Functional Groups
Functional Groups
Definition
Functional groups are specific groups of atoms within molecules that are responsible for the characteristic chemical reactions of those molecules.
Importance
Determine the properties and reactivity of organic compounds.
Serve as the basis for classifying organic molecules.
Common Functional Groups
1. Hydroxyl Group (-OH)
Structure: R-OH
Properties: Polar, can form hydrogen bonds.
Example: Alcohols (e.g., ethanol).
2. Carbonyl Group (C=O)
Structure: R-CO-R' (ketone) or R-CHO (aldehyde)
Properties: Polar, can participate in nucleophilic addition reactions.
Example: Ketones (e.g., acetone), Aldehydes (e.g., formaldehyde).
3. Carboxyl Group (-COOH)
Structure: R-COOH
Properties: Acts as an acid (donates H+), polar.
Example: Carboxylic acids (e.g., acetic acid).
4. Amino Group (-NH2)
Structure: R-NH2
Properties: Acts as a base (accepts H+), polar.
Example: Amines (e.g., aniline).
5. Sulfhydryl Group (-SH)
Structure: R-SH
Properties: Can form disulfide bonds, polar.
Example: Thiols (e.g., cysteine).
6. Phosphate Group (-PO4)
Structure: R-PO4^2-
Properties: Contributes negative charge, involved in energy transfer (ATP).
Example: Nucleotides (e.g., ATP).
7. Methyl Group (-CH3)
Structure: R-CH3
Properties: Nonpolar, hydrophobic.
Example: Methylated compounds (e.g., methylated DNA).
Summary of Functional Group Properties
Functional Group Polarity Acid/Base Example | |||
Hydroxyl | Polar | Neutral | Ethanol |
Carbonyl | Polar | Neutral |