Q47.In Reimer - Tiemann reaction, phenol is converted into salicylaldehyde through an intermediate. The structure of intermediate is _____ (1) (2) (3) (4)
What This Question Tests
This question tests the understanding of the Reimer-Tiemann reaction, specifically identifying the key intermediate formed when phenol is converted to salicylaldehyde.
Concepts Tested
📚 NCERT Sections This Tests
7.18 — Explain The Following With An Example.
Chemistry Class 12 · Chapter 7
7.18 Explain the following with an example. (i) Kolbe’s reaction. (ii) Reimer-Tiemann reaction. (iii) Williamson ether synthesis. (iv) Unsymmetrical ether.
7.21 — Name The Reagents Used In The Following Reactions:
Chemistry Class 12 · Chapter 7
7.21 Name the reagents used in the following reactions: (i) Oxidation of a primary alcohol to carboxylic acid. (ii) Oxidation of a primary alcohol to aldehyde. (iii) Bromination of phenol to 2,4,6-tribromophenol. (iv) Benzyl alcohol to benzoic acid. (v) Dehydration of propan-2-ol to propene. (vi) Butan-2-one to butan-2-ol.
7.17 — Give Equations Of The Following Reactions:
Chemistry Class 12 · Chapter 7
7.17 Give equations of the following reactions: (i) Oxidation of propan-1-ol with alkaline KMnO4 solution. (ii) Bromine in CS2 with phenol. (iii) Dilute HNO3 with phenol. (iv) Treating phenol wih chloroform in presence of aqueous NaOH.
📋 Question Details
- Chapter
- Alcohols Phenols Ethers
- Topic
- Reimer-Tiemann reaction mechanism
- Year
- 2024
- Shift
- 06 Apr Shift 1
- Q Number
- Q47
- Type
- MCQ
- NCERT Ref
- Class 12 Chemistry Ch 11: Alcohols Phenols Ethers
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