The kinetics of reactions of chlorine, bromine, bromine monochloride, iodine monochloride, and iodine monobromide with phenyltrimethylsilane

1979 ◽  
pp. 117 ◽  
Author(s):  
John R. Chipperfield ◽  
Ronald Z. Fernandez ◽  
David E. Webster
Keyword(s):  
Iodine Monochloride ◽  
Iodine Monobromide ◽  
Kinetics Of

scholarly journals Spectroscopic Studies of Charge Transfer Complexes. VII. Acrylonitrile and Iodine, Iodine Monochloride and Iodine Monobromide.

1963 ◽  
Vol 17 ◽  
pp. 1179-1180 ◽  
Author(s):  
Peter Klæboe ◽  
Einar Jacobsen ◽  
Eeva-Liisa Syväoja ◽  
Armi Alivaara ◽  
M. Trætteberg
Keyword(s):  
Charge Transfer ◽  
Spectroscopic Studies ◽  
Charge Transfer Complexes ◽  
Iodine Monochloride ◽  
Iodine Monobromide

ChemInform Abstract: Kinetics of the Iodine Monochloride Reaction with Iodide Measured by the Pulsed-Accelerated-Flow Method.

ChemInform ◽  
1987 ◽  
Vol 18 (15) ◽  
Author(s):  
D. W. MARGERUM ◽  
P. N. DICKSON ◽  
J. C. NAGY ◽  
K. KUMAR ◽  
C. P. BOWERS ◽  
...  
Keyword(s):  
Iodine Monochloride ◽  
Flow Method ◽  
Accelerated Flow ◽  
Kinetics Of

A Comparative Study of the Kinetics of Electrophilic Substitution in Aromatic Substrates by Iodine Monochloride and Iodine in Potassium Iodide

1980 ◽  
Vol 35 (2) ◽  
pp. 254-255
Author(s):  
T. S. Rao ◽  
R. N. Jukar
Keyword(s):  
Comparative Study ◽  
Potassium Iodide ◽  
Electrophilic Substitution ◽  
Iodine Monochloride ◽  
Electrophilic Attack ◽  
Aromatic Substrates ◽  
Kinetics Of

Abstract Electrophilic substitution in aromatic substrates by iodine monochloride is about 105 times faster than by iodine in potassium iodide. This is due to the permanent dipole in the iodine monochloride, with iodine as the positive end, which greatly facilitates electrophilic attack.

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