Ozonolysis of the given compound yields:

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(D) The given compound is bicyclo[$3.3$.$0$]oct$-1-$ene. Ozonolysis involves the cleavage of the carbon-carbon double bond $(C=C)$ followed by oxidati

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(D) The given compound is bicyclo[$3.3$.$0$]oct$-1-$ene. Ozonolysis involves the cleavage of the carbon-carbon double bond $(C=C)$ followed by oxidation to form carbonyl compounds. In this case,the double bond is at the bridgehead position. Upon ozonolysis,the ring opens to form a $1,6$-dicarbonyl compound,specifically $1,6$-cyclodecanedione.

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