्त होता है — लेकिन चूंकि आयतन (2.51) में केवल 3 सार्थक अंक हैं, इसलिए अंतिम उत्तर को भी 3 सार्थक अंकों तक पूर्णांकित (Round off) करना होगा:

    \[ \text{घनत्व} = \frac{4.237\text{ g}}{2.51\text{ cm}^3} = 1.69 \text{ g cm}^{-3} \]
    अंक “5” को पूर्णांकित करने का नियम (Rounding off rule for 5)

    यदि छोड़ा जाने वाला अंक ठीक 5 हो और उसके बाद कोई अंक न हो, तो पूर्ववर्ती अंक को निकटतम सम अंक (Even digit) में बदल दिया जाता है। उदाहरण के लिए 2.745 → 2.74 (क्योंकि 4 पहले से सम है), परंतु 2.735 → 2.74 (3 विषम था, इसलिए बढ़ाकर सम 4 कर दिया गया)।


    1.4भौतिक राशियों की विमाएं (Dimensions)

    किसी भी भौतिक राशि को मूल राशियों के संयोजन के रूप में व्यक्त किया जा सकता है — मुख्य रूप से द्रव्यमान [M], लंबाई [L], और समय [T] (तथा आवश्यकतानुसार धारा, ताप आदि)। इस संयोजन को उस राशि की विमा (Dimension) कहते हैं।

    विमाओं की तुलना किसी पकवान की सामग्री से करें जिस प्रकार कोई रेसिपी यह बताती है कि “इस डिश में आटा, चीनी और अंडे चाहिए” बिना सटीक मात्रा बताए, उसी प्रकार विमीय सूत्र यह बताता है कि “यह राशि द्रव्यमान, लंबाई और समय से बनी है” बिना उसके आगे की संख्या बताए।

    उदाहरण के लिए, चाल “प्रति इकाई समय में तय की गई दूरी” है, इसलिए इसकी विमा लंबाई को समय से भाग देने पर प्राप्त होती है:

    \[ [\text{चाल}] = [\text{L}][\text{T}]^{-1} \]

    बल = द्रव्यमान × त्वरण = द्रव्यमान × (लंबाई / समय²), इसलिए:

    \[ [\text{बल}] = [\text{M}][\text{L}][\text{T}]^{-2} \]

    1.5विमीय सूत्र एवं विमीय समीकरण

    जब हम किसी भौतिक राशि को उसकी विमाओं के पदों में व्यक्त करते हैं, तो इसे विमीय सूत्र (Dimensional Formula) कहते हैं। जब इसे समीकरण के रूप में लिखा जाता है, तो यह विमीय समीकरण (Dimensional Equation) कहलाता है।

    भौतिक राशिविमीय सूत्र
    आयतन (Volume)\([\text{M}^0\text{L}^3\text{T}^0]\)
    चाल / वेग (Speed/Velocity)\([\text{M}^0\text{L}^1\text{T}^{-1}]\)
    बल (Force)\([\text{M}^1\text{L}^1\text{T}^{-2}]\)
    द्रव्यमान घनत्व (Mass Density)\([\text{M}^1\text{L}^{-3}\text{T}^0]\)

    1.6विमीय विश्लेषण और इसके उपयोग

    विमीय विश्लेषण का मुख्य आधार विमाओं की समांगता का सिद्धांत (Principle of Homogeneity of Dimensions) है: “हम केवल उन्हीं भौतिक राशियों को जोड़ या घटा सकते हैं जिनकी विमाएं समान हों।” आप “5 किग्रा” में “3 मीटर” नहीं जोड़ सकते — यह भौतिक रूप से निरर्थक है।

    उपयोग 1: समीकरण की सत्यता की जांच करना

    मुख्य नियम यदि किसी समीकरण के दोनों पक्षों के प्रत्येक पद की विमाएं समान हैं, तो समीकरण विमीय रूप से सही (Consistent) है। परंतु ध्यान दें: विमीय रूप से सही समीकरण का पूरी तरह सही होना आवश्यक नहीं है — लेकिन यदि विमाएं समान नहीं हैं, तो समीकरण निश्चित रूप से गलत है।
    हल किया गया उदाहरण — \(\frac{1}{2}mv^2 = mgh\) की जांच

    वामावर्त पक्ष (LHS): \([\text{M}][\text{L}\text{T}^{-1}]^2 = [\text{M}\text{L}^2\text{T}^{-2}]\)

    दक्षिणावर्त पक्ष (RHS): \([\text{M}][\text{L}\text{T}^{-2}][\text{L}] = [\text{M}\text{L}^2\text{T}^{-2}]\)

    चूंकि दोनों पक्षों की विमाएं समान हैं, इसलिए यह समीकरण विमीय रूप से सत्य है (यह गिरती हुई वस्तु के लिए ऊर्जा संरक्षण का समीकरण है)।

    उपयोग 2: विभिन्न भौतिक राशियों के बीच संबंध (सूत्र) स्थापित करना

    यदि हमें यह अनुमान हो कि कोई भौतिक राशि किन-किन अन्य राशियों पर निर्भर करती है, तो विमीय विश्लेषण के उपयोग से हम उनके बीच का सूत्र व्युत्पन्न कर सकते हैं — हालांकि यह सूत्र में आने वाले आंकिक नियतांक (Numerical Constant) का मान नहीं बता सकता।

    हल किया गया उदाहरण — सरल लोलक का आवर्तकाल

    मान लीजिए कि आवर्तकाल \(T\) लोलक की लंबाई \(l\), द्रव्यमान \(m\), और गुरुत्वीय त्वरण \(g\) पर निर्भर करता है:

    \[ T = k\, l^x g^y m^z \]

    दोनों पक्षों की विमाओं की तुलना करने पर हमें \(x = \frac{1}{2}\), \(y = -\frac{1}{2}\), तथा \(z = 0\) प्राप्त होता है — अर्थात लोलक का द्रव्यमान आवर्तकाल को बिल्कुल प्रभावित नहीं करता! इससे हमें निम्नलिखित सूत्र प्राप्त होता है:

    \[ T = k\sqrt{\frac{l}{g}} \]

    विमीय विश्लेषण यह नहीं बता सकता कि नियतांक \(k = 2\pi\) है — इसके लिए प्रयोगों या सैद्धांतिक निगमन की आवश्यकता होती है। परंतु इसने सूत्र की संपूर्ण संरचना का सटीक अनुमान लगा लिया।

    विमीय विश्लेषण की सीमाएं (Limitations)

    • यह सूत्र में आने वाले बीजीय नियतांकों (जैसे 2, ½, या π) का मान ज्ञात नहीं कर सकता।
    • यह उन विभिन्न राशियों के बीच भेद नहीं कर सकता जिनकी विमाएं समान होती हैं (उदाहरण के लिए: कार्य और बल-आघूर्ण दोनों का विमीय सूत्र समान है, परंतु वे भौतिक रूप से भिन्न हैं)।
    • यह केवल तभी कार्य करता है जब आपको पहले से ज्ञात हो कि कौन-कौन सी राशियां प्रक्रिया में शामिल हैं।
    • त्रिकोणमितीय, चरघातांकी (exponential) और लघुगणकीय (logarithmic) पदों वाले सूत्रों का निगमन इससे नहीं किया जा सकता।

    संक्षेप में (Quick Recap)

