What will be the product in the following reaction?
$1$-chloro-$1$-methylcyclohexane $\xrightarrow{H_2O}$ ?

  • A
    $1-$methylcyclohexanol
  • B
    $1-$isopropylcyclohexanol
  • C
    $2,2-$dimethylcyclohexanol
  • D
    $1-$methylcyclohexanol (with rearrangement)

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Most reactive for $S_{N}1$ reaction is

In $S_{N}2$ reactions,the correct order of reactivity for the following compounds:

Hydrolysis of a gem-dihalide gives $....$.

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Identify the major product for the following reaction:
$1$-fluoro-$1$-methylcyclohexane $\xrightarrow[\Delta]{Alc. KOH}$ ?

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For the following compounds,the correct statement$(s)$ with respect to nucleophilic substitution reactions is(are):
$I$: Benzyl bromide $(C_6H_5CH_2Br)$
$II$: Cyclohexylmethyl bromide $(C_6H_{11}CH_2Br)$
$III$: tert-Butyl bromide $((CH_3)_3CBr)$
$IV$: $1-$Phenylethyl bromide $(C_6H_5CH(CH_3)Br)$
$A$. $I$ and $III$ follow $S_{N}1$ mechanism
$B$. $I$ and $II$ follow $S_{N}2$ mechanism
$C$. Compound $IV$ undergoes inversion of configuration
$D$. The order of reactivity for $I$,$III$ and $IV$ is: $IV > I > III$

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