The major product expected from the following reaction is:
$2-(\text{carbamoyl})-3-(\text{hydroxymethyl})-6-(\text{hydroxy})\text{benzoic acid} \xrightarrow{HCl_{(g)} / CCl_4} ?$

Ethanol on reaction with acetic anhydride gives

Statement $(A)$: Carboxylic acid can be obtained by the reaction of $R-C \equiv N$ with $H_3O^+$ under mild reaction conditions.
Statement $(B)$: Hydrolysis of $R-C \equiv N$ in alkaline aqueous medium gives $R-COONa$ and $NH_3$ as products.
The correct answer is:

Find out the major products $A$ and $B$ from the following reaction sequence.

Give the conversion of the following:
$(i)$ Phthalimide from $o-xylene$
$(ii)$ Ethanol from Ethanoic anhydride

At which value of $n$ does the formation of a six-membered ring take place in the following reaction?
$Br-(CH_2)_n-CH_2-Br + CH_2(CO_2Et)_2 \xrightarrow{NaOEt, EtOH} \text{cyclic product}$