Identify the major product.

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(A) The reaction involves the acid-catalyzed rearrangement of the given alcohol. $1$. Protonation of the hydroxyl group occurs,followed by the loss of

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(A) The reaction involves the acid-catalyzed rearrangement of the given alcohol. $1$. Protonation of the hydroxyl group occurs,followed by the loss of a water molecule to form a carbocation. $2$. The carbocation undergoes a ring expansion (or rearrangement) to form a more stable resonance-stabilized carbocation. $3$. Finally,the loss of a proton leads to the formation of the ketone product as shown in the mechanism.

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