The product (C) of the reaction is: | vedclass

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(C) $1$. The starting material is bicyclopentylidene. Ozonolysis $(O_3/Zn)$ of this alkene cleaves the double bond to form two molecules of cyclopenta

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Cyclopentene

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(C) $1$. The starting material is bicyclopentylidene. Ozonolysis $(O_3/Zn)$ of this alkene cleaves the double bond to form two molecules of cyclopentanone $(A)$.$2$. Reduction of cyclopentanone $(A)$ with $H_2/Ni$ or $LiAlH_4$ yields cyclopentanol $(B)$.$3$. Acid-catalyzed dehydration of cyclopentanol $(B)$ with $H^+/\Delta$ results in the formation of cyclopentene $(C)$.

The product $(C)$ of the reaction is:

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