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Aldehydes, Ketones and Carboxylic Acids

NEET (UG) 2019MCQMediumNot asked in last 5 yrs+4−1
Ques. 1NEET (UG) 2019

The major product of the following reaction is : [figure]

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]

Answer

(4) [figure]

Solution

As per NCERT, carboxylic acids react with ammonia to give ammonium salts, which on further heating at high temperature give amides. Phthalic acid gives phthalamide, which on strong heating loses ammonia to form phthalimide.

[figure]

The major product is phthalimide.

Answer: (4)

Keep practising — Aldehydes, Ketones and Carboxylic Acids

Ques. 2NEET 2018

Compound A, C8H10O, is found to react with NaOI (produced by reacting Y with NaOH) and yields a yellow precipitate with characteristic smell. A and Y are respectively

  1. [figure] and I2
  2. [figure] and I2
  3. [figure] and I2
  4. [figure] and I2
Ques. 3NEET 2018

Carboxylic acids have higher boiling points than aldehydes, ketones and even alcohols of comparable molecular mass. It is due to their

  1. formation of intramolecular H-bonding
  2. formation of carboxylate ion
  3. more extensive association of carboxylic acid via van der Waals' forces of attraction
  4. formation of intermolecular H-bonding
Ques. 4NEET 2017

Of the following, which is the product formed when cyclohexanone undergoes aldol condensation followed by heating?

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
Ques. 5NEET 2017

Consider the reactions, [figure] Identify A, X, Y and Z.

  1. A-Methoxymethane, X-Ethanol, Y-Ethanoic acid, Z-Semicarbazide.
  2. A-Ethanal, X-Ethanol, Y-But-2-enal, Z-Semicarbazone.
  3. A-Ethanol, X-Acetaldehyde, Y-Butanone, Z-Hydrazone.
  4. A-Methoxymethane, X-Ethanoic acid, Y-Acetate ion, Z-Hydrazine.
Ques. 6NEET 2016 (Phase 1)

Which of the following reagents would distinguish cis-cyclopentane-1,2-diol from the trans-isomer?

  1. MnO2
  2. Aluminium isopropoxide
  3. Acetone
  4. Ozone
Ques. 7NEET 2016 (Phase 1)

The product formed by the reaction of an aldehyde with a primary amine is

  1. carboxylic acid
  2. aromatic acid
  3. Schiff's base
  4. ketone
Ques. 8NEET 2016 (Phase 2)

The correct order of the strengths of the carboxylic acids [figure] is

  1. I > II > III
  2. II > III > I
  3. III > II > I
  4. II > I > III
Ques. 9NEET 2016 (Phase 2)

The correct structure of the product 'A' formed in the reaction [figure]

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]
Ques. 10AIPMT 2015

Reaction of a carbonyl compound with one of the following reagents involves nucleophilic addition followed by elimination of water. The reagent is

  1. hydrazine in presence of feebly acidic solution
  2. hydrocyanic acid
  3. sodium hydrogen sulphate
  4. a Grignard reagent.
Ques. 11AIPMT 2015

Which one of the following esters gets hydrolysed most easily under alkaline conditions?

  1. [figure]
  2. [figure]
  3. [figure]
  4. [figure]

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