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IUPAC Nomenclature for Transformations

The IUPAC Nomenclature for Transformations is a methodology for naming a chemical reaction. Traditionally a chemical reaction especially in organic chemistry is named after its inventor, the so called named reaction, to name just a few: Knoevenagel condensation, Wittig reaction or Diels-Alder reaction. A lot of reactions derive their name from the reagent involved like bromination or acylation. On rare occasions the reaction is named after the company responsible like in the Wacker process or the name only hints to the process involved like in the halogen dance rearrangement.The related IUPAC nomenclature is designed for naming organic compounds themselves.

The IUPAC Nomenclature for Transformations was developed in 1981 and presents a clear cut methodology for naming an organic reaction. It incorporates the reactant and product in a chemical transformation together with one of three transformation types:

  • substitutions have the infix -de- example: methoxy-de-bromination for the chemical reaction of a bromo-alkane to an alkoxy-alkane
  • additions end with -addition example: hydro-bromo-addition for the hydrobromination of an alkene
  • eliminations. end with -elimination example: dibromo-elimination.


  • Nomenclature for organic chemical transformations. Jones, R.A.Y. Bunnett, J.F. Pure Applied Chemistry 1989, 61, 725 - 768
  • Advanced Organic Chemistry Jerry March John Wiley ISBN 0-471-85472-7
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "IUPAC_Nomenclature_for_Transformations". A list of authors is available in Wikipedia.
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