Question: In the problem-solving feature above, methylcyclohexanone was seen to react at its unsubstituted carbon. Try to write a mechanism for the same reaction at

In the problem-solving feature above, methylcyclohexanone was seen to react at its unsubstituted α carbon. Try to write a mechanism for the same reaction at the methyl-substituted carbon atom, and explain why this regiochemistry is not observed.

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