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.

List-$I$	List-$II$
$A$. Phenol $\rightarrow$ Salicylaldehyde	$I$. $Br_2$ in $CS_2$
$B$. Phenol $\rightarrow$ Benzene	$II$. $Na_2Cr_2O_7/H_2SO_4$
$C$. Phenol $\rightarrow$ $p$-Benzoquinone	$III$. $Zn$
$D$. Phenol $\rightarrow$ $p$-Bromophenol	$IV$. $CHCl_3/NaOH$

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

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