Microwave spectra and conformation of trans-2-butenoic acid
β Scribed by Junji Shibano; Tomoaki Matsumoto; Tomoko Ishida; Masao Onda; Takeshi Sakaizumi; Osamu Ohashi; Ichiro Yamaguchi
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 487 KB
- Volume
- 190
- Category
- Article
- ISSN
- 0022-2860
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π SIMILAR VOLUMES
Aqueous iodination of trans-2-butenoic acid proceeds via hydrolysis of 12 to form HOI and I-, then rapid addition of HOI across the double bond to form the iodohydrin product. In the presence of iodate to keep iodide concentration low, the reaction proceeds a t a conveniently measurable rate. The ra
## Abstract Proton magnetic resonance spectral parameters of acrylic, __trans__βcrotonic and 3βbutenoic acids, their methyl esters and the corresponding alcohols (COOH substituted by CH~2~OH) have been measured for 5% (w/v) solutions in carbon tetrachloride and in pyridineβ__d__~5~ at 33Β·5 Β°C. The