CBSE Class 12 Chemistry Aldehydes Ketones And Carboxylic Acids Board Exam Notes

Download the latest CBSE Class 12 Chemistry Aldehydes Ketones And Carboxylic Acids Board Exam Notes in PDF format. These Class 12 Chemistry revision notes are carefully designed by expert teachers to align with the 2025-26 syllabus. These notes are great daily learning and last minute exam preparation and they simplify complex topics and highlight important definitions for Class 12 students.

Chapter-wise Revision Notes for Class 12 Chemistry Unit 8 Aldehydes, Ketones and Carboxylic Acids

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Unit 8 Aldehydes, Ketones and Carboxylic Acids Revision Notes for Class 12 Chemistry

 

♦ Form aldehyde cannot be prepared by Rosenmund's reaction since formyl chloride is unstable at room temperature.

CBSE Class 12 Chemistry Aldehydes Ketones and Carboxylic Acids Board Exam Notes-1

 

VERY SHORT ANSWER TYPE QUESTIONS 
 
Q 1. Arrange the following compounds in an increasing order of their reactivity towards nucleophilic addition reaction.
 
CBSE Class 12 Chemistry Aldehydes Ketones and Carboxylic Acids Board Exam Notes-2
 
Q2. Name the reagent which is used to convert allyl alcohol to propanol.
Ans. PCC (Pyridinium Chlorochromate)
 
Q3. Name the aldehyde which does not give Fehling solution test.
Ans. Benzaldehyde.
 
Q4. Write IUPAC name of the compound
CBSE Class 12 Chemistry Aldehydes Ketones and Carboxylic Acids Board Exam Notes-3
Ans. 3‐Oxopent‐4‐ enoic acid
 
Q5. Complete the reaction:
Ans.
 
CBSE Class 12 Chemistry Aldehydes Ketones and Carboxylic Acids Board Exam Notes-4

ASSERTION - REASON TYPE QUESTIONS
A statement of assertion is followed by a statement of reason. Mark the correct choice from the options given below.
(a) Both assertion and reason are true and reason is the correct explanation of assertion.
(b) Both assertion and reason are true but reason is not the correct explanation of assertion.
(c) Assertion is true but reason is false.
(d) Both assertion and reason are false.

1. Assertion : Carbonyl compounds take part in nucleophilic addition reactions.
Reason : These reactions are initiated by nucleophilic attack at the electron deficient carbon atom. ( Ans - a)

2. Assertion : All aldehydes do not take part in aldol condensation.
Reason : In the aldol condensation, cabanion is generated by the abstraction of α - H atom by base. (Ans - b)

3. Assertion : Acetone is less reactive towards nucleophilic addition than acetaldehyde.
Reason : The alkyl groups hinder the nucleophilic attack on carbonyl carbon atom. ( Ans - a)

4. Assertion : The α - H atom in carbonyl compounds is less acidic.
Reason : The anion formed after the loss of α - H atom is not resonance stabilized. ( Ans - d)

5. Assertion : Aldehydes and ketones both react with Tollen’s reagent to form silver mirror.
Reason : Both aldehydes and ketones contain a carboxylic group. ( Ans - d)

One - word answer
1. Name the reagent used to distinguish between methanoic acid and ethanoic acid.
( Ans - Tollen’ s reagent)

2. Name the product obtained by reaction of hydroxylamine with carbonyl compound?
( Ans - Oxime)

SHORT ANSWER TYPE QUESTIONS (2‐ MARKS)
Q1. Write chemical equation to illustrate following name reactions:‐
(a) Cannizzaro's reaction
(b) Hell‐Volhard‐ Zelinsky reaction
Ans. (a) Cannizzaro's reaction

CBSE-Class-12-Chemistry-Aldehydes-Ketones-and-Carboxylic-Acids-Board-Exam-Notes

Q2. Givea chemical test to distinguish between thefollowing pairs:‐

(i) Phenol and benzoic acid
(ii) Benzaldehyde and Acetophenone

Ans. (i) Benzoic acid reacts with NaHCO3 giving CO2 gas with effervescence where as phenol does not . C6H5 COOH + NaHCO3 →C6H5COONa + H2O + CO2
(ii) Acetophenone on reacting with hot NaOH / I2 gives yellow ppt of CHI3while Benzophenone does not .CH3COC6H5 NaOH/I2 CHI3 + C6H5COONa

Q3. Account for the following :‐
(i) Chloroacetic acid Cl‐CH2COOH is a stronger acid than acetic acid CH3COOH.
(ii) Carboxylic acids do not give the reaction of carbonyl group.
Ans. (i) The –I effect of Cl atom in ClCH2 COOH stabiles the ClCH COOion while +I e ffect of CH ‐ group in CH3 COOH destabilizes the CH3COO0.
(ii) In the resonating structures of carboxylic acid and carbonyls, the carbonyl carbon of carboxylic acid is less electro‐positive (less electrophile) than carbonyl carbon in aldehydes and ketones. Therefore carboxylic acids do not give the reaction of carbonyl group

Q4. Arrange the following.
(i) C6H5COOH, FCH2COOH, NO2CH2COOH( decreasing order of their acidic character)
(ii) Ethanal, Propanal, Propanone, Butanone reaction (increasing order of their nucleophilic addition reaction)
Ans. (i) NO2‐CH2‐COOH> F‐CH2‐COOH >C6H5‐COOH
(ii) Butanone < Propanone < Propanal < Ethanal

Q5. An organic compound 'A' with molecular formula C8H8O gives positive DNP and iododorm test. It does not reduce Tollens' or Fehling's reagent and does not decolourise bromine water also . On oxidation with chromic acid, it gives a carboxylic acid 'B' with molecular formula C7H6O2. Deduce the structures A and B.
Ans. Since A does not give Fehling's or Tollen‘s test but gives iodoform test and 2,4‐ DNP test so it has CH3 CO‐ group. Hence:

CBSE-Class-12-Chemistry-Aldehydes-Ketones-and-Carboxylic-Acids-Board-Exam-Notes

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CBSE Class 12 Chemistry Unit 8 Aldehydes, Ketones and Carboxylic Acids Notes

Students can use these Revision Notes for Unit 8 Aldehydes, Ketones and Carboxylic Acids to quickly understand all the main concepts. This study material has been prepared as per the latest CBSE syllabus for Class 12. Our teachers always suggest that Class 12 students read these notes regularly as they are focused on the most important topics that usually appear in school tests and final exams.

NCERT Based Unit 8 Aldehydes, Ketones and Carboxylic Acids Summary

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Unit 8 Aldehydes, Ketones and Carboxylic Acids Complete Revision and Practice

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