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Question

(D) The reaction involves the reduction of the carbonyl group of $2$-bromoacetophenone by $NaBH_4$ to form an alkoxide intermediate. This intermediate

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phenyloxirane

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(D) The reaction involves the reduction of the carbonyl group of $2$-bromoacetophenone by $NaBH_4$ to form an alkoxide intermediate. This intermediate then undergoes an intramolecular nucleophilic substitution reaction,where the alkoxide oxygen attacks the carbon bearing the bromine atom,displacing the bromide ion to form an epoxide ring. Thus,the final product is phenyloxirane.

The major product of the following reaction is:

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