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C
C
C

Functional Groups

World C — Carbon Chemistry

36.A — THE FOUNDATION

R
-FG
R36.01 The "Active Site"
  • An atom or group of atoms attached to a hydrocarbon chain ($R$).
  • Dictates the physical and chemical properties of the entire molecule.
  • The hydrocarbon chain forms the skeleton; the functional group provides the behavior.
R36.10 Homologous Series
  • A family of organic compounds with the *same* functional group.
  • Successive members differ by a $-CH_2-$ unit.
  • Same chemical properties, gradual change in physical properties (boiling point increases).
-COOH (Acid)
>C=O (Ketone)
-OH (Alcohol)
R36.11 Nomenclature Priority
  • When multiple groups are present, IUPAC uses a priority list.
  • Highest priority determines the suffix (e.g., *-oic acid*).
  • Lower priority groups become prefixes (e.g., *hydroxy-*).
Alcohol (R-OH)
VS
Ether (R-O-R)
R36.12 Functional Isomerism
  • Same molecular formula, entirely different functional groups.
  • E.g., $C_2H_6O$ can be Ethanol (liquid, drinkable) or Dimethyl Ether (gas, anesthetic).

36.B — OXYGEN-CONTAINING GROUPS

R36.02 Alcohols (-OH)
  • Contains the Hydroxyl group.
  • Suffix: -ol (e.g., Methanol, Ethanol).
  • Can form hydrogen bonds (high boiling points, soluble in water).
  • Used as solvents, fuels, and beverages.
R36.03 Aldehydes (-CHO)
  • Carbonyl group ($C=O$) located at the end of a chain.
  • Suffix: -al (e.g., Methanal/Formaldehyde, Ethanal).
  • Often have strong, pungent odors. Used in preservatives and resins.
R36.04 Ketones (>C=O)
  • Carbonyl group ($C=O$) located in the middle of a chain.
  • Suffix: -one (e.g., Propanone/Acetone).
  • Excellent solvents for organic compounds (nail polish remover).
R36.05 Carboxylic Acids (-COOH)
  • Contains Carbonyl and Hydroxyl on the same terminal carbon.
  • Suffix: -oic acid (e.g., Ethanoic acid/Acetic acid/Vinegar).
  • Weak acids; donate a proton ($H^+$) in water.

36.C — HALOGENS, AMINES & DERIVATIVES

R36.06 Haloalkanes (-X)
  • One or more Hydrogens replaced by Halogens ($F, Cl, Br, I$).
  • Prefix used: Fluoro-, Chloro-, Bromo-, Iodo-.
  • Used as refrigerants, solvents, and anesthetics.
R36.07 Amines (-NH₂)
  • Derivatives of Ammonia ($NH_3$).
  • Suffix: -amine. Nitrogen has a lone pair of electrons.
  • Act as weak organic bases. Crucial in amino acids and proteins.
R36.08 Esters (-COO-)
  • Formed by reacting a Carboxylic Acid with an Alcohol.
  • Suffix: -oate.
  • Famous for distinct sweet, fruity smells (used in perfumes and flavorings).
R36.09 Ethers (-O-)
  • An oxygen atom bonded to two alkyl groups.
  • Names usually end in ether (e.g., Diethyl ether).
  • Highly flammable, historically used as early anesthetics.