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(A) The reaction of methylenecyclohexane with $BH_3$ followed by oxidation with $H_2O_2/OH^-$ is a Hydroboration-Oxidation $(HBO)$ reaction.This react

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Cyclohexylmethanol

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(A) The reaction of methylenecyclohexane with $BH_3$ followed by oxidation with $H_2O_2/OH^-$ is a Hydroboration-Oxidation $(HBO)$ reaction.This reaction proceeds via the anti-Markovnikov addition of water $(H-OH)$ across the double bond.In methylenecyclohexane,the exocyclic double bond is between the ring carbon and the terminal $CH_2$ group.The $OH$ group attaches to the less substituted carbon (the terminal $CH_2$ group),resulting in the formation of cyclohexylmethanol.

Suppose the following reaction,the major product will be:

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$I$. $(CH_3)_2 C=CH_2 \xrightarrow{KMnO_4 / H^{+}} X + CO_2 + H_2 O$
$II$. $CH_3-CH=CH-CH_3 \xrightarrow{KMnO_4 / H^{+}} Y$
The functional groups in $X$ and $Y$ are respectively

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Which of the following alkenes is the most stable?

Select the suitable reagent for the conversion shown below:

The major products $P$ and $Q$ in the following reaction sequence are:

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