Which one of the following compounds gives ac | vedclass

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(D) Ozonolysis of an alkene involves the cleavage of the $C=C$ double bond to form carbonyl compounds. If the alkene has the structure $R_2C=CR'_2$,th

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isopropylidenecyclohexane

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(D) Ozonolysis of an alkene involves the cleavage of the $C=C$ double bond to form carbonyl compounds. If the alkene has the structure $R_2C=CR'_2$,the products will be $R_2C=O$ and $R'_2C=O$. To obtain acetone $(CH_3)_2C=O$,the starting alkene must contain an isopropylidene group,i.e.,$(CH_3)_2C=$ moiety. Among the given options,isopropylidenecyclohexane has the structure where a cyclohexyl ring is double-bonded to a carbon atom that is also attached to two methyl groups. Upon ozonolysis,the $C=C$ bond breaks to yield cyclohexanone and acetone $(CH_3)_2C=O$.

Which one of the following compounds gives acetone $(CH_3)_2C=O$ as one of the products of its ozonolysis?

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