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  Home > JCE Print > Journal of Chemical Education > Issues > 2000  > July  >
In the Laboratory
The Discovery Approach to NMR: Development of Chemical-Shift Additivity Tables and Application to Product Identification
Eric Bosch
Department of Chemistry, Southwest Missouri State University, Springfield, MO 65804-0087

Cover
July 2000
Vol. 77 No. 7
p. 890

Abstract
A discovery-based approach to the preparation and application of chemical-shift additivity tables is presented to give students insight into the development of NMR spectral prediction software. The chemical shift of each proton in meta-dinitrobenzene is first assigned on the basis of the expected coupling constants (ortho, meta, and para) around a benzene ring. These chemical shifts are used to determine the chemical shift additivity for a nitro group ortho, meta, or para to hydrogen on a benzene nucleus. The chemical shift additivities obtained are then used to predict the NMR spectrum of the product of nitration of methylbenzoate.
More Information
*  Citation
Bosch, Eric. J. Chem. Educ. 2000 77 890.
*  Keywords
Internet; Laboratory Computing / Interfacing; Laboratory Instruction; NMR Spectrometry; Inquiry-Based / Discovery Method
*  History
Created:
Last Updated:
June 2, 2000
April 15, 2005
  Home > JCE Print > Journal of Chemical Education > Issues > 2000 > July > Page 890


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