    • मात्रक ही संख्याओं को भौतिक अर्थ प्रदान करते हैं; SI प्रणाली वैश्विक रूप से स्वीकृत प्रणाली है जिसमें 7 मूल मात्रक हैं।
    • सार्थक अंक यह दर्शाते हैं कि मापन कितना यथार्थ है — मापक यंत्र की क्षमता से अधिक यथार्थता नहीं लिखनी चाहिए।
    • गुणा/भाग करते समय न्यूनतम सार्थक अंक तथा योग/घटाव करते समय न्यूनतम दशमलव स्थानों का ध्यान रखें।
    • विमाएं यह बताती हैं कि कोई राशि द्रव्यमान, लंबाई, समय आदि के किस संयोजन से बनी है।
    • केवल समान विमाओं वाली राशियों को ही आपस में जोड़ा या घटाया जा सकता है।
    • विमीय विश्लेषण गलत समीकरणों को पकड़ने और सूत्रों का रूप निर्धारित करने में सहायक है — परंतु यह आंकिक नियतांक का मान ज्ञात नहीं कर सकता।
    © abhishek.io.in

  • C9.Chapter 6: How Forces Affect Motion

    Chapter 6: How Forces Affect Motion — Detailed Notes | Class 9 Science
    Class 9 · Science · NCERT Exploration

    Chapter 6: How Forces Affect Motion

    Complete Study Notes Newton’s Three Laws, Friction & Momentum Exam-Ready Format

    1. The Concept of Force

    A force can: (i) make an object move from rest, (ii) change the speed or direction of a moving object, and (iii) change the shape of an object (e.g., kicking a ball, striking a ball with a bat, squeezing a lemon).

    Force is a Vector Quantity Like position, displacement, velocity, and acceleration, force needs both magnitude and direction to be fully specified (e.g., friction acts opposite to motion; gravity acts downward; buoyant force acts upward). SI unit: newton (N) — written with a small “n” as a word, but capital “N” as a symbol.
    Exam Tip Common slip: writing “Newton” for the unit name or “n” for the symbol. Correct: unit name = newton (lowercase), symbol = N (uppercase) — this rule applies to any unit named after a person (e.g., kelvin/K, pascal/Pa).

    1.1 Measuring the Magnitude of a Force

    A spring balance measures the force with which you pull on the spring inside it — it can measure weight (gravitational force) or force in general.

    Threads of Curiosity — Scale of Forces Everyday smallest perceivable forces: order of millinewtons ($10^{-3}$ N, e.g., a light touch). Scientists can measure forces as small as yoctonewtons ($10^{-24}$ N) in specialised experiments.

    2. Balanced and Unbalanced Forces

    Usually, more than one force acts on an object simultaneously (e.g., pushing a box: applied force + friction; a floating ball: gravity + buoyant force).

    Balanced Forces

    Equal in magnitude, opposite in direction → net force = 0. Object’s motion does not change (e.g., tug-of-war with equal pulling teams — rope doesn’t move).

    Unbalanced Forces

    Net force ≠ 0 → causes a change in the object’s state of motion. The object moves/accelerates in the direction of the larger force.

    2.1 Calculating Net Force

    6 N
    10 N
    Same direction → Net force = sum of magnitudes, along that direction. Opposite directions → Net force = difference of magnitudes, along the larger force’s direction.
    Solved Example 6.1 — Net Force on a Block Two forces, 10 N and 6 N, act on a block. Find the net force in each case:
    (a) Both acting right: $F_{net} = 10 + 6 = 16\ \text{N}$, towards the right.
    (b) 10 N right, 6 N left: $F_{net} = 10 – 6 = 4\ \text{N}$, towards the right (direction of larger force).
    (c) 6 N right, 10 N left: $F_{net} = 10 – 6 = 4\ \text{N}$, towards the left.
    Exam Tip Key line for definitions: forces equal in magnitude and opposite in direction are called balanced forces; the rope in tug-of-war “does not move if forces are balanced, but moves if forces are unbalanced” — a favourite fill-in-the-blank/reasoning line.
    Beyond the Basics Forces that act at an angle to each other (not parallel/opposite), and equal-and-opposite forces applied to two ends of an extended object (causing rotation — e.g., turning a handlebar or a tap), are studied in higher grades.

    3. The Force of Friction

    Friction is the force that opposes relative motion (or attempted motion) between two surfaces in contact. It always acts opposite to the direction of motion.

    Note — Multiple Forces, One Net Effect Multiple forces may act on an object (applied force, friction, gravity/weight, normal force), but its motion depends only on the net force. Weight (downward) and normal force (upward, perpendicular to surface) are balanced for an object on a horizontal surface — they don’t affect horizontal motion.

    3.1 Activities 6.1 & 6.2 — Friction Depends on Surface Nature

    Key Experimental Finding

    A stack of coins launched by a stretched rubber band travels different distances on different surfaces (wooden table < laminated table < polished marble/tile) even though launched with the same force each time.

    Conclusion: smoother surfaces → smaller force of friction → object decelerates more slowly → travels farther before stopping. A spring balance pulling a block confirms this directly: a smaller spring-balance reading (force needed to just start motion) = smaller friction on that surface.

    Exam Tip — “What If” Reasoning If friction disappeared entirely: once set in motion, objects would continue moving forever at constant velocity (per Newton’s First Law) — nothing would ever naturally come to rest by sliding to a stop. This is a classic HOTS/thought-experiment question.

    4. Newton’s First Law of Motion (Law of Inertia)

    Statement An object at rest remains at rest, and an object in motion continues to move with a constant velocity, unless a net force acts upon it.

    If net force = 0 → acceleration = 0 → object cannot begin to move or change its velocity.

    Galileo Galilei

    Through thought experiments, argued (17th century) that if a body moves on a horizontal plane with all impediments (friction) removed, it will continue moving indefinitely — challenging the old belief that force is needed to sustain motion.

    Isaac Newton

    Introduced the term inertia — the tendency of objects to resist a change in their state of rest or uniform motion. Framed the First Law using this idea; presented all three laws of motion in 1687 (Principia).

    Exam Tip — Position-Time & Velocity-Time Graphs (No Net Force) At rest: position-time graph = horizontal line at a fixed position; velocity-time graph = horizontal line at $v=0$.
    Constant velocity: position-time graph = straight sloped line; velocity-time graph = horizontal line at some non-zero $v$.
    This is one of the most frequently asked graph-sketching questions in this chapter.
    Solved Example 6.2 A person pushes a moving box forward with a force exactly equal to friction. Will the box stop or keep moving?
    Answer: The two forces are equal and opposite → balanced → net force = 0 → by Newton’s First Law, the box continues moving with constant velocity (it does NOT stop, and does NOT speed up).

    5. Newton’s Second Law of Motion

    A force produces acceleration. Experiments (pulling a cart with varying weights via a pulley system) show:

    • For a fixed mass, acceleration increases as net force increases (larger force → larger acceleration)
    • For a fixed force, acceleration decreases as mass increases (larger mass → smaller acceleration)
    Statement When a net force acts on an object, the object accelerates in the direction of the net force. The magnitude of acceleration is directly proportional to net force and inversely proportional to mass.
    Newton’s Second Law $$a = \frac{F}{m} \qquad \text{or} \qquad F = ma$$
    Definition of the Newton (N) If $m = 1\ \text{kg}$ and $a = 1\ \text{m s}^{-2}$: $F = 1\ \text{kg} \times 1\ \text{m s}^{-2} = 1\ \text{kg m s}^{-2} = 1\ \text{N}$
    One newton is the force that produces an acceleration of $1\ \text{m s}^{-2}$ on a mass of $1\ \text{kg}$.
    Gravitational Force / Weight $$F = mg \qquad g \approx 9.8\ \text{m s}^{-2}\ (\text{take}\ 10\ \text{m s}^{-2}\ \text{for quick estimates})$$ $g$ does NOT depend on the mass of the object.
    Threads of Curiosity — Real vs. Ideal In real experiments, doubling force doesn’t exactly double acceleration (and vice versa for mass) due to measurement errors and friction between the cart’s wheels and the surface — a good explanation to cite for “why did your experimental ratio not match theory” type questions.
    Beyond the Basics — Momentum Form Momentum = mass × velocity (direction same as velocity). The more complete Second Law: the rate of change of momentum of an object is proportional to the net force and occurs in the direction of the net force. This form applies even when mass is not constant.

