A chemist obtains a mass spectrum of an unknown compound and notices a profound M+2 of...
A chemist obtains a mass spectrum of an unknown compound and notices a profound M+2 of approximately 33% intensity. What compound could this be?
A: 3-chloropentane
B: 2-bromohexane
C: T-butyl alcohol
D: HExane
E: 2-iodohexane
Please walk me through arriving to the right answer thx
Homework Answers
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A chemist obtains a mass spectrum of an unknown compound and
notices a profound M+2 of...
Intensity MASS SPECTRAL DATA Unknown m/e Relative Intensity Mass Spectrum (мм) 90 18.4 0.83 92 0.09 29 90 I5 60 m/...
Intensity MASS SPECTRAL DATA Unknown m/e Relative Intensity Mass Spectrum (мм) 90 18.4 0.83 92 0.09 29 90 I5 60 m/e 2. Based on the mass spectrum, do you think your compound has a nitrogen atom? Explain. Propose at least two molecular formulas based on the mass spectrum and calculate the exact mass of the parent ion. Is one of your formula more likely than the other? If so, explain. 3.
A compound of unknown structure gave the following spectroscopic data: Mass spectrum: M+ = 88.1 IR:...
A compound of unknown structure gave the following
spectroscopic data:
Mass spectrum: M+ = 88.1
IR: 3600cm-1
1H NMR: 1.4 (2H, quartet, J=7Hz); 1.2 (6H, singlet); 1.0 (1H,
singlet); 0.9 (3H, triplet, J=7Hz)
13C NMR: 74, 35, 27, 25
a. assuming that the compound contains C and H but may or may not
contain O, give three possible molecular formulas.
b. how many protons (H) does the compound contain?
c. what functional group(s) does the compound contain?
d. how many...
The low‐resolution mass spectrum and m/z data obtained for an unknown compound seized during the raid...
The low‐resolution mass spectrum and m/z data obtained for an
unknown compound seized during
the raid on a clandestine laboratory are provided. Ignore the
signals below m/z 70 and the small
clusters of signals at about m/z 85 and 93. The significant signals
(m/z) and their signal intensities
(%I) from the mass spectrum are: (72,2), (73,5), (74,16),
(75,35), (76,8), (77,5), (78,1),
(111,51),
(112,6), (113,17), (114,2),
(139,100), (140,9),
(141,31), (142,3), (155,50),
(156,5), (157,16),
(158,2).
Subsequent analysis of the same compound using...
Below are the mass spectrum, IR spectrum, and 1H NMR spectrum for an unknown compound X....
Below are the mass spectrum, IR spectrum, and 1H NMR spectrum
for an unknown compound X. Identify and give the systematic name
for X. For full marks, rationalize every piece of
data.
Spectroscopy Lab Below are the mass spectrum, IR spectrum, and 1H NMR spectrum for an unknown compound X. Identify and give the systematic name for X. For full marks, rationalize every piece of data. 0.15 -0.45 A (9) 0.40 0.10 +0.35 10.05 ЛОО 0.30 - 0.00 0.25 4.19...
13. What can you say about an unknown compound that gave a pouldve test with 2...
13. What can you say about an unknown compound that gave a pouldve test with 2 hydrazine and a positive test with the Jones Reseat? now compound that gave a pouldve test with 2,4-dinitrophenyl 14 What can you say about sa unknown compound when dissolved in distilled water and tested with peper, pave an estimated pH of about 81. 15. What can you say about an unknown compound that turned a wet plece al blue litmus red? 16. What can...
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....
8. The nass spectrum of which compound has M and N+2 peaks of approxinately equal intensity?...
8. The nass spectrum of which compound has M and N+2 peaks of approxinately equal intensity? A) 3-bromopentane B) 3-pentanol C) pentane D) 3-chloropentane E) 3-iodopentane 9. Consider the structure isomers. 1-bromopropane (A) and 2-bromopropane (B) respectively. How many unique proton peaks are in es H NMR? A) A: 4 types, B: 4 types B) A: 3 types, B: 2 types C) A: 2 types, B: 3 types D) A: 8 types, B: 8 types E A: 4 types, B:...
Unknown 315-S20-2 Can someone help me fill out the table on the right side please IR...
Unknown 315-S20-2
Can someone help me fill out the table on the right side
please
IR Spectrum:
Unknown # 315-S20-2 Mol. Wt. = 181.0 g/mol C-33.17% H=5.01% 0 = 17.68% Molecular Formula Degree of Unsaturation = Mass Spectrum IR spectrum (liquid film) 100- Relative Intensity 150 175 25 50 75 100 125 m/z Based on the M.W., circle & label the molecular ion peak (M). Spectrum Region Frequency (cm ) Peak Shape (sharp, broad) MAVUTO Peak Intensity (strong, med., weak)...
