JEE Exam  >  JEE Notes  >  Chemistry Main & Advanced  >  Aldehydes, Ketones and Carboxylic Acids: JEE Main Previous Year Questions (2021-2026)

Aldehydes, Ketones and Carboxylic Acids: JEE Main Previous Year Questions (2021-2026)

Download, print and study this document offline
Please wait while the PDF view is loading
 Page 1


JEE Main Previous Year Questions (2021-2026): 
Aldehydes, Ketones and Carboxylic Acids  
 
(January 2026) 
 
Q1: The correct order of acidic strength of the major products formed in the given 
reactions, is: 
 
Choose the correct answer from the options given below: 
A: C > A > D > B 
B: A > D > C > B 
C: A > D > B > C 
D: C > B > A > D 
Answer: A 
Explanation: 
Correct order of acidic strength of major product formed in the given reaction is 
Page 2


JEE Main Previous Year Questions (2021-2026): 
Aldehydes, Ketones and Carboxylic Acids  
 
(January 2026) 
 
Q1: The correct order of acidic strength of the major products formed in the given 
reactions, is: 
 
Choose the correct answer from the options given below: 
A: C > A > D > B 
B: A > D > C > B 
C: A > D > B > C 
D: C > B > A > D 
Answer: A 
Explanation: 
Correct order of acidic strength of major product formed in the given reaction is 
 
 
C > A > D > B 
 
Q2: Which of the following reaction is NOT correctly represented? 
A:  
B:  
C:  
D:  
Page 3


JEE Main Previous Year Questions (2021-2026): 
Aldehydes, Ketones and Carboxylic Acids  
 
(January 2026) 
 
Q1: The correct order of acidic strength of the major products formed in the given 
reactions, is: 
 
Choose the correct answer from the options given below: 
A: C > A > D > B 
B: A > D > C > B 
C: A > D > B > C 
D: C > B > A > D 
Answer: A 
Explanation: 
Correct order of acidic strength of major product formed in the given reaction is 
 
 
C > A > D > B 
 
Q2: Which of the following reaction is NOT correctly represented? 
A:  
B:  
C:  
D:  
Answer: A 
Explanation:  
 
 
Major product of reaction (1) will be 
 
Page 4


JEE Main Previous Year Questions (2021-2026): 
Aldehydes, Ketones and Carboxylic Acids  
 
(January 2026) 
 
Q1: The correct order of acidic strength of the major products formed in the given 
reactions, is: 
 
Choose the correct answer from the options given below: 
A: C > A > D > B 
B: A > D > C > B 
C: A > D > B > C 
D: C > B > A > D 
Answer: A 
Explanation: 
Correct order of acidic strength of major product formed in the given reaction is 
 
 
C > A > D > B 
 
Q2: Which of the following reaction is NOT correctly represented? 
A:  
B:  
C:  
D:  
Answer: A 
Explanation:  
 
 
Major product of reaction (1) will be 
 
As 3° radical more stable 
 
Q3: Given below are two statements for the following reaction sequence. 
 
Statement I : Compound ‘Z’ will give yellow precipitate with NaOI . 
Statement II : Compound Q has two different types of H atoms (aromatic : 
aliphatic) in the ratio 1 : 3. 
In the light of the above statements, choose the correct answer from the options 
given below : 
A: Statement I is true but Statement II is false 
B: Both Statement I and Statement II are true 
C: Statement I is false but Statement II is true 
D: Both Statement I and Statement II are false 
Answer: B 
Explanation: 
 
 
Page 5


JEE Main Previous Year Questions (2021-2026): 
Aldehydes, Ketones and Carboxylic Acids  
 
(January 2026) 
 
Q1: The correct order of acidic strength of the major products formed in the given 
reactions, is: 
 
Choose the correct answer from the options given below: 
A: C > A > D > B 
B: A > D > C > B 
C: A > D > B > C 
D: C > B > A > D 
Answer: A 
Explanation: 
Correct order of acidic strength of major product formed in the given reaction is 
 
 
C > A > D > B 
 
Q2: Which of the following reaction is NOT correctly represented? 
A:  
B:  
C:  
D:  
Answer: A 
Explanation:  
 
 
Major product of reaction (1) will be 
 
As 3° radical more stable 
 
Q3: Given below are two statements for the following reaction sequence. 
 
