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A-LevelChemistryHydrocarbons9701/12 · Feb/Mar 2023 · Q391 Mark

Cyclohexa-1,4-diene is treated with a solution of bromine in tetrachloromethane in the dark. [Figure 39.1: Structure of cyclohexa-1,4-diene.] Which product is formed?

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ACyclic six-membered ring with two Br on adjacent carbons and one double bond remaining. (1,2-dibromocyclohex-4-ene)
BCyclic six-membered ring with four Br atoms, all single bonds. (1,2,4,5-tetrabromocyclohexane)
CCyclic six-membered ring with two Br atoms on carbons separated by one carbon, and one double bond remaining. (1,4-dibromocyclohex-2-ene)
DCyclic six-membered ring with four Br atoms on adjacent carbons, all single bonds. (1,2,3,4-tetrabromocyclohexane)

✓ Correct answer

B: Cyclic six-membered ring with four Br atoms, all single bonds. (1,2,4,5-tetrabromocyclohexane)

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About this question

Topic
Hydrocarbons, A-Level Chemistry (syllabus 9701). Multiple choice, 1 mark.
Source
A-Level Chemistry, Feb/Mar 2023 Paper 1 Variant 2, question 39.

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