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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

Principles of Instrumental Analysis
Principles of Instrumental Analysis
7th Edition
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Chapter15: Molecular Luminescence Spectrometry
Section: Chapter Questions
Problem 15.6QAP
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1. Draw the sketal structure from the mass spectrometry chart given 

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
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
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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