About Hydrocarbons in A Level Chemistry
Hydrocarbons is one of the 18 main topics in our A Level Chemistry (Cambridge (CAIE) 9701) question bank, and about 6% of its real questions come from it. Tayyari Karo has 36 real questions on this topic from 2021 to 2026, from Paper 1, Paper 2, Paper 4; 26 are multiple choice and marked instantly, and the rest are structured questions with a model answer. By difficulty: 20 hard, 13 medium, 3 easy.
Work through the questions below, then open the explanation for each one. Redo the ones you missed a few days later.
Try 6 real questions
These are real past-paper questions. Think of your answer first, then open the explanation.
May/June 2026 · Paper 1 · Hydrocarbons
Which compound will decolourise Br2(aq) in the dark?
- CH3CH2CH2CH2CH2CO2H
- CH3CH2CHOHCH2CH2CH3
- CH3CH=CHCH2CH2CH2OH
- CH3CH2CH2CO2CH2CH3
Show answer and explanation
Answer: C. CH3CH=CHCH2CH2CH2OH
Only the alkene undergoes electrophilic addition with bromine water in the dark.
May/June 2025 · Paper 1 · Hydrocarbons
The structural formula of hept-1,4,5-triene is CH2=CH-CH2-CH=C=CH-CH3. How many of the carbon atoms in one molecule of hept-1,4,5-triene are sp2 hybridised?
- 4
- 5
- 6
- 7
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Answer: A. 4
Carbons in a C=C double bond are normally sp2, but the central carbon of the cumulated diene (C=C=C, at C5) is sp hybridised, not sp2; only C1, C2, C4 and C6 are sp2 hybridised, giving 4.
October/November 2025 · Paper 1 · Hydrocarbons
The fumes from petrol-burning car exhausts contain: 1 unburnt hydrocarbons, 2 nitrogen dioxide, 3 carbon monoxide. Which pollutants are removed by oxidation in a catalytic converter?
- 1, 2 and 3
- 1 and 2 only
- 1 and 3 only
- 2 and 3 only
Show answer and explanation
Answer: C. 1 and 3 only
In a catalytic converter, unburnt hydrocarbons and carbon monoxide are removed by oxidation (to CO2 and H2O); nitrogen dioxide/oxides are removed by reduction (to N2), not oxidation.
May/June 2023 · Paper 1 · Hydrocarbons
Which equation represents a reaction that proceeds through initiation, propagation and termination steps?
- C4H10 + Cl2 → C4H9Cl + HCl
- C5H11Br + NaOH → C5H11OH + NaBr
- C6H12 + H2O → C6H13OH
- C6H13CHO + HCN → C6H13CH(OH)CN
Show answer and explanation
Answer: A. C4H10 + Cl2 → C4H9Cl + HCl
Free-radical substitution of an alkane by chlorine (initiated by UV light, homolytic fission) proceeds via initiation, propagation and termination steps; the other reactions are ionic/nucleophilic mechanisms.
October/November 2023 · Paper 1 · Hydrocarbons
The hydrocarbon C17H36 can be cracked. Which compound is the least likely to be produced in this reaction?
- C3H8
- C4H8
- C8H16
- C16H34
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Answer: D. C16H34
Cracking C17H36 breaks it into smaller fragments; a product with 16 carbons (C16H34) is far too close to the original chain length to be a plausible cracking product, unlike the smaller alkane/alkene fragments in A–C.
May/June 2021 · Paper 1 · Hydrocarbons
Which compound would produce two different carboxylic acids when treated with hot, concentrated, acidified manganate(VII) ions? A: CH3CH=C(CH3)CH(CH3)2; B: CH3CH=CHCH(CH3)2; C: cyclohexene; D: (CH3)2CHCH=CHCH(CH3)2
- CH3CH=C(CH3)CH(CH3)2
- CH3CH=CHCH(CH3)2
- cyclohexene
- (CH3)2CHCH=CHCH(CH3)2
Show answer and explanation
Answer: B. CH3CH=CHCH(CH3)2
In B both alkene carbons bear one H, so oxidative cleavage gives CH3COOH and (CH3)2CHCOOH (two different acids); A has a trisubstituted alkene carbon (gives a ketone), C is cyclic (gives one diacid), D is symmetric (gives two identical acids).