Ozonolysis
From Proteopedia
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[[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, O<sub>3</sub>. | [[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, O<sub>3</sub>. | ||
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<applet load='1ea5' size='500' frame='true' align='right' caption='Insert caption here' /> | <applet load='1ea5' size='500' frame='true' align='right' caption='Insert caption here' /> | ||
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| + | This is <scene name='Ozonolysis/Ozonolysis_step_1/1'>step one</scene> of ozonolysis. | ||
Revision as of 12:52, 27 April 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
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This is of ozonolysis.
