A reverse __ortho__ effect is observed for the ^13^ C NMR chemical shifts of the carboxyl carbon (__δ__~co~) in benzoic acids measured in aprotic solvents of varying polarity. The __ortho__ effect on __δ__~co~ is best described by a combination of the reverse field and steric accelerating effects of
✦ LIBER ✦
Influence of Aprotic Solvents on the Transmission of Anomalous Substituent Effects on13C NMR Chemical Shifts at the Carboxyl Carbon (δco) inMeta-Substituted Benzoic Acids: A Strong Evidence for π-Polarization Mechanism
✍ Scribed by Susanta K. Sen Gupta; Ruchi Shrivastava
- Book ID
- 113051900
- Publisher
- Springer Vienna
- Year
- 2011
- Tongue
- English
- Weight
- 347 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0937-9347
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## Abstract The results of measurements of substituent induced chemical shifts of carboxyl carbons (δ~CO~) of dichloro‐ and difluorobenzoic acids, including the monosubstituted ones with substituents at __meta‐__ and/or __ortho‐__ positions, in chloroform‐d and strengths of these acids (log K) in c