Organic Chemistry Basics Quiz

Grade 11 · Science · Quiz

10 questions on carbon chemistry, hydrocarbon classes, functional groups, isomers, and reaction types.

Questions

  1. Which hydrocarbon class contains only single carbon-carbon bonds?

    1. Alkene
    2. Alkyne
    3. Alkane
    4. Aromatic
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    Answer: Alkane

    Alkanes are saturated hydrocarbons with only C-C single bonds; formula CₙH₂ₙ₊₂.

  2. Ethanol (CH₃CH₂OH) belongs to which functional group class?

    1. Ester
    2. Alcohol
    3. Aldehyde
    4. Amine
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    Answer: Alcohol

    The −OH (hydroxyl) group defines alcohols. Ethanol is the most common alcohol.

  3. Which hydrocarbon type contains a triple bond?

    1. Alkane
    2. Alkene
    3. Alkyne
    4. Aromatic
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    Answer: Alkyne

    Alkynes contain at least one C≡C triple bond; general formula CₙH₂ₙ₋₂.

  4. The fruity aromas of many fruits result from which functional group?

    1. Amines
    2. Esters
    3. Carboxylic acids
    4. Aldehydes
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    Answer: Esters

    Esters (−COO−) produce characteristic fruity scents. Isoamyl acetate gives bananas their smell.

  5. Butane (C₄H₁₀) and isobutane both have the formula C₄H₁₀ but different structures. They are:

    1. Isotopes
    2. Structural isomers
    3. Geometric isomers
    4. Identical compounds
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    Answer: Structural isomers

    Structural isomers have the same molecular formula but different connectivity of atoms. Butane is a straight chain; isobutane is branched.

  6. Which reaction type removes atoms to create a new double bond?

    1. Addition
    2. Substitution
    3. Elimination
    4. Condensation
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    Answer: Elimination

    Elimination reactions remove atoms from adjacent carbons, forming a new pi (double) bond. E.g., alcohol → alkene + water.

  7. Aromatic compounds like benzene are characterized by:

    1. Only single bonds
    2. A triple bond in the ring
    3. Delocalized pi electrons in a ring
    4. High reactivity with water
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    Answer: Delocalized pi electrons in a ring

    Benzene's six pi electrons are delocalized around the ring, giving it exceptional stability — the hallmark of aromaticity.

  8. Amino acids link together by releasing water. This is a:

    1. Addition reaction
    2. Elimination reaction
    3. Condensation reaction
    4. Substitution reaction
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    Answer: Condensation reaction

    Condensation reactions join two molecules with the release of a small molecule (water). This is how peptide bonds form.

  9. Which functional group makes carboxylic acids weakly acidic?

    1. −OH alone
    2. −NH₂
    3. −COOH (both C=O and −OH)
    4. C=C double bond
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    Answer: −COOH (both C=O and −OH)

    The carboxyl group's C=O withdraws electron density, making the −OH proton more acidic and easily donated.

  10. How many valence electrons does carbon have?

    1. 2
    2. 3
    3. 4
    4. 6
    Show answer

    Answer: 4

    Carbon is in Group 14 and has 4 valence electrons, enabling it to form 4 covalent bonds and create enormous structural diversity.

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