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JEE • CHEMISTRY • ALDEHYDES & KETONES & CARBOXYLIC ACIDS
Aldehydes & ketones & carboxylic acids practice · Easy
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Practice format and chapter quiz
These sets use single-correct-answer MCQs. They do not cover every JEE Main or JEE Advanced question format and are not full-length mock papers.
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1
Easy
1 of 56
Understanding
+4 | -1
Carboxylic acids dimerise due to
View answer and explanation
Correct option: C
Intermolecular hydrogen bonding
The correct answer is C (Intermolecular hydrogen bonding) because carboxylic acids form dimers through intermolecular hydrogen bonds between the carbonyl oxygen and the hydroxyl hydrogen of two molecules.
2
Easy
2 of 56
Analyzing
+4 | -1
The most acidic among the following is:
View answer and explanation
Correct option: C
Option C () is correct because carboxylic acids are generally more acidic than alcohols and phenols due to resonance stabilization of the carboxylate anion.
3
Easy
3 of 56
Understanding
+4 | -1
Acetic acid will be obtained on oxidation of
View answer and explanation
Correct option: A
Ethanol
Option A (Ethanol) is correct because the oxidation of ethanol yields acetic acid.
4
Easy
4 of 56
Analyzing
+4 | -1
Which of the following is a better reducing agent for the following reduction?
View answer and explanation
Correct option: D
Option D (B2H6/H3O+) is correct because diborane is a selective reducing agent that reduces carboxylic acids to primary alcohols without affecting other functional groups.
5
Easy
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Remembering
+4 | -1
General formula of carbonyl compound is:
View answer and explanation
Correct option: A
Option A () is correct because carbonyl compounds (aldehydes and ketones) have the general formula .
6
Easy
6 of 56
Remembering
+4 | -1
Action of acetylene on dilute gives
View answer and explanation
Correct option: B
Acetaldehyde
Option B (Acetaldehyde) is correct because acetylene reacts with dilute sulfuric acid in the presence of mercuric sulfate to form acetaldehyde.
7
Easy
7 of 56
Remembering
+4 | -1
The term hypnone is used for:
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Correct option: B
Acetophenone
Option B (Acetophenone) is correct because Acetophenone is known as hypnone due to its hypnotic properties.
8
Easy
8 of 56
Understanding
+4 | -1
Which of the following will not undergo aldol condensation?
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Correct option: C
Benzaldehyde
Option C is correct because benzaldehyde lacks an alpha-hydrogen, which is required for aldol condensation to occur.
9
Easy
9 of 56
Understanding
+4 | -1
Hydrolysis of acetamide produces which of the following.
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Correct option: A
Acetic acid
The correct answer is A (Acetic acid) because hydrolysis of acetamide in the presence of a base produces acetic acid and ammonia.
10
Easy
10 of 56
Understanding
+4 | -1
Acetic acid on heating with urea gives:
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Correct option: A
Acetamide, carbon dioxide and ammonia
Option A (Acetamide, carbon dioxide and ammonia) is correct because acetic acid reacts with urea upon heating to produce acetamide, carbon dioxide, and ammonia.
11
Easy
11 of 56
Remembering
+4 | -1
Composition of Fehling solution and Fehling solution is
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Correct option: A
an aqueous copper sulphate and alkaline sodium potassium tartarate (Rochelle salt) respectively
Option A (an aqueous copper sulphate and alkaline sodium potassium tartarate (Rochelle salt) respectively) is correct because Fehling's solution A is aqueous copper sulfate, and Fehling's solution B is alkaline sodium potassium tartrate (Rochelle salt).
12
Easy
12 of 56
Remembering
+4 | -1
Which of the following contain an aldehyde?
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Correct option: D
All of these
Option D (All of these) is correct because vanilla beans, meadowsweet, and cinnamon all contain aldehydes, specifically vanillin, salicylaldehyde, and cinnamaldehyde, respectively.
13
Easy
13 of 56
Remembering
+4 | -1
Chloral belongs to the class of:
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Correct option: B
Aldehydes
Option B (Aldehydes) is correct because Chloral has the formula , which contains the -CHO functional group characteristic of aldehydes.
14
Easy
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Remembering
+4 | -1
Formalin is:
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Correct option: C
Formaldehyde + methanol + water
Option C (Formaldehyde + methanol + water) is correct because formalin is a solution of formaldehyde in water, typically stabilized with methanol to prevent polymerization.
15
Easy
15 of 56
Remembering
+4 | -1
Diborane easily reduce the functional group such as
View answer and explanation
Correct option: A
acid
Option A is correct because diborane () readily reduces carboxylic acids to primary alcohols.
