![/tmp/Hussein-2012.jpg Mass Spectrometry (not shown): [M] 156 (75 % ) , [ M+ 2] = 158 (100 % ) , [M+ 4] 160 (25 % ) m/ Infrare](http://img.homeworklib.com/questions/af930460-715b-11ea-b4b4-15143d9a99c7.png?x-oss-process=image/resize,w_560)
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Mass Spectrometry (not shown): [M)-146 m/z Infrared Spectroscopy (not shown): 2988, 1752, 1723, 1221 cm H...
Based on mass spectrometry, infrared spectroscopy, H NMR and CNMR, what could the following two unknowns...
Based on mass spectrometry, infrared spectroscopy, H NMR and
CNMR, what could the following two unknowns be?
1.2.
Mass Spectrometry (not shown): [M] = 134 m/z Infrared Spectroscopy (not shown): 3073, 2924, 1714, cm 'H Nuclear Magnetic Resonance. 3 5H PPM 2H Sc Nuclear Magnetic Resonance. 220 200 180 160 140 120 100 80 60 40 20 0 Mass Spectrometry (not shown): [M] = 156 (75%), [M+2] = 158 (100%), (M+4) = 160 (25%) m/z Infrared Spectroscopy (not shown): 2966,...
Based on mass spectrometry, infrared spectroscopy, H NMR and CNMR, what could the following unknown be?...
Based on mass spectrometry, infrared spectroscopy, H NMR and
CNMR, what could the following unknown be?
Mass Spectrometry (not shown): [M] = 156 (75%), [M+2] = 158 (100%), [M+4] = 160 (25%) m/z Infrared Spectroscopy (not shown): 2966, 2910 cm H Nuclear Magnetic Resonance. quin 2 2H PPM 1 0 4 2H 2H 13C Nuclear Magnetic Resonance. 20 35 25 PPM 15 45 40 30 10
Mass Spectrometry (not shown: [M]-200 (50%) IM+2]- 202 (100%) M4]-204 (50%) m/z Infrared Spectroscopy (not shown):...
Mass Spectrometry (not shown: [M]-200 (50%) IM+2]- 202 (100%) M4]-204 (50%) m/z Infrared Spectroscopy (not shown): 2968, 2906 cm H Nuclear Magnetic Resonance. t 221 "C Nuclear Magnetic Resonance. part of the spectrum Mass Spectrometry (not shown): M-146 m/ Infrared Spectroscopy (not shown): 2967,1739, 1164 am H Nuclear Magnetic Resonance. SH "C Nuclear Magnetic Resonance. 180 40 20 160 140 120 80 PPM
Mass Spectrometry (not shown): [M] = 134 m/z Infrared Spectroscopy (not shown): 3073, 2924, 1714, cm...
Mass Spectrometry (not shown): [M] = 134 m/z Infrared Spectroscopy (not shown): 3073, 2924, 1714, cm 'H Nuclear Magnetic Resonance. PPM 2н c Nuclear Magnetic Resonance. 220 .200 . 180 . 160 .140 . 120 100 . 80 . 60 . 40
Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are...
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 'H 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...
Spectroscopy Unknown What is the Structure? Information: Each spectra below was obtained from a pure compound....
Spectroscopy Unknown
What is 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 cm 'H 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...
Information: Each spectra below was obtained from a pure compound Mass Spectrum parent peaks (M) are listed for all ex...
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 *H 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...
What structure would these create? Please explain how to solve this, thanks. Mass Spectrometry (not shown):...
What structure would these
create? Please explain how to solve this, thanks.
Mass Spectrometry (not shown): [M] = 108 m/z Infrared Spectroscopy (not shown): 3033, 3003, 2957, 2945, 2836, 1601, 1498, 1248, 1041 cm "H Nuclear Magnetic Resonance. mm 2H 3H PPM 3H 13C Nuclear Magnetic Resonance. 160 ' 140 120 100 80 60 40 20 o PPM
Draw the structure of the molecule given in the following information: Mass Spectrometry (not shown): [M]...
Draw the structure of the molecule given in the following
information:
Mass Spectrometry (not shown): [M] = 146 m/z Infrared Spectroscopy (not shown): 2967, 1739, 1164 cm 'H Nuclear Magnetic Resonance. 13c Nuclear Magnetic Resonance. 180 . 160 .140 . 120 . 109.,' 80 ' 60 ' 40
Draw the Skeletal Structure of the unknown compound. Formal skeletal structures do not include hydrogens on...
