The reaction of compound $$P$$ with $$C{H_3}MgBr$$ (excess) in $${\left( {{C_2}{H_5}} \right)_2}O$$ followed by addition of $${H_2}O$$ gives $$Q.$$ The compound $$Q$$ on treatment with $${H_2}S{O_4}$$ at $${0^ \circ }C$$ gives $$R.$$ The reaction of $$R$$ with $$C{H_3}COCl$$ in the presence of anhydrous $$AlC{l_3}$$ in $$C{H_2}C{l_2}$$ followed by treatment with $${H_2}O$$ producess compound $$S.$$ [$$Et$$ in compound $$P$$ is ethyl group]

The reactions, $$Q$$ to $$R$$ and $$R$$ to $$S,$$ are

The reaction of compound $$P$$ with $$C{H_3}MgBr$$ (excess) in $${\left( {{C_2}{H_5}} \right)_2}O$$ followed by addition of $${H_2}O$$ gives $$Q.$$ The compound $$Q$$ on treatment with $${H_2}S{O_4}$$ at $${0^ \circ }C$$ gives $$R.$$ The reaction of $$R$$ with $$C{H_3}COCl$$ in the presence of anhydrous $$AlC{l_3}$$ in $$C{H_2}C{l_2}$$ followed by treatment with $${H_2}O$$ producess compound $$S.$$ [$$Et$$ in compound $$P$$ is ethyl group]

The product $$S$$ is

Columns 1, 2 and 3 contain starting materials, reaction conditions, and type of reactions, respectively.

	Column 1		Column 2		Column 3
(I)	Toluene	(i)	NaOH/Br2	(P)	Condensation
(II)	Acetophenone	(ii)	Br2/hv	(Q)	Carboxylation
(III)	Benzaldehyde	(iii)	(CH3CO)2O/ CH3COOK	(R)	Substitution
(IV)	Phenol	(iv)	NaOH/CO2	(S)	Haloform

For the synthesis of benzoic acid, the only CORRECT combination is

Columns 1, 2 and 3 contain starting materials, reaction conditions, and type of reactions, respectively.

	Column 1		Column 2		Column 3
(I)	Toluene	(i)	NaOH/Br2	(P)	Condensation
(II)	Acetophenone	(ii)	Br2/hv	(Q)	Carboxylation
(III)	Benzaldehyde	(iii)	(CH3CO)2O/ CH3COOK	(R)	Substitution
(IV)	Phenol	(iv)	NaOH/CO2	(S)	Haloform

The only CORRECT combination in which the reaction proceeds through radical mechanism is :