    5.1 Newton’s Second Law in Everyday Life

    • Catching a fast ball: pulling hands back while catching increases the time over which velocity drops to zero → reduces acceleration → reduces force on hands (less injury)
    • Airbags: increase the time of impact during a collision → reduce deceleration → reduce force on the passenger
    • Cracking a coconut: very short stopping time on hitting the ground → very large force → shell breaks
    Quick Recall: Longer stopping/impact time → smaller force (catching, airbags, landing mats). Shorter stopping time → larger force (coconut cracking, bullet penetration).

    Solved Numericals — Newton’s Second Law

    Example 6.4 — Weightlifter’s Force Barbell: 10 kg on each side + 10 kg bar = 30 kg total.
    $$F = mg = 30 \times 9.8 = 294\ \text{N (downward, due to gravity)}$$ To hold it steady, the weightlifter applies an equal and opposite force of 294 N upward.
    Example 6.5 — Pushing a Block Against Friction Block mass = 25 kg; max friction = 50 N.
    (i) Applied force = 50 N → balances friction exactly → net force = 0 → block stays stationary.
    (ii) Applied force = 55 N → $F_{net} = 55 – 50 = 5\ \text{N}$ $$a = \frac{F}{m} = \frac{5}{25} = 0.2\ \text{m s}^{-2}$$ $$s = ut + \frac{1}{2}at^2 = (0)(2) + \frac{1}{2}(0.2)(2)^2 = 0.4\ \text{m (forward)}$$
    Example 6.6 — Force from a Velocity-Time Graph Sports car, mass 1500 kg. Graph: 0–5 s (0 → 10 m/s), 5–10 s (constant 10 m/s), 10–15 s (10 → 0 m/s).
    0–5 s: $a = \frac{v-u}{t} = \frac{10-0}{5} = 2\ \text{m s}^{-2}$;   $F = ma = 1500 \times 2 = 3000\ \text{N}$ (towards east)
    5–10 s: constant velocity → $a = 0$ → $F = 0$ N
    10–15 s: $a = \frac{0-10}{5} = -2\ \text{m s}^{-2}$;   $F = 1500 \times (-2) = -3000\ \text{N}$ (negative sign → force acts towards west, opposite to motion)

    6. Newton’s Third Law of Motion

    Statement Whenever one object exerts a force on a second object, the second object simultaneously exerts an equal and opposite force on the first object.
    Exam Tip — Critical Distinction Action-reaction force pairs act on two different objects — so they never cancel each other (they cannot “balance” since they act on different bodies). This is distinct from balanced forces (which act on the same object).

    6.1 Everyday Applications

    Paddle → water
    Water → paddle & canoe
    Canoeing: paddle pushes water backward; water pushes paddle (and canoe) forward with equal force. Pushing harder → larger forward force → higher canoe velocity.
    • Walking/running: feet push the ground backward; the ground pushes feet forward (via friction) — here friction helps motion rather than opposing it
    • Climbing a tree: legs push the trunk down; friction pushes the person up — harder on smooth (low-friction) trunks
    • Rocket launch: engine expels gas downward; gas exerts equal-opposite force on rocket upward; when this exceeds the rocket’s weight, it lifts off
    • Chandrayaan-3’s Vikram lander: fired its engine in the direction of motion (forward) to produce a backward reaction force, slowing it down for a soft lunar landing
    Exam Tip — Grooves & Treads Grooves on footwear soles and treads on vehicle tyres increase friction between the surfaces — necessary for the reaction force (via friction) that pushes us/vehicles forward. This is why it’s hard to walk on wet polished floors/ice, and risky to drive on wet/snowy roads (friction, hence reaction force, is too low).

    6.2 Newton’s Third Law Applies to All Force Types

    Not just contact forces — also applies to non-contact forces: two magnets repel/attract each other equally; two charged balloons apply equal electrostatic forces; the Earth and a fruit apply equal gravitational forces on each other.

    Note — Equal Forces, Unequal Accelerations Forces in a third-law pair are always equal in magnitude, but they generally do NOT produce equal accelerations, because $a = F/m$ — if the masses of the two objects differ, their accelerations differ too.
    Example 6.7 — Why Doesn’t the Earth Move Towards the Fruit? The Earth and a falling fruit exert equal and opposite gravitational forces on each other. But the Earth’s mass is astronomically larger than the fruit’s, so $a_{Earth} = F/m_{Earth}$ is extremely tiny — undetectably small — while the fruit visibly accelerates towards Earth.
    Example 6.8 — Gun Recoil 0.1 kg bullet fired from a 5 kg gun; force = 2 N.
    By Newton’s Third Law, recoil force on gun = 2 N (equal, opposite). $$a_{gun} = \frac{2\ \text{N}}{5\ \text{kg}} = 0.4\ \text{m s}^{-2} \qquad a_{bullet} = \frac{2\ \text{N}}{0.1\ \text{kg}} = 20\ \text{m s}^{-2}$$ Equal forces, but very different accelerations because the masses differ hugely.

    7. Forces on a System of Objects

    For two objects connected by a string (e.g., two boxes, masses $m_1$ and $m_2$, pulled by external force $F$), treat them as a single system: internal forces (tension $T$) cancel out within the system; only the external force $F$ matters.

    Acceleration of a Connected System $$a = \frac{F}{\text{mass of system}} = \frac{F}{m_1 + m_2}$$
    Exam Tip The system also has external gravitational force $(m_1+m_2)g$ downward, balanced by normal force $(N_1+N_2)$ upward from the ground — these don’t affect horizontal acceleration. This “treat connected objects as one system” trick massively simplifies numerical problems on connected bodies/systems.

    8. Quick Summary Table — All Three Laws

    Table 8.1 — Newton’s Laws at a Glance
    LawStatement (essence)Key formulaReal-life cue
    First (Inertia)No change in motion without net force$F_{net}=0 \Rightarrow a=0$Object slides to rest only due to friction
    SecondNet force produces acceleration, proportional to F, inverse to m$F=ma$Catching a ball softly (increase time, reduce force)
    ThirdEvery action has an equal & opposite reaction (on a different body)$F_{12} = -F_{21}$Rowing a canoe, rocket launch, walking

    9. Exam Question Bank

    A. MCQ / Assertion–Reason (1 mark each)

    1. A table moved at constant velocity by force $F$ across a floor — frictional force = $F$ (equal and opposite, since velocity is constant → net force = 0).[1]
    2. Two identical spring balances connected and pulled from both ends show the same reading — confirms Newton’s Third Law experimentally.[1]

    B. Short Answer (2–3 marks)

    1. Why does a canoe move forward when the canoeist pushes water backward with the paddle? Why does it move faster with a harder push?[3]
    2. Explain why airbags reduce injury in a car crash, using Newton’s Second Law.[3]
    3. Distinguish between balanced and unbalanced forces with one example each.[2]
    4. Why do treads on tyres and grooves on shoe soles help us move rather than slip?[2]

