## Abstract ^1^H, ^13^C and ^17^O NMR spectra for 22 substituted nitropyridines were measured and their ^1^H NMR spectra were analysed. The most significant variations in the NMR parameters are found for isomeric hydroxy derivatives, owing to the possibility of keto–enol tautomerism. The prevalence
13C, 17O and 1H NMR study of the protonation of acetone in water
✍ Scribed by Lian-fang Shen; You-Ru Du; Qian-fen Shao; Shi-zhen Mao
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 339 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
The protonation of acetone in water for a wide range of compositions of the binary mixture was studied by multinuclear NMR spectroscopy. Formation constants (Ill and K2) and 13C, "0 and 'H chemical shifts of the 1: 1 and 1:2 complexes were evaluated. The correlation of the 'H chemical shift of uncombined water with its concentration, 6,"~" = A + B In [H20b,, recently derived for the trimethyl phosphatewater system, was verified. A measure of the fraction of monomer species existing in the uncombined water at each composition was obtained. The results are discussed with respect to the structure of water.
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