Oxygen-containing organic compounds are fundamental in organic chemistry. They include applications in industries, pharmaceuticals, and biological processes. These compounds have functional groups such as alcohols, ethers, aldehydes, ketones, carboxylic acids, esters, and others. Here’s a detailed overview:
Important Points to Remember
1. Oxidation:
Alcohols can be oxidized to aldehydes, ketones, or carboxylic acids.
Example reaction:
Ethanol (CH3CH2OH) → Acetaldehyde (CH3CHO) → Acetic Acid (CH3COOH).
2. Reduction:
Aldehydes and ketones can be reduced to alcohols.
Example:
Acetone (CH3COCH3) → Isopropanol (CH3CHOHCH3).
3. Esterification:
Carboxylic acids react with alcohols to form esters in the presence of acid.
Example: Acetic acid + Ethanol → Ethyl acetate.
4. Nucleophilic Substitution Reactions:
Carboxylic acids and derivatives (like esters) undergo substitution reactions.
Example: Hydrolysis of ethyl acetate to acetic acid and ethanol.
Addition Reactions:
Aldehydes and ketones undergo nucleophilic addition due to the polar C=O bond.
Example: Formaldehyde + HCN → Cyanohydrin.
(Session 2025 - 26)