Question:

What will be the correct decreasing order of acid strength of the hydroxybenzoic acids? (Symbols and notations carry their usual meanings)

Updated On: Jun 14, 2022
  • $ p $-Hydroxybenzoic acid $ > $ benzoic acid $ > m $-hydroxybenzoic acid $ > o $-hydroxybenzoic acid
  • $ o $-Hydroxybenzoic acid $ > m $-hydroxybenzoic acid $ > $ benzoic acid $ > p $-hydroxybenzoic acid
  • $ o $-Hydroxybenzoic acid $ > $ benzoic acid $ > m $-hydroxybenzoic acid $ > p $-hydroxybenzoic acid
  • $ m $-Hydroxybenzoic acid $ > $ benzoic acid $ > o $-hydroxybenzoic acid $ > p $ -hydroxybenzoic acid
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The Correct Option is B

Solution and Explanation

In case of hydroxybenzoic acids, they display both kind of effect and there is a decrease in electron density at all positions due to inductive effect of $-OH$ group, but increase in electron density at $o$- and $p$- positions due to resonance effect by $-OH$ group . So, $o$- p-hydroxybenzoic acids should be weaker than m-hydroxybenzoic acid, but $o$-hydroxybenzoic acid is strongest due to stabilisation of anion by hydrogen bonding


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Concepts Used:

Aldehydes, Ketones, and Carboxylic Acids

Aldehydes, Ketones, and Carboxylic Acids are carbonyl compounds that contain a carbon-oxygen double bond. These organic compounds are very important in the field of organic chemistry and also have many industrial applications.

Aldehydes:

Aldehydes are organic compounds that have the functional group -CHO.

Preparation of Aldehydes

Acid chlorides are reduced to aldehydes with hydrogen in the presence of palladium catalyst spread on barium sulfate.

Ketones:

Ketones are organic compounds that have the functional group C=O and the structure R-(C=O)-R’.

Preparation of Ketones

Acid chlorides on reaction with dialkyl cadmium produce ketones. Dialkyl cadmium themselves are prepared from Grignard reagents.

Carboxylic Acid:

Carboxylic acids are organic compounds that contain a (C=O)OH group attached to an R group (where R refers to the remaining part of the molecule).

Preparation of Carboxylic Acids

Primary alcohols are readily oxidized to carboxylic acids with common oxidizing agents such as potassium permanganate in neutral acidic or alkaline media or by potassium dichromate and chromium trioxide in acidic media.