## Abstract The 220 MHz spectra of the title compounds are reported and values for the internal ring dihedral angle, __Ψ__, formed between the C‐2C‐1 and C‐3C‐4 bonds, calculated using the R‐value method. The trimethyltetralone exists in a conformer having __Ψ__ = 51° and the 4‐methyl group in th
100 MHz n.m.r. spectra and conformational analysis of some methyl and trimethyl derivatives of 1-tetralone
✍ Scribed by Knut Bergesen; Michael J. Cook; Teh Kim Hock
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 505 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The 100 MHz spectra of 2‐methyl‐, 4‐methyl‐, 4,5,8‐trimethyl‐ and 4,5,7‐trimethyl‐1‐tetralones have been analysed as 8‐spin systems using iterative computation. The monomethyl derivatives exist in inverting half‐chair conformations, the 2‐methyl group favouring the equatorial site and the 4‐methyl group showing equal preference for both axial and equatorial environments. The 5‐methyl substituent of the trimethyl derivatives constrains the 4‐methyl group to the axial site of rings which adopt non‐half‐chair conformations. The n.m.r. spectrum of 3‐methyl‐1‐tetralone is also discussed.
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