Question:

Why does an old sample of benzaldehyde turn blue litmus red?

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Aldehydes slowly react with atmospheric oxygen on standing, and benzaldehyde forms acidic benzoic acid this way.
Updated On: Jul 3, 2026
  • Due to the conversion of benzaldehyde to phenol
  • Due to the presence of acid impurity with benzaldehyde
  • Due to aerial oxidation of benzaldehyde
  • Benzaldehyde is acidic in nature
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The Correct Option is C

Solution and Explanation

Step 1: Benzaldehyde does not have a hydrogen directly bonded to its carbonyl oxygen, so pure benzaldehyde itself is essentially neutral and will not turn blue litmus red.
Step 2: Aldehydes are air-sensitive. On standing in contact with atmospheric oxygen over time, an aldehyde slowly undergoes autoxidation at the carbonyl carbon-hydrogen bond.
Step 3: For benzaldehyde this aerial oxidation converts some of the sample into benzoic acid: \[C_6H_5CHO + \tfrac{1}{2}O_2 \xrightarrow{\text{air}} C_6H_5COOH\]
Step 4: Benzoic acid is a genuine carboxylic acid, so once it accumulates in an old, air-exposed sample of benzaldehyde, it turns blue litmus red.
Step 5: The root cause is the slow reaction of benzaldehyde with atmospheric oxygen, aerial oxidation.
\[\boxed{\text{Aerial oxidation of benzaldehyde to benzoic acid}}\]
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