Energy disposal by the four-centered unimolecular hydrogen chloride elimination reaction

1978 ◽  
Vol 82 (23) ◽  
pp. 2461-2468 ◽  
Author(s):  
B. E. Holmes ◽  
D. W. Setser
Keyword(s):  
Hydrogen Chloride ◽  
Elimination Reaction ◽  
Chloride Elimination

Redox Chloride Elimination Reaction: Facile Solution Route for Indium-Free, Low-Voltage, and High-Performance Transistors

2017 ◽  
Vol 3 (3) ◽  
pp. 1600513 ◽  
Author(s):  
Ao Liu ◽  
Zidong Guo ◽  
Guoxia Liu ◽  
Chundan Zhu ◽  
Huihui Zhu ◽  
...  
Keyword(s):  
High Performance ◽  
Low Voltage ◽  
Elimination Reaction ◽  
Solution Route ◽  
Chloride Elimination

The kinetics and mechanisms of the gas phase pyrolyses of exo-2-norbornyl chloride and cyclopentyl chloride

1979 ◽  
Vol 57 (19) ◽  
pp. 2621-2625 ◽  
Author(s):  
J. L. Holmes ◽  
D. L. McGillivray ◽  
D. Yuan
Keyword(s):  
Gas Phase ◽  
Hydrogen Chloride ◽  
Isotope Effect ◽  
Deuterium Isotope Effect ◽  
Temperature Range ◽  
Elimination Reactions ◽  
Chloride Elimination ◽  
Kinetics Of

The gas phase pyrolyses of exo-2-norbornyl chloride and cyclopentyl chloride were studied in the temperature range 570–670 K. The results obtained show that these compounds behave as typical secondary halides insofar as the kinetics of their hydrogen chloride elimination reactions are concerned. Labelling experiments showed that in the formation of both norbornene and cyclopentene, a cis-1,2 elimination with a deuterium isotope effect of ∼3 was involved. Nortricyclene also was produced from exo-2-norbornyl chloride, via a trans 1,3 elimination; this process is analogous to a fragmentation of the ionized molecule. No gas phase Wagner–Meerwein rearrangement was involved in the formation of either norbornene or nortricyclene.

ChemInform Abstract: Regiospecific Hydrogen Chloride Elimination from α,β- Dichloroalkyl Phenyl Sulfides.

ChemInform ◽  
2010 ◽  
Vol 26 (23) ◽  
pp. no-no
Author(s):  
F. BELLESIA ◽  
F. GHELFI ◽  
U. M. PAGNONI ◽  
A. PINETTI
Keyword(s):  
Hydrogen Chloride ◽  
Chloride Elimination
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