Mass Spectrometry (not shown): [M] = 158 m/z -1 Infrared Spectroscopy (not shown): 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm*¹ ¹H Nuclear Magnetic Resonance. 3 1³C Nuclear Magnetic Resonance. 180 4H 160 140 2 120 m 4HPPM 100 PPM 80 6H 60 40 20 O
Mass Spectrometry (not shown): [M] = 158 m/z -1 Infrared Spectroscopy (not shown): 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm*¹ ¹H Nuclear Magnetic Resonance. 3 1³C Nuclear Magnetic Resonance. 180 4H 160 140 2 120 m 4HPPM 100 PPM 80 6H 60 40 20 O
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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1. Draw the sketal structure from the mass spectrometry chart given
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
![Mass Spectrometry (not shown): [M] = 158 m/z
-1
Infrared Spectroscopy (not shown): 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm
¹H Nuclear Magnetic Resonance.
3
1³C Nuclear Magnetic Resonance.
180
4H
<
160
2
|_____||
120
140
4HPPM
100
PPM
t
80
6H
60
40
20
O](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fd7323f76-5a9c-46b6-9930-86cefe6607d1%2F162bf990-feb8-4c86-9ca1-68a0a6b95c6e%2Fubzk9lx_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Mass Spectrometry (not shown): [M] = 158 m/z
-1
Infrared Spectroscopy (not shown): 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm
¹H Nuclear Magnetic Resonance.
3
1³C Nuclear Magnetic Resonance.
180
4H
<
160
2
|_____||
120
140
4HPPM
100
PPM
t
80
6H
60
40
20
O
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