Mass Spectrometry (not shown): [M] = 170 (100%) , [M+2] = 172 (100%) m/z Infrared Spectroscopy (not shown): 3064, 3031, 2968 cm ¹H Nuclear Magnetic Resonance. 8 m 5H 13C Nuclear Magnetic Resonance. 140 120 100 5 2H PPM 80 PPM 60 -3₂ 40 2 20 0 0

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Draw the sketal structure from the mass spec chart given. 

Mass Spectrometry (not shown): [M] = 170 (100%), [M+2] = 172 (100%) m/z
-1
Infrared Spectroscopy (not shown): 3064, 3031, 2968 cm ¹¹
¹H Nuclear Magnetic Resonance.
8
m
5H
1³C Nuclear Magnetic Resonance.
140
120
100
5
2H PPM
80
PPM
60
3
40
2
20
0
Transcribed Image Text:Mass Spectrometry (not shown): [M] = 170 (100%), [M+2] = 172 (100%) m/z -1 Infrared Spectroscopy (not shown): 3064, 3031, 2968 cm ¹¹ ¹H Nuclear Magnetic Resonance. 8 m 5H 1³C Nuclear Magnetic Resonance. 140 120 100 5 2H PPM 80 PPM 60 3 40 2 20 0
Unknown Number:
Draw the Skeletal Structure of the Unknown Compound.
Note - Formal skeletal structures do not include hydrogens on
521
any carbons (including the aldehyde C).
You should not need the X button to draw your answer
Transcribed Image Text:Unknown Number: Draw the Skeletal Structure of the Unknown Compound. Note - Formal skeletal structures do not include hydrogens on 521 any carbons (including the aldehyde C). You should not need the X button to draw your answer
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