An alkene (X) on ozonolysis followed by reduc | vedclass

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(A) Ozonolysis cleaves $C=C$ bonds to form carbonyl compounds.Given products are $2$ moles of $HCHO$ (formaldehyde), $HCOCHO$ (glyoxal), and $CH_3COCO

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(A) Ozonolysis cleaves $C=C$ bonds to form carbonyl compounds.Given products are $2$ moles of $HCHO$ (formaldehyde), $HCOCHO$ (glyoxal), and $CH_3COCOCH_3$ (butane$-2,3-$dione).By analyzing the fragments, we can reconstruct the original cyclic alkene structure.$HCHO$ comes from terminal $=CH_2$ groups.$HCOCHO$ and $CH_3COCOCH_3$ represent the internal segments of the ring.By connecting these fragments, we find that the structure corresponds to $1,2,4,5$-tetramethylenecyclohexane or a similar derivative based on the provided options. Based on the standard chemical analysis of such ozonolysis products, the structure is identified as option $A$.

An alkene $(X)$ on ozonolysis followed by reduction gives the following products: $H-CHO$ ($2$ moles), $H-CO-CHO$, and $CH_3-CO-CO-CH_3$. The alkene $(X)$ is:

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