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The major product of the following reaction is
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A. image
B. image
C. image
D. image

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Alkyl halides undergo nucleophilic substitution more readily than aryl halides. Hence substitution occurs more readily in the side chain rather than in the ring. `PhS^(-)` is a strong nucleophile and dimethyl formamide (DMF) is a higher aprotic solvent conditions indicate that nucleophilic substitution `(S_(N^(2)))` takes place at `2^(@)` benzylic place, stero chemically it involves inversion of configuration
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