The proton NMR spectrum of a compound with formula C7H12O3 is shown. the coupling constant for the triplet at 1.25 ppm is of the same magnitude as the one for the the quartet at 4.15 ppm. The pair of distorted triplets at 2.56 and 2.75 ppm are coupled to each other. The infrared spectrum displays strong bands at 1720 and 1738 cm-1. The normal carbon-13 and the DEPT experimental results are tabulated. Draw the structure of this compound.
The proton NMR spectrum of a compound with formula C7H12O3 is shown. the coupling constant for the triplet at 1.25 ppm is of the same magnitude as the one for the the quartet at 4.15 ppm. The pair of distorted triplets at 2.56 and 2.75 ppm are coupled to each other. The infrared spectrum displays strong bands at 1720 and 1738 cm-1. The normal carbon-13 and the DEPT experimental results are tabulated. Draw the structure of this compound.
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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The proton NMR spectrum of a compound with formula C7H12O3 is shown. the coupling constant for the triplet at 1.25 ppm is of the same magnitude as the one for the the quartet at 4.15 ppm. The pair of distorted triplets at 2.56 and 2.75 ppm are coupled to each other. The infrared spectrum displays strong bands at 1720 and 1738 cm-1. The normal carbon-13 and the DEPT experimental results are tabulated. Draw the structure of this compound.
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