Q63.The product B formed in the following reaction sequence is : (1) (2) (3) (4)
What This Question Tests
This question requires identifying the product of a multi-step organic reaction sequence, demanding knowledge of common reagents and their mechanisms for functional group transformations. (Note: The actual reaction scheme is missing from the prompt, so the chapter is chosen based on general organic chemistry context).
Concepts Tested
๐ NCERT Sections This Tests
8.17 โ Complete Each Synthesis By Giving Missing Starting Material, Reagent Or Products
Chemistry Class 12 ยท Chapter 8
8.17 Complete each synthesis by giving missing starting material, reagent or products
7.21 โ Name The Reagents Used In The Following Reactions:
Chemistry Class 12 ยท 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.
7.7 โ Predict The Major Product Of Acid Catalysed Dehydration Of
Chemistry Class 12 ยท Chapter 7
7.7 Predict the major product of acid catalysed dehydration of (i) 1-methylcyclohexanol and (ii) butan-1-ol
๐ Question Details
- Chapter
- Organic Chemistry
- Topic
- Reaction mechanisms and product prediction
- Year
- 2025
- Shift
- 28 Jan Shift 2
- Q Number
- Q63
- Type
- MCQ
- NCERT Ref
- Class 12 Chemistry Ch 10: Haloalkanes & Haloarenes
More from this Chapter
Q58.The major product obtained in the following reaction is (1) (2) (3) (4)
Q41.The principle of column chromatography is: (1) Differential adsorption of the substances on the (2) Differential absorption of the substances on the solid phase. solid phase. (3) Gravitational force. (4) Capillary action
Q47. Consider the above reaction and identify the Product P : JEE Main 2021 (27 Jul Shift 1) JEE Main Previous Year Paper (1) (2) (3) (4)
Q45. hv (C7H5O2)2 โ[X] โ2หC6H5 + 2 CO2 Consider the above reaction and identify the intermediated ' X' (1) (2) (3) (4)