A molozonide (or "molecular ozonide") is a 1,2,3-trioxolane, which can also be considered a cyclic disubstituted trioxidane derivative.[1] 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]
YouTube Encyclopedic
-
1/3Views:26 5231 1476 757
-
Ozonolysis of Alkenes Reaction, Product Trick, and Mechanism: Alkene Reactions 12
-
Dihalogénation et Ozonolyse des Alcynes
-
Organic Chemistry 51B. Lecture 15. Reduction and Oxidation, Part 3.
Transcription
References
- ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "molozonides". doi:10.1351/goldbook.M04004
- ^ McMurry, John (2004). Organic Chemistry, 6th ed. Belmont: Brooks/Cole. p. 225. ISBN 978-0-534-38999-4.
 | This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it. |
This page was last edited on 1 March 2023, at 01:02