determine
the neutral organic compound from the following spectra
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determine
the neutral organic compound from the following spectra
M+ 151 Mass Spectrum - Neutral Solid...
Identify which of these four mass spectra indicate the presence of sulfur, chlorine, bromine, iodine, or...
Identify which of these four mass spectra indicate the presence of sulfur, chlorine, bromine, iodine, or nitrogen. Suggest a molecular formula for each. 100 abundance 8 $ 38 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160 mily abundance 10 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160 z 8 8 8 abundance $ 8 LL 10 20 30 40 50 60 70 80 90 100 110...
8. (10 points) The following spectra correspond to compounds AE listed below con pound to its...
8. (10 points) The following spectra correspond to compounds AE listed below con pound to its corresponding spestre Label very simal on the spectrum (as Co . ctc.). Spectrum CDCI, 190 160 170 160 150 140 130 120 110 100 80 80 Spectrum 2 70 80 50 40 30 20 10 O le CDCI, 190 180 170 180 150 140 130 120 110 100 90 80 70 60 50 40 30 20 10 O de CDCI, 190 180 170 180...
Identify which of these four mass spectra indicate the presence of sulfur, chlorine, bromine, iondine, nitrogen....
Identify which of these four mass spectra indicate the
presence of sulfur, chlorine, bromine, iondine, nitrogen. suggest a
molecular formula for each.
2otten breaks sh ass spec er be mass PROBLEM 12-7 Identify which of these four mass spectra indicate the presence of sulfur, chlorine bromine, iodine, or nitrogen. Suggest a molecular formula for each. AA gIve the lonica 100 77 80 156 158 (a) 60 40 20 Fragn 10 20 30 40 50 60 70 80 100 110 120...
2. . An unknown, non-branched saturated hydrocarbon has the mass spectrum s below. What is the...
2. . An unknown, non-branched saturated hydrocarbon has the mass spectrum s below. What is the structure of the unknown hydrocarbon? 100) 3. "19 127 141 158 189 188 107 211 225 241 20 40 60 80 100 120 140 160 180 200 220 240 An unknown compound with formula C H100, RVO negative tent with 2.4 dinitrophenylhydrazine; however, the unknown tested positive with the Jones reagent. When added to a solution of bromine dissolved in methylene, the reddin solution...
Use the spectra below to determine the molecular formula and chemical structure of the unknown compound....
Use the spectra below to determine the molecular formula and
chemical structure of the unknown compound.
MASS 142 % of Base Peak 1147 40 50 70 80 5 100 % Transmittance Jari- 3000 1000 4000 'H NMR 300 MERE 2000 Wavenumber (cm) 3.0 25 20 15 Ppm 4.0 3.5 C/DEPT NMR 75.5 MHz ppm 60 50 40 80 70 90 100 110 120 170 160 150 140 130 ppm 4.5 4.0 3.5 3.0 2.5 2.0 1.5 ppm COSY 300 MHz...
Use the mass spectrum and either the NMR spectrum or the IR spectrum to deduce the...
Use the mass spectrum and either the NMR spectrum or the IR
spectrum to deduce the structure of the following compound
(c) C8HO3H NMR, 300 MHz, 6.1 ppm (singlet, 2H), 6.9 ppm (doublet, 1H), and 7.3 ppm (singlet, 1H), 7.4 ppm (doublet, 1H), 9.8 ppm (singlet, 1H); significant IR absorbances at 1687, 1602, 1449, 1264, 1038, 929, and 815 cm1. 100 149 (150) 80 60 40 121 63 20 65 91 0 15 20 25 30 35 40 45 50...
The mass spectrum of 3-bromopropanoic acid is shown below. Four peaks are labeled with A, B,...
The mass spectrum of 3-bromopropanoic acid is shown below. Four peaks are labeled with A, B, C, and D. Select the label for the base peak(s). 45 55 18 26 on 10 20 30 40 50 60 70 80 90 100 MIZ 110 120 130 140 150 160 170 The mass spectrum of 3-bromopropanoic acid is shown below. Four peaks are labeled with A, B, C, and D. Select the label for the M peak(s) (unfragmented parent). 135 27 45...
Instructions: Write the structure of each molecular formula using the IR and Mass Spec spectra. Important...
Instructions: Write the structure of each molecular formula using the IR and Mass Spec spectra. Important that you justify with at least two arguments in each spectrum for which you present that structure. CH 3500 3000 1500 1000 2500 2000 Wavenumber(cm-1) 20 30 40 50 60 70 80 90 100 110 120 CHBr 100 Transmittance 3500 3000 2500 2000 Wavenumber(cm-1) 1500 1000 119 135 100 110 120 130 140 150 160 170 180 190 10 20 30 40 50 60...
Match each compound (d) to its mass spectrum (1-4). ) Relativel y 30 40 50 60...
Match each compound (d) to its mass spectrum (1-4). ) Relativel y 30 40 50 60 70 80 90 100 110 120 18 Mars plastic 2 STAEDTLER Revente 20 30 40 50 60 70 80 90 100 110 120 130 Relative intensy 10 20 30 40 50 60 70 80 90 100 110 120 130
Consider the data provided in appendix B containing the mass spectrum, the IR spectrum and the...
