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Revision: Aldehydes, Ketones and Carboxylic Acids >> Aldehydes and Ketones Chemistry HSC Science (General) 12th Standard Board Exam Maharashtra State Board

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Key Points

Key Points: Nomenclature of Aldehydes and Ketones

In IUPAC system in aldehyde the suffix ‘e’ of alkane is replaced by ‘al’, e.g.,
CH₃—CH₂—CH=O; Propanal

\[ \underset{\text{2-methylpropanal}}{\mathrm{CH}_3 - \underset{\underset{\displaystyle \mathrm{CH}_3}{|}}{\mathrm{CH}} - \mathrm{CH} = \mathrm{O}} \]

In ketones, the suffix ‘e’ of alkane is replaced by ‘one’.

For example,

\[ \underset{\text{Butan-2-one}}{\mathrm{CH}_3 - \mathrm{CH}_2 - \overset{\displaystyle \mathrm{O}}{\overset{||}{\mathrm{C}}} - \mathrm{CH}_3} \quad \quad \underset{\text{Propanone (Acetone)}}{\mathrm{CH}_3\mathrm{COCH}_3} \]

Key Points: Physical Properties of Aldehydes and Ketones
  • Most aldehydes are liquids (except HCHO = gas); ketones of lower order are colourless liquids with a pleasant odour.
  • Higher BP than corresponding hydrocarbons but lower than alcohols (no H-bonding between molecules, but dipole-dipole interactions).
  • Lower members are soluble in water (H-bonding with water); higher members are insoluble (large alkyl groups).
Key Points: Chemical Reactions of Aldehydes and Ketones - Nucleophilic Addition Reactions

Addition of HCN:

\[\text{HCN} + \text{OH}^- \rightleftharpoons :\text{CN}^- + \text{H}_2\text{O}\]

Addition of NaHSO3:

Addition of Grignard reagent:

Addition of alcohols:

Key Points: Uses of Aldehydes and Ketones
  • Formaldehyde: Used in making Bakelite (phenol-formaldehyde resin), as a preservative (formalin = 40% HCHO).
  • Acetaldehyde: Used in the preparation of acetic acid and ethanol.
  • Acetone: Solvent (nail polish remover), used in the manufacture of chloroform.
  • Benzaldehyde: Used in perfumes and dyes.

Important Questions [31]

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