What will be obtained by the hydrolysis of th | vedclass

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(A) The hydrolysis of the given compound proceeds via an $S_{N}1$ mechanism involving the formation of a carbocation intermediate.Upon the loss of the

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$A$ mixture of $(K)$ and $(L)$

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(A) The hydrolysis of the given compound proceeds via an $S_{N}1$ mechanism involving the formation of a carbocation intermediate.Upon the loss of the chloride ion,a secondary carbocation is formed.This carbocation can undergo a $1,2$-hydride shift to form a more stable carbocation,which is stabilized by the electron-donating methoxy group $(-OCH_3)$ on the phenyl ring.The initial carbocation leads to the formation of product $(K)$ upon attack by water.The rearranged carbocation leads to the formation of product $(L)$ upon attack by water.Therefore,a mixture of $(K)$ and $(L)$ is obtained as the final product.

What will be obtained by the hydrolysis of the following compound in aqueous acetone?

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