The reaction shown above is a Baeyer-Villiger | vedclass

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(A) The reaction is a Baeyer-Villiger oxidation of a ketone. In this rearrangement,an oxygen atom is inserted into the bond between the carbonyl carbo

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(A) The reaction is a Baeyer-Villiger oxidation of a ketone. In this rearrangement,an oxygen atom is inserted into the bond between the carbonyl carbon and the more substituted alkyl group (migratory aptitude: tertiary alkyl > secondary alkyl > primary alkyl > methyl). For the given $2$-substituted cyclohexanone,the oxygen inserts between the carbonyl carbon and the more substituted carbon (the one bearing the $R$ group) to form a lactone. Thus,the product is the one where the oxygen is inserted between the carbonyl carbon and the carbon with the $R$ substituent,which corresponds to option $A$.

Column $I$	Column $II$
$A$. $C_6H_5CHO$	$p$. gives precipitate with $2, 4-$dinitrophenylhydrazine
$B$. $CH_3C \equiv CH$	$q$. gives precipitate with $AgNO_3$
$C$. $CN^{-}$	$r$. is a nucleophile
$D$. $I^{-}$	$s$. is involved in cyanohydrin formation

The reaction shown above is a Baeyer-Villiger rearrangement of an asymmetric ketone with magnesium monoperoxyphthalate hexahydrate (in the drawing,$Mg^{+2}$ is omitted for clarity). Identify the major product.

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