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IUPAC Naming of Organic Compounds

Apr 8, 2025

Understanding IUPAC Nomenclature for Organic Compounds

Introduction

  • Chemists, pharmacists, and scientists need to interpret and name organic compounds.
  • IUPAC (International Union of Pure and Applied Chemistry) provides systematic naming rules.

Hydrocarbons

Alkanes

  • Definition: Hydrocarbons with only carbon and hydrogen, all bonds between carbons are single.
  • Saturation: Alkanes are saturated; all carbon atoms form maximum single bonds.
  • Sources: Found in fossil fuels like coal, crude oil, and natural gas.
  • Naming:
    • Root name from the longest carbon chain.
    • Ends with the suffix "-ane".
    • E.g., Butane (4 carbon atoms), Ethane (2 carbon atoms).

Naming Rules for Alkanes

  • Linear Alkanes: Root name indicates carbon atoms in the chain.
  • Branched Alkanes:
    • Identify the longest chain for the root.
    • Number the chain from the end closest to the branch.
    • Side chains are called alkyl groups, named with "-yl".
    • Use numbers and hyphens for side chain positions.
    • Prefixes like di-, tri-, tetra- indicate multiple side chains.

Unsaturated Hydrocarbons

Alkenes and Alkynes

  • Alkenes:
    • Contain carbon-carbon double bonds.
    • Named with "-ene" suffix.
  • Alkynes:
    • Contain carbon-carbon triple bonds.
    • Named with "-yne" suffix.
  • Naming:
    • Include double/triple bonds in the longest chain.
    • Indicate position of the bond with numbers.
  • Examples: Naming includes position and type of side chains.

Halogenoalkanes

  • Definition: Alkanes with halogen atoms (e.g., bromine or chlorine).
  • Naming: Similar to alkanes, with halogens indicated by prefixes like bromo- or chloro-.
  • Example: 2-bromo-1-chloro-4-methylpentane.

Alcohols

  • Definition: Compounds with hydroxy groups (-OH).
  • Naming:
    • End with "-ol".
    • Number chain from the closest end to the hydroxy group.
  • Examples: Butan-1-ol and Butan-2-ol.

Carbonyl Compounds

Types

  • Aldehydes:
    • Carbonyl group at the end of the chain.
    • Named with "-al" suffix.
    • No number needed for position.
  • Ketones:
    • Carbonyl group within the chain.
    • Named with "-one" suffix.
    • Position indicated if multiple possibilities.
  • Carboxylic Acids:
    • Contain carboxy group (-COOH).
    • Named with "-oic acid" suffix.
    • No position number needed as always at the end.

Summary of IUPAC Rules

  • Longest carbon chain determines root name.
  • Functional group type gives specific suffix.
  • Number the chain to have the smallest numbers for functional groups.
  • Indicate positions with numbers and hyphens.
  • Branched chains or halogens are prefixed and listed alphabetically.