Absolute rate constants and Arrhenius parameters for the reaction of bromine atoms with ethane

1970 ◽  
Vol 66 ◽  
pp. 2794 ◽  
Author(s):  
Keith D. King ◽  
David M. Golden ◽  
Sidney W. Benson
1979 ◽  
Vol 57 (18) ◽  
pp. 2484-2490 ◽  
Author(s):  
J. A. Howard ◽  
J. H. B. Chenier

Rate constants and Arrhenius parameters for reaction of the tert-butylperoxy radical with 1-bromo-2-methylbutane and 1-bromo-3-methylbutane in solution from 30–80 °C have been estimated. The magnitude of these kinetic parameters are consistent with activation of the tertiary hydrogen vicinal to the bromine substituent and the involvement of a "bridged" transition state in the hydrogen atom transfer reaction.Chloro, trimethylsilyl, and trimethylstannyl substituents also activate a vicinal tertiary hydrogen and activation increases in the order trimethylsilyl ∼ trimethylstannyl < chloro < bromo.


1978 ◽  
Vol 9 (20) ◽  
Author(s):  
V. MADHAVAN ◽  
R. H. SCHULER ◽  
R. W. FESSENDEN

1965 ◽  
Vol 61 (0) ◽  
pp. 1417-1424 ◽  
Author(s):  
G. E. Adams ◽  
J. W. Boag ◽  
B. D. Michael

1971 ◽  
Vol 49 (12) ◽  
pp. 2178-2182 ◽  
Author(s):  
J. A. Howard ◽  
S. Korcek

Absolute rate constants for the liquid phase autoxidation of some organic sulfides at 30 °C have been measured. The reactivities of organic sulfides towards t-butylperoxy radicals are equal to or somewhat less than the reactivities of structurally analogous ethers. The α-alkylthiylalkylperoxy radicals appear to be about 3–5 times more reactive in hydrogen atom abstraction than the α-alkoxyalkylperoxy radicals.


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