Statement I : Compound ‘Z’ will give yellow precipitate with NaOI . 
Statement II : Compound Q has two different types of H atoms (aromatic : 
aliphatic) in the ratio 1 : 3. 
In the light of the above statements, choose the correct answer from the options 
given below : 
A: Statement I is true but Statement II is false 
B: Both Statement I and Statement II are true 
C: Statement I is false but Statement II is true 
D: Both Statement I and Statement II are false 
Answer: B 
Explanation: 
 
 
Q4: Given below are the four isomeric compounds (P, Q, R, S) 
 
Identify correct statements from below. 
A. Q, R and S will give precipitate with 2, 4-DNP. 
B. P and Q will give positive Bayer's test. 
C. Q and R will give sooty flame. 
D. R and S will give yellow precipitate with I 2/NaOH. 
E. Q alone will deposit silver with Tollen's reagent 
Choose the correct option. 
A: C and E only 
B: A and E only 
C: A, B, D and E only 
D: A, C and E only 
Answer: D 
Explanation: 
(A) Q, R and S give the 2, 4-DNP test because each of them contains a carbonyl group 
(> C = O) of aldehyde/ketone. In this test, aldehydes and ketones form an orange/yellow 
precipitate of the 2, 4-dinitrophenylhydrazone. 
(C) Q and R give a sooty flame because they contain an aromatic ring. Aromatic 
compounds have a higher carbon content, so they burn with incomplete combustion and 
produce a smoky (sooty) flame. 
(E) Only Q gives Tollens’ test because Q is an aldehyde. Aldehydes reduce Tollens’ 
reagent (ammoniacal silver nitrate) to metallic silver, so a silver deposit/mirror is 
obtained. Ketones (R and S) do not give this test. 
 
Q5: The unsaturated ether on acidic hydrolysis produces carbonyl compounds as 
shown below: 
 
Based on this, predict the solution/reagent that will help to distinguish "P" and 
"Q" obtained in the following reaction:- 
Read More

FAQs on Aldehydes, Ketones and Carboxylic Acids: JEE Main Previous Year Questions (2021-2026)

1. What are the key differences between aldehydes and ketones?
Ans. The primary difference between aldehydes and ketones lies in their molecular structure. Aldehydes contain a carbonyl group (C=O) that is located at the end of the carbon chain, whereas ketones have the carbonyl group within the carbon chain. This structural distinction leads to differing chemical properties and reactivity; aldehydes are generally more reactive than ketones due to the presence of the terminal carbonyl group.
2. How can carboxylic acids be identified in a laboratory setting?
Ans. Carboxylic acids can be identified through several methods in a laboratory. One common method is the use of litmus paper; carboxylic acids will turn blue litmus paper red due to their acidic nature. Another method involves adding sodium bicarbonate (NaHCO₃) which will produce effervescence (bubbles of carbon dioxide) if a carboxylic acid is present. Additionally, infrared spectroscopy can be utilised to identify the characteristic O-H and C=O stretching vibrations in the carboxylic acid functional group.
3. What is the significance of the carbonyl group in organic compounds?
Ans. The carbonyl group (C=O) is a functional group that is crucial in organic chemistry as it imparts distinct chemical properties to the molecules it is part of. It plays a vital role in the reactivity of aldehydes, ketones, and carboxylic acids, allowing them to participate in various chemical reactions such as nucleophilic addition and condensation reactions. The presence of the carbonyl group also affects the physical properties, such as boiling and melting points, due to its ability to form hydrogen bonds.
4. What are some common uses of ketones in everyday products?
Ans. Ketones are widely used in various everyday products due to their solvent properties and chemical reactivity. Acetone, for instance, is a common solvent found in nail polish removers, paint thinners, and cleaning products. Other ketones, such as methyl ethyl ketone (MEK), are used in the manufacture of plastics, textiles, and adhesives. Additionally, certain ketones are used in the food industry as flavouring agents and in the production of pharmaceuticals.
5. How do the boiling points of carboxylic acids compare to those of aldehydes and ketones?
Ans. Carboxylic acids generally have higher boiling points than aldehydes and ketones of similar molecular weight. This is primarily due to the ability of carboxylic acids to form strong hydrogen bonds between their molecules, which requires more energy to break during boiling. In contrast, aldehydes and ketones, while they can also form dipole-dipole interactions, do not engage in hydrogen bonding to the same extent, resulting in lower boiling points compared to carboxylic acids.
Explore Courses for JEE exam
Related Searches
MCQs, Previous Year Questions with Solutions, ppt, Sample Paper, Exam, Semester Notes, Ketones and Carboxylic Acids: JEE Main Previous Year Questions (2021-2026), Ketones and Carboxylic Acids: JEE Main Previous Year Questions (2021-2026), Summary, past year papers, Viva Questions, shortcuts and tricks, practice quizzes, Extra Questions, Objective type Questions, study material, mock tests for examination, Aldehydes, Important questions, Ketones and Carboxylic Acids: JEE Main Previous Year Questions (2021-2026), Free, pdf , Aldehydes, video lectures, Aldehydes;