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(C) The rate of $S_N1$ reaction depends on the stability of the carbocation intermediate formed during the rate-determining step.In $(C_6H_5)_3CCl$,th

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$(C_6H_5)_3CCl$

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(C) The rate of $S_N1$ reaction depends on the stability of the carbocation intermediate formed during the rate-determining step.In $(C_6H_5)_3CCl$,the carbocation formed is $(C_6H_5)_3C^+$,which is highly stabilized by resonance with three phenyl groups.This carbocation is significantly more stable than the allyl carbocation $(CH_2=CH-CH_2^+)$,the benzyl carbocation $(C_6H_5CH_2^+)$,or the phenyl cation $(C_6H_5^+)$.Therefore,$(C_6H_5)_3CCl$ undergoes hydrolysis most rapidly via the $S_N1$ mechanism.

Which of the following compounds is most rapidly hydrolysed by $S_N1$ mechanism?

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