✦ LIBER ✦
Conformational preference of aromatic ketones and aldehydes determined by nuclear overhauser effect difference spectroscopy indicates aromatic π-electron density
✍ Scribed by Lawrence I. Kruse; Jin K. Cha
- Book ID
- 104217377
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 168 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
NOE difference spectra of aromatic aldehydes and ketones demonstrate the carbonyl group favors an s-trans orientation to the ortho position of highest double bond character.