## Abstract An accurate measurement of the chemical shifts and the coupling constants of some disubstituted acetophenones has been made. The acetophenones studied contained nitro, bromo or amino groups substituted in either the 3,4 or 2,5 positions. For compounds with no substituent adjacent to the
1H magnetic resonance spectroscopy of some substituted acetophenones
✍ Scribed by J. Bloxsidge; J. R. Jones; R. E. Marks
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- English
- Weight
- 141 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Measurements are reported on the nuclear magnetic resonance spectra of the acetyl protons of a series of substituted acetophenones. Although the extreme values of the chemical shifts, δ for the meta‐ and para‐ substituted compounds differ only by 0·2 units, the values themselves are linearly related to the Hammett substituent constants. No such relationship exists for the ortho‐substituted compounds. The magnitude of the chemical shift is independent of substrate concentration over a five‐fold variation.
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