Ozonolysis
From Proteopedia
(Difference between revisions)
| Line 7: | Line 7: | ||
[[Image:Ozonolysis stepone.jpg]] | [[Image:Ozonolysis stepone.jpg]] | ||
| - | This is <scene name='Ozonolysis/Ozonolysis_step_1/4'>step one</scene> of ozonolysis. | ||
| - | |||
| - | This is <scene name='Ozonolysis/Ozonolysis_step_2/1'>step two</scene> of ozonolysis. | ||
| - | |||
| - | This is <scene name='Ozonolysis/Ozonolysis_step_3/1'>step three</scene> of ozonolysis. | ||
| - | |||
| - | This is <scene name='Ozonolysis/Ozonolysis_step_4/1'>step four</scene> of ozonolysis. | ||
| - | |||
| - | This is the <scene name='Ozonolysis/Ozonolysis_step_1_fix/2'>test scene</scene> | ||
| - | |||
| - | This should do something <scene name='Ozonolysis/Ozonolysis_step_1_fix/3'>test scene</scene> | ||
This should forgo transition <scene name='Ozonolysis/Ozonolysis_step_1_fix/6'>test scene</scene> | This should forgo transition <scene name='Ozonolysis/Ozonolysis_step_1_fix/6'>test scene</scene> | ||
| - | [[Image:Ozonolysis mechanism1.jpg]] | ||
Revision as of 08:37, 28 May 2008
Ozonolysis is a type of cycloaddition which destroys bonds. It starts with a 1,3-dipolar cycloaddition but eventually becomes a method of cleaving π bonds in an oxidative fashion, so that they end up as two carbonyl groups. The reagent for this reaction is ozone, O3.
Reaction
|
This should forgo transition
Acknowledgements
The animations of the ozonolysis reaction, as well as the 2D images of the reaction mechanism, were created by Nick Greeves. Many more reactions are viewable in an intuitive manner at http://www.chemtube3d.com.
