## Abstract The additivity of chloro and hydroxy substituent effects on the formyl proton spin‐spin coupling constants with the __meta__ ring proton, ^5^__J__(HH), has been tested with 15 chlorinated benzaldehydes and hydroxybenzaldehydes by multiple linear regression analysis. No general additivit
The effects of substituents on the 5J long-range spin-spin coupling constants in substituted benzaldehydes
✍ Scribed by R. H. Contreras; D. G. de Kowalewski; A. Osella
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 189 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Proton magnetic resonance spectra of several mono‐ and disubstituted benzaldehydes were studied using CW, INDOR and double resonance techniques. It was verified that substitution in the para position has no effect on the long‐range coupling of the aldehydic proton with the ring protons five bonds away. Substitution in the ortho and meta positions (with the exception of 2,4‐dinitrobenzaldehyde) follows closely the additivity rule effects of the substituents.
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