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Overview of typical 1H NMR shifts. Note: alkene region modified from earlier handout.
H NMR tables. Overview of typical 1H NMR shifts . 1H NMR Tables . FROM TABLE 14.4 (LABBOOK) OR TABLE H.6 (SPEC BOOK) Substituted Alkanes 1. 1.
A GUIDE TO 1H NMR CHEMICAL SHIFT VALUES. Nuclear Magnetic Resonance (NMR) is a commonly used technique for organic compound structure determination. In 1H NMR, applying an external magnetic field causes the nuclei spin to flip.
1H-NMR Chemical Shift Table 10.5 9.0 8.0 6.5 13.0 10.0 7.8 6.5 8.0 5.0 8.8 7.6 14 13.5 13 12.5 12 11.5 11 10.5 10 9.5 9 8.5 8 7.5 7 6.5 6 ppm H H O OH O H HO N H O N H. Title: Chemical Shift Table.xls Author: Matt Bowman Created Date:
If a protic deuterated solvent is used (e.g., D2O or CD3OD), then the NH and OH protons will exchange with the deuterium and the peaks will shrink or disappear entirely, since D (2H) does not show up in the 1H NMR spectrum.
AROMATIC RING PEAK SHAPES AND DISTRIBUTIONS FOR AROMATIC RINGS WITH ONE GROUP ATTACHED. There are generally three possible ways for aromatic peaks to appear in a H NMR spectrum when only one group is attached the ring. STRONG DEACTIVATING GROUPS have a partially positive atom attached directly to ring. These include C=O, NO2, CN and S=O groups.
1.1 Scope and Organization. The present data collection is intended to serve as an aid in the interpretation of molecular spectra for the elucidation and confirmation of the structure of organic compounds. It consists of reference data, spectra, and empirical correlations from.
