Which of the following is product A in the ab | vedclass

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(B) The reaction involves the acid-catalyzed dehydration of an alcohol using $Conc. H_2SO_4$. $1$. The hydroxyl group is protonated to form an oxonium

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(B) The reaction involves the acid-catalyzed dehydration of an alcohol using $Conc. H_2SO_4$. $1$. The hydroxyl group is protonated to form an oxonium ion,which then leaves as $H_2O$ to form a carbocation. $2$. The resulting carbocation undergoes a cyclization reaction where the double bond of the cyclohexenyl ring attacks the carbocation center. $3$. This forms a bicyclic carbocation intermediate. $4$. Finally,the loss of a proton $(H^+)$ from the intermediate leads to the formation of the most stable alkene,which is the major product $A$.

Which of the following is product $A$ in the above reaction?

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