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, 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...
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...
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...
determine
the neutral organic compound from the following spectra
M+ 151 Mass Spectrum - Neutral Solid Unknown 140 150 160 100 110 120 130 70 80 90 40 50 60 20 30
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...
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 2,6-dimethylheptan-4-ol is shown in appendix A. a) Draw the structure of this compound. b) Propose structures for the fragments at m/z 87, 111 and 126. 100 80 60 abundance 40 87 20 111 126 0 10 III 100'110' 120' 130 140 150 160 20 30 40 50 60 70 80 90 m/z.
Question 1: Predict a reasonable molecular formula for the following mass spectra (12 pts) (1 bonus point each for drawing a reasonable structure) a) 100- rel. int. 11 50- 43 109 27 1101 135 55 136 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160
Draw a structure that is consistent with the MS, IR, and NMR spectra in Figures 1-3. abundance اسلام سال M 73 10' 20' 30' 40'50' 60' 70' 80' 90 '100' 110' 120 130 140 150 160 m/z 25 3.5 4 4.5 wavelength (mm) 5 5.5 6 7 8 9 10 11 12 13 14 15 16 ECZO-EESZOW 4000 3500 3000 2500 1400 1200 1000 800 600 2000 1800 1600 wavenumber (cm) wavenumber (cm" 100 80 200 180 160 140 120...
2. Answer the following questions for an unknown with molecular formula C HBrO2 given the spectral data below: (a) Calculate the molecular weight and the exact mass of the compound. (b) Deduce the structure. Relative Abundance percent) (166) Om 10 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160 170 triplets