$3$-Phenylpropene on reaction with $HBr$ gives (as a major product)

In the given pairs of alkyl halides,in which pair is the first compound more reactive than the second compound toward $S_N2$ reaction?

Given below are two statements:
Statement $I$: $(CH_3)_3C-CH_2-Cl$ will undergo $S_N1$ reaction even though it is a primary halide.
Statement $II$: It will not undergo $S_N2$ reaction very easily even though it is a primary halide.
In the light of the above statements,choose the most appropriate answer from the options given below:

What is the major product of the following reaction?
$1\text{-methylcyclohexene} \xrightarrow{Br_2, H_2O} ?$

$A$ solution of $D(+)-1-$chloro$-1-$phenylethane in toluene racemises slowly in the presence of a small amount of $SbCl_5$,due to the formation of:

Among the following chlorides, the compounds which will be hydrolysed most easily and most slowly in aqueous $NaOH$ solution are respectively:
$1$. Methoxymethyl chloride $(CH_3OCH_2Cl)$
$2$. Benzyl chloride $(C_6H_5CH_2Cl)$
$3$. Neopentyl chloride $((CH_3)_3CCH_2Cl)$
$4$. Propyl chloride $(CH_3CH_2CH_2Cl)$