The following compound on hydrolysis in aqueo | vedclass

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(A) The reaction proceeds via an $S_N1$ mechanism involving the formation of a carbocation intermediate.$1$. The initial loss of the chloride ion $(Cl

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Mixture of $(K)$ and $(L)$

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(A) The reaction proceeds via an $S_N1$ mechanism involving the formation of a carbocation intermediate.$1$. The initial loss of the chloride ion $(Cl^-)$ generates a secondary carbocation.$2$. This secondary carbocation can undergo a hydride shift (rearrangement) to form a more stable benzylic carbocation.$3$. The initial secondary carbocation can be attacked by water to form product $(K)$.$4$. The rearranged,more stable benzylic carbocation can be attacked by water to form product $(L)$.$5$. Therefore,the hydrolysis results in a mixture of $(K)$ and $(L)$.

The following compound on hydrolysis in aqueous acetone will give:

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