    C. Numerical Problems

    1. A bullet of mass 50 g moving at 100 m/s penetrates 50 cm into a wooden block and stops. Estimate the stopping force (assume constant deceleration).[3]
    2. A footballer kicks a 0.4 kg ball to a speed of 108 km/h with a force of 800 N. Find the time of contact between foot and ball.[3]
    3. An object of mass 2 kg moving at constant 10 m/s enters a rough patch where friction (7 N) plus an additional opposing force (3 N) act. Find the distance travelled before it stops.[3]
    4. A 0.1 kg bullet is fired from a 5 kg gun with a force of 2 N. Find the initial accelerations of the bullet and the gun.[3]

    D. Long Answer / HOTS (4–5 marks)

    1. A tractor pulls a harrow of mass $m_1$ with force $F$ giving acceleration $a_1$, and separately pulls a trolley of mass $m_2$ with the same force $F$ giving acceleration $a_2$. If the tractor now pulls both together (trolley + harrow) with the same force $F$, derive the resulting acceleration in terms of $a_1$ and $a_2$.[5]
    2. Explain, using Newton’s third law, why a bar magnet brought near a compass causes the compass needle to move but the bar magnet appears stationary — even though the forces are equal and opposite.[4]
    3. A sailor jumps forward from a small boat onto the shore. Explain, using Newton’s laws, whether the boat moves, and in which direction.[3]
    4. Explain why a landing mat or sand bed is used in a high jump event, linking your answer to the concept of impact time and force.[3]

    At a Glance — Chapter Summary

    • Force is a vector — needs magnitude AND direction; SI unit = newton (N); measured using a spring balance.
    • Balanced forces → net force = 0 → no change in motion. Unbalanced forces → net force ≠ 0 → causes acceleration.
    • Friction opposes relative motion; depends on the nature of the surfaces in contact.
    • Newton’s First Law: An object at rest stays at rest, an object in motion continues with constant velocity, unless acted on by a net force (Law of Inertia).
    • Newton’s Second Law: $F = ma$ — acceleration ∝ net force, inversely ∝ mass. $F=mg$ gives weight ($g \approx 9.8\ \text{m s}^{-2}$).
    • Newton’s Third Law: Every action has an equal and opposite reaction, acting on a different object — hence these paired forces never balance each other.
    • Connected objects can be treated as a single system: $a = F/(m_1+m_2)$ using only external forces.
    • Real-life applications: catching a ball, airbags, rocket propulsion, walking/rowing (friction/reaction helps motion), tyre treads and shoe grooves.
    © abhishek.io.in  ·  Class 9 Science Notes  ·  Chapter 6: How Forces Affect Motion
  • C9. Chapter 8: Journey Inside the Atom

    Chapter 8: Journey Inside the Atom — Detailed Notes | Class 9 Science
    Class 9 · Science · NCERT Exploration

    Chapter 8: Journey Inside the Atom

    Complete Study Notes Atomic Models, Subatomic Particles & Isotopes Exam-Ready Format

    1. The Ancient Origins of Atomic Theory

    Over 2,000 years ago, thinkers in both ancient India and ancient Greece independently asked: What is everything made up of?

    Acharya Kanada (India)

    Proposed that matter (dravya) divided repeatedly reaches a stage of smallest, indivisible particles called parmanus, recorded in the Vaisesika Sutras. Parmanus combine to form dyads (pairs) and triads (groups of three), building up the entire material universe.

    Leucippus & Democritus (Greece)

    Proposed similar indivisible particles called atomos (Greek for “indivisible”) — the origin of the modern word “atom”.

    Exam Tip Remember: both ideas were philosophical/imaginary, not based on experiments. The first scientific, experiment-based atomic theory came from John Dalton in 1808. This distinction (imaginary vs experimental) is a favourite 1-mark question.
    Dalton’s Atomic Theory (1808) All matter is composed of indivisible particles called atoms — the fundamental building blocks of matter that cannot be broken into smaller parts. This became the starting point for modern atomic theory, though we now know atoms ARE divisible.

    Following Dalton, scientists sought answers to: What are atoms made of? What would they look like? What makes atoms of one element different from another?


    2. Evolution of Atomic Models

    Discovery of radioactivity (certain elements emitting invisible energy/particles called radiation) in the late 19th century proved that atoms are not indivisible — they must contain smaller particles.

    2.1 Thomson’s Model (1897) — “Plum Pudding”

    The Discovery of the Electron

    J. J. Thomson studied conduction of electricity through gases at very low pressure using a cathode ray tube (two electrodes in a glass tube with high voltage). He observed rays moving from cathode (–) to anode (+), called cathode rays. Studying their behaviour in electric/magnetic fields, he concluded these are streams of negatively charged particles — much lighter than atoms — later named electrons.

    Key finding: the nature of cathode rays was independent of the cathode material and the gas used — proving electrons are a fundamental component of all atoms. Charge of an electron = $-1.602 \times 10^{-19}\,\text{C}$, taken as $-1$ by convention.

    Since atoms are neutral overall, Thomson had to explain where the positive charge sits. He proposed the atom as a sphere of positive charge with electrons embedded in it — like a pudding studded with plums, or seeds in a watermelon.

    2.2 Testing Thomson’s Model — The Gold Foil Experiment (1911)

    Geiger–Marsden Experiment (under Rutherford)

    A beam of alpha (α) particles (positively charged; later shown to be helium nuclei — 2 protons + 2 neutrons) was fired at an extremely thin gold foil.

    Expected (per Thomson’s model): particles pass straight through or deflect only slightly, since positive charge is spread evenly.

    Observed: most particles passed straight through undeflected; some were sharply deflected; a few bounced straight back. This deflection is called scattering — hence also called the α-ray scattering experiment.

    Exam Tip — Classic Reasoning Question Why did most α-particles pass through undeflected, while a few bounced back? Most of the atom is empty space (→ undeflected passage); the positive charge and mass are concentrated in a tiny, dense region (→ occasional sharp deflection/bounce-back when an α-particle happens to approach this dense region head-on).

    2.3 Rutherford’s Nuclear (Planetary) Model

    Based on the gold foil results, Rutherford proposed:

    • Most of an atom is empty space
    • All positive charge and most mass is concentrated in a tiny, dense central region — the nucleus
    • Electrons revolve around the nucleus like planets around the Sun — the planetary model
    Scale of the Atom Diameter of atom $\approx 10^{-10}\,\text{m}$; diameter of nucleus $\approx 10^{-15}\,\text{m}$ — the nucleus is about $10^{5}$ (one lakh) times smaller than the whole atom. If an atom were the size of a cricket ground (~100 m across), the nucleus would be a tiny pepper grain at its centre!
    Limitation of Rutherford’s Model A revolving (accelerating) electron should continuously lose energy, spiral inward, and eventually crash into the nucleus — meaning atoms should collapse. But atoms are stable in reality. This is the single biggest weakness of Rutherford’s model, and it’s exactly what Bohr’s model fixed. This “why doesn’t the electron fall into the nucleus” question is extremely common.

    Discovery of the Proton

    Rutherford showed the nucleus carries positive charge from particles called protons — much heavier than electrons, with charge equal and opposite to an electron’s. For a neutral atom: number of protons = number of electrons.

