Which of the following undergoes nucleophilic | vedclass

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(C) $S_{N}1$ mechanism depends on the stability of the carbocation intermediate formed during the reaction.Benzyl chloride $(C_6H_5CH_2Cl)$ forms a be

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Benzyl chloride

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(C) $S_{N}1$ mechanism depends on the stability of the carbocation intermediate formed during the reaction.Benzyl chloride $(C_6H_5CH_2Cl)$ forms a benzyl carbocation $(C_6H_5CH_2^+)$ upon the loss of a chloride ion.This carbocation is highly stabilized by resonance with the benzene ring.Therefore,benzyl chloride readily undergoes $S_{N}1$ reaction compared to the other options provided.

Which of the following undergoes nucleophilic substitution reaction according to the $S_{N}1$ mechanism?

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