Polarographic Behavior of Organic Compounds. XIV. Carbon—Halogen Bond Fission in System Acid—Anion—Ester; Estimation of Acid Half-wave Potentials

1952 ◽  
Vol 74 (23) ◽  
pp. 6112-6113 ◽  
Author(s):  
Isadore Rosenthal ◽  
Ching-Siang Tang ◽  
Philip J. Elving
2009 ◽  
Vol 74 (11-12) ◽  
pp. 1777-1789 ◽  
Author(s):  
Petr Zuman

There are two possibilities how to follow equilibria of organic compounds established in aqueous solutions using polarography: for very fast reactions, information can be obtained from shifts of half-wave potentials. For slowly established equilibria, the changes in the limiting current are followed. In both cases variation of the half-wave potentials or limiting currents with concentration of a reactant, present in excess, is followed. The types of reactions, which had been followed in this way, are as follows: hydration–dehydration equilibria, additions of hydroxide ion to carbonyl and nitroso compounds, the role of slowly established acid–base equilibria involving C-acids; further also reactions involving the addition of ammonia, primary amines, hydroxylamine, and hydrazine to carbonyl compounds.


1950 ◽  
Vol 72 (7) ◽  
pp. 3241-3243 ◽  
Author(s):  
William J. Seagers ◽  
Philip J. Elving

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