



To determine which pair of structures will give different products on ozonolysis, let's understand the ozonolysis reaction. Ozonolysis is a reaction where ozone (O3) cleaves the carbon-carbon double bonds in alkenes to form carbonyl compounds (aldehydes or ketones).
Consider the fact that the double bonds in the structures are rigid and not delocalized, meaning the stereochemistry around the double bond can lead to different products depending on the substitution pattern.
Let us evaluate each pair:
Based on this analysis, the third pair will give different products on ozonolysis because of the distinct substitution pattern around the double bonds in the two structures.
Conclusion: The correct answer is the third pair
as they will produce different carbonyl products upon ozonolysis.
Aman has been asked to synthesise the molecule:

Using an aldol condensation reaction. He found a few cyclic alkenes in his laboratory.
He thought of performing ozonolysis reaction on the alkene to
produce a dicarbonyl compound followed by aldol reaction to prepare "x".
Predict the suitable alkene that can lead to the formation of "x".
