## Abstract Carbon‐13, proton coupling constants have been measured in eighteen different 2‐substituted propanes. ^1^__J__(C‐2,H) shows variations similar to those observed previously for monosubstituted methanes. ^2^__J__(C‐2,H) is essentially independent of the substituent at C‐2, while ^2^__J__(
Geminal carbon-proton spin-spin coupling constants in ethyl, isopropyl and tert-butyl compounds
✍ Scribed by Tom Spoormaker; Marius J. A. de Bie
- Book ID
- 104588236
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 364 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
The geminal ^13^C^1^H coupling constants in ethyl, isopropyl and tert‐butyl compounds having elements of the first row of the Periodic Table and halogens as substituents are determined by single resonance ^13^C FT NMR spectroscopy. In addition, the values of directly bonded ^13^C^13^C coupling constants are given. The substituent electronegativity dependence of the geminal ^13^C^1^H coupling constant is discussed. It is concluded that the influence exerted by a β‐methyl substituent on the geminal ^13^C^1^H coupling constant of 13C^α^‐C^β^‐^1^H fragments is not constant and hence no simple additivity relation can be established for this coupling constant.
📜 SIMILAR VOLUMES
## Abstract The increments in ^3^__J__(CH) for substituents attached to C^γ^ in the ^13^C^α^‐C^β^‐C^γ^‐^1^H coupling pathway, with respect to ^3^__J__(CH) in propane are calculated for equal C^β^‐C^γ^ rotamer population from ^3^__J__(CH) observed in the corresponding neopentyl compounds. From th