Absolute rate constants for the additions of halophenylcarbenes to alkenes: a reactivity-selectivity relation
β Scribed by D.Phillip Cox; Ian R. Gould; Nigel P. Hacker; Robert A. Moss; Nicholas J. Turro
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 214 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The absolute rate constants determined for the additions of FCPh, ClCPh, and BrCPh to Me2C=CMez, MepC=CHMe, trans-MeCH=CHEt, and n-BuCH=CH2 appear to follow a reactivity/selectivity pattern of the "normal" (inverse) type.
π SIMILAR VOLUMES
Absolute rate constants and their temperature dependencies were determined for the addition of hydroxymethyl radicals ( C H 2 0 H ) to 20 monoor 1,l-disubstituted alkenes (CH2 = C X Y ) in methanol by time-resolved electron spin resonance spectroscopy. With the alkene substituents the rate constants