Aldehydes and ketones
Section 1: Introduction to Aldehydes and Ketones
- Named under the class of carbonyl compounds, both aldehydes and ketones contain a carbonyl group (C=O).
- Aldehydes have a carbonyl group at the end of the carbon chain while ketones have it within the carbon chain.
- Generally, both compounds are polar due to the carbonyl group, resulting in relatively high melting and boiling points.
- Aldehydes and ketones can be produced through oxidation of alcohols.
Section 2: Physical Properties of Aldehydes and Ketones
- Both groups of compounds are characterised by the presence of a dipole across the carbonyl group, enhancing intermolecular forces.
- Since they do not form hydrogen bonds, they have lower boiling points than alcohols and carboxylic acids.
- Both aldehydes and ketones are soluble in organic solvents and in water if the carbon chain is short.
Section 3: Chemical Reactions of Aldehydes and Ketones
- Aldehydes can be oxidised to form carboxylic acids unlike ketones.
- Both aldehydes and ketones are susceptible to nucleophilic addition reactions, often involving a nucleophile attacking the carbon atom of the carbonyl group.
- Aldehydes and ketones form hydrates, hemiketals, hemiacetals, and undergo Aldol condensation under certain conditions.
- Frequently used in Cannizzaro’s reaction, aldehydes without alpha-hydrogens are treated with a base to form a primary alcohol and a carboxylic acid.
Section 4: Identification of Aldehydes and Ketones
- The Tollens’ reagent test can identify aldehydes as they oxidise to form silver mirrors while ketones do not react.
- The Fehling’s solution test and the Schiff’s test can also distinguish between the two.
- The Iodoform test helps to identify methyl ketones specifically.
Section 5: Uses of Aldehydes and Ketones
- Aldehydes and ketones find extensive use in the perfume and flavour industry.
- These compounds are also fundamental in polymer industry and in the synthesis of pharmaceuticals.
- They also serve as important solvents in a variety of chemical reactions.