✦ LIBER ✦

Influence of substituent electronegativities on conformational preferences in 1,2-disubstituted ethanes

✍ Scribed by Leo Radom; Peter J. Stiles; Mark A. Vincent

Book ID: 118330258
Publisher: Elsevier Science
Year: 1978
Tongue: English
Weight: 817 KB
Volume: 48
Category: Article
ISSN: 0022-2860
DOI: 10.1016/0022-2860(78)87253-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Conformational studies on 2-fluoro-1,2-d

Conformational studies on 2-fluoro-1,2-disubstituted ethanes by NMR spectroscopy. Influence of electronegativity on vicinal proton–proton and fluorine–proton coupling constants

✍ Sylvain Hamman; Claude Béguin; Claude Charlon; Cuong Luu-Duc 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 English ⚖ 570 KB

The gauche effect : On the nature of the

The gauche effect : On the nature of the interaction between electronegative substituents in trans-1,2-disubstituted cyclohexanes

✍ Nikolai S. Zefirov; V.V. Samoshin; O.A. Subbotin; V.I. Baranenkov; Saul Wolfe 📂 Article 📅 1978 🏛 Elsevier Science 🌐 French ⚖ 567 KB

On the structural differences of conform

On the structural differences of conformers (a study of 1,2-disubstituted ethanes and ethenes)

✍ Peter Scharfenberg; István Hargittai 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 422 KB

Is There a General Rule for the Gauche E

Is There a General Rule for the Gauche Effect in the Conformational Isomerism of 1,2-Disubstituted Ethanes?

✍ Freitas, Matheus P.; Rittner, Roberto 📂 Article 📅 2007 🏛 American Chemical Society 🌐 English ⚖ 97 KB

Solute−Solvent Interactions in Liquid No

Solute−Solvent Interactions in Liquid Noble Gases As Probed by the Conformational Equilibrium of Some 1,2-Disubstituted Ethanes

✍ Herrebout, W. A.; van der Veken, B. J. 📂 Article 📅 1996 🏛 American Chemical Society 🌐 English ⚖ 669 KB

Conformational Preferences of Alkyl Subs

Conformational Preferences of Alkyl Substituents in 5-Me-5-R-1, 2, 3-Trithianes

✍ G. Goor; M. Anteunis 📂 Article 📅 2010 🏛 Wiley (John Wiley & Sons) ⚖ 136 KB

## Abstract Variable temperature ^1^H‐NMR‐study of 5‐Me‐5‐R‐1,2,3‐trithianes shows an axial preference for linear and α‐branched groups; this preference is disfavoured by β‐substitution. The Ph‐group takes exclusively the equatorial position.