Which among the following is most reactive via $S_N2$ mechanism?

What is the major product of the following reaction?
$1\text{-methylcyclopentene} \xrightarrow[\text{Peroxide}]{\text{HBr}} ?$

Under the specified conditions,substrate $X$ undergoes substitution and elimination reactions to give products $A - D$. $A$ and $B$ are stereoisomers,but not enantiomers. $C$ and $D$ are enantiomers. $A$ is not an isomer of $C$. Which of the following could be the starting material $X$ ?
$X \xrightarrow[\Delta]{H_2O} A + B + C + D$

What is the product formed when $n$-propyl bromide is reacted with ethanolic potassium hydroxide?

Consider the following reaction sequence:
$Cyclohexylidene-methane$ $\xrightarrow[CH_3OH]{Br_2} A$ $\xrightarrow{KCN} B$
Identify the correct structures for $A$ and $B$ from the given options:
$A$ is:
$A) \text{ 1-(bromomethyl)-1-methoxycyclohexane}$
$B) \text{ 1-(methoxymethyl)-1-bromocyclohexane}$
$B$ is:
$C) \text{ 1-(bromomethyl)-1-methoxycyclohexane}$
$D) \text{ 1-(cyanomethyl)-1-methoxycyclohexane}$

$S_N^1$ and $S_N^2$ reactions are