$A$ $(C_3H_6O)$ $\xrightarrow{NaCN/H_2SO_4}$ cyanohydrin of $A$. If the cyanohydrin is optically active,then the possible structure of $A$ is:

The reagent used in the Wolff-Kishner reduction is:

Which compound does not form iodoform with alkali and iodine?

Which of the following gives the iodoform test?

Match the reactions in Column-$I$ with their products in Column-$II$.
| Column-$I$ (Reagents) | Column-$II$ (Product) |
| :--- | :--- |
| $(A) \ CH_3CHO + 2C_2H_5OH \xrightarrow{HCl_{(g)}} $ | $(i) \ (CH_3)_2C(OCH_2)_2$ |
| $(B) \ CH_3COCH_3 + CH_2OH-CH_2OH \xrightarrow{HCl_{(g)}} $ | $(ii) \ CH_3CH(OH)CN$ |
| $(C) \ CH_3CHO + HCN$ $\xrightarrow{OH^-}$ $\xrightarrow{H_3O^+}$ | $(iii) \ CH_3CH(OC_2H_5)_2$ |
| $(D) \ CH_3CHO + HCN \xrightarrow{OH^-} $ | $(iv) \ CH_3CH(OH)COOH$ |

In the given reaction sequence,$Z$ is a mixture of alcohol and acid. The reaction for the conversion of $Y$ to $Z$ is:
$CH_3CH_2OH$ $\xrightarrow[443 \ K]{\text{Conc. } H_2SO_4} X$ $\xrightarrow[(2) \ Zn/H_2O]{(1) \ O_3} Y$ $\xrightarrow[(ii) \ H^+]{(i) \ \text{Conc. } NaOH} Z$