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![f. NMR Spectrum a [~2.5ppm Aromatic proton [ 7 - 8 ppm] Asomatte protoo 11 10 9 N ppm](http://img.homeworklib.com/questions/63061e90-de98-11eb-ba52-8d071627cdf6.png?x-oss-process=image/resize,w_560)
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Please label the peaks of the following graphs for the compound
Acetophenone
100 Relative Intensity 100...
15. The mass spectrum of a compound appears below. The molecular ion, M+1, and M+2 peaks...
15. The mass spectrum of a compound appears below. The molecular ion, M+1, and M+2 peaks have intensities of 100, 6.8, and 31.8 respectively. Use the information provided to determine the formula of the compound 100 MS-NW-5495 80 60 40 20 шшшl 110 10 20 30 40 50 60 70 80 90 100 m/z Relative Intensity
15. The mass spectrum of a compound appears below. The molecular ion, M+1, and M+2 peaks have intensities of 100, 6.8, and 31.8 respectively....
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...
Please match the compound to its spectrum and explain why cpd 22 Spectrum A 100- 60...
Please match the compound to its spectrum and explain
why
cpd 22 Spectrum A 100- 60 40 20 100 125 50 75 m/z Spectrum B 100 80- 60 40 20- 10 20 30 40 50 60 70 0 90 100 110 120 m/z (6 points) Match EOT Spectrum C 100- 80- 60 40 75 100 125 50 m/z Spectrum D 100 80 60- 40 20- 25 50 75 100 125 m/z Spectrum E 100 80 60 20 10 20 30...
Propose a reasonable structure for this compound based on the mass spec, IR, and NMR data....
Propose a reasonable structure for this compound based on the mass spec, IR, and NMR data. 100 Relative Intensity M+ 10 20 30 40 60 70 80 90 50 m/z LUU TRINETTRICET 4000 3000 2000 cm1 1500 1000 500 ЗН Зн 2H тттттттттттттттттт 11 10 9 8 7 6 5 4 ppm 200 180 160 140 120 80 60 40 20 100 ppm
t-Butylbenzene was reacted with 1-bromopropane in the presence of AlCl3 as a catalyst ACl The product was bel...
t-Butylbenzene was reacted with 1-bromopropane in the presence of AlCl3 as a catalyst ACl The product was believed to be one of the following isomers В D A single product was isolated from the reaction mixture and the 1c-NMR spectrum of the compound was obtained Which of the candidate product structures is most consistent with the spectrum? 140 100 120 160 80 PPM 60 20 Compound X,ttre, was isolated from early batches of a new craft beer. This compound is...
For part B also calculate degree of unsaturation and use the MS and 13CNMR spectra...
For part B also calculate degree of
unsaturation and use the MS and 13CNMR spectra to identify the
molecule. Label the graphs with the information gained.
9. Identify the compound with give molecular formula that gives the IR and 'H NMR spectra shown. Label the IR peaks with the type of functional group. Draw the structure of the compound and label the signals on the structure using letters (a, b, c, etc.) then label the signals on the 'H...
Please help with identifying this compound? Need to draw the structure 14.01 Mass Spectrum 13C-NMR Spectrum...
Please help with identifying this compound? Need to draw the
structure
14.01 Mass Spectrum 13C-NMR Spectrum CHO M**= 60 Relative Intensity 10 15 20 25 30 40 45 50 35 m/z 55 60 200 180 160 140 120 80 60 40 20 100 ppm IR Spectrum 1H-NMR Spectrum o Chem. shift Ret area Porto age are 3.5822.00 226 157 094 Singlet (hare some into the rest 1.00 2.00 3.00 1466 3333 2963 11 10 Ppm
Use the IR and MS data to elucidate the structures of the compounds below. Identify the...
Use the IR and MS data to elucidate the structures of the compounds below. Identify the M and other necessary peaks in the mass spectra below. Give the functional group responsible for the IR signals. IR: (1 709) sharp, strong (1607-1653) weak MS: ID 4 peaks 100- Relative Intensity orta pripreme 10 20 30 40 50 60 70 80 90 100 m/z 110 120 IR: (1753) strong (1602 - 1658) weak MS: ID 4 peaks 100 MS-NU-18 Relative Intensity 10...
evaluate if the compound is cyclopentene or cyclihexyl bromide. label each part C IR 100 D...
evaluate if the compound is cyclopentene or cyclihexyl
bromide.
label each part
C IR 100 D j000 530 3000 00 VENUREI- Mass Spec. 100 80- 60 40 20 0 175 100 125 150 75 50 25 m/z Relative Intensity H-NMR quintet, 1H multiplet, 2H multiplet, 6H multiplet, 2H 0 PPM "C-NMR 30 10 40 0 20 PPM 50
Answer the following questions about the provided spectra: The Molecular Weight of the compound is 88...
