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Aldehydes, Ketones and Carboxylic Acids · Question 21

JEE Main 2026 (Online) 22nd January Morning ShiftMatchingEasy📈 Topic in 10% papers+4−1
1

Match the LIST-I with LIST-II Choose the correct answer from the options given below :

  1. A-IV, B-III, C-II, D-I
  2. A-III, B-I, C-IV, D-II
  3. A-II, B-I, C-IV, D-III
  4. A-III, B-IV, C-I, D-II

Answer

(2) A-III, B-I, C-IV, D-II

Solution

A. NH2NH2 then KOH (heat in ethylene glycol): >C=O → >CH2, Wolff-Kishner reduction III

B. [Ag(NH3)2]OH is Tollens' reagent (silver mirror with aldehydes) I

C. Aqueous CuSO4 (Fehling solution A) + alkaline sodium potassium tartrate (Fehling solution B) is Fehling's reagent (red-brown Cu2O with aliphatic aldehydes) IV

D. Zn-Hg / conc. HCl: >C=O → >CH2, Clemmensen reduction II

A-III, B-I, C-IV, D-II

Answer: (2)

JEE Main 2026 (Online) 22nd January Morning Shift

Keep practising — Aldehydes, Ketones and Carboxylic Acids

2

The compound A, C8H8O2 reacts with acetophenone to form a single product via cross-Aldol condensation. The compound A on reaction with conc. NaOH forms a substituted benzyl alcohol as one of the two products. The compound A is :

  1. 2-hydroxy acetophenone
  2. 4-hydroxy benzaldehyde
  3. 4-methyl benzoic acid
  4. 4-methoxy benzaldehyde
JEE Main 2026 (Online) 22nd January Evening Shift
3

An organic compound "P" of molecular formula C6H12O3 gives positive iodoform test but negative Tollens' test. When "P" is treated with dilute acid, it produces "Q". "Q" gives positive Tollens' test and also iodoform test. The structure of "P" is :

  1. H- O \|C-CH2-CH2- OCH3 |CH-OCH3
  2. CH3- O \|C- OCH3 |CH- OCH3 |CH2
  3. CH3- O \|C-CH2- OCH3 |CH-OCH3
  4. CH3- O \|C- OCH3 | OCH3 |C-CH3
JEE Main 2026 (Online) 21st January Morning Shift
4

Match List - I with List - II. Choose the correct answer from the options given below :

  1. A-II, B-III, C-IV, D-I
  2. A-IV, B-III, C-I, D-II
  3. A-IV, B-I, C-II, D-III
  4. A-II, B-IV, C-I, D-III
JEE Main 2026 (Online) 21st January Evening Shift
5

A [(ii) H3O+](i) NaOH B [(ii) H2SO4, ](i) EtOH C 'A' shows positive Lassaigne's test for N and its molar mass is 121. 'B' gives effervescence with aq NaHCO3. 'C' gives fruity smell. Identify A, B and C from the following.

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
JEE Main 2025 (Online) 8th April Evening Shift
6

When [figure] undergoes intramolecular aldol condensation, the major product formed is :

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
JEE Main 2025 (Online) 8th April Evening Shift
7

Which of the following compounds is least likely to give effervescence of CO2 in presence of aq. NaHCO3?

  1. Ph- NH3 Cl
  2. [figure]
  3. [figure]
  4. [figure]
JEE Main 2025 (Online) 7th April Morning Shift
8

"P" is an optically active compound with molecular formula C6H12O. When "P" is treated with 2,4-dinitrophenylhydrazine, it gives a positive test. However, in presence of Tollens' reagent, "P" gives a negative test. Predict the structure of "P".

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
JEE Main 2025 (Online) 7th April Evening Shift
9

Aldol condensation is a popular and classical method to prepare , -unsaturated carbonyl compounds. This reaction can be both intermolecular and intramolecular. Predict which one of the following is not a product of intramolecular aldol condensation?

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
JEE Main 2025 (Online) 4th April Morning Shift
10

Which among the following compounds give yellow solid when reacted with NaOI/NaOH? Choose the correct answer from the options given below :

  1. (A) and (C) Only
  2. (C) and (D) Only
  3. (B), (C) and (E) Only
  4. (A), (C) and (D) Only
JEE Main 2025 (Online) 4th April Evening Shift
11

Number of molecules from below which cannot give iodoform reaction is : Ethanol, Isopropyl alcohol, Bromoacetone, 2-Butanol, 2-Butanone, Butanal, 2-Pentanone, 3-Pentanone, Pentanal and 3-Pentanol.

  1. 4
  2. 3
  3. 5
  4. 2
JEE Main 2025 (Online) 3rd April Morning Shift

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