The base peak in mass specrum is the peak with 100% relative abundance . It need not necessarily be the parent ion( equatl to molar mass).
Here in the given spectrum the base peak is at m/z =73 (100%, on y- axis) PEAK A
The molecular ion is 152 and all the peaks are accompanied by M+2 peaks with equal abundance due to the presence of Br(Br has two isotopes 79 and 81 with equal abundance).
The base peak at 73 is due to the loss of Br ( M+ - Br)
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 M peak(s) (unfragmented parent). 135 27 45 55 18 26 10 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160 170 MIZ
Suggest a composition for the halogen compound whose mass spectrum is shown below and assign the labeled peaks. 127 100 173 160 158 162 25 48 TITTHTT 160 170 91 208 79 35 160 173 30 40 50 60 70 80 90 100 110 120 130 140 150 160 170 180 190 200 210 m/z 127 100 173 160 158 162 25 48 TITTHTT 160 170 91 208 79 35 160 173 30 40 50 60 70 80 90 100...
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...
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...
Deduce the ester compound structure with M/Z=136 on this mass spectrum; significant peaks at 51, 77, 105, 136. Relative Abundance M(136) 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100 105 110 115 120 125 130 135 140 mz
Spectroscopy of C5H10O 1. Correctly label 2 peaks in the IR spectrum with the appropriate functional group. 2. Correctly label 1 peak in the 13C NMR spectrum. 3. Draw some possible structures (isomers) as you analyze the 'H NMR spectrum. 4. Draw your final choice of structure to match the IR. 13C NMR, and H NMR 5. Label the different types of hydrogens on your structure as a, b, c, etc. Label the peaks in the 'H NMR spectrum with...
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...
4. As discussed earlier fatty acids are often identified from the mass spectrum of the corresponding methyl ester. Identify the fatty acid methyl ester (draw its structure) whose spectrum is shown below. Include the reasoning used to make your decision Abundance 143 w.w. Christie 155 L 50 ubom 80 90 101 129 o 100 110 120 130 140 150 160 17 180 160 170*180*** 60 70
4. As discussed earlier fatty acids are often identified from the mass spectrum of the corresponding methyl ester. Identify the fatty acid methyl ester (draw its structure) whose spectrum is shown below. Include the reasoning used to make your decision. Abundance 143 Ww. Christie 101 hul_ IS 80 90 100 110 120 130 140 155 186 150 160 170 180 50 60 70 m/z
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...