Answer the following questions about the provided spectra: The Molecular Weight of the compound is 88 g/mol. A) (1 point) The broad peak at -3100 cm and the strong peak at 1700 cm' combined indicate the presence of what functional group? B) (1 point) How many hydrogen neighbors does the septet at 2.6 ppm in the 'H NMR spectrum have? C) (1 point) What functional group is indicated by the peak at 184 ppm in the C spectrum? D) (1...
15. The mass spectrum of a compound appears below. The molecular ion, M+1, and M+2 peaks have intensities of 100, 6.8, and 31.8 respectively. Use the information provided to determine the formula of the compound 100 MS-NW-5495 80 60 40 20 шшшl 110 10 20 30 40 50 60 70 80 90 100 m/z Relative Intensity
15. The mass spectrum of a compound appears below. The molecular ion, M+1, and M+2 peaks have intensities of 100, 6.8, and 31.8 respectively....
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...
Please match the compound to its spectrum and explain
why
cpd 22 Spectrum A 100- 60 40 20 100 125 50 75 m/z Spectrum B 100 80- 60 40 20- 10 20 30 40 50 60 70 0 90 100 110 120 m/z (6 points) Match EOT Spectrum C 100- 80- 60 40 75 100 125 50 m/z Spectrum D 100 80 60- 40 20- 25 50 75 100 125 m/z Spectrum E 100 80 60 20 10 20 30...
Propose a reasonable structure for this compound based on the mass spec, IR, and NMR data. 100 Relative Intensity M+ 10 20 30 40 60 70 80 90 50 m/z LUU TRINETTRICET 4000 3000 2000 cm1 1500 1000 500 ЗН Зн 2H тттттттттттттттттт 11 10 9 8 7 6 5 4 ppm 200 180 160 140 120 80 60 40 20 100 ppm
t-Butylbenzene was reacted with 1-bromopropane in the presence of AlCl3 as a catalyst ACl The product was believed to be one of the following isomers В D A single product was isolated from the reaction mixture and the 1c-NMR spectrum of the compound was obtained Which of the candidate product structures is most consistent with the spectrum? 140 100 120 160 80 PPM 60 20 Compound X,ttre, was isolated from early batches of a new craft beer. This compound is...
For part B also calculate degree of
unsaturation and use the MS and 13CNMR spectra to identify the
molecule. Label the graphs with the information gained.
9. Identify the compound with give molecular formula that gives the IR and 'H NMR spectra shown. Label the IR peaks with the type of functional group. Draw the structure of the compound and label the signals on the structure using letters (a, b, c, etc.) then label the signals on the 'H...
Please help with identifying this compound? Need to draw the
structure
14.01 Mass Spectrum 13C-NMR Spectrum CHO M**= 60 Relative Intensity 10 15 20 25 30 40 45 50 35 m/z 55 60 200 180 160 140 120 80 60 40 20 100 ppm IR Spectrum 1H-NMR Spectrum o Chem. shift Ret area Porto age are 3.5822.00 226 157 094 Singlet (hare some into the rest 1.00 2.00 3.00 1466 3333 2963 11 10 Ppm
Use the IR and MS data to elucidate the structures of the compounds below. Identify the M and other necessary peaks in the mass spectra below. Give the functional group responsible for the IR signals. IR: (1 709) sharp, strong (1607-1653) weak MS: ID 4 peaks 100- Relative Intensity orta pripreme 10 20 30 40 50 60 70 80 90 100 m/z 110 120 IR: (1753) strong (1602 - 1658) weak MS: ID 4 peaks 100 MS-NU-18 Relative Intensity 10...
evaluate if the compound is cyclopentene or cyclihexyl
bromide.
label each part
C IR 100 D j000 530 3000 00 VENUREI- Mass Spec. 100 80- 60 40 20 0 175 100 125 150 75 50 25 m/z Relative Intensity H-NMR quintet, 1H multiplet, 2H multiplet, 6H multiplet, 2H 0 PPM "C-NMR 30 10 40 0 20 PPM 50
Answer the following questions about the provided spectra: The Molecular Weight of the compound is 88 g/mol. A) (1 point) The broad peak at -3100 cm and the strong peak at 1700 cm' combined indicate the presence of what functional group? B) (1 point) How many hydrogen neighbors does the septet at 2.6 ppm in the 'H NMR spectrum have? C) (1 point) What functional group is indicated by the peak at 184 ppm in the C spectrum? D) (1...
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