Home
Class 12
CHEMISTRY
pK(a) value of 4-nitrobenzoic acid is l...

`pK_(a)` value of 4-nitrobenzoic acid is lower than that of benzoic acid. Why ?

Text Solution

AI Generated Solution

To understand why the pKa value of 4-nitrobenzoic acid is lower than that of benzoic acid, we can break down the explanation into a series of steps: ### Step 1: Understand the Structures - **4-Nitrobenzoic Acid**: This compound has a carboxylic acid group (-COOH) and a nitro group (-NO2) attached to a benzene ring. The nitro group is located at the para position relative to the carboxylic acid group. - **Benzoic Acid**: This compound has only the carboxylic acid group attached to the benzene ring without any substituents. ### Step 2: Define pKa - The pKa value is a measure of the acidity of a compound. A lower pKa value indicates a stronger acid, meaning it more readily donates protons (H⁺ ions). ...
Doubtnut Promotions Banner Mobile Dark
|

Topper's Solved these Questions

Similar Questions

Explore conceptually related problems

Account for the following : (a) Aromatic carboxylic acids do not undergo Friedel-Crafts reaction. (b) pK_(a) value of 4-nitrobenzoic acid is lower than that of benzoic acid .

How is benzoic acid converted to m-nitrobenzoic acid

How is benzoic acid converted to m-nitrobenzoic acid

How is benzoic acid converted to m-nitrobenzoic acid

Give reasons : (i) CH_(3)-CHO is more reactive than CH_(3)COCH_(3) towards HCN. (ii) 4-nitrobenzoic acid is more acidic than benzoic acid.

Why benzoic acid is a stronger acid than acetic acid?

How is benzoic acid converted to Benzoic anhydride

Explain why formic acid is stronger acid than benzoic acid.

Assertion:The pK_(a) of acetic acid is lower than that of phenol. Reason:Phenoxide ion is more resonance stablised.

Why is benzoic acid less soluble in water than acetic acid?