    2.4 Bohr’s Model (1913) — Fixed Energy Levels

    Niels Bohr proposed that electrons:

    • Move only in fixed circular paths called stationary states, orbits, or shells — not randomly
    • Each shell has a definite energy — hence called energy levels, labelled K, L, M, N… (or $n = 1, 2, 3, 4…$)
    • Do not lose energy while moving in a fixed shell (this is the key postulate that fixes Rutherford’s stability problem)
    • K-shell ($n=1$, closest to nucleus) has the least energy; energy increases with distance from the nucleus
    • An electron changes shells only by absorbing or releasing energy exactly equal to the difference between the two shells’ energies
    • Each shell holds only a limited number of electrons
    Quick Recall: Dalton (indivisible ball) → Thomson (plum pudding — + sphere with e⁻) → Rutherford (nucleus + empty space, but unstable) → Bohr (fixed energy shells, stable) → Modern (electron cloud/quantum model).
    Dalton (1808)

    Solid indivisible sphere

    Thomson (1897)

    Plum pudding model

    Rutherford (1911)

    Nucleus + empty space

    Bohr (1913)

    Fixed energy shells

    Modern Model

    Quantum electron cloud

    Threads of Curiosity — Why K, L, M, N? The naming came from physicist Charles Barkla’s early X-ray experiments — he called the first observed X-ray line “K”, leaving room (unused, as it turned out) for a possible earlier series. Bohr adopted the same notation for atomic shells.

    3. Discovery of the Neutron & the Three Subatomic Particles

    A puzzle remained: a helium atom (2 protons) has about 4× the mass of a hydrogen atom (1 proton) — not 2×. This suggested another mass-contributing particle existed.

    James Chadwick (1932)

    Discovered the neutron — mass nearly equal to a proton’s, but electrically neutral (no charge). Found in the nucleus of all atoms except ordinary hydrogen ($^1_1\text{H}$). Neutrons also help bind the nucleus together by countering the mutual repulsion between protons (the nuclear force) — this is why heavier atoms need proportionally more neutrons.

    Table 3.1 — The Three Subatomic Particles
    ParticleSymbolRelative ChargeLocationDiscovered by
    Electron$e^-$−1Revolves around nucleusJ. J. Thomson (1897)
    Proton$p^+$+1Inside nucleusErnest Rutherford (1911)
    Neutron$n^0$0Inside nucleusJames Chadwick (1932)

    4. Symbols of Elements

    Dalton (1803) introduced pictorial symbols. Berzelius (1813) proposed deriving symbols from Latin names — giving us modern alphabetic symbols. Today, IUPAC approves all element names/symbols internationally.

    Rules for Writing Symbols

    • Often the first letter, or first two letters, of the element’s name
    • First letter always capital; second letter (if any) always lowercase — e.g., Aluminium = Al (not AL), Cobalt = Co (not CO)
    • Some symbols use a letter other than the second letter — e.g., Chlorine = Cl, Zinc = Zn
    • Some come from Latin/Greek/German names — Iron = Fe (Latin ferrum), Mercury = Hg (Greek hydrargyros), Tungsten = W (German wolfram)
    Exam Tip Common mistake: writing AL for aluminium or CO for cobalt (which is actually carbon monoxide!). Always: first letter capital, second letter small.

    5. Atomic Number, Mass Number & Notation

    Definitions Atomic Number $(Z)$ = Number of protons in the nucleus $=$ Number of electrons (in a neutral atom)

    Mass Number $(A)$ = Number of protons $+$ Number of neutrons  (protons and neutrons together = nucleons)

    Standard notation for an atom:

    $$\ ^{A}_{Z}\text{Symbol} \quad\quad \text{e.g., for Carbon:} \quad\ ^{12}_{6}\text{C}$$
    Table 5.1 — First 18 Elements: Composition & Electron Distribution
    ElementSymbolZProtonsNeutronsElectronsKLM
    HydrogenH11011––
    HeliumHe22222––
    LithiumLi334321–
    BerylliumBe445422–
    BoronB556523–
    CarbonC666624–
    NitrogenN777725–
    OxygenO888826–
    FluorineF9910927–
    NeonNe1010101028–
    SodiumNa11111211281
    MagnesiumMg12121212282
    AluminiumAl13131413283
    SiliconSi14141414284
    PhosphorusP15151615285
    SulfurS16161616286
    ChlorineCl17171817287
    ArgonAr18182218288

    5.1 Bohr–Bury Rules for Electron Distribution

    • Maximum electrons in a shell $= 2n^2$ (where $n$ = shell number): K-shell ($n=1$) → 2; L-shell ($n=2$) → 8; M-shell ($n=3$) → 18
    • Maximum electrons in the outermost shell = 8 (except when it’s the only shell, which holds max 2)
    • Shells fill stepwise from innermost outward (K → L → M → N…); a shell fills completely before the next one starts
    Solved Example Q: Write the electronic configuration of Magnesium (Z = 12).
    A: 12 electrons to distribute: K-shell takes 2 (full) → 10 remain; L-shell takes 8 (full) → 2 remain; M-shell takes the remaining 2.
    Configuration: 2, 8, 2

    6. Valency — Combining Capacity

    Key Terms Valence shell = outermost shell containing electrons. Valence electrons = electrons in that shell. Octet = 8 electrons in the outermost shell (a stable, largely unreactive configuration; for the first shell, 2 electrons = stable, as in helium).

    Valency = number of electrons an atom gains, loses, or shares to complete its octet (achieve stability).

    Fewer than 4 valence electrons

    Tends to lose electrons. E.g., Sodium (2, 8, 1) loses 1 electron → valency 1.

    More than 4 valence electrons

    Tends to gain electrons. E.g., Oxygen (2, 6) gains 2 electrons → valency 2.

    Exactly 4 valence electrons (e.g., Carbon: 2, 4) → tends to share 4 electrons → valency 4.

    Exam Tip Elements with a complete octet already (like Neon, Argon) are stable and generally do not lose/gain/share electrons — this is why noble gases are largely unreactive.

    7. Isotopes and Isobars

    7.1 Isotopes

    Isotopes are atoms of the same element (same atomic number $Z$, same number of protons/electrons) but with different numbers of neutrons, hence different mass numbers $A$.

    Table 7.1 — Isotopes of Hydrogen
    IsotopeNotationProtonsNeutronsElectronsNatural abundance
    Protium$^1_1\text{H}$101~99.98%
    Deuterium$^2_1\text{H}$111~0.015%
    Tritium$^3_1\text{H}$121traces
    Exam Tip Isotopes have identical chemical properties (same number of electrons/valence electrons) but different physical properties (e.g., boiling/melting points), because chemical behaviour depends on valence electrons, while physical properties depend on mass.

    Applications of Isotopes

    • $^{235}_{92}\text{U}$ — fuel in nuclear reactors (electricity generation)
    • $^{60}_{27}\text{Co}$ — radiotherapy for cancer treatment
    • $^{131}_{53}\text{I}$ — treatment of goitre and thyroid cancer
    • $^{14}_{6}\text{C}$ — radiocarbon dating of fossils/artefacts in archaeology and geology

    Average (Weighted) Atomic Mass

    Since isotopes don’t occur in equal proportions, the atomic mass of an element is calculated as a weighted average, not a simple average.

    Solved Example — Chlorine Chlorine has two isotopes: $^{35}\text{Cl}$ (75% abundance) and $^{37}\text{Cl}$ (25% abundance). $$\text{Average atomic mass} = \left(35 \times \frac{75}{100}\right) + \left(37 \times \frac{25}{100}\right)$$ $$= \frac{105}{4} + \frac{37}{4} = \frac{142}{4} = 35.5\ \text{u}$$ Interpretation: No single chlorine atom weighs 35.5 u — but in 1 million chlorine atoms, about 7.5 lakh would be $^{35}\text{Cl}$ and 2.5 lakh would be $^{37}\text{Cl}$, giving this weighted average.

