Kinetics of Aromatic Halogenation. III.1The Iodination of p-Chloroaniline with Iodine Monochloride

1956 ◽  
Vol 78 (15) ◽  
pp. 3632-3637 ◽  
Author(s):  
Ernst Berliner
ChemInform ◽  
1987 ◽  
Vol 18 (15) ◽  
Author(s):  
D. W. MARGERUM ◽  
P. N. DICKSON ◽  
J. C. NAGY ◽  
K. KUMAR ◽  
C. P. BOWERS ◽  
...  

1980 ◽  
Vol 35 (2) ◽  
pp. 254-255
Author(s):  
T. S. Rao ◽  
R. N. Jukar

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.


1986 ◽  
Vol 25 (27) ◽  
pp. 4900-4904 ◽  
Author(s):  
Dale W. Margerum ◽  
Peter N. Dickson ◽  
Julius C. Nagy ◽  
Krishan Kumar ◽  
Conrad P. Bowers ◽  
...  

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