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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 cm¹ ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (/-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): 2982, 1731, 1717, 1149 cm² ¹H Nuclear Magnetic Resonance. "C Nuclear Magnetic Resonance. 220 2H 200 180 160 140 3H PPM 120 100 9H 80 8 8 20

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 cm¹ ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (/-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): 2982, 1731, 1717, 1149 cm² ¹H Nuclear Magnetic Resonance. "C Nuclear Magnetic Resonance. 220 2H 200 180 160 140 3H PPM 120 100 9H 80 8 8 20

Organic Chemistry: A Guided Inquiry
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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determine the chemical structure and name the structure.

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 cm¹ ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (/-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): 2982, 1731, 1717, 1149 cm³¹ ¹H Nuclear Magnetic Resonance. 1³C Nuclear Magnetic Resonance. 220 2H 200 180 160 140 2 3H PPM 120 PPM 100 9H 80 60 40 8 o
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 cm¹ ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (/-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): 2982, 1731, 1717, 1149 cm³¹ ¹H Nuclear Magnetic Resonance. 1³C Nuclear Magnetic Resonance. 220 2H 200 180 160 140 2 3H PPM 120 PPM 100 9H 80 60 40 8 o
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So which way do you write it? Like this or this? Also, what is the name of the structure.

N مهلا Methyl-4,4-dimethyl-3-oxopentanoate
Transcribed Image Text:N مهلا Methyl-4,4-dimethyl-3-oxopentanoate
ChemNMR ¹3³C Estimation 30.3 220 200.4 H3C 50.6 28.7 CH3 81.8-CH328.7 H₂ 166.4 CH3 28.7 200 180 160 140 120 100 PPM 80 60 40 20
Transcribed Image Text:ChemNMR ¹3³C Estimation 30.3 220 200.4 H3C 50.6 28.7 CH3 81.8-CH328.7 H₂ 166.4 CH3 28.7 200 180 160 140 120 100 PPM 80 60 40 20
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