Question:

The following carboxylic acids have a general formula, R-COOH.
(i) HCOOH
(ii) CH\(_3\) - COOH
(iii) ClCH\(_2\) - COOH
(iv) CF\(_3\) - COOH
Which one of the following represents the decreasing order of their respective pK\(_a\) values?

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Electronegative groups, especially halogens, lower the pK\(_a\) of carboxylic acids by making the hydrogen easier to lose, thus increasing acidity.
Updated On: Dec 4, 2025
  • i > ii > iii > iv
  • ii > i > iv > iii
  • iv > iii > i > ii
  • iv > iii > ii > i
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The Correct Option is B

Solution and Explanation

To arrange the given carboxylic acids in decreasing order of their pKa values, we need to understand the relationship between the structure of carboxylic acids and their acidity.

The pKa value is a measure of the strength of an acid. The lower the pKa, the stronger the acid. This is because a strong acid dissociates more completely in solution, releasing more protons (H+ ions).

In carboxylic acids, the presence of electron-withdrawing groups increases acidity (thus lowering the pKa) by stabilizing the negative charge on the conjugate base (carboxylate ion) through resonance or induction. Conversely, electron-donating groups decrease acidity (thus increasing the pKa).

  1. HCOOH (Formic acid): This acid has no additional groups attached besides the carboxyl group, so it exhibits the baseline acidity of carboxylic acids.
  2. CH3COOH (Acetic acid): The CH3 group is slightly electron-donating, which makes acetic acid less acidic than formic acid. Hence, it has a higher pKa than formic acid.
  3. ClCH2COOH (Chloroacetic acid): The Cl group is highly electronegative and acts as an electron-withdrawing group through induction, thus making chloroacetic acid more acidic than both formic and acetic acids.
  4. CF3COOH (Trifluoroacetic acid): The CF3 group is even more electron-withdrawing than the Cl group because F is more electronegative and there are three F atoms, making trifluoroacetic acid the most acidic among these compounds. Therefore, it has the lowest pKa value.

Thus, the order of decreasing pKa values (i.e., increasing acidity) is as follows:

  • CH3COOH (ii) > HCOOH (i) > CF3COOH (iv) > ClCH2COOH (iii)

Hence, the correct order is indeed ii > i > iv > iii.

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