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(B) The reaction with hot $KMnO_4/H^+$ is an oxidative cleavage reaction,similar to oxidative ozonolysis.It cleaves double bonds to form carboxylic ac

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$3-$vinylcyclohex$-1-$ene

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(B) The reaction with hot $KMnO_4/H^+$ is an oxidative cleavage reaction,similar to oxidative ozonolysis.It cleaves double bonds to form carboxylic acids or ketones,and terminal double bonds are oxidized to $CO_2$ and $H_2O$.The product shown is a substituted pentanedioic acid derivative with a $CO_2$ byproduct.Analyzing the structure of the product,it corresponds to the oxidative cleavage of $3$-vinylcyclohex-$1$-ene (Option $B$).The double bond in the ring at position $1$ and the vinyl group at position $3$ are cleaved to yield the observed dicarboxylic acid and $CO_2$.

Which of the following compounds was the starting material for the oxidation shown below?

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