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 oftenconnected 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.

13C-NMR spectroscopy is mainly used for the identification of carbon skeletal present in the organic…

Answered: Draw an isomer of C5H11CI that would be…

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

Principles of Modern Chemistry

8th Edition

ISBN:9781305079113

Author:David W. Oxtoby, H. Pat Gillis, Laurie J. Butler

Publisher:David W. Oxtoby, H. Pat Gillis, Laurie J. Butler

Chapter20: Molecular Spectroscopy And Photochemistry

Section: Chapter Questions

Problem 51AP

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Concept explainers

NMR Spectroscopy

NMR stands for Nuclear Magnetic Resonance in which the study of different molecules is done based on the interaction of radiofrequency electromagnetic radiations with the nuclei of molecules placed in a strong magnetic field. A precise study of spectra of visible light and all bands of electromagnetic radiation is called spectroscopy.

Question

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.

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