The product (P) of the given reaction is: | vedclass

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(B) The reaction involves the treatment of $2$-hydroxy$-2-$cyclohexylacetic acid with $3$ equivalents of $EtLi$. First,$2$ equivalents of $EtLi$ act a

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(B) The reaction involves the treatment of $2$-hydroxy$-2-$cyclohexylacetic acid with $3$ equivalents of $EtLi$. First,$2$ equivalents of $EtLi$ act as a base,deprotonating both the carboxylic acid group and the hydroxyl group to form a dianion. The third equivalent of $EtLi$ then acts as a nucleophile,attacking the carboxylate carbon. Upon acidic workup $(H_3O^+)$,the intermediate forms a gem-diol,which is unstable and loses water to form a ketone. The final product is $1$-cyclohexyl$-2-$hydroxybutan$-1-$one,which corresponds to the structure in option $B$.

The product $(P)$ of the given reaction is:

Similar Questions

In the following reactions,what are $B$ and $X$ respectively?
$C_2H_5MgBr$ $\xrightarrow{ClCN} C_2H_5CN$ $\xrightarrow{H_3O^+} B$
$CH_3COCH_3$ $\xrightarrow[NaOH]{I_2} X + CHI_3$ $\xrightarrow{Ag} Y$
$C_6H_5NH_2$ $\xrightarrow[HCl]{NaNO_2} P$ $\xrightarrow{CuCN} Q$ $\xrightarrow{+4H} R$

The major product in the following reaction is

Hydrolysis of an ester gives a carboxylic acid which on Kolbe's electrolysis yields ethane. The ester is

The product $(A)$ of the reaction is:

The correct order of acidity for the following compounds is:

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