    7.2 Isobars

    Isobars are atoms of different elements with the same mass number but different atomic numbers.

    Table 7.2 — Example: Isobars with Mass Number 40
    ElementAtomic Number (Z)Mass Number (A)
    Argon1840
    Potassium1940
    Calcium2040
    Do Not Confuse: Isotopes → SAME element, SAME protons, DIFFERENT neutrons/mass number. Isobars → DIFFERENT elements, DIFFERENT protons, SAME mass number.

    8. Beyond Bohr — The Modern View

    Bohr’s model, too, was eventually found incomplete. Electrons do not follow fixed, well-defined circular paths. The modern quantum mechanical model describes electrons as existing in “electron clouds” — regions around the nucleus where an electron is most likely to be found, rather than an exact, predictable path. (Detailed treatment is reserved for higher grades.)


    9. Scientists to Remember

    J. J. Thomson

    Discovered the electron via cathode ray studies; Nobel Prize in Physics, 1906; headed the Cavendish Laboratory, Cambridge, and mentored Ernest Rutherford.

    Ernest Rutherford

    Born in New Zealand; known as the “Father of Nuclear Physics”; discovered the atomic nucleus and the proton; Nobel Prize in Chemistry, 1908; his portrait appears on New Zealand’s $100 banknote.

    Niels Bohr

    Proposed fixed energy levels/shells to explain atomic stability; Nobel Prize in Physics, 1922.

    James Chadwick

    Discovered the neutron in 1932 while working under Rutherford at the Cavendish Laboratory; Nobel Prize in Physics, 1935.

    Homi Jehangir Bhabha

    “Father of the Indian nuclear programme”; established the Tata Institute of Fundamental Research (TIFR) and the Bhabha Atomic Research Centre (BARC) for peaceful uses of atomic energy — electricity generation, agriculture, medical treatment.


    10. Exam Question Bank

    A. MCQ / Assertion–Reason (1 mark each)

    1. The gold foil experiment showed most alpha particles pass undeflected, proving that most of the atom is empty space (NOT evidence of neutrons — neutrons were discovered separately by Chadwick in 1932).[1]
    2. Assertion: Electrons do not fall into the nucleus in Bohr’s model. Reason: Electrons in a stationary state (fixed shell) do not lose energy. — Both true, R correctly explains A.[1]
    3. The maximum number of electrons in the M-shell is $2n^2 = 2(3)^2 = 18$.[1]

    B. Short Answer (2–3 marks)

    1. State the postulates of Bohr’s model of the atom that explain the stability of atoms.[3]
    2. Differentiate between isotopes and isobars with one example each.[3]
    3. Why do atoms of the same element have the same chemical properties even when they are different isotopes?[2]
    4. Explain why the gold foil experiment’s results could not be explained by Thomson’s model.[3]

    C. Numerical Problems

    1. An atom has atomic number 26 and 56 nucleons. Find the number of electrons, protons, and neutrons.[2]
    2. An atom has 18 neutrons and atomic number 17. Find its mass number.[2]
    3. Bromine has two isotopes: $^{79}_{35}\text{Br}$ (49.7%) and $^{81}_{35}\text{Br}$ (50.3%). Calculate its average atomic mass.[3]
    4. An atom $^{23}A$ has 11 electrons. Find the number of neutrons in it.[2]

    D. Long Answer / HOTS (4–5 marks)

    1. Trace the historical development of atomic models from Dalton to the modern quantum mechanical model, highlighting the key experimental evidence that led to each revision.[5]
    2. Explain, with reasoning, why Rutherford’s model failed to explain atomic stability, and how Bohr’s model resolved this issue.[4]
    3. For an element with mass number 35 and 18 neutrons: (i) find protons and electrons, (ii) find atomic number, (iii) identify the element, (iv) write its electronic configuration, (v) state its valency.[5]
    4. Explain why isotopes of an element have the same valency but the weighted average atomic mass of the element is often a non-whole number.[4]

    At a Glance — Chapter Summary

    • Atomic theory origins: Acharya Kanada’s parmanu and Democritus’s atomos — imaginative, not experimental. Dalton (1808) gave the first scientific atomic theory.
    • Model evolution: Dalton (indivisible sphere) → Thomson (plum pudding — electrons in positive sphere) → Rutherford (nucleus, mostly empty space, but unstable) → Bohr (fixed energy shells, stable) → Modern (quantum/electron cloud model).
    • Gold foil experiment (Geiger–Marsden, under Rutherford) → discovered the nucleus via α-particle scattering.
    • Three subatomic particles: electron ($e^-$, −1, Thomson), proton ($p^+$, +1, Rutherford), neutron ($n^0$, 0, Chadwick).
    • Atomic number ($Z$) = number of protons; Mass number ($A$) = protons + neutrons (nucleons).
    • Bohr–Bury rule: max electrons per shell = $2n^2$; outermost shell max = 8.
    • Valency = electrons lost/gained/shared to complete the octet.
    • Isotopes: same element, same $Z$, different $A$ (different neutrons) — same chemical, different physical properties.
    • Isobars: different elements, same $A$, different $Z$.
    • Average atomic mass = weighted average based on natural isotopic abundance.
    © abhishek.io.in  ·  Class 9 Science Notes  ·  Chapter 8: Journey Inside the Atom
  • C9. Chapter 3: Tissues in Action Notes

    Chapter 3: Tissues in Action — Detailed Notes | Class 9 Science
    Class 9 · Science · NCERT Exploration

    Chapter 3: Tissues in Action

    Complete Study Notes Plant & Animal Tissues Exam-Ready Format

    1. Introduction — The Idea of a Tissue

    A tissue is a group of cells that are similar in structure and work together to perform a specific function. The formation of tissues creates division of labour in the body, which increases efficiency and allows complex life processes to occur.

    Hierarchy of Organisation Cell → Tissue → Organ → Organ System → Organism

    In unicellular organisms (e.g., Amoeba), a single cell performs all life functions. In multicellular organisms (plants and animals), different groups of specialised cells carry out different functions — this is why tissues exist.

    Exam Tip A very common 1-mark/2-mark question: “Define tissue and give one example each from a plant and an animal.” Answer: Tissue = group of similar cells performing a specific function. Plant example: xylem (conducts water). Animal example: muscle tissue (movement).

    Why Are Plant and Animal Tissues Different?

    Table 1.1 — Key structural/functional differences
    BasisPlantsAnimals
    MovementFixed in one place; need support to stay uprightGenerally capable of movement (except a few like sponges)
    Cell wallPresent — gives rigidity and strengthAbsent — allows change of shape, aiding locomotion
    Mode of nutritionAutotrophic — tissues help utilise solar energy via photosynthesisHeterotrophic — tissues help digest food from external sources
    Growth patternLocalised growth (only at meristems) — growth continues throughout lifeGeneralised growth — occurs throughout the body, but growth stops after a point

    2. Tissues for Growth in Plants

    Plants grow in three distinct ways:

    • Increase in length — height of stem and depth of roots
    • Increase in girth — thickness of the stem
    • Regrowth — after cutting of branches or grazing by animals

    All three types of growth depend on actively dividing cells, collectively called meristematic tissue. There are three types, based on location and function.

