A. Determine the M+ peak (Which m/z peak represents the M+ peak). B. Determine the chemical formula. Determine the degrees of unsaturation. What functional group does this compound contain? C. Identify the structure for the M+ peak and the base peak (tallest peak). Hint: Look for the most stable carbocation. dibero lu 100 llame eve 80 [S+M] S JOY ONDE Relative Intensity 60 40 20 0 10 seenq sinagotin 20 belom besod Tuoy to exurio 30 40 50 m/z 60 70 80 twelver

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
ChapterL3: Carbon (13c) Nmr Spectroscopy
Section: Chapter Questions
Problem 14CTQ
Question
The compound being investigated only has carbons and hydrogens.
A. Determine the M+ peak (Which m/z peak represents the M+ peak).
B. Determine the chemical formula. Determine the degrees of unsaturation. What
functional group does this compound contain?
C. Identify the structure for the M+ peak and the base peak (tallest peak). Hint: Look for
the most stable carbocation.
ibero lut
100-
llame eve
Relative Intensity
80-
[S+M] 00
JOY ORDE
bruct
60
40
20
0
10
elubelom
20
30
0001 Tuoy to exurio
40
50
m/z
60
70
80
welven
Jorn
sed eri
Transcribed Image Text:A. Determine the M+ peak (Which m/z peak represents the M+ peak). B. Determine the chemical formula. Determine the degrees of unsaturation. What functional group does this compound contain? C. Identify the structure for the M+ peak and the base peak (tallest peak). Hint: Look for the most stable carbocation. ibero lut 100- llame eve Relative Intensity 80- [S+M] 00 JOY ORDE bruct 60 40 20 0 10 elubelom 20 30 0001 Tuoy to exurio 40 50 m/z 60 70 80 welven Jorn sed eri
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