Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

Jump to content

Molozonide

From Wikipedia, the free encyclopedia
General chemical structure of molozonides

A molozonide (short for "molecular ozonide"; 1,2,3-trioxolane) is a cyclic molecule containing a five-membered ring consisting of two adjacent carbon atoms and three adjacent oxygen atoms.[1] They are thus cyclic disubstituted trioxidane derivatives. Molozonides are formed by cycloaddition of ozone and an alkene during ozonolysis, as a transient intermediate which quickly rearranges to give the ozonide (1,2,4-trioxolane), the relatively stable product generated immediately prior to reductive or oxidative cleavage to form alcohols, carbonyl compounds, or derivatives thereof.[2]

References

[edit]
  1. IUPAC, Compendium of Chemical Terminology, 5th ed. (the "Gold Book") (2025). Online version: (2006) "molozonides". doi:10.1351/goldbook.M04004
  2. McMurry, John (2004). Organic Chemistry, 6th ed. Belmont: Brooks/Cole. p. 225. ISBN 978-0-534-38999-4.