    2.1 Apical Meristem — Growth in Length

    Key Experiment: Activity 3.1 (Onion Root Growth)

    Two onion bulbs are placed in water-filled jars (Jar A and Jar B). Root growth is measured daily. On Day 3, the root tips of Jar B are cut by about 1 cm.

    Observation: Roots in Jar A continue growing in length steadily. Roots in Jar B stop growing after their tips are removed.

    Conclusion: Roots grow only from their tips, which contain cells that divide continuously (confirmed earlier by observing mitosis in onion root tips).

    This growth zone at the tips of roots and shoots is called the apical meristem. It is responsible for increase in length of the plant.

    Exam Tip — Diagram-Based Question Be ready to label a sapling diagram showing shoot apical meristem (tip of shoot) and root apical meristem (tip of root). This is a frequently asked 2-mark diagram question.

    2.2 Lateral Meristem — Growth in Girth

    Located along the circumference of the stem (in a ring), this meristem produces new cells inside and outside in a concentric manner, increasing the stem’s diameter. This is called the lateral meristem (also linked to formation of annual growth rings seen in a cut tree trunk).

    Application: Age of a Tree Counting annual rings lets scientists estimate a tree’s age and the climatic conditions (favourable/unfavourable years) it experienced — wide rings = good growth year; narrow rings = poor growth year.

    2.3 Intercalary Meristem — Regrowth After Cutting

    Located at the base of the internode, or just above a node (the point where branches/leaves arise). When the tip of a stem is cut, growth in length stops, but new branches sprout from the nodes — this is why hedges become bushier after trimming and grass regrows after mowing/grazing.

    Quick Recall — 3 Meristems: Apical (tip → length) · Lateral (ring → girth) · Intercalary (node/base → regrowth after cutting)

    Characteristics of Meristematic Cells

    • Small in size, with thin cell walls
    • Large, prominent nucleus and dense cytoplasm rich in organelles
    • Vacuoles generally absent
    • Tightly packed with little/no intercellular space

    These features allow rapid and continuous cell division.

    Differentiation Cells that lose the ability to divide undergo structural/functional change to become specialised — this process is called differentiation. Meristematic tissue becomes permanent tissue through differentiation.

    3. Permanent Tissues in Plants

    Permanent tissues are classified as:

    • Simple — composed of only one type of cell (parenchyma, collenchyma, sclerenchyma)
    • Complex — composed of more than one type of cell working together (xylem, phloem)

    3.1 Protective Tissue — Epidermis

    The epidermis is the outermost layer of the plant body — a single, tightly packed layer of flat, rectangular cells. It is covered by a waxy layer called the cuticle, which reduces water loss. In roots, epidermal projections form root hairs that increase surface area for water/mineral absorption. In leaves, the epidermis contains pores called stomata, which allow gaseous exchange and transpiration (evaporation of water vapour), creating a transpiration pull that helps move water up through the xylem.

    HOTS Question Why is a thick cuticle advantageous for a desert plant but disadvantageous for an underwater plant? — A thick cuticle minimises water loss by transpiration (vital in dry conditions), but an aquatic plant needs gas exchange directly through its surface, so a thick waterproof cuticle would hinder that exchange.

    3.2 Supporting Tissues (Simple Permanent Tissues)

    Table 3.1 — Parenchyma, Collenchyma, Sclerenchyma compared
    FeatureParenchymaCollenchymaSclerenchyma
    Cell natureLiving, thin-walledLiving, unevenly thickened corners (pectin)Mostly dead, thick walls (lignin)
    PackingLoosely packed, intercellular spaces presentFairly compactCompact, no intercellular space
    FunctionFood storage; photosynthesis in green parts; aquatic forms have air spaces for floatingProvides flexibility — allows stems/tendrils to bend without breakingProvides strength & rigidity (woody structure)
    Location exampleCortex, pithPetioles, young stemsStems, leaf veins, seed/nut coverings (coconut husk, walnut shell)
    Exam Tip Classic assertion-reason style question: fresh green twigs bend (collenchyma provides flexibility) but dry/woody twigs snap (sclerenchyma is rigid due to lignin, cannot bend).

    3.3 Conducting Tissues (Complex Permanent Tissues)

    Xylem
    • Transports water and minerals from roots upward
    • Also gives mechanical strength
    • Components: tracheids, vessels, xylem parenchyma, xylem fibres
    • Only xylem parenchyma is living; tracheids, vessels, fibres are sclerenchymatous (dead, thick-walled)
    Phloem
    • Transports food (organic nutrients) from leaves to rest of plant
    • Mostly made of living cells
    • Components: sieve tubes, companion cells, phloem parenchyma, phloem fibres
    • Companion cells regulate loading/unloading of sugars in sieve tubes
    Frequently Confused Xylem = water/minerals, mostly dead cells (except xylem parenchyma). Phloem = food, mostly living cells. If a question says “food transport tissue malfunctioning” → answer is Phloem, not Xylem.

    3.4 Plant Tissue Systems

    All plant tissues are organised into three larger tissue systems:

    1. Dermal tissue system — outer covering; protects and reduces water loss (epidermis)
    2. Ground tissue system — main body between dermal and vascular tissue; includes parenchyma, collenchyma, sclerenchyma
    3. Vascular tissue system — conducting tissues: xylem and phloem

    4. Animal Tissues

    Animal tissues are broadly of four types: Epithelial, Connective, Muscular, and Nervous.

    4.1 Epithelial Tissue

    Forms the outer covering of the body (skin) and lines internal organs (mouth, lungs, blood vessels, intestine). Cells are closely packed with minimal intercellular space, preventing entry of germs and reducing water loss.

    Table 4.1 — Types of Epithelial Tissue (structure–function relationship)
    FunctionStructureLocation
    Exchange (diffusion of gases/liquids)Single layer of thin, flat cells (squamous)Lining of blood vessels, lungs
    ProtectionMany layers; outer cells flat and tightly packed (stratified)Skin, mouth, oesophagus
    SecretionCuboidal/columnar cells specialised for producing & releasing substancesSalivary glands, sweat glands, stomach lining
    Sensory functionSpecialised receptor cells with hair-like ciliaNostrils, taste buds, inner ear
    AbsorptionSingle layer of tall, pillar-like (columnar) cells, often with hair-like structuresLining of small intestine
    Exam Tip Why is epithelium lining the lungs/blood vessels only one cell thick? — To allow rapid/efficient diffusion of gases and liquids across the tissue; a thicker layer would slow down exchange.

    4.2 Connective Tissue

    Connects and supports other tissues/organs. Composition varies in the matrix (the substance between cells) — from fluid (blood) to hard (bone).

    Table 4.2 — Types of Connective Tissue
    TissueMatrix / StructureFunction
    BloodFluid matrix (plasma ~55%); contains RBCs, WBCs, plateletsTransports nutrients, gases, hormones, wastes
    BoneHard, rigid matrix (calcium and phosphorus compounds)Gives strength, support, and protection; forms the skeleton
    CartilageSoft, jelly-like matrixProvides flexibility; cushions bone ends (e.g., nose, ear)
    TendonTough fibrous connective tissueConnects muscle to bone; transmits force for movement
    LigamentFibrous connective tissueConnects bone to bone; provides stability, limits movement, prevents dislocation
    Quick Recall: “Tendon = To bone (from muscle)” and “Ligament = bone to bone, Limits movement.” Do not mix them up — a very common 1-mark error.

