## Abstract ^13^C FT single resonance spectra are obtained for two isomers of 2,6‐dichloro‐1,4‐oxathiane; one of the isomers is a racemic mixture. From a combined study of the various long‐range carbon‐proton coupling constants the conformations of both isomers could be determined. Each isomer exis
✦ LIBER ✦
A Penney—Dirac bond order study of the geminal proton—carbon-13 coupling constants in unsaturated systems
✍ Scribed by P. Mohanakrishnan
- Book ID
- 119116910
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 569 KB
- Volume
- 149
- Category
- Article
- ISSN
- 0166-1280
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## Abstract Orientation effects of electronegative substituents on vicinal carbon‐proton coupling constants are studied in 1,2‐disubstituted propanes and are found to resemble those on vicinal proton‐proton coupling constants. Known relations for the orientation effect of substituents on synclinal