Which alkene undergoes ozonolysis to produce | vedclass

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(D) Ozonolysis of an alkene involves the cleavage of the $C=C$ double bond to form carbonyl compounds.For a cyclic alkene,ozonolysis results in an ope

Vedclass · Accepted Answer

$1,2-$dimethylcyclohexene

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(D) Ozonolysis of an alkene involves the cleavage of the $C=C$ double bond to form carbonyl compounds.For a cyclic alkene,ozonolysis results in an open-chain dicarbonyl compound.$2,6-$heptanedione is a $7-$carbon chain with ketone groups at positions $2$ and $6$.The structure is $CH_3-CO-CH_2-CH_2-CH_2-CO-CH_3$.This indicates that the original alkene was a cyclic compound with a $7-$carbon ring containing a double bond,specifically $1,2-$dimethylcyclohexene,where the double bond is between the carbons bearing the methyl groups. Upon ozonolysis,the $C=C$ bond breaks,and the ring opens to form the $7-$carbon chain with carbonyls at the ends of the original double bond positions.

Which alkene undergoes ozonolysis to produce $2,6-$heptanedione?

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