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| Column - $(I)$ Product | Column - $(II)$ Preparation Process |
| $(A)$ Butan$-1-$ol | $(i)$ Hydration of propene in the presence of dilute sulfuric acid |
| $(B)$ Propan$-2-$ol | $(ii)$ Reaction of propanone with methylmagnesium bromide followed by hydrolysis |
| $(C)$ $2-$Methylpropan$-2-$ol | $(iii)$ Hydroboration of propene followed by reaction with $(NaOH + H_2O_2)$ |
| $(D)$ Propan$-1-$ol | $(iv)$ Catalytic reduction of butanal |
| Column-$I$ (Reaction) | Column-$II$ (Electrophile) |
| $A$. $C_6H_6 + CH_3Cl \xrightarrow{AlCl_3} C_6H_5CH_3$ | $P$. $CO_2$ |
| $B$. $C_6H_5OH + CO_2 \xrightarrow[H^+]{NaOH} \text{Salicylic acid}$ | $Q$. $:CCl_2$ |
| $C$. $C_6H_5OH + CHCl_3 \xrightarrow{KOH} \text{Salicylaldehyde}$ | $R$. $\stackrel{+}{C}H_3$ |
| $D$. $C_6H_6 + SO_3 \xrightarrow{H_2SO_4} C_6H_5SO_3H$ | $S$. $\stackrel{+}{S}O_3H$ |
| $T$. $SO_3$ |
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