An unknown compound has the molecular formula C7H14O, and its 1H NMR and 13C NMR spectra are shown here. Determine the structure of the unknown compound and draw it below. Note that there are no peaks above 3 ppm in the 1H NMR, and the numbers present on the 1H NMR are the integration values for each set of peaks. (Also note that the protons responsible for causing the splitting pattern seen for the "9 peak" multiplet have similar coupling constants.)
An unknown compound has the molecular formula C7H14O, and its 1H NMR and 13C NMR spectra are shown here. Determine the structure of the unknown compound and draw it below. Note that there are no peaks above 3 ppm in the 1H NMR, and the numbers present on the 1H NMR are the integration values for each set of peaks. (Also note that the protons responsible for causing the splitting pattern seen for the "9 peak" multiplet have similar coupling constants.)
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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An unknown compound has the molecular formula C7H14O, and its 1H NMR and 13C NMR spectra are shown here. Determine the structure of the unknown compound and draw it below. Note that there are no peaks above 3 ppm in the 1H NMR, and the numbers present on the 1H NMR are the integration values for each set of peaks. (Also note that the protons responsible for causing the splitting pattern seen for the "9 peak" multiplet have similar coupling constants.)
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