The conversion of cyclohexene to HO-(CH_2)_6- | vedclass

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(D) The target molecule is hexane$-1,6-$diol. Let's analyze the options:$1$. $O_3, Zn/H_2O$ (reductive ozonolysis) converts cyclohexene to hexane$-1,6

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All of these

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(D) The target molecule is hexane$-1,6-$diol. Let's analyze the options:$1$. $O_3, Zn/H_2O$ (reductive ozonolysis) converts cyclohexene to hexane$-1,6-$dial. Subsequent reduction with $LiAlH_4$ gives hexane$-1,6-$diol.$2$. $O_3/H_2O_2$ (oxidative ozonolysis) converts cyclohexene to adipic acid (hexane$-1,6-$dioic acid). Subsequent reduction with $LiAlH_4$ gives hexane$-1,6-$diol.$3$. Cold dil. $KMnO_4$ (Baeyer's reagent) converts cyclohexene to cyclohexane$-1,2-$diol. Treatment with $HIO_4$ (periodic acid) cleaves the diol to hexane$-1,6-$dial. Subsequent reduction with $LiAlH_4$ gives hexane$-1,6-$diol.Since all three pathways lead to the desired product,the correct answer is $D$.

List-$I$	List-$II$
$A.$ Butane $\to$ Isobutane	$(a).$ Cracking
$B.$ Butane $\to$ Lower hydrocarbons	$(b).$ Isomerisation
$C.$ $n-$Heptane $\to$ Toluene	$(c).$ Reed reaction
$D.$ Propane $\to CH_3CH_2CH_2SO_2Cl$	$(d).$ Aromatization

The conversion of cyclohexene to $HO-(CH_2)_6-OH$ can be achieved by:

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