Identify the major product of the following r | vedclass

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(B) The reaction proceeds via the protonation of the double bond in the cyclohexenyl group to form a stable carbocation intermediate. Following this,t

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(B) The reaction proceeds via the protonation of the double bond in the cyclohexenyl group to form a stable carbocation intermediate. Following this,the terminal amino group $(-NH_2)$ of the semicarbazide moiety acts as a nucleophile and attacks the carbocation. This intramolecular cyclization leads to the formation of a cyclic structure where the nitrogen atom is bonded to the same carbon atom of the cyclohexane ring,resulting in the final major product shown in option $B$.

Identify the major product of the following reaction:

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