A compound of formula C4H8Cl2 exhibits two signals in its ¹³C NMR. There are only primary RX (no secondary or tertiary) substituents. Provide the structure of this compound and calculate its degree of unsaturation.

A compound of formula C4H8Cl2 exhibits two signals in its ¹³C NMR. There are only primary RX (no secondary or tertiary) substituents. Provide the structure of this compound and calculate its degree of unsaturation.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.20P

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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

A compound of formula C4H8Cl2 exhibits two signals in its ¹³C NMR. There are
only primary RX (no secondary or tertiary) substituents. Provide the structure of this
compound and calculate its degree of unsaturation.

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