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 $A$.

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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