A Levels Chemistry (9701)•9701/12/O/N/20

Explanation
Radical Intermediates in Chlorination of Ethane Steps:
- Chlorine radicals form via homolytic cleavage of Cl₂.
- A chlorine radical abstracts a hydrogen from ethane (CH₃CH₃), forming HCl and an ethyl radical (CH₃CH₂•).
- The ethyl radical reacts with Cl₂ to form chloroethane (CH₃CH₂Cl) and regenerate Cl•.
- Termination steps involve radical combinations, but propagation generates the key alkyl radical.
Why B is correct:
- CH₃CH₂• is the alkyl radical produced when Cl• abstracts H from ethane, per the propagation step in free radical substitution.
Why the others are wrong:
- A: CH₃• forms from methane (CH₄), not ethane.
- C: CH₃Cl• is a radical from chloromethane, unrelated to ethane chlorination.
- D: CH₃CHCl• arises in secondary chlorination of chloroethane, not the primary reaction with ethane.
Final answer: B
Topic: Hydrocarbons
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