A Study of the Formation of Haloamines and Cyclic Amines by the Free Radical Chain Decomposition of N-Haloammonium Ions (Hofmann-Löffler Reaction)1

1960 ◽  
Vol 82 (7) ◽  
pp. 1657-1668 ◽  
Author(s):  
E. J. Corey ◽  
Walter R. Hertler
Keyword(s):  
Free Radical ◽  
Radical Chain ◽  
Chain Decomposition ◽  
Cyclic Amines

The thermal dissociation and pyrolysis of ethane

1963 ◽  
Vol 275 (1361) ◽  
pp. 190-199 ◽  
Keyword(s):  
Free Radical ◽  
Thermal Dissociation ◽  
Experimental Results ◽  
Methane Formation ◽  
Methyl Radicals ◽  
Order Process ◽  
Radical Chain ◽  
Chain Decomposition ◽  
First Order ◽  
Kinetics Of

The kinetics of methane formation during the pyrolysis of ethane have been examined experimentally. It has been shown that under the conditions commonly used for the pyrolysis of hydrocarbons, the dissociation of ethane into methyl radicals is a first-order process of velocity constant log 10 k 1 = (17.45 ±0.82) - 91740 ±1400/2.303 RT (S -1 ) The kinetics of the free-radical chain decomposition of ethane are interpreted in the light of this and other experimental results.

ChemInform Abstract: New Free-Radical Chain Processes Involving Substitution of Vinyl and Aryl Chlorides by Alkanes, Alkenes, Esters, and Ethers.

ChemInform ◽  
2010 ◽  
Vol 28 (4) ◽  
pp. no-no
Author(s):  
S. ARANEO ◽  
R. ARRIGONI ◽  
H.-R. BJOERSVIK ◽  
F. FONTANA ◽  
L. LIGUORI ◽  
...  
Keyword(s):  
Free Radical ◽  
Radical Chain ◽  
Aryl Chlorides ◽  
Chain Processes

scholarly journals The detection and inhibition of free radical chain reactions

1942 ◽  
Vol 180 (982) ◽  
pp. 237-256 ◽  
Keyword(s):  
Nitric Oxide ◽  
Free Radical ◽  
Chemical Analysis ◽  
Diethyl Ether ◽  
Pressure Increase ◽  
Stationary States ◽  
Decomposition Rates ◽  
Radical Chain ◽  
Chain Reactions ◽  
Limiting Values

Part I. Comparison of nitric oxide and propylene as inhibitors The reduction by propylene of the rate of pressure increase in the decomposition of propaldehyde at 550° has been shown by chemical analysis to represent a true inhibition of the reaction, and not to be due n an important degree to an induced polymerization of the propylene. With propaldehyde and with diethyl ether the limiting values to which the decomposition rates are reduced by nitric oxide and by propylene respectively are the same, although much more propylene is required to produce a given degree of inhibition. From this it is concluded that the limiting rates are more probably those of independent non-chain processes, than those characteristic of stationary states where the inhibitor starts and stops chains with equal efficiency.

The reaction of thionitrites with barton esters: a convenient free radical chain reaction for decarboxylative nitrosation

Tetrahedron ◽  
1999 ◽  
Vol 55 (12) ◽  
pp. 3573-3584 ◽  
Author(s):  
Pierre Girard ◽  
Nadine Guillot ◽  
William B. Motherwell ◽  
Robyn S. Hay-Motherwell ◽  
Pierre Potier
Keyword(s):  
Free Radical ◽  
Chain Reaction ◽  
Radical Chain ◽  
Free Radical Chain Reaction ◽  
Radical Chain Reaction
Sign in / Sign up

Export Citation Format

Share Document