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⚗️ class 12 chemistry · chapter 8

Aldehydes, Ketones and Carboxylic Acids

~8 marks in boardshard~5 hrs to master14 NCERT topics

Aldehydes, Ketones and Carboxylic Acids is Chapter 8 of Class 12 CBSE Chemistry, worth around 8 marks of the 70-mark board paper. It's one of the tougher chapters — plan roughly 5 hours to cover it properly. The NCERT chapter has 14 topics across 3 broad areas: aldehydes and ketones — preparation, reactions of aldehydes and ketones, carboxylic acids. Examiner's note: Aldol condensation, Cannizzaro reaction — name reactions matter.

What's in this chapter

part 1

Aldehydes and Ketones — Preparation

  • Nomenclature of aldehydes and ketones
  • Preparation from alcohols, alkenes, alkynes
  • Preparation using Grignard reagent
  • Physical properties

part 2

Reactions of Aldehydes and Ketones

  • Nucleophilic addition reactions
  • Addition of HCN, NH₂OH, hydrazine, Grignard reagent
  • Aldol condensation
  • Cannizzaro reaction
  • Oxidation and reduction reactions
  • Tests to distinguish aldehydes from ketones

part 3

Carboxylic Acids

  • Nomenclature and preparation of carboxylic acids
  • Physical and chemical properties
  • Acidity of carboxylic acids and factors affecting it
  • Reactions — with bases, PCl₅, LiAlH₄, decarboxylation
  • Uses of carboxylic acids

Must-know formulas

Aldol condensation

2CH₃CHO → (NaOH) CH₃CH(OH)CH₂CHO → (−H₂O) CH₃CH=CHCHO

board favourite

Tollens' test (silver mirror)

RCHO + 2[Ag(NH₃)₂]⁺ → RCOO⁻ + 2Ag↓

board favourite

Fehling's test

RCHO + 2Cu²⁺ → RCOO⁻ + Cu₂O↓ (red ppt)

board favourite

Iodoform test (methyl ketones)

RCOCH₃ + I₂/NaOH → CHI₃↓ (yellow) + RCOONa

board favourite

Nucleophilic addition to C=O

Nu⁻ attacks C of C=O → tetrahedral intermediate → product

frequently asked

Cannizzaro reaction (non-enolisable)

2HCHO → (NaOH) CH₃OH + HCOONa

frequently asked

Clemmensen reduction

C=O → CH₂ (Zn-Hg/HCl)

frequently asked

Wolff-Kishner reduction

C=O → CH₂ (NH₂NH₂/KOH/Δ)

frequently asked

Hell-Volhard-Zelinsky (HVZ) reaction

RCOOH + Br₂/(P) → RCH(Br)COOH

frequently asked

see all 10 formulas for this chapter →

Mistakes that cost marks

"Ketones oxidise as easily as aldehydes"ketones RESIST mild oxidation (no H on the carbonyl carbon) — that's the whole point of Tollens'/Fehling's tests.
"Carboxylic acids give Tollens'/Fehling's positive too"they don't; the –COOH carbon is already fully oxidised.
"Any carbonyl compound can do aldol condensation"aldol needs an α-HYDROGEN; HCHO and benzaldehyde can't self-aldol (hence Cannizzaro/cross-aldol).
"Alcohols and carboxylic acids have similar acidityboth have O–H" — carboxylate resonance (two equivalent O) makes acids ~10¹¹ times stronger.

Real board questions from this chapter

CBSE 20243 marksDistinguishing Tests

Give a simple chemical test to distinguish between: (i) acetaldehyde and acetone, (ii) benzaldehyde and acetophenone, (iii) formic acid and acetic acid.

CBSE 20242 marksCannizzaro Reaction

What is the Cannizzaro reaction? Write the reaction of benzaldehyde with concentrated NaOH and name the products formed.

CBSE 20235 marksNucleophilic Addition

Explain the mechanism of nucleophilic addition of HCN to acetaldehyde. Compare the reactivity of acetaldehyde and acetone towards nucleophilic addition. Give reasons.

CBSE 20233 marksAcidity of Carboxylic Acids

Arrange the following in increasing order of acid strength and justify: benzoic acid, 4-nitrobenzoic acid, 4-methoxybenzoic acid, 3,4-dinitrobenzoic acid.

CBSE 20223 marksAldol Condensation

What is aldol condensation? Write the reaction of acetaldehyde undergoing aldol condensation. Under what conditions does cross-aldol condensation occur?

CBSE 20225 marksConversions

How will you convert: (i) propan-2-ol to propanone, (ii) benzaldehyde to benzoic acid, (iii) acetic acid to acetaldehyde, (iv) toluene to benzaldehyde, (v) ethanal to but-2-enal?

CBSE 20212 marksReactivity

Explain why aldehydes are more reactive than ketones towards nucleophilic addition reactions.

CBSE 20203 marksName Reactions

Write the products and name the reaction: (i) benzaldehyde treated with HCHO and NaOH, (ii) acetone treated with dilute Ba(OH)₂, (iii) acetaldehyde treated with Tollens' reagent.

CBSE 20191 markAcidity

Why is the boiling point of a carboxylic acid higher than that of an alcohol of comparable molecular mass?

CBSE 20185 marksNucleophilic Addition Mechanism

(a) Write the mechanism of acid-catalysed nucleophilic addition of an alcohol to acetaldehyde to form an acetal. (b) An organic compound with molecular formula C₃H₆O gives a positive iodoform test but does not reduce Tollens' reagent. Identify the compound and write the reactions.

Quick answers

How many marks is Aldehydes, Ketones and Carboxylic Acids worth in the Class 12 board exam?

Around 8 marks of the 70-mark CBSE Chemistry theory paper, based on the official unit-wise weightage. Aldol condensation, Cannizzaro reaction — name reactions matter.

Is Aldehydes, Ketones and Carboxylic Acids easy or hard?

It's rated hard — one of the tougher chapters in Class 12 Chemistry. Most students need about 5 hours to cover it well.

What are the important topics in Aldehydes, Ketones and Carboxylic Acids?

The chapter covers 14 NCERT topics in 3 areas: Aldehydes and Ketones — Preparation; Reactions of Aldehydes and Ketones; Carboxylic Acids.

What questions come from Aldehydes, Ketones and Carboxylic Acids in board exams?

Between 2018–2024, CBSE board papers asked questions from this chapter on Distinguishing Tests, Cannizzaro Reaction, Nucleophilic Addition, Acidity of Carboxylic Acids — 1- to 5-mark questions.

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