Functional Groups

Note: This is a learning resource and may simplify some concepts for educational purposes.

Why Functional Groups Matter

  • They determine chemical reactivity (how the molecule behaves).
  • They affect polarity and solubility (whether it dissolves in water or oil).
  • They influence biological activity (how drugs interact with the body).

What are Functional Groups?

Functional groups are specific groups of atoms within molecules that are responsible for the characteristic chemical reactions of those molecules. The same functional group will undergo the same or similar chemical reactions regardless of the size of the molecule it is a part of.

1. Hydrocarbons

C C

Alkanes (C-C)

Saturated hydrocarbons with single bonds. Unreactive.

Example: View Alkanes

C C

Alkenes (C=C)

Unsaturated hydrocarbons with double bonds. Rigid.

Example: View Alkenes

C C

Alkynes (C≡C)

Unsaturated hydrocarbons with triple bonds.

Example: View Alkynes

Arenes (Aromatic)

Cyclic structures like Benzene with stabilized electron rings.

Example: View Arenes

2. Halogen-Containing

R X

Alkyl Halides (R-X)

Alkane with a halogen substituent (where X = F, Cl, Br, or I).

Example: View Alkyl Halides

3. Oxygen-Containing

R OH

Alcohols (R-OH)

Hydroxyl group attached to a carbon.

Example: View Alcohols

R O R'

Ethers (R-O-R)

Oxygen atom bonded to two carbons.

Example: View Ethers

R C H O

Aldehydes (R-CHO)

Carbonyl group at the end of a chain.

Example: View Aldehydes

R C R' O

Ketones (R-CO-R)

Carbonyl group in middle of chain.

Example: View Ketones

R C OH O

Carboxylic Acids (-COOH)

Acidic functional group.

Example: View Acids

R C O R' O

Esters (-COO-)

Often fragant. Derivative of CA.

Example: View Esters

R C NH₂ O

Amides (-CONH₂)

Amino group bonded to carboxyl C.

Example: View Amides

4. Nitrogen-Containing

R NH₂

Amines (-NH₂)

Derivatives of ammonia (NH₃).

Example: View Amines

R C N

Nitriles (-C≡N)

Contain a cyano group.

Example: View Nitriles

R NO₂

Nitro Compounds

Contain a nitro group.

Example: View Nitro

5. Sulfur-Containing

R SH

Thiols (-SH)

Sulfur analogue of alcohols. Strong odor.

Example: View Thiols

R S R'

Sulfides (Thioethers)

Sulfur analogue of ethers (R-S-R).

Example: View Sulfides

6. Phosphorus-Containing

P O O⁻ O⁻ RO

Phosphate Esters

Essential in biochemistry (DNA, ATP).

Example: View Phosphates

7. Special Groups

C R¹ H OR² OR³

Acetals

Carbon bonded to two -OR groups.

Example: View Acetals

Related Topic Reading Structures
Want to see real examples of functional groups? Search "Ethanol"
Last updated: 2026-01-13

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