**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
Transition State Geometry and Polar Effect in the Addition of Peroxyl Radicals to Olefins
β Scribed by T. G. Denisova; N. S. Emel'yanova
- Publisher
- Springer
- Year
- 2005
- Tongue
- English
- Weight
- 85 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0023-1584
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π SIMILAR VOLUMES
THE study of the direction of addition of reagents to unsymmetrically substituted open chain olefins has a long history, but until recently,' very rXh less information has been available concerning the effects of substituents on the direction of addition of reagents to cyclic olefinic bonds in a pla
We have reported' that photochemical addition of toluene and substituted toluenes to 9, lo-phenanthrenequinone (PQ) proceeds in a 1, Z-manner to give derivatives (I) of 9,10-dihydro-9-hydroxy-H. H. Lee, J. Chem. Sot., 2500 (1964). (9) Satisfactory analytical data and spectroscopic properties were o