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16
Easy
16 of 56
Understanding
+4 | -1
Acetaldehyde cannot show
View answer and explanation
Correct option: B
Lucas test
Option B is correct because the Lucas test is specific to alcohols and is used to differentiate between primary, secondary, and tertiary alcohols, not aldehydes.
17
Easy
17 of 56
Analyzing
+4 | -1
Oxidation of which compound is not possible?
View answer and explanation
Correct option: A
Option A () is correct because carboxylic acids are already in a high oxidation state and are generally resistant to further oxidation.
18
Easy
18 of 56
Analyzing
+4 | -1
An organic acid when heated strongly with , gave rise to a colourless gas which burns with a pale blue flame. The acid is:
View answer and explanation
Correct option: B
Formic acid
Option B (Formic acid) is correct because formic acid, when heated with , dehydrates to produce carbon monoxide, which burns with a pale blue flame.
19
Easy
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Remembering
+4 | -1
Pyroligneous acid contains:
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Correct option: C
10% acetic acid
Option C (10% acetic acid) is correct because pyroligneous acid, obtained from the destructive distillation of wood, contains approximately 10% acetic acid.
20
Easy
20 of 56
Remembering
+4 | -1
Imine derivatives of aldehyde and ketone is called as
View answer and explanation
Correct option: C
Schiff’s base
Option C (Schiff’s base) is correct because imine derivatives of aldehydes and ketones are known as Schiff's bases.
21
Easy
21 of 56
Remembering
+4 | -1
Which of the following have pleasant smell?
View answer and explanation
Correct option: D
Hexanal
Option D (Hexanal) is correct because as the size of the aldehyde molecule increases, the odor becomes less pungent and more fragrant.
22
Easy
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Understanding
+4 | -1
Arrange the following compounds in their acidic strength order.
I. Ethanoic acid
II. Propanoic acid
III. Butanoic acid
I. Ethanoic acid
II. Propanoic acid
III. Butanoic acid
View answer and explanation
Correct option: A
I II III
Option A is correct because the acidic strength decreases as the alkyl chain length increases due to the +I inductive effect, so ethanoic acid is the strongest.
23
Easy
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Analyzing
+4 | -1
can be distinguished by:
View answer and explanation
Correct option: D
All of these
Option D (All of these) is correct because and differ in physical state, solubility, and flame characteristics.
24
Easy
24 of 56
Remembering
+4 | -1
Lindlar’s catalyst is:
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Correct option: B
Option B () is correct because Lindlar's catalyst is palladium supported on calcium carbonate, poisoned with barium sulfate or quinoline.
25
Easy
25 of 56
Understanding
+4 | -1
What is the neutralization equivalent of benzoic acid?
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Correct option: A
122
Option A (122) is correct because benzoic acid is a monobasic acid, so its molecular weight equals its neutralization equivalent.
26
Easy
26 of 56
Remembering
+4 | -1
Stinges of bees, red ant and wasps contain:
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Correct option: B
Formic acid
Option B (Formic acid) is correct because the stings of bees, red ants, and wasps contain formic acid.
27
Easy
27 of 56
Analyzing
+4 | -1
Which of the following reagents reacts differently with and
View answer and explanation
Correct option: D
The correct answer is D (NH3) because HCHO forms hexamethylenetetramine, CH3CHO forms acetaldehyde ammonia trimer, and CH3COCH3 forms ketimine, showing different reaction patterns with NH3.
28
Easy
28 of 56
Understanding
+4 | -1
Which method is not used in the preparation of ketone?
View answer and explanation
Correct option: C
Acid hydrolysis of alkyl cyanide
The correct answer is D (Reaction of acid chloride with Grignard reagents) because this reaction leads to a tertiary alcohol, not a ketone.
29
Easy
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Understanding
+4 | -1
Why the aromatic carboxylic acids do not undergo Friedel-Crafts reaction?
View answer and explanation
Correct option: B
Carboxyl group act as a deactivating and ortho-directing group
Option D is correct because the carboxyl group deactivates the benzene ring and the catalyst (AlCl3) coordinates with the carboxyl group, preventing it from acting as a Lewis acid.
30
Easy
30 of 56
Remembering
+4 | -1
Liquid obtained by distillation of red ant is
View answer and explanation
Correct option: C
Formic acid
Option C (Formic acid) is correct because formic acid is obtained by the distillation of red ants.
Revision notes and key takeaways
Review ALDEHYDES & KETONES & CARBOXYLIC ACIDS in your textbook or class notes, then use this set to check your understanding.
Key Takeaways
- ✓ This set contains 56 single-correct-answer MCQs on ALDEHYDES & KETONES & CARBOXYLIC ACIDS.
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Showing 1-30 of 56 questions
