The structure of product (A) is: | vedclass

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Question

(A) The reaction involves a nucleophilic substitution reaction. The nucleophile $PhS^-$ attacks the electrophilic carbon of the $-CH_2Cl$ group,which

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$4-$bromobenzyl phenyl sulfide

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(A) The reaction involves a nucleophilic substitution reaction. The nucleophile $PhS^-$ attacks the electrophilic carbon of the $-CH_2Cl$ group,which is a primary benzylic halide. The $-Br$ group attached directly to the benzene ring is much less reactive towards nucleophilic substitution under these conditions compared to the benzylic chloride. Therefore,the $PhS^-$ group replaces the $-Cl$ atom to form $4$-bromobenzyl phenyl sulfide as the major product $(A)$.

The structure of product $(A)$ is:

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