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Identify 5 of the major peaks on each spectrum
Liquid T MS 100 80 60 40-...
what are possible structures for each spectra 100 MS 80 - 60 Relative Intensity 40 20-...
what are possible structures for each spectra
100 MS 80 - 60 Relative Intensity 40 20- 0 10 20 30 40 60 70 80 50 m/z 100- 80 Relative Intensity 40 20 0 10 15 20 25 30 35 40 50 55 60 65 70 75 80 45 m/z
is is the mass spectrum of 2-pentanol. 100 MS-NW-8471 6 80 60 40 20 omt 10...
is is the mass spectrum of 2-pentanol. 100 MS-NW-8471 6 80 60 40 20 omt 10 20 30 40 60 70 80 50 m/z Provide a reasonable fragmentation pathway for the indicated fragments. Make sure that you discuss the relative intensity of the same fragments. | m/z 27.0 7.6 29.0 5.3 31.0 5.0 41.0 5.8 43.0 13.7 44.0 7.5 45.0 100.0 55.0 18.7 73.0 7.1
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...
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 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...
Organic Chemistry - Using the following IR anaylsis identify the major peaks and possible functio...
Organic Chemistry - Using the following IR anaylsis identify the
major peaks and possible functional group identity. Using the two
NMR spectra, discuss the integration of peaks, chemical shifts, and
splitting. Using the mass spectra, identify molecular weight and
important fragments to confirm the structure. Draw the fragments
that correspond to each peak in the mass spectra. Draw the
structure of the unknown that corresponds to all available data.
additional information: Unknown ‘J’ is a alkane.
H-NMR multiplet, 1OH triplet,...
label peaks Butane MASS SPECTRUM 100 Molar mass- 58.12 q/mol 80 40 20 0.0 10 20...
label peaks
Butane MASS SPECTRUM 100 Molar mass- 58.12 q/mol 80 40 20 0.0 10 20 30 40 50 m/z IST Char:-. 60 60 Rel. Intensity
3. Identify each compound in the following questions and make assignments in the 1H NMR. e)...
3. Identify each compound in the following questions and make
assignments in the 1H NMR.
e) Compound-5-with-1H-NMR-and-mass-spectrum-given. 100 MS-NW-3193 80 60 otrophittttttttttttt 10 20 30 40 50 60 70 m/z 80 t 90 100
The following is the mass spectrum of Niacin. Can you please interpret each of the peaks...
The following is the mass spectrum of Niacin. Can you please
interpret each of the peaks seen in the mass spectrum and what they
correspond to on the Niacin compound?
Niacin Mass Spectrum Relative Intensity LES .45 1718 2025262728 No 89 9495 III. 6162366566768 70 60 72757 11,80 80 122| 20 30 40 50 70 100 1 10 120 m/z
Please label the peaks of the following graphs for the compound Acetophenone 100 Relative Intensity 100...
Please label the peaks of the following graphs for the compound
Acetophenone
100 Relative Intensity 100 110 120 Ortofritt 10 20 30 40 50 60 70 80 90 m/z f. NMR Spectrum: 11 10 9 8 5 4 2 1 ppm g. IR Spectrum: THESE TERCEIP HAVENUMERI
what are possible structures for each spectra
100 MS 80 - 60 Relative Intensity 40 20- 0 10 20 30 40 60 70 80 50 m/z 100- 80 Relative Intensity 40 20 0 10 15 20 25 30 35 40 50 55 60 65 70 75 80 45 m/z
is is the mass spectrum of 2-pentanol. 100 MS-NW-8471 6 80 60 40 20 omt 10 20 30 40 60 70 80 50 m/z Provide a reasonable fragmentation pathway for the indicated fragments. Make sure that you discuss the relative intensity of the same fragments. | m/z 27.0 7.6 29.0 5.3 31.0 5.0 41.0 5.8 43.0 13.7 44.0 7.5 45.0 100.0 55.0 18.7 73.0 7.1
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...
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 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...
Organic Chemistry - Using the following IR anaylsis identify the
major peaks and possible functional group identity. Using the two
NMR spectra, discuss the integration of peaks, chemical shifts, and
splitting. Using the mass spectra, identify molecular weight and
important fragments to confirm the structure. Draw the fragments
that correspond to each peak in the mass spectra. Draw the
structure of the unknown that corresponds to all available data.
additional information: Unknown ‘J’ is a alkane.
H-NMR multiplet, 1OH triplet,...
label peaks
Butane MASS SPECTRUM 100 Molar mass- 58.12 q/mol 80 40 20 0.0 10 20 30 40 50 m/z IST Char:-. 60 60 Rel. Intensity
3. Identify each compound in the following questions and make
assignments in the 1H NMR.
e) Compound-5-with-1H-NMR-and-mass-spectrum-given. 100 MS-NW-3193 80 60 otrophittttttttttttt 10 20 30 40 50 60 70 m/z 80 t 90 100
The following is the mass spectrum of Niacin. Can you please
interpret each of the peaks seen in the mass spectrum and what they
correspond to on the Niacin compound?
Niacin Mass Spectrum Relative Intensity LES .45 1718 2025262728 No 89 9495 III. 6162366566768 70 60 72757 11,80 80 122| 20 30 40 50 70 100 1 10 120 m/z
Please label the peaks of the following graphs for the compound
Acetophenone
100 Relative Intensity 100 110 120 Ortofritt 10 20 30 40 50 60 70 80 90 m/z f. NMR Spectrum: 11 10 9 8 5 4 2 1 ppm g. IR Spectrum: THESE TERCEIP HAVENUMERI
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