| Column-$I$ (Reaction) | Column-$II$ (Condition) |
|---|---|
| $(A)$ $CH_3-CH(OH)-CH_3 \rightarrow CH_3-CH=CH_2$ | $(i)$ $20\% \ H_3PO_4, 358 \ K$ |
| $(B)$ $CH_3-C(CH_3)_2-OH \rightarrow CH_3-C(CH_3)=CH_2$ | (ii) $Cu, 573 \ K$ |
| $(C)$ $CH_3CH_2OH \rightarrow CH_2=CH_2 + H_2O$ | (iii) $85\% \ H_3PO_4, 440 \ K$ |
| $(D)$ $R-CH(OH)-R' \rightarrow R-CO-R'$ | (iv) $H_2SO_4, 443 \ K$ |
Explore More
| Column-$I$ | Column-$II$ |
| $A$. Methanol | $p$. Conversion of phenol to salicylic acid |
| $B$. Kolbe's reaction | $q$. Wood spirit |
| $C$. Williamson's reaction | $r$. Vapours are passed over heated copper at $573 \ K$ |
| $D$. Conversion of $2^\circ$ alcohol to ketone | $s$. Reaction of alkyl halide with sodium alkoxide |
| Column $(I)$ | Column $(II)$ |
| $(A)$ Kolbe's reaction | $(i)$ Salicylaldehyde |
| $(B)$ Reimer-Tiemann reaction | $(ii)$ Ethers |
| $(C)$ Williamson synthesis | $(iii)$ Ethanol |
| $(D)$ Fermentation | $(iv)$ Salicylic acid |
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