(A) Styrene on reaction with HBr gives 1-bromo-1-phenyl ethane.
(R) Benzyl radical is more stable than alkyl radical.

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Both (A) and (R) are correct and (R) isthe correct explanation of (A)

(A) is True but (R) is False

Both (A) and (R) are false

Both (A) and (R) are correct but (R) is not the correct explanation of (A)

answer is A.

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Detailed Solution

HBr adds to the double bond of the styrene forming 1−bromo−1−phenylethane.

Benzyl radical is more stable than alkyl radical because of resonance in benzyl radicals.

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