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Functional groups: classification of organic compounds practice questions.

135 exam-style questions on Functional groups: classification of organic compounds — topic S3.2 of Structure 3: Classification of matter in the IB Chemistry syllabus — with answers and explanations. Samples below; the full set is free with an account.

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About this topic

Syllabus code
S3.2
Subject
IB Chemistry
Concept
S3 · Structure 3: Classification of matter
Questions
135 with worked answers
Question types
96 fill-in-the-gap questions · 24 multiple-choice questions · 7 true/false questions · 5 flashcards · 2 matching tasks · 1 structured question
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Sample questions on Functional groups: classification of organic compounds

In the mass spectrum of a compound, what does the peak at the highest m/z value (the molecular ion peak, M+) tell you?

  • The number of hydrogen atoms
  • The relative molecular mass of the compound
  • The total number of carbon atoms in the molecule
  • The boiling point

Answer: The relative molecular mass of the compound

The molecular ion peak (M+) corresponds to the whole molecule that has lost one electron. Its m/z value equals the relative molecular mass of the compound. Fragment peaks at lower m/z arise when the molecular ion breaks apart, helping to deduce structure.

A broad absorption at about 3200-3550 cm-1 in an infrared spectrum indicates the presence of which functional group?

  • C=O (carbonyl, a sharp absorption near 1700)
  • O-H (hydroxyl or acid)
  • C-H (alkane)
  • C=C (alkene)

Answer: O-H (hydroxyl or acid)

A broad absorption around 3200-3550 cm-1 is characteristic of the O-H bond stretch in alcohols (and even broader for carboxylic acids). The C=O carbonyl stretch appears near 1700 cm-1, so IR distinguishes functional groups by their absorption ranges.

What is the general formula of the alkanes?

  • CₙH₂ₙ
  • CₙH₂ₙ₊₂
  • CₙH₂ₙ₋₂
  • CₙHₙ

Answer: CₙH₂ₙ₊₂

Saturated hydrocarbons follow CₙH₂ₙ₊₂ (e.g. methane CH₄, ethane C₂H₆). Alkenes, which have one double bond, follow CₙH₂ₙ.

By which mechanism does a tertiary halogenoalkane undergo nucleophilic substitution?

  • SN1
  • SN2
  • electrophilic addition
  • free-radical substitution

Answer: SN1

A tertiary halogenoalkane forms a relatively stable tertiary carbocation, favouring the two-step SN1 mechanism. Primary halogenoalkanes favour the one-step SN2 mechanism.

Identify the functional group present in the compound CH3CH2CHO.

  • Hydroxyl (alcohol)
  • Carbonyl of an aldehyde
  • Carbonyl group in the middle of a ketone
  • Carboxyl

Answer: Carbonyl of an aldehyde

The -CHO group is a carbonyl at the end of the chain, characteristic of an aldehyde (propanal).

State the class of organic compound represented by the general formula R-O-R', where R and R' are alkyl groups.

  • Ester
  • Ether
  • Ketone
  • Amine

Answer: Ether

An oxygen atom bonded between two alkyl (carbon) groups, R-O-R', defines an ether.

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