IUPAC nomenclature for organic chemical 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 name 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 at the process involved like in the halogen dance rearrangement. The related IUPAC nomenclature is designed for naming organic compounds themselves.[citation needed]
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.
Notes and references
 | This article includes a list of references, related reading, or external links, but its sources remain unclear because it lacks inline citations. (March 2016) |
- Jones, R.A.Y. Bunnett, J.F. (1989). "Nomenclature for organic chemical transformations" (Free fulltext). Pure Appl. Chem. 61: 725–768. doi:10.1351/pac198961040725. S2CID 98538653.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - March, Jerry (1985). Advanced organic chemistry: reactions, mechanisms, and structure. New York: Wiley. ISBN 0-471-85472-7.