- A$B{r_2}$ in bright sunlight (in the absence of a catalyst)
- ✓$C{l_2}$ in bright sunlight (in the absence of a catalyst)
- C$C{H_3}Cl$ in the presence of anhydrous $AlC{l_3}$
- D$COC{l_2}$ in the presence of anhydrous $AlC{l_3}$

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$(i) \,\,\begin{array}{*{20}{c}}
{C{H_3}\,\,\,\,\,\,\,\,\,\,\,} \\
{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} \\
{C{H_3} - C - CH - C{H_3}} \\
{\,\,\,\,\,|} \\
{\,\,\,\,\,\,\,\,\,\,\,\,OH}
\end{array}\,\xrightarrow{{{H^ + }/heat}}\,\,\mathop A\limits_{[Major\,product]} \, + \,\mathop B\limits_{[Minor\,product]} $
$(ii)\,\, A\xrightarrow[{in\,\,absence\,\,\,of\,peroxide}]{{HBr,\,dark}}\,\,\mathop C\limits_{[Major\,product]} \, + \,\mathop D\limits_{[Minor\,product]} $
the major products $(A)$ and $(C)$ are respectively
(Image)
$IUPAC$ name of Compound $A$ is $4-$ chloro-$1$, $3$-dinitrobenzene:
(Image)
$IUPAC$ name of Compound $B$ is
$4$-ethyl-$2$-methylaniline.
In the light of the above statements, choose the most appropriate answer from the options given below:
