Draw all constitutional isomers of molecular formula C3H6Cl2. a. How many signals does each isomer exhibit in its 1H NMR spectrum? b. How many lines does each isomer exhibit in its 13C NMR spectrum? c.When only the number of signals in both 1H and 13C NMR spectroscopy is considered, is it possible to distinguish all of these constitutional isomers?

Draw all constitutional isomers of molecular formula C3H6Cl2. a. How many signals does each isomer exhibit in its 1H NMR spectrum? b. How many lines does each isomer exhibit in its 13C NMR spectrum? c.When only the number of signals in both 1H and 13C NMR spectroscopy is considered, is it possible to distinguish all of these constitutional isomers?

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

Chapter13: Nuclear Magnetic Resonance Spectroscopy

Section13.7: Chemical Shift

Problem 13.5P: Following are two constitutional isomers with the molecular formula C4H8O2. (a) Predict the number...

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Following are two constitutional isomers with the molecular formula C4H8O2. (a) Predict the number of signals in the 1H-NMR spectrum of each isomer. (b) Predict the ratio of areas of the signals in each spectrum. (c) Show how you can distinguish between these isomers on the basis of chemical shift.
Draw all constitutional isomers of molecular formula C3H6Cl2.a. How many signals does each isomer exhibit in its 1H NMR spectrum?b. How many lines does each isomer exhibit in its 13C NMR spectrum?c. When only the number of signals in both 1H and 13C NMR spectroscopy is considered, is it possible to distinguish all of these constitutional isomers?
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