New Findings in the Electrophilic Addition of Halogens to Olefins
β Scribed by Priv.-Doz. Dr. Rainer Herges
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 322 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
**The presence of a negative partial charge on the benzylic carbon atom in the transition state** __(1)__ can be deduced from the experimentally determinable Hammett Ο± values. Alkyl radicals R^Λ^ are accordingly seen to develop nucleophilic properties during addition to olefins. equation image
The title reaction has been studied with 2-methoxypropene, (E)-cyclooctene, ethoxyethene, 1,3-cyclopentadiene, 3methylenecyclohexene, styrene and isoprene as the olefinic substrates. This sequence is one of decreasing reactivity of the substrates towards 2-oxido-2-cyclopenten-1-ylium (1) if [4 + 3]