    Components of Blood

    • Plasma — fluid part (~55% of volume); carries dissolved substances
    • RBCs (Red Blood Cells) — contain haemoglobin (iron-rich protein, gives red colour); lifespan ~4 months
    • WBCs (White Blood Cells) — fight infection; collect at infected sites causing pus/inflammation
    • Platelets — help in blood clotting at injury sites

    4.3 Muscular Tissue

    Table 4.3 — Three Types of Muscle
    TypeCell shapeNucleiStriationsControlLocation
    Skeletal (striated)Long, cylindrical, unbranchedMultinucleatePresent (striated)VoluntaryAttached to skeleton (limbs, etc.)
    Smooth (unstriated)Spindle-shapedSingle nucleusAbsentInvoluntaryStomach, intestines (slow, continuous movement)
    CardiacCylindrical, branchedSingle nucleusFaint striationsInvoluntaryOnly in the heart
    Exam Tip — Assertion/Reason style Assertion: Cardiac muscle can contract continuously without fatigue. Reason: Cardiac muscle cells have abundant mitochondria and a rich blood supply, sustaining continuous energy production. (Both true and R correctly explains A.)

    4.4 Nervous Tissue

    Forms the body’s control and coordination network. Made up of neurons (nerve cells), specialised to receive, process, and transmit messages.

    Structure of a Neuron (label carefully for diagram questions)

    • Cell body — contains nucleus; controls cell activities
    • Dendrites — receive signals from other neurons
    • Axon — long fibre carrying messages away from the cell body, ending in axon terminals that transmit signals to other cells

    5. The Musculoskeletal System

    Made up of bones, muscles, joints, cartilage, tendons, and ligaments. It helps the body stand upright, move, maintain posture, and protect delicate organs — functioning under control of the nervous system. Muscles pull on bones via tendons; muscle contraction → tendon transmits force → movement at a joint.

    Quick Fact On average, the adult human skeleton makes up about 12–15% of body weight (varies with age, gender, body composition).

    5.1 Types of Joints

    Table 5.1 — Joint types, movement, and location
    Joint TypeMovement AllowedExample Location
    Ball and socketFree movement — forward, backward, sideways, circularShoulder (rounded arm bone fits shoulder bone hollow)
    HingeMovement in one direction only (like a door hinge)Elbow, knee
    PivotSide-to-side rotation (like a doorknob)Joint between skull and backbone (neck)
    FixedNo movementSkull bones (protect brain)
    Common Mistake to Avoid Assertion: In a hinge joint, movement occurs primarily in one plane. Reason: The bone ends are shaped to allow sliding in all directions. — This Reason is FALSE; hinge joints restrict movement to one plane precisely because the bone ends do NOT allow sliding in all directions (that describes a ball-and-socket joint).

    5.2 Skeletal System — Backbone & Rib Cage

    • Vertebral column (backbone) — series of small bones called vertebrae; supports the body, allows upright posture. Cartilage discs between vertebrae cushion and allow flexibility while protecting the spinal cord.
    • Rib cage — 12 pairs of ribs; attached to the spine (back) and sternum/breast bone (front) via flexible cartilage. This flexibility allows the rib cage to expand/contract during breathing.

    6. Important Named Concepts & Scientists

    Totipotency (F. C. Steward, 1958)

    Demonstrated that single cells from carrot phloem could regenerate an entire plant. Phloem cells first dedifferentiate (regain ability to divide) forming an unspecialised cell mass, which then divides and redifferentiates into roots, shoot, and a complete plant. This ability of a mature cell to give rise to a whole organism is called totipotency, and such cells are totipotent cells — similar to how a zygote develops into a full organism.

    Crown Gall Disease

    Caused by the bacterium Agrobacterium tumefaciens; produces tumour-like swellings on stems due to uncontrolled cell division. Scientists studied how this bacterium transfers genetic material into plant cells — this knowledge is now used as a tool in plant tissue culture and genetic engineering to introduce useful genes into crops.

    B. G. L. Swamy

    Renowned Indian botanist known for contributions to plant morphology and anatomy; authored Hasuru Honnu (Kannada), which won the Kendra Sahitya Akademi Award (1978).

    Sipra Guha Mukherjee & S. C. Maheshwari

    Achieved a breakthrough in plant tissue culture — developed a complete plant through anther culture using an artificial nutrient medium under controlled conditions, contributing significantly to crop improvement.


    7. Exam Question Bank

    A. Multiple Choice / Assertion-Reason (1 mark each)

    1. Meristematic tissues can divide repeatedly because their cells have thin walls, dense cytoplasm, and a large prominent nucleus (NOT because they have thick walls or large vacuoles).[1]
    2. If a plant cannot transport food from leaves to roots, the malfunctioning tissue is Phloem.[1]
    3. Epithelial tissue lining internal organs is usually one/few cells thick to allow quick exchange of materials by diffusion.[1]
    4. Bending knees and ankles involves a Hinge joint.[1]

    B. Short Answer (2–3 marks)

    1. Distinguish between xylem and phloem on the basis of function and cell nature (living/dead).[3]
    2. Why does a fresh green twig bend without breaking, while a dry twig snaps? Name the tissues responsible.[2]
    3. Differentiate between a tendon and a ligament with one example/function of each.[2]
    4. Explain why cardiac muscle can work continuously throughout life without fatigue.[2]
    5. What is meant by differentiation in the context of meristematic tissue?[2]

    C. Long Answer / HOTS (4–5 marks)

    1. An elephant severely debarks a tree to feed on its bark. (a) Which function(s) of the tree are hampered? (b) Which tissue would be further affected if damage continues beneath the bark? (c) What function would be hampered if tissue beneath the bark is severely damaged? — Hint: bark removal damages phloem (just under the bark), disrupting food transport; further damage into the wood affects xylem (water transport) and the lateral meristem (girth growth).[5]
    2. Explain the totipotency experiment of F. C. Steward using carrot phloem cells. What does this reveal about the potential of mature plant cells?[5]
    3. With reference to Sohan’s sugarcane cutting experiment (Type A vs Type B), identify the likely difference between the cuttings (presence of a node/bud with meristematic tissue) and explain why only Type B could sprout.[4]
    4. Explain the three types of meristematic tissues with their location and function. How do they together account for a plant’s overall growth in length, girth, and branching?[5]
    5. Describe the structure and function of a neuron, and explain how nervous tissue coordinates both voluntary and involuntary muscle activity.[4]

    D. Numerical / Graph-Based

    1. Using the teak tree data (age vs. diameter vs. annual rings), plot the graph and explain the relationship between diameter and number of annual rings formed. Identify the tissue responsible for girth and its location.[5]

    At a Glance — Chapter Summary

    • Tissue = group of similar cells performing specific functions; enables division of labour.
    • Plant tissues: Meristematic (dividing: apical, lateral, intercalary) and Permanent (differentiated: simple & complex).
    • Simple permanent tissues: parenchyma (storage), collenchyma (flexibility), sclerenchyma (strength).
    • Complex permanent tissues: xylem (water/minerals, mostly dead) and phloem (food, mostly living).
    • Animal tissues: Epithelial (covering/lining), Connective (support/connect — blood, bone, cartilage, tendon, ligament), Muscular (movement — skeletal, smooth, cardiac), Nervous (control/coordination — neurons).
    • Musculoskeletal system = bones + muscles + joints + cartilage + tendons + ligaments, under nervous system control.
    • Joint types: ball & socket (free movement), hinge (one direction), pivot (rotation), fixed (no movement).
    • Totipotency: a mature plant cell’s ability to regenerate a whole organism (F. C. Steward, carrot phloem, 1958).
    © abhishek.io.in  ·  Class 9 Science Notes  ·  Chapter 3: Tissues in Action