CBSE Class 12 Chemistry: Aldehydes & Ketones — Notes 2026
Tushar Parik
Author
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
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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