The structure of the product P of the followi | vedclass

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(D) The reaction is a Kolbe-Schmitt reaction. $1$. $4$-Methoxyphenol reacts with $NaOH$ to form sodium $4$-methoxyphenoxide. $2$. The phenoxide ion is

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(D) The reaction is a Kolbe-Schmitt reaction. $1$. $4$-Methoxyphenol reacts with $NaOH$ to form sodium $4$-methoxyphenoxide. $2$. The phenoxide ion is highly reactive towards electrophilic aromatic substitution. $3$. The $-O^-$ group is a strong ortho/para directing group. Since the para position is already occupied by the $-OMe$ group, the electrophile $(CO_2)$ attacks the ortho position relative to the $-O^-$ group. $4$. Subsequent acidification with $H_3O^+$ yields the final product, $2$-hydroxy-$5$-methoxybenzoic acid.

The structure of the product $P$ of the following reaction is

Similar Questions

Assertion : Phenol is a stronger acid than ethanol.
Reason : Groups with $+M$ effect decrease acidity at $p-$position.

The major product of the following reaction is:

Arrange the following in increasing order of acidic character.

The product $(B)$ will be:

Which compound has the highest value of $pK_{a}$?

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