CM23 Ме CI Br i) Sketch the 'H NMR spectrum of the molecule. You must annotate your spectra with "Jxy notation and suggest approximate chemical shifts. ii) Sketch the 19F NMR spectrum of the molecule. You must annotate your spectra with "Jxy notation.

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
Chapter14: Mass Spectrometry
Section: Chapter Questions
Problem 14.27P: Following is the mass spectrum of an unknown compound. The two highest peaks are at m/z 120 and 122....
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The structure of a molecule is shown below. The fluorines are diastereotopic.
F.
CM23
Me
CI
Br
i)
Sketch the H NMR spectrum of the molecule. You must annotate your
spectra with "Jxy notation and suggest approximate chemical shifts.
ii)
Sketch the 19F NMR spectrum of the molecule. You must annotate
your spectra with "Jxy notation.
Transcribed Image Text:The structure of a molecule is shown below. The fluorines are diastereotopic. F. CM23 Me CI Br i) Sketch the H NMR spectrum of the molecule. You must annotate your spectra with "Jxy notation and suggest approximate chemical shifts. ii) Sketch the 19F NMR spectrum of the molecule. You must annotate your spectra with "Jxy notation.
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