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Sodium Bicarbonate Test: Detection of Carboxylic Acids | Chemca

Sodium Bicarbonate Test: Detection of Carboxylic Acids | Chemca
Organic Chemistry

Sodium Bicarbonate Test: Identifying Carboxylic Acids

By Chemca Editorial Team Last Updated: January 2026 6 min read

The Sodium Bicarbonate Test (or Sodium Hydrogen Carbonate test) is the primary qualitative test used to detect the presence of Carboxylic Acids ($R-COOH$). It relies on the acidity difference between carboxylic acids and carbonic acid.

1. General Reaction

When a carboxylic acid reacts with aqueous Sodium Bicarbonate ($NaHCO_3$), it displaces the weaker carbonic acid, which decomposes to release Carbon Dioxide ($CO_2$) gas.

$$ R-COOH + NaHCO_3 \longrightarrow R-COO^-Na^+ + H_2O + \underbrace{CO_2 \uparrow}_{\text{Brisk Effervescence}} $$

Observation: The rapid evolution of colorless, odorless gas bubbles (Brisk Effervescence) indicates a positive test.

2. The Principle: Acid Strength

Rule of Displacement

A stronger acid displaces a weaker acid from its salt.
Reaction occurs if: $\text{Acidity of Reactant Acid} > \text{Acidity of } H_2CO_3$.

Acidity Order ($pK_a$)

  • Sulfonic Acids ($R-SO_3H$): $pK_a \approx -2$ (Very Strong)
  • Carboxylic Acids ($R-COOH$): $pK_a \approx 4-5$ (Stronger)
  • Carbonic Acid ($H_2CO_3$): $pK_a \approx 6.4$ (Weak)
  • Phenols ($Ph-OH$): $pK_a \approx 10$ (Weaker)
  • Alcohols ($R-OH$): $pK_a \approx 16$ (Weakest)

3. Distinguishing Phenols from Acids

This is the most common application in exams.

Carboxylic Acids

Since $RCOOH$ is stronger than $H_2CO_3$, it protonates the bicarbonate ion.
Result: $CO_2$ Evolved.

Phenols

Simple phenols are weaker acids than $H_2CO_3$. They cannot protonate the bicarbonate ion.
Result: No Reaction.

Important Exception: Picric Acid

Picric Acid (2,4,6-Trinitrophenol) and 2,4-Dinitrophenol are phenols, but due to strong electron-withdrawing $-NO_2$ groups, they are stronger acids than Carbonic acid.
Observation: They give a Positive Sodium Bicarbonate test despite being phenols.

4. Mechanism

It is a simple Brønsted-Lowry acid-base reaction.

$$ R-COOH + HCO_3^- \rightleftharpoons R-COO^- + H_2CO_3 $$ $$ H_2CO_3 \rightleftharpoons H_2O + CO_2 \uparrow $$

5. Solved Examples

Compound Reaction with $NaHCO_3$ Reason
Acetic Acid Positive ($CO_2 \uparrow$) $pK_a (4.7) < 6.4$
Benzoic Acid Positive ($CO_2 \uparrow$) $pK_a (4.2) < 6.4$
Phenol Negative $pK_a (10) > 6.4$
Picric Acid Positive ($CO_2 \uparrow$) $pK_a (0.38) \ll 6.4$
Benzenesulfonic Acid Positive ($CO_2 \uparrow$) Very Strong Acid

Bicarbonate Test Quiz

Test your concepts on Acidity. 10 MCQs with explanations.

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