Consider the data provided in appendix B containing the mass spectrum, the IR spectrum and the 'H NMR of an unknown compound. Determine the structure of this compound base on the data provided. (Make sure to show your work). 100 80 117 M 60 abundance 40 20 . = . 0 10 20 30 40 50 60 70 80 90 100 110 120 130' 140' 150 160 3.5 wavelength (um) 5.5 4.5 6 7 8 9 10 11 12 13...
Identify which of these four mass spectra indicate the presence of sulfur, chlorine, bromine, iodine, or nitrogen. Suggest a molecular formula for each. 100 abundance 8 $ 38 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160 mily abundance 10 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160 z 8 8 8 abundance $ 8 LL 10 20 30 40 50 60 70 80 90 100 110...
8. (10 points) The following spectra correspond to compounds AE listed below con pound to its corresponding spestre Label very simal on the spectrum (as Co . ctc.). Spectrum CDCI, 190 160 170 160 150 140 130 120 110 100 80 80 Spectrum 2 70 80 50 40 30 20 10 O le CDCI, 190 180 170 180 150 140 130 120 110 100 90 80 70 60 50 40 30 20 10 O de CDCI, 190 180 170 180...
Identify which of these four mass spectra indicate the
presence of sulfur, chlorine, bromine, iondine, nitrogen. suggest a
molecular formula for each.
2otten breaks sh ass spec er be mass PROBLEM 12-7 Identify which of these four mass spectra indicate the presence of sulfur, chlorine bromine, iodine, or nitrogen. Suggest a molecular formula for each. AA gIve the lonica 100 77 80 156 158 (a) 60 40 20 Fragn 10 20 30 40 50 60 70 80 100 110 120...
2. . An unknown, non-branched saturated hydrocarbon has the mass spectrum s below. What is the structure of the unknown hydrocarbon? 100) 3. "19 127 141 158 189 188 107 211 225 241 20 40 60 80 100 120 140 160 180 200 220 240 An unknown compound with formula C H100, RVO negative tent with 2.4 dinitrophenylhydrazine; however, the unknown tested positive with the Jones reagent. When added to a solution of bromine dissolved in methylene, the reddin solution...
Use the spectra below to determine the molecular formula and
chemical structure of the unknown compound.
MASS 142 % of Base Peak 1147 40 50 70 80 5 100 % Transmittance Jari- 3000 1000 4000 'H NMR 300 MERE 2000 Wavenumber (cm) 3.0 25 20 15 Ppm 4.0 3.5 C/DEPT NMR 75.5 MHz ppm 60 50 40 80 70 90 100 110 120 170 160 150 140 130 ppm 4.5 4.0 3.5 3.0 2.5 2.0 1.5 ppm COSY 300 MHz...
Use the mass spectrum and either the NMR spectrum or the IR
spectrum to deduce the structure of the following compound
(c) C8HO3H NMR, 300 MHz, 6.1 ppm (singlet, 2H), 6.9 ppm (doublet, 1H), and 7.3 ppm (singlet, 1H), 7.4 ppm (doublet, 1H), 9.8 ppm (singlet, 1H); significant IR absorbances at 1687, 1602, 1449, 1264, 1038, 929, and 815 cm1. 100 149 (150) 80 60 40 121 63 20 65 91 0 15 20 25 30 35 40 45 50...
The mass spectrum of 3-bromopropanoic acid is shown below. Four peaks are labeled with A, B, C, and D. Select the label for the base peak(s). 45 55 18 26 on 10 20 30 40 50 60 70 80 90 100 MIZ 110 120 130 140 150 160 170 The mass spectrum of 3-bromopropanoic acid is shown below. Four peaks are labeled with A, B, C, and D. Select the label for the M peak(s) (unfragmented parent). 135 27 45...
Instructions: Write the structure of each molecular formula using the IR and Mass Spec spectra. Important that you justify with at least two arguments in each spectrum for which you present that structure. CH 3500 3000 1500 1000 2500 2000 Wavenumber(cm-1) 20 30 40 50 60 70 80 90 100 110 120 CHBr 100 Transmittance 3500 3000 2500 2000 Wavenumber(cm-1) 1500 1000 119 135 100 110 120 130 140 150 160 170 180 190 10 20 30 40 50 60...
Match each compound (d) to its mass spectrum (1-4). ) Relativel y 30 40 50 60 70 80 90 100 110 120 18 Mars plastic 2 STAEDTLER Revente 20 30 40 50 60 70 80 90 100 110 120 130 Relative intensy 10 20 30 40 50 60 70 80 90 100 110 120 130
Consider the data provided in appendix B containing the mass spectrum, the IR spectrum and the 'H NMR of an unknown compound. Determine the structure of this compound base on the data provided. (Make sure to show your work). 100 80 117 M 60 abundance 40 20 . = . 0 10 20 30 40 50 60 70 80 90 100 110 120 130' 140' 150 160 3.5 wavelength (um) 5.5 4.5 6 7 8 9 10 11 12 13...
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