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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Question
![HA
29. Draw a splitting diagram for HA and indicate the expected splitting pattern.
Hc
Draw splitting diagrams for complex splitting patterns.
30. Determine the structure of the compound C10H14 whose 13C NMR spectrum is shown below.
16.12 OBJ:
REF:
n oomp 0
0.
50.
Chemical shift (ppm)
120](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fea9cc4aa-6448-4354-8c80-3956c9525a82%2F5470aafa-4604-4e42-ba7e-f07333ce36e8%2F4xnu5nt_processed.jpeg&w=3840&q=75)
Transcribed Image Text:HA
29. Draw a splitting diagram for HA and indicate the expected splitting pattern.
Hc
Draw splitting diagrams for complex splitting patterns.
30. Determine the structure of the compound C10H14 whose 13C NMR spectrum is shown below.
16.12 OBJ:
REF:
n oomp 0
0.
50.
Chemical shift (ppm)
120
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In the proton NMR the splitting of signals is always due to non-equivalent neighboring proton and they are usually at two or three bond distance.
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