Draw the Skeletal Structure of the unknown compound. Formal
skeletal structures do not include hydrogens on any carbons
(including the aldehyde C).
Mass Spectrometry (not shown): [M] = 122 (100%), [M+2] = 124 (100%) m/z Infrared Spectroscopy (not shown): 2988, 2973 cm 'H Nuclear Magnetic Resonance. ET 3 PPM 2H 2 GH " Nuclear Magnetic Resonance. Mass Spectrometry (not shown): [M] = 147 (100%), (M+2] = 149 (100%) m/z Infrared Spectroscopy (not shown): 2969, 2935, 2249 cm 'H Nuclear Magnetic...
Based on mass spectrometry, infrared spectroscopy, H NMR and
CNMR, what could the following two unknowns be?
1.2.
Mass Spectrometry (not shown): [M] = 134 m/z Infrared Spectroscopy (not shown): 3073, 2924, 1714, cm 'H Nuclear Magnetic Resonance. 3 5H PPM 2H Sc Nuclear Magnetic Resonance. 220 200 180 160 140 120 100 80 60 40 20 0 Mass Spectrometry (not shown): [M] = 156 (75%), [M+2] = 158 (100%), (M+4) = 160 (25%) m/z Infrared Spectroscopy (not shown): 2966,...
Based on mass spectrometry, infrared spectroscopy, H NMR and
CNMR, what could the following unknown be?
Mass Spectrometry (not shown): [M] = 156 (75%), [M+2] = 158 (100%), [M+4] = 160 (25%) m/z Infrared Spectroscopy (not shown): 2966, 2910 cm H Nuclear Magnetic Resonance. quin 2 2H PPM 1 0 4 2H 2H 13C Nuclear Magnetic Resonance. 20 35 25 PPM 15 45 40 30 10
Mass Spectrometry (not shown: [M]-200 (50%) IM+2]- 202 (100%) M4]-204 (50%) m/z Infrared Spectroscopy (not shown): 2968, 2906 cm H Nuclear Magnetic Resonance. t 221 "C Nuclear Magnetic Resonance. part of the spectrum Mass Spectrometry (not shown): M-146 m/ Infrared Spectroscopy (not shown): 2967,1739, 1164 am H Nuclear Magnetic Resonance. SH "C Nuclear Magnetic Resonance. 180 40 20 160 140 120 80 PPM
Mass Spectrometry (not shown): [M] = 134 m/z Infrared Spectroscopy (not shown): 3073, 2924, 1714, cm 'H Nuclear Magnetic Resonance. PPM 2н c Nuclear Magnetic Resonance. 220 .200 . 180 . 160 .140 . 120 100 . 80 . 60 . 40
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 'H 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...
Spectroscopy Unknown
What is 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 cm 'H 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...
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 *H 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...
What structure would these
create? Please explain how to solve this, thanks.
Mass Spectrometry (not shown): [M] = 108 m/z Infrared Spectroscopy (not shown): 3033, 3003, 2957, 2945, 2836, 1601, 1498, 1248, 1041 cm "H Nuclear Magnetic Resonance. mm 2H 3H PPM 3H 13C Nuclear Magnetic Resonance. 160 ' 140 120 100 80 60 40 20 o PPM
Draw the structure of the molecule given in the following
information:
Mass Spectrometry (not shown): [M] = 146 m/z Infrared Spectroscopy (not shown): 2967, 1739, 1164 cm 'H Nuclear Magnetic Resonance. 13c Nuclear Magnetic Resonance. 180 . 160 .140 . 120 . 109.,' 80 ' 60 ' 40
Draw the Skeletal Structure of the unknown compound. Formal
skeletal structures do not include hydrogens on any carbons
(including the aldehyde C).
Mass Spectrometry (not shown): [M] = 122 (100%), [M+2] = 124 (100%) m/z Infrared Spectroscopy (not shown): 2988, 2973 cm 'H Nuclear Magnetic Resonance. ET 3 PPM 2H 2 GH " Nuclear Magnetic Resonance. Mass Spectrometry (not shown): [M] = 147 (100%), (M+2] = 149 (100%) m/z Infrared Spectroscopy (not shown): 2969, 2935, 2249 cm 'H Nuclear Magnetic...
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