What is the product 'A' in the following reac | vedclass

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(B) The reaction involves the acid-catalyzed ring opening of an epoxide. $1$. The oxygen atom of the epoxide is protonated by $H_3O^{\oplus}$ to form

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(B) The reaction involves the acid-catalyzed ring opening of an epoxide. $1$. The oxygen atom of the epoxide is protonated by $H_3O^{\oplus}$ to form a better leaving group. $2$. The ring opens to form a more stable carbocation intermediate. In this specific structure,the epoxide ring is fused to a five-membered ring. $3$. The nucleophilic attack by water $(H_2O)$ occurs at the more substituted carbon of the epoxide,followed by deprotonation to yield the diol product. $4$. The structure corresponds to a cyclopentane ring with a $-CH_2OH$ group at the top position and a tertiary alcohol group ($-OH$ and $-CH_3$) at the adjacent carbon. Therefore,the correct product is represented by option $B$.

What is the product '$A$' in the following reaction?
(Image of an epoxide ring fused to a cyclopentane ring with an exocyclic double bond,reacting with $H_3O^{\oplus}$ to form $A$.)

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What is the product '$A$' in the following reaction?(Image of an epoxide ring fused to a cyclopentane ring with an exocyclic double bond,reacting with $H_3O^{\oplus}$ to form $A$.)