Identify the reaction schemes A, B, C for the | vedclass

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(C) The starting material is vinylcyclohexane. Let's analyze the products:$1$. Product $A$ is $2$-cyclohexylethanol,which is an anti-Markovnikov produ

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$II, III, I$

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(C) The starting material is vinylcyclohexane. Let's analyze the products:$1$. Product $A$ is $2$-cyclohexylethanol,which is an anti-Markovnikov product. This is formed by hydroboration-oxidation $(II)$.$2$. Product $B$ is $1$-cyclohexylethanol,which is a Markovnikov product formed without rearrangement. This is characteristic of oxymercuration-demercuration $(III)$.$3$. Product $C$ is $1$-ethyl$-1-$cyclohexanol,which is a Markovnikov product formed via rearrangement (carbocation intermediate). This is characteristic of acid-catalyzed hydration $(I)$.Therefore,the sequence $A, B, C$ corresponds to $II, III, I$.

Identify the reaction schemes $A, B, C$ for the conversion of vinylcyclohexane to the respective alcohols,given the following methods:
$I-$ Acid-catalyzed hydration
$II-$ Hydroboration-oxidation $(HBO)$
$III-$ Oxymercuration-demercuration

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Identify the reaction schemes $A, B, C$ for the conversion of vinylcyclohexane to the respective alcohols,given the following methods:$I-$ Acid-catalyzed hydration$II-$ Hydroboration-oxidation $(HBO)$$III-$ Oxymercuration-demercuration