## Abstract Electrochemical oxidation of various __para__‐ and __meta__‐substituted benzylamines in different mole fractions of 2‐methylpropan‐2‐ol in water has been investigated in the presence of 0.1 M sulfuric acid as supporting electrolyte. The oxidation potential data of benzylamines correlate
Solvent and substituent effects on the electrochemical oxidation of para- and meta-substituted anilines
✍ Scribed by D. S. Bhuvaneshwari; K. P. Elango
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 293 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Electrochemical oxidation of 15 para‐ and meta‐substituted anilines in different mole fractions of water in 2‐methylpropan‐2‐ol has been investigated in the presence of 0.1 M sulfuric acid as a supporting electrolyte. The oxidation potential data of anilines correlate well with the Brown–Okamoto's substituent constants affording a negative reaction constant. The effect of para‐ and meta‐substituents on the oxidation potential confirms to Swain's F and R, affording negative reaction constants. The oxidation potential values also correlate satisfactorily with macroscopic solvent parameter such as relative permittivity, ε~r~. The results of Kamlet–Taft multiple correlation analysis show that specific solute–solvent interactions play a dominant role in governing the reactivity. © 2007 Wiley Periodicals, Inc. Int J Chem Kinet 39: 289–297, 2007
📜 SIMILAR VOLUMES
## Abstract The solvent effect on a nucleophilic substitution reaction of 2‐ and 4‐chloro‐3,5‐dinitrobenzotrifluoride with substituted anilines was studied in methanol, acetonitrile, and toluene at 25°C. This reaction is of second order, except 2‐chloro‐3,5‐dinitrobenzotrifluoride in toluene shows
## Abstract The imidazolium fluorochromate (IFC) oxidation of __meta__‐ and __para__‐substituted anilines, in seven organic solvents, in the presence of __p__‐toluenesulfonic acid (TsOH) is first order in IFC and TsOH and is zero order with respect to substrate. The IFC oxidation of 15 __meta__‐ an
The effect of substituents on the activation energy for primary dissociation processes in the molecular ions of mono-andparu and meta di-substituted benzenes has been examined. Where the daughter ion retains the substituent group, variation of the energy of activation derives from a combination of t
The aniline molecule is nonplanar, with its NH 2 group lying at an angle θ of approximately 42 • to the plane of the benzene ring. Substituents on the phenyl ring alter this out-of-plane angle as well as other molecular properties such as the ring bond lengths and angles, the barrier to inversion E
## Abstract Pyridiniumchlorochromate (PCC) oxidizes aniline and substituted anilines except nitro anilines smoothly in chlorobenzene–nitrobenzene mixtures in the presence of dichloroacetic acid. The reaction has unit dependence on each of the aniline, PCC, and dichloroacetic acid concentrations. El