The major product of the following reaction i | vedclass

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(B) The reaction involves the acid-catalyzed dehydration of a $\beta$-hydroxy ketone. $1$. The hydroxyl group $(-OH)$ is protonated by $H^+$ to form a

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$3-$isopropylcyclopent$-2-$en$-1-$one

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(B) The reaction involves the acid-catalyzed dehydration of a $\beta$-hydroxy ketone. $1$. The hydroxyl group $(-OH)$ is protonated by $H^+$ to form a good leaving group $(-OH_2^+)$. $2$. Water is eliminated,creating a carbocation at the carbon atom. $3$. The carbocation undergoes rearrangement or elimination to form a stable conjugated system. $4$. In this specific case,the elimination of water leads to the formation of a double bond conjugated with the carbonyl group,resulting in $3$-isopropylcyclopent-$2$-en-$1$-one as the major product.

The major product of the following reaction is:

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