The increasing rate of $S_N1$ reaction in the following compounds is:

The order of reactivity of the following compounds towards dilute aqueous $KOH$ in $SN_1$ reaction is
$I$. $CH_3CH_2CH_2CH_2Br$
$II$. $CH_3CH_2CHBrCH_3$
$III$. $(CH_3)_2CHCH_2Br$
$IV$. $(CH_3)_3CBr$

Which of the following statements is correct for optically active alkyl halides,upon reaction with nucleophiles?

	$S_{N}1$	$S_{N}2$
$(a)$	Retention of configuration	Inversion of configuration
$(b)$	Racemisation	Inversion of configuration
$(c)$	Inversion of configuration	Retention of configuration
$(d)$	Racemisation	Retention of configuration

The reaction of $3$-bromocyclohexene with $HBr$ yields $P_1$ and $P_2$ as major dibromo products. What is the relationship between $P_1$ and $P_2$?

The major product of the reaction is:

Which compound in each of the following pairs will react faster in $S_N2$ reaction with $OH^{-}$?
$(i)$ $CH_3-Br$ or $CH_3-I$
$(ii)$ $CH_3-C(CH_3)_2-Cl$ or $CH_3-Cl$