(a) Draw all six isomers of formula C4H8 (including stereoisomers).(b) For each structure, show how many types of H would appear in the proton NMR spectrum.(c) For each structure, show how many types of C would appear in the 13C NMR spectrum.(d) If an unknown compound of formula C4H8 shows two types of H and three types of C, can you determine its structurefrom this information?

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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(a) Draw all six isomers of formula C4H8 (including stereoisomers).
(b) For each structure, show how many types of H would appear in the proton NMR spectrum.
(c) For each structure, show how many types of C would appear in the 13C NMR spectrum.
(d) If an unknown compound of formula C4H8 shows two types of H and three types of C, can you determine its structure
from this information?

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