| Column-$I$: Compound / Reagent | Column-$II$: Other name / Chemical / Process |
|---|---|
| $A$. Methanol | $I$. Lucas reagent |
| $B$. $ZnCl_2$ / Conc. $HCl$ | $II$. Baeyer's reagent |
| $C$. Rectified spirit | $III$. Wood spirit |
| $D$. Dil. $KMnO_4$ | $IV$. $95 \% C_2H_5OH$ |
| - | $V$. $75 \% C_2H_5OH$ |
| - | $VI$. $90 \% C_3H_7OH$ |
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| Column-$I$ | Column-$II$ |
|---|---|
| $(i)$ $2-$methylphenol | $(a)$ Hydroquinone |
| $(ii)$ Benzene$-1,2-$diol | $(b)$ Phenetole |
| $(iii)$ Benzene$-1,3-$diol | $(c)$ Catechol |
| $(iv)$ Benzene$-1,4-$diol | $(d)$ $o$-Cresol |
| $(v)$ Methoxybenzene | $(e)$ Quinone |
| $(vi)$ Ethoxybenzene | $(f)$ Resorcinol |
| $(g)$ Anisole |
| Column-$I$ (Reaction) | Column-$II$ (Mechanism) |
| $A$. $CH_3OCH_2CH_3 + HI \to CH_3I + CH_3CH_2OH$ | $i$. $S_{E}2$ Aromatic |
| $B$. $(CH_3)_3COCH_3 + HI \to CH_3OH + (CH_3)_3CI$ | $ii$. $S_{N}1$ |
| $C$. $C_6H_5OCH_3 + Br_2(CH_3COOH) \to p$-Bromoanisole | $iii$. Elimination $(\beta)$ |
| $D$. $CH_3CH_2OH + H_2SO_4 (443 \ K) \to CH_2=CH_2$ | $iv$. $S_{N}2$ |
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