33. Propose a structure for Compound X, which has M -120 and (M+2)-122 of approximately equal...
33. Propose a structure for Compound X, which has M -120 and (M+2)-122 of approximately equal intensity in its mass spectrum and has the following "C NMR spectral data: (5 points) Broadband decoupled "C NMR: 32.6, 118.8, 134.3 ppm DEPT-90: 134.3 ppm DEPT-135: positive peaks at 134.3 ppm; negative peaks at 32.6, 118.8 ppm
1. What is the chemical formula of the unknown? 2. what is the mass of the...
1. What is the chemical formula of the unknown?
2. what is the mass of the unknown?
3. What is the HDI?
4. According to IR spectra, what functional groups are
present?
5. What is the structure of the molecule?
138 PRACTICAL SPECTROSCOPY Compound 80 is a liquid (boiling point 212 C), that can be prepared by the reaction of Compound 79 with acidic, anhydrous ethanol. The Mass, IR, and 'H NMR spectra, along with C NMR data, are given...
Intensity MASS SPECTRAL DATA Unknown m/e Relative Intensity Mass Spectrum (мм) 90 18.4 0.83 92 0.09 29 90 I5 60 m/e 2. Based on the mass spectrum, do you think your compound has a nitrogen atom? Explain. Propose at least two molecular formulas based on the mass spectrum and calculate the exact mass of the parent ion. Is one of your formula more likely than the other? If so, explain. 3.
A compound of unknown structure gave the following
spectroscopic data:
Mass spectrum: M+ = 88.1
IR: 3600cm-1
1H NMR: 1.4 (2H, quartet, J=7Hz); 1.2 (6H, singlet); 1.0 (1H,
singlet); 0.9 (3H, triplet, J=7Hz)
13C NMR: 74, 35, 27, 25
a. assuming that the compound contains C and H but may or may not
contain O, give three possible molecular formulas.
b. how many protons (H) does the compound contain?
c. what functional group(s) does the compound contain?
d. how many...
The low‐resolution mass spectrum and m/z data obtained for an
unknown compound seized during
the raid on a clandestine laboratory are provided. Ignore the
signals below m/z 70 and the small
clusters of signals at about m/z 85 and 93. The significant signals
(m/z) and their signal intensities
(%I) from the mass spectrum are: (72,2), (73,5), (74,16),
(75,35), (76,8), (77,5), (78,1),
(111,51),
(112,6), (113,17), (114,2),
(139,100), (140,9),
(141,31), (142,3), (155,50),
(156,5), (157,16),
(158,2).
Subsequent analysis of the same compound using...
Below are the mass spectrum, IR spectrum, and 1H NMR spectrum
for an unknown compound X. Identify and give the systematic name
for X. For full marks, rationalize every piece of
data.
Spectroscopy Lab Below are the mass spectrum, IR spectrum, and 1H NMR spectrum for an unknown compound X. Identify and give the systematic name for X. For full marks, rationalize every piece of data. 0.15 -0.45 A (9) 0.40 0.10 +0.35 10.05 ЛОО 0.30 - 0.00 0.25 4.19...
13. What can you say about an unknown compound that gave a pouldve test with 2 hydrazine and a positive test with the Jones Reseat? now compound that gave a pouldve test with 2,4-dinitrophenyl 14 What can you say about sa unknown compound when dissolved in distilled water and tested with peper, pave an estimated pH of about 81. 15. What can you say about an unknown compound that turned a wet plece al blue litmus red? 16. What can...
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....
8. The nass spectrum of which compound has M and N+2 peaks of approxinately equal intensity? A) 3-bromopentane B) 3-pentanol C) pentane D) 3-chloropentane E) 3-iodopentane 9. Consider the structure isomers. 1-bromopropane (A) and 2-bromopropane (B) respectively. How many unique proton peaks are in es H NMR? A) A: 4 types, B: 4 types B) A: 3 types, B: 2 types C) A: 2 types, B: 3 types D) A: 8 types, B: 8 types E A: 4 types, B:...
Unknown 315-S20-2
Can someone help me fill out the table on the right side
please
IR Spectrum:
Unknown # 315-S20-2 Mol. Wt. = 181.0 g/mol C-33.17% H=5.01% 0 = 17.68% Molecular Formula Degree of Unsaturation = Mass Spectrum IR spectrum (liquid film) 100- Relative Intensity 150 175 25 50 75 100 125 m/z Based on the M.W., circle & label the molecular ion peak (M). Spectrum Region Frequency (cm ) Peak Shape (sharp, broad) MAVUTO Peak Intensity (strong, med., weak)...
33. Propose a structure for Compound X, which has M -120 and (M+2)-122 of approximately equal intensity in its mass spectrum and has the following "C NMR spectral data: (5 points) Broadband decoupled "C NMR: 32.6, 118.8, 134.3 ppm DEPT-90: 134.3 ppm DEPT-135: positive peaks at 134.3 ppm; negative peaks at 32.6, 118.8 ppm
1. What is the chemical formula of the unknown?
2. what is the mass of the unknown?
3. What is the HDI?
4. According to IR spectra, what functional groups are
present?
5. What is the structure of the molecule?
138 PRACTICAL SPECTROSCOPY Compound 80 is a liquid (boiling point 212 C), that can be prepared by the reaction of Compound 79 with acidic, anhydrous ethanol. The Mass, IR, and 'H NMR spectra, along with C NMR data, are given...
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