Organic Chemistry I For Dummies, 2nd Edition
Book image
Explore Book Buy On Amazon

Ozonolysis is a way of cleaving carbon-carbon double bonds into two fragments using ozone (O3) as a reagent. The fragments formed are either aldehydes or ketones, depending on the nature of the R groups attached to the double bond, as shown here.

The ozonolysis of an alkene.
The ozonolysis of an alkene.

If both R groups on one side of the double bond are alkyl groups, that side of the double bond will become a ketone fragment; if only one R group is an alkyl group and the other R is a hydrogen, that side of the double bond will become an aldehyde fragment.

A quick way of determining the products of ozonolysis is to visually snip the double bond as shown in the next figure, and then to cap both sides with oxygens to make the carbonyl compounds.

Determining products of ozonolysis.
Determining products of ozonolysis.

A common exam problem is one that asks you to determine the structure of the starting alkene given the products of ozonolysis. If you remember how to determine the products of ozonolysis and then work backward from that reaction (snip off the oxygens, and then smoosh the two pieces together), you get the starting alkene.

About This Article

This article is from the book:

About the book author:

Arthur Winter, PhD, is a chemistry professor at Iowa State University.

This article can be found in the category: