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CBSE Class 12 Chemistry: Aldehydes & Ketones — Notes 2026

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Tushar Parik

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2 min read

CBSE Class 12 Chemistry: Aldehydes & Ketones — Notes 2026

This comprehensive guide from Bright Tutorials covers everything you need to know — with clear explanations, exam tips, and key points for board exam preparation.

In This Article

  1. Structure and Nomenclature
  2. Preparation Methods
  3. Nucleophilic Addition Reactions
  4. Distinction Tests
  5. Aldol Condensation
  6. Cannizzaro Reaction
  7. CBSE Board Focus

Structure and Nomenclature

  • Aldehyde: −CHO group; carbonyl carbon attached to H and organic group; methanal (HCHO), ethanal (CH₃CHO)
  • Ketone: >C=O; carbonyl between two carbon atoms; propanone (CH₃COCH₃)
  • IUPAC: parent chain includes C=O; suffix -al (aldehyde), -one (ketone); number from closest end to C=O

Preparation Methods

  • Oxidation: 1° alcohol → aldehyde (PCC, Cr₂O₃); 2° alcohol → ketone (Na₂Cr₂O₇/H₂SO₄)
  • Rosenmund reduction: RCOCl + H₂ (Pd/BaSO₄) → RCHO + HCl; Baeyer-Villiger: ketone → ester with peracid
  • Ozonolysis: alkene + O₃ → ozonide → RCHO + R₂CO (reductive workup) or RCOOH + R₂C=O (oxidative)

Nucleophilic Addition Reactions

  • C=O is electrophilic (carbonyl C); Nu⁻ attacks → tetrahedral intermediate → protonation → product
  • Addition of HCN: gives cyanohydrin; RCHO + HCN → RCH(OH)CN (α-hydroxy nitrile)
  • Grignard: RMgX + RCHO → 2° alcohol; R₂CO → 3° alcohol; HCHO → 1° alcohol

Distinction Tests

  • Tollens' test (silver mirror): aldehydes oxidised to carboxylate; ketones do not respond
  • Fehling's test: Benedict's/Fehling's solution (Cu²⁺); aliphatic aldehydes give brick red precipitate; aromatic aldehydes do not
  • Iodoform test: CH₃CO− group → CHI₃ (yellow precipitate); acetaldehyde, acetone, ethanol (oxidised to acetaldehyde)

Aldol Condensation

  • Self-condensation of aldehydes with α-H in base: 2 CH₃CHO → CH₃CH(OH)CH₂CHO (aldol)
  • Aldol: β-hydroxy carbonyl compound; on heating → α,β-unsaturated carbonyl (aldol dehydration)
  • Cross-aldol: two different carbonyl compounds; mixture of products; industrial use in synthesis

Cannizzaro Reaction

  • Aldehydes without α-H (HCHO, benzaldehyde) undergo disproportionation in base
  • 2 RCHO + NaOH → RCOO⁻Na⁺ + RCH₂OH; one oxidised, one reduced
  • Industrial use: HCHO → methanol + formate; benzaldehyde → benzyl alcohol + benzoic acid

CBSE Board Focus

  • Aldehydes & Ketones: 6–8 marks; Tollens'/Fehling's/iodoform tests, aldol condensation mechanism
  • Numerical/mechanism: nucleophilic addition steps for HCN addition to ethanal
  • Distinguish aldehyde from ketone: 4 tests; at least 2 with equations in CBSE

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