The major products $A$ and $B$ in the following set of reactions are:

The final product $[D]$ of the reaction is
$CHCl_3$ $\xrightarrow[hv]{O_2} [A]$ $\xrightarrow{EtOH} [B]$ $\xrightarrow{2 \ mole \ MeMgBr} [C]$ $\xrightarrow{CaOCl_2} [D]$ $\xrightarrow{\Delta} CH_3-C(=O)-CH_3$

An organic compound $[A]$,molecular formula $C_{10}H_{20}O_2$,was hydrolyzed with dilute sulphuric acid to give a carboxylic acid $[B]$ and an alcohol $[C]$. Oxidation of $[C]$ with $CrO_3-H_2SO_4$ produced $[B]$. Which of the following structures are not possible for $[A]$?

Which of the following undergoes decarboxylation most readily on being heated?

Choose the response that matches the correct functional group classification with the following group of structural formulas.

The desired product $X$ $(\text{Ph-C(Me)(Ph)-COOH})$ can be prepared by reacting the major product of the reactions in List-$I$ with one or more appropriate reagents in List-$II$. (Given,order of migratory aptitude: $\text{aryl} > \text{alkyl} > \text{hydrogen}$)
| List-$I$ | List-$II$ |
| :--- | :--- |
| $P$. $\text{Ph}_2\text{C(OH)-C(OH)Me}_2 + \text{H}_2\text{SO}_4$ | $1$. $\text{I}_2, \text{NaOH}$ |
| $Q$. $\text{Ph}_2\text{C(NH}_2\text{)-CH(OH)Me} + \text{HNO}_2$ | $2$. $[\text{Ag(NH}_3)_2]\text{OH}$ |
| $R$. $\text{PhC(OH)(Me)-C(OH)(Ph)Me} + \text{H}_2\text{SO}_4$ | $3$. $\text{Fehling solution}$ |
| $S$. $\text{Ph}_2\text{C(Br)-CH(OH)Me} + \text{AgNO}_3$ | $4$. $\text{HCHO, NaOH}$ |
| | $5$. $\text{NaOBr}$ |