Question:

What is the major organic product obtained when phenol undergoes the Reimer-Tiemann reaction?

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The Reimer-Tiemann reaction introduces a formyl group (-CHO) to the aromatic ring of phenol at the ortho position, producing o-hydroxybenzaldehyde (salicylaldehyde).
Updated On: Apr 12, 2025
  • Benzaldehyde
  • o-Hydroxybenzaldehyde (Salicylaldehyde)
  • p-Hydroxybenzoic acid
  • o-Nitrophenol
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The Correct Option is B

Solution and Explanation

The Reimer-Tiemann reaction is used to introduce a formyl group (-CHO) at the ortho position to the hydroxyl group on a benzene ring. When phenol undergoes this reaction, the major product formed is o-hydroxybenzaldehyde, also known as salicylaldehyde, which has both a hydroxyl group and an aldehyde group on the aromatic ring. - Option (A) is incorrect because the reaction does not lead to the formation of benzaldehyde. - Option (C) is incorrect because p-Hydroxybenzoic acid is not formed in this reaction. - Option (D) is incorrect as o-Nitrophenol is unrelated to this reaction. Therefore, the correct answer is option (B).
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