## 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 Brow
Substituent effects in mass spectrometry—II. The effect of substituents on the dissociation of para and meta disubstituted benzenes
✍ Scribed by F. Benoit
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- English
- Weight
- 316 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
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 the effects of substituents on the ionisation potential of the molecular ion and the appearance potential of the daughter ion. An equation relating the energy of activation for the fragmentation of the molecular ion of a mono-substituted benzene to that of related para and ineta di-substituted benzenes is presented.
📜 SIMILAR VOLUMES
## Abstract Three empirical equation which have been used to calculate ionisation potentials of para and __meta__ disubstituted benzenes are evalyated according to their ability to predict the IP's of __para__ and __meta__ YC~6~H~4~COX, (where x OH, NH~2~, CL).
## Abstract In __para__‐disubstituted benzenes, the effect of one substituent is transferred to the other composite substituent group and its decreased influence on the __ortho__ and __meta__ protons is reflected in their chemical shifts. A graphical presentation of this linear non‐additive depende
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