Which of the reactants given below is/are sui | vedclass

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(B) For the preparation of Methoxybenzene $(C_6H_5OCH_3)$,the Williamson ether synthesis is used.In reaction $(x)$,$C_6H_5Br + CH_3ONa$,the $C-Br$ bon

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Only $y$

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(B) For the preparation of Methoxybenzene $(C_6H_5OCH_3)$,the Williamson ether synthesis is used.In reaction $(x)$,$C_6H_5Br + CH_3ONa$,the $C-Br$ bond in bromobenzene has partial double bond character due to resonance,making it resistant to nucleophilic substitution. Thus,it does not undergo the reaction.In reaction $(y)$,$C_6H_5ONa + CH_3Br$,sodium phenoxide acts as a nucleophile and attacks the methyl bromide $(CH_3Br)$ via an $S_N2$ mechanism to form Methoxybenzene. Therefore,only reaction $(y)$ is suitable.

Which of the reactants given below is/are suitable for the preparation of Methoxybenzene?
$(x)$ $C_6H_5Br + CH_3ONa$
$(y)$ $C_6H_5ONa + CH_3Br$

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Which of the reactants given below is/are suitable for the preparation of Methoxybenzene?$(x)$ $C_6H_5Br + CH_3ONa$$(y)$ $C_6H_5ONa + CH_3Br$