Explain two differences between haloalkanes and haloarenes.

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(N/A) The two main differences between haloalkanes and haloarenes are as follows:
$1$. Structure: In haloalkanes,the halogen atom is bonded to an $sp^3$ hybridized carbon atom of an alkyl group. In haloarenes,the halogen atom is directly bonded to an $sp^2$ hybridized carbon atom of an aromatic ring.
$2$. Reactivity towards Nucleophilic Substitution: Haloalkanes are generally more reactive towards nucleophilic substitution reactions compared to haloarenes. Haloarenes show low reactivity due to resonance effects,which give the $C-X$ bond partial double bond character,and the instability of the phenyl cation.

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Identify the correct order of reactivity for the following pairs towards the respective mechanism:
$(A)$ $S_{N}2$: Isobutyl bromide > tert-Butyl bromide
$(B)$ $S_{N}1$: Benzyl bromide > $2-$Phenylethyl bromide
$(C)$ Electrophilic substitution: Chlorobenzene > $1-$Chloro$-4-$nitrobenzene
$(D)$ Nucleophilic substitution: Bromobenzene < $1-$Bromo$-4-$nitrobenzene
Choose the correct answer from the options given below:

Match the reactants in Column-$(I)$ with the products formed in Column-$(II)$.
Column-$(I)$ (Reactants)Column-$(II)$ (Major Products)
$(A)$ $C_6H_5CH_3 + X_2 \xrightarrow{Fe, \text{dark}}$$(i)$ $C_6H_5CH(Br)CH_3$
$(B)$ $C_6H_5NH_2 \xrightarrow{NaNO_2, HX, 273-278 \ K}$$(ii)$ $C_6H_5N_2^+X^-$
$(C)$ $C_6H_5N_2^+X^- \xrightarrow{Cu_2X_2}$$(iii)$ $p-X-C_6H_4CH_3 + o-X-C_6H_4CH_3$
$(D)$ $C_6H_5CH_2CH_3 \xrightarrow{Br_2, \Delta \text{ or } UV \text{ light}}$$(iv)$ $C_6H_5X$

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The total number of hydrogen atoms in product $A$ and product $B$ is $ . . . . . . $.

In the given reaction,$[X]$ will be:

The product$(s)$ formed during the following reaction is/are:
$Ph-CH_2-C^*H_2-OTs \xrightarrow{AcONa, AcOH} \text{Product(s)} \ [C^* = \text{isotopic carbon}]$

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