Which of the following halides undergoes hydr | vedclass

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(D) The rate of hydrolysis of alkyl halides via the $S_N1$ mechanism depends on the stability of the carbocation intermediate formed. In the given opt

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$(C_6H_5)_3CCl$

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(D) The rate of hydrolysis of alkyl halides via the $S_N1$ mechanism depends on the stability of the carbocation intermediate formed. In the given options,$(C_6H_5)_3CCl$ forms a triphenylmethyl carbocation $(C_6H_5)_3C^+$. This carbocation is highly stabilized by resonance due to the presence of three phenyl rings. Since the carbocation formed from $(C_6H_5)_3CCl$ is the most stable,it undergoes hydrolysis most rapidly.

Which of the following halides undergoes hydrolysis most rapidly?

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