To use all functions of this page, please activate cookies in your browser.
With an accout for my.chemeurope.com you can always see everything at a glance – and you can configure your own website and individual newsletter.
- My watch list
- My saved searches
- My saved topics
- My newsletter
Additional recommended knowledge
For example, two of the following isomers of norbornene violate Bredt's rule, which makes them too unstable to prepare:
In the figure, the bridgehead atoms involved in Bredt's rule violation are highlighted in red.
Bredt's rule is a consequence of the fact that having a double bond on a bridgehead would be equivalent to having a trans double bond on a ring, which is not possible for small rings (fewer than eight atoms) due to ring strain, and angle strain in particular.
Bredt's rule can be useful for predicting which isomer is obtained from an elimination reaction in a bridged ring system. It can also be applied to reaction mechanisms that go via carbocations and, to a lesser degree, via free radicals, because these intermediates, like carbon atoms involved in a double bond, prefer to have a planar geometry with 120 degree angles and sp2 hybridization.
An anti-bredt molecule is one that is found to exist and be stable (within certain parameters) despite this rule. A recent (2006) example such a molecule is 2-quinuclidonium tetrafluoroborate.
The first publication of what would later become known as Bredt's rule was in an article by Julius Bredt in 1924 about the chemistry of naturally occurring bicyclic terpenes. For an extensive review of this topic, see the article by Shea.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Bredt's_rule". A list of authors is available in Wikipedia.|