1 Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Mass Spectrometry (not shown): [M] = 158 m/z Infrared Spectroscopy (not shown): 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm³ -1 ¹H Nuclear Magnetic Resonance. 3 180 t 13C Nuclear Magnetic Resonance. 160 4H 140 120 m 4HPPM 100 PPM 80 6H 60 40 20
1 Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Mass Spectrometry (not shown): [M] = 158 m/z Infrared Spectroscopy (not shown): 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm³ -1 ¹H Nuclear Magnetic Resonance. 3 180 t 13C Nuclear Magnetic Resonance. 160 4H 140 120 m 4HPPM 100 PPM 80 6H 60 40 20
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
ChapterL2: Mass Spectrometry
Section: Chapter Questions
Problem 3E
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please answer with structure and name of chemical compound!
![Information: Each spectra below was obtained from a pure compound.
Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm³¹
¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to
the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum.
Mass Spectrometry (not shown): [M] = 158 m/z
Infrared Spectroscopy (not shown): 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm³¹
¹H Nuclear Magnetic Resonance.
3
1³C Nuclear Magnetic Resonance.
180
4H
160
140
120
m
4HPPM
100
PPM
80
t
6H
60
40
20
0
0](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa451162e-14ac-4cfd-a2c6-1eae7f4a5f1a%2Fd720bb80-e6c9-41de-bd93-ac9e1adbedf2%2Fgxl0ba_processed.png&w=3840&q=75)
Transcribed Image Text:Information: Each spectra below was obtained from a pure compound.
Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm³¹
¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to
the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum.
Mass Spectrometry (not shown): [M] = 158 m/z
Infrared Spectroscopy (not shown): 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm³¹
¹H Nuclear Magnetic Resonance.
3
1³C Nuclear Magnetic Resonance.
180
4H
160
140
120
m
4HPPM
100
PPM
80
t
6H
60
40
20
0
0
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