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Draw an isomer of C5H11CI that would be expected to have three resonances in its 1³C NMR spectrum

Draw an isomer of C5H11CI that would be expected to have three resonances in its 1³C NMR spectrum

Chemistry
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
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Draw an isomer of C5H11Cl that would be expected to have three resonances in its 1³C NMR spectrum.
Transcribed Image Text:Draw an isomer of C5H11Cl that would be expected to have three resonances in its 1³C NMR spectrum.
13C NMR spectroscopy provides valuable information about the environments of a molecule's carbon atoms. Because carbon atoms are often connected to hydrogen atoms, which could split the carbon signal through spin-spin coupling, the coupling between C and H is often "turned off" through the use of broadband decoupling, causing each C signal to appear as a singlet.
Transcribed Image Text:13C NMR spectroscopy provides valuable information about the environments of a molecule's carbon atoms. Because carbon atoms are often connected to hydrogen atoms, which could split the carbon signal through spin-spin coupling, the coupling between C and H is often "turned off" through the use of broadband decoupling, causing each C signal to appear as a singlet.
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