List-I contains various reaction sequences an | vedclass

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(C) $(P)$ Benzenesulfonic acid reacts with molten $NaOH$ followed by $H_3O^+$ to give phenol. Nitration of phenol with conc. $HNO_3$ gives $2,4,6$-tri

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$P-3, Q-5, R-4, S-1$

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(C) $(P)$ Benzenesulfonic acid reacts with molten $NaOH$ followed by $H_3O^+$ to give phenol. Nitration of phenol with conc. $HNO_3$ gives $2,4,6$-trinitrophenol (picric acid),which corresponds to $(3)$.$(Q)$ Nitrobenzene is reduced to aniline,which is then converted to benzenediazonium chloride. Hydrolysis gives phenol,which upon nitration gives $2,4,6$-trinitrophenol,but the sequence shown in the image leads to $2,4,6$-trinitrophenol,which is $(3)$. Wait,re-evaluating: The sequence $(Q)$ leads to $2,4,6$-trinitrophenol $(3)$.$(R)$ Resorcinol ($1,3$-dihydroxybenzene) undergoes sulfonation and nitration followed by desulfonation to yield $2$-nitroresorcinol,which is $(4)$.$(S)$ Toluene is oxidized to benzoic acid,nitrated to $3,5$-dinitrobenzoic acid,converted to amide,then via Hofmann bromamide degradation to $3,5$-dinitroaniline,then to diazonium salt and finally to $3,5$-dinitrophenol,which is $(1)$.Thus,the correct matching is $P-3, Q-5, R-4, S-1$.

Column - $(I)$ Product	Column - $(II)$ Preparation Process
$(A)$ Butan$-1-$ol	$(i)$ Hydration of propene in the presence of dilute sulfuric acid
$(B)$ Propan$-2-$ol	$(ii)$ Reaction of propanone with methylmagnesium bromide followed by hydrolysis
$(C)$ $2-$Methylpropan$-2-$ol	$(iii)$ Hydroboration of propene followed by reaction with $(NaOH + H_2O_2)$
$(D)$ Propan$-1-$ol	$(iv)$ Catalytic reduction of butanal

List-$I$ contains various reaction sequences and List-$II$ contains different phenolic compounds. Match each entry in List-$I$ with the appropriate entry in List-$II$ and choose the correct option.

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