Q47. Consider the above reaction, the product A and product B respectively are (1) (2) (3) (4)
What This Question Tests
This question requires recognizing a two-step reaction sequence involving the hydrolysis of an ester followed by decarboxylation of the resulting dicarboxylic acid.
Concepts Tested
📚 NCERT Sections This Tests
8.17 — Complete Each Synthesis By Giving Missing Starting Material, Reagent Or Products
Chemistry Class 12 · Chapter 8
8.17 Complete each synthesis by giving missing starting material, reagent or products
7.7 — Predict The Major Product Of Acid Catalysed Dehydration Of
Chemistry Class 12 · Chapter 7
7.7 Predict the major product of acid catalysed dehydration of (i) 1-methylcyclohexanol and (ii) butan-1-ol
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.
📋 Question Details
- Chapter
- Aldehydes Ketones Carboxylic Acids
- Topic
- Reactions of Carboxylic Acids and Esters
- Year
- 2022
- Shift
- 29 Jun Shift 1
- Q Number
- Q47
- Type
- MCQ
- NCERT Ref
- Class 12 Chemistry Ch 12: Aldehydes, Ketones and Carboxylic Acids
More from this Chapter
Q80.The increasing order of the rate of HCN addition to compounds A −D is (A) HCHO (B) CH3COCH3 (C) PhCOCH3 (D) PhCOPh (1) A < B < C < D (2) D < B < C < A (3) D < C < B < A (4) C < D < B < A
Q78. In the following sequence of reactions, the compound ' D ' is (1) butanal (2) n−butyl alcohol (3) n−propyl alcohol (4) propanal
Q57.In Cannizzaro reaction qiven below (1) the attack of : OH at the carboxyl group (2) the transfer of hydride to the carbonyl group (3) the abstraction of proton from the carboxylic (4) the deprotonation of PhCH2OH group JEE Main 2009 JEE Main Previous Year Paper
Q58.A liquid was mixed with ethanol and a drop of concentrated H2SO4 was added. A compound with a fruity smell was formed. The liquid was: (1) CH3OH (2) HCHO (3) CH3COCH3 (4) CH3COOH