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A statistical study of the additivity of substituent effects on the 5J(HH) long-range coupling constant of the formyl proton in substituted benzaldehydes

✍ Scribed by E. Kolehmainen; J. Knuutinen; P. J. Salovaara


Publisher
John Wiley and Sons
Year
1982
Tongue
English
Weight
167 KB
Volume
20
Category
Article
ISSN
0749-1581

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✦ Synopsis


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 additivity rule was detected with whole data. Using benzaldehyde as the reference substance, a good correlation was achieved for p‐hydroxybenzaldehydes. The same reference compound was not suitable for o‐hydroxy derivatives; a much better correlation was observed using o‐hydroxybenzaldehyde as a reference compound in the latter case.


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The effects of substituents on the 5J lo
✍ R. H. Contreras; D. G. de Kowalewski; A. Osella 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 189 KB 👁 1 views

## 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 prot