Acetophenone (PhCOCH_3) reacts with perbenzoi | vedclass

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(C) Acetophenone $(PhCOCH_3)$ reacts with perbenzoic acid to undergo Baeyer-Villiger oxidation to form phenyl acetate $(PhOCOCH_3)$ as compound $X$. W

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tert-Butyl alcohol and phenol

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(C) Acetophenone $(PhCOCH_3)$ reacts with perbenzoic acid to undergo Baeyer-Villiger oxidation to form phenyl acetate $(PhOCOCH_3)$ as compound $X$. When $X$ $(PhOCOCH_3)$ reacts with excess $CH_3MgBr$,the ester undergoes nucleophilic acyl substitution followed by addition to the resulting ketone. $1$. $PhOCOCH_3 + CH_3MgBr \rightarrow PhOMgBr + CH_3COCH_3$ (acetone). $2$. The formed acetone further reacts with another equivalent of $CH_3MgBr$ to form tert-butoxide $( (CH_3)_3COMgBr )$. $3$. Upon treatment with aqueous acid $(H_3O^+)$,the products are phenol $(PhOH)$ and tert-butyl alcohol $((CH_3)_3COH)$.

Acetophenone $(PhCOCH_3)$ reacts with perbenzoic acid to produce a compound $X$. Reaction of $X$ with excess $CH_3MgBr$ followed by treatment with aqueous acid predominantly produces

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