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.

Group-$I$ (Compound)	Group-$II$ (Use)
$A$. Alcohol	$1$. Antiseptic
$B$. Phenol	$2$. Perfumes
$C$. Ether	$3$. Detergents
$D$. Amine	$4$. Dyes

Column-$I$	Column-$II$
$A$. Methanol	$p$. Conversion of phenol to salicylic acid
$B$. Kolbe's reaction	$q$. Wood spirit
$C$. Williamson's reaction	$r$. Vapours are passed over heated copper at $573 \ K$
$D$. Conversion of $2^\circ$ alcohol to ketone	$s$. Reaction of alkyl halide with sodium alkoxide

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

Similar Questions

Based on the provided reaction scheme,determine the total number of stereoisomers of $B$.

What is the product of the reaction shown below?

Match the compounds in Group-$I$ with their uses in Group-$II$. Find the correct match for Group-$I$ from Group-$II$.

Group-$I$ (Compound) Group-$II$ (Use)

$A$. Alcohol $1$. Antiseptic

$B$. Phenol $2$. Perfumes

$C$. Ether $3$. Detergents

$D$. Amine $4$. Dyes

Which of the following reactions involves the formation of a carbene intermediate?

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