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Mass Spectrometry (not shown): [M] = 134 m/z Infrared Spectroscopy (not shown): 3073, 2924, 1714, cm...
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,...
Mass Spectrometry (not shown): [M)-146 m/z Infrared Spectroscopy (not shown): 2988, 1752, 1723, 1221 cm H...
Mass Spectrometry (not shown): [M)-146 m/z Infrared Spectroscopy (not shown): 2988, 1752, 1723, 1221 cm H Nuclear Magnetic Resonance. 3 1H PPM 3H "C Nuclear Magnetic Resonance. 20 40 80 60 100 PPM 120 140 160 180 /tmp/Hussein-2012.jpg Mass Spectrometry (not shown): [M] 156 (75 % ) , [ M+ 2] = 158 (100 % ) , [M+ 4] 160 (25 % ) m/ Infrared Spectroscopy (not shown): 2966, 2910 cm H Nuclear Magnetic Resonance. t t quin 3 1...
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
Draw the structure of the molecule given in the following information: Mass Spectrometry (not shown): (M) = 112 m/z Inf...
Draw the structure of the molecule given in the following
information:
Mass Spectrometry (not shown): (M) = 112 m/z Infrared Spectroscopy (not shown): 2860, 1699 cm 'H Nuclear Magnetic Resonance. 8H PPM c Nuclear Magnetic Resonance. 220 '200' 180 160 . 140 120 100.80.60.40.200
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
Please draw a potential structure based on the [M], IR, H NMR, and C NMR Mass...
Please draw a potential structure based on the [M], IR, H NMR,
and C NMR
Mass Spectrometry (not shown): [M] = 148 m/z Infrared Spectroscopy (not shown): 3062, 2964, 2934, 1687, 1449, 1214 cm 'H Nuclear Magnetic Resonance. 8 7 6 2H 1H2H 5 4 PPM 2H - 2H 3H * Nuclear Magnetic Resonance. 220 .200 .180 .160 .140 120 100 .80 .60 40 20
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
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
Please draw a structure which matches the [M], IR, H NMR, and C NMR - Thank...
Please draw a structure which matches the [M], IR, H NMR, and C
NMR - Thank you!!!
Mass Spectrometry (not shown): [M] = 150 m/z Infrared Spectroscopy (not shown): 3035,2966, 1743, 1381, 1363, 1229, 1027 cm 'H Nuclear Magnetic Resonance. 24 PM BA PPM c Nuclear Magnetic Resonance. 180 160 140 120 100 80 60 40 20 PPM
Draw the Skeletal Structure of the Unknown Compound. Note - Formal skeletal structures do not include hydrogens on any c...
Draw the Skeletal Structure of the Unknown Compound.
Note - Formal skeletal structures do not include
hydrogens on any carbons (including the aldehyde C)
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...
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,...
Mass Spectrometry (not shown): [M)-146 m/z Infrared Spectroscopy (not shown): 2988, 1752, 1723, 1221 cm H Nuclear Magnetic Resonance. 3 1H PPM 3H "C Nuclear Magnetic Resonance. 20 40 80 60 100 PPM 120 140 160 180 /tmp/Hussein-2012.jpg Mass Spectrometry (not shown): [M] 156 (75 % ) , [ M+ 2] = 158 (100 % ) , [M+ 4] 160 (25 % ) m/ Infrared Spectroscopy (not shown): 2966, 2910 cm H Nuclear Magnetic Resonance. t t quin 3 1...
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
Draw the structure of the molecule given in the following
information:
Mass Spectrometry (not shown): (M) = 112 m/z Infrared Spectroscopy (not shown): 2860, 1699 cm 'H Nuclear Magnetic Resonance. 8H PPM c Nuclear Magnetic Resonance. 220 '200' 180 160 . 140 120 100.80.60.40.200
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
Please draw a potential structure based on the [M], IR, H NMR,
and C NMR
Mass Spectrometry (not shown): [M] = 148 m/z Infrared Spectroscopy (not shown): 3062, 2964, 2934, 1687, 1449, 1214 cm 'H Nuclear Magnetic Resonance. 8 7 6 2H 1H2H 5 4 PPM 2H - 2H 3H * Nuclear Magnetic Resonance. 220 .200 .180 .160 .140 120 100 .80 .60 40 20
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
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
Please draw a structure which matches the [M], IR, H NMR, and C
NMR - Thank you!!!
Mass Spectrometry (not shown): [M] = 150 m/z Infrared Spectroscopy (not shown): 3035,2966, 1743, 1381, 1363, 1229, 1027 cm 'H Nuclear Magnetic Resonance. 24 PM BA PPM c Nuclear Magnetic Resonance. 180 160 140 120 100 80 60 40 20 PPM
Draw the Skeletal Structure of the Unknown Compound.
Note - Formal skeletal structures do not include
hydrogens on any carbons (including the aldehyde C)
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...
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