The order of reactivity of alkyl halides for dehydrohalogenation is:

What will be the reduction products of the following reactions:
$CHCl_3 \xrightarrow[Zn/HCl \text{ (alc.)}]{+2H}$
$CHCl_3 \xrightarrow[Zn/HCl \text{ (aq.)}]{+4H}$
$CHCl_3 \xrightarrow[Zn/H_2O]{+6H}$

Which alkyl halide has maximum density?

The major product formed when $1$-Bromo-$3$-chlorocyclobutane reacts with metallic sodium in dry ether is

Which of the following haloalkanes reacts with aqueous $KOH$ most easily? Explain giving reason.
$(i)$ $1$-Bromobutane
$(ii)$ $2$-Bromobutane
$(iii)$ $2$-Bromo-$2$-methylpropane
$(iv)$ $2$-Chlorobutane

The mechanism of $S_{N}1$ reaction is given as:
$R-X$ $\rightarrow R^{\oplus} X^{\ominus}$ $\rightarrow R^{\oplus} | X^{\ominus}$ $\xrightarrow{Y^{\ominus}} R-Y + X^{\ominus}$
(Ion pair) (Solvent separated ion pair)
$A$ student writes general characteristics based on the given mechanism as:
$(a)$ The reaction is favoured by weak nucleophiles
$(b)$ $R^{\oplus}$ would be easily formed if the substituents are bulky
$(c)$ The reaction is accompanied by racemization
$(d)$ The reaction is favoured by non-polar solvents.
Which observations are correct?