could you please help me to explain the problem with answers and explain why peak c is 3h triplets ?
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could you please help me to explain the problem with
answers and explain why peak c...
A compound, C,H100, shows an IR peak at 1690 cm. Its 'H NMR spectrum has peaks...
A compound, C,H100, shows an IR peak at 1690 cm. Its 'H NMR spectrum has peaks at delta 7.9 (2H, multiplet), 7.6-7.4 (3H, multiplet), 2.95 (2H, quartet, J = 7 Hz), 1.25 (3H, triplet, J= 7 Hz). Draw its structure in the window below. . You do not have to consider stereochemistry. ChemDoodle A compound, C3H100, exhibits IR absorption at 1730 cm-1. Its carbon NMR shifts and substitution, determined by DEPT, are given below. 13C NMR: 822.6 (3), 23.6 (1),...
In this NMR handout, you will get practice interpreting NMR spectra. Refer to the NMR tutorial/theory for chemica...
In this NMR handout, you will get practice interpreting NMR spectra. Refer to the NMR tutorial/theory for chemical shifts and descriptions of peak splitting. There are 4 NMR problems. For each problem, you have been given the chemical formula as well as the IR and NMR spectra. Draw the structure for each unknown compound and provide sufficient reasoning as to why you think it has that structure. To get full credit, determine the structure of the unknown compound, calculate the...
Question 3) Propose a structure consistent with the following spectral data for a compound C H..0,...
Question 3) Propose a structure consistent with the following spectral data for a compound C H..0, IR 3100 (broad, strong). 1710 (strong) cm '; 'H NMR: 1.05 (triplet, 3H), 2.40 (triplet: 2H), 3.46 (quartet, 2H), 3.61 (triplet, 2H), 12.01 (broad singlet, IH) (10 points)
(c) Compound C has molecular formula C9H10O. The mass spectrum shows a parent ion (M+) peak...
(c) Compound C has molecular formula C9H10O. The mass spectrum shows a parent ion (M+) peak at 134 and a base peak (largest peak) at 105 atomic mass units. The IR spectrum shows major signals at 3029, 2925, 2721, 1708, 1495, 1452, 1375, 1152, 745, and 699 cm-1. The 1H-NMR spectrum shows signals at 2.35 (singlet, 3H), 3.65 (doublet, 2H), 7.11 (doublet 2H), 7.18 (doublet, 2H), and 9.73 (triplet, 1H) ppm. The 13C-NMR spectrum shows signals at 21.1, 50.2, 128.7,...
Compound C has molecular formula C9H10O. The mass spectrum shows a parent ion (M+) peak at...
Compound C has molecular formula C9H10O. The mass spectrum shows a parent ion (M+) peak at 134 and a base peak (largest peak) at 105 atomic mass units. The IR spectrum shows major signals at 3029, 2925, 2721, 1708, 1495, 1452, 1375, 1152, 745, and 699 cm-1. The 1H-NMR spectrum shows signals at 2.35 (singlet, 3H), 3.65 (doublet, 2H), 7.11 (doublet 2H), 7.18 (doublet, 2H), and 9.73 (triplet, 1H) ppm. The 13C-NMR spectrum shows signals at 21.1, 50.2, 128.7, 129.5,...
formula is C4H10O 1. Fill in the table below. (7 pts.) Peak letter Chemical shift Splitting...
formula is C4H10O
1. Fill in the table below. (7 pts.) Peak letter Chemical shift Splitting pattern Integration # Type of H that made the peak (i.e CH) 2. Calculate the degree of unsaturation for your compound. (3 pts.) 3. Predict a structure for your unknown compound. (5 pts.) 4. Label the hydrogens in your structure with the letter of the NMR peak with which they correspond. (5pts.) 5. Explain how you arrived at your predicted structure. For example, "The...
Compound 3: Use the information provided below and the IR and NMR spectra on the next...
Compound 3: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. a) An MS was taken of compound 3 and the table is given below. Determine the molecular formula of 3 from the MS given below. . relative abundance m/z 152 100 153 9.7 154 4.5 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 'H- and 13C-NMR spectra...
if you can explain to me step by step how to come up with the answer....
if you can explain to me step by step how to come up with the
answer.
Versic Part 8 (15 Points Total) An unknown compound was found to have the molecular formula C.HCIO using high resolution mass spectrometry (m/z = 149.9680). An Infrared spectrum of this compound includes an absorbance at 1715 cm 1H NMR, TMS = Oppm 3H Зн 1H, quartet PPM (3 Points) How many units of unsaturation are in this unknown compound? (2 Points) What functional group...
Spectroscopy Problems For each problem, you must: 1) Calculate the degree of unsaturation. 2) Assign the principal...
Spectroscopy Problems For each problem, you must: 1) Calculate the degree of unsaturation. 2) Assign the principal IR absorption bands above 1500 cm-1 3) Draw the structure of the compound 4) Label the protons on your structure with letters and assign them to peaks on the NMR spectrum (see the example below). в OHD 3.5- 3. 2.5 1.0 PPM 0.5 Each problem contains the formula of the compound, the IR spectrum (with axes in cm vs. % transmission), and the...
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)...
A compound, C,H100, shows an IR peak at 1690 cm. Its 'H NMR spectrum has peaks at delta 7.9 (2H, multiplet), 7.6-7.4 (3H, multiplet), 2.95 (2H, quartet, J = 7 Hz), 1.25 (3H, triplet, J= 7 Hz). Draw its structure in the window below. . You do not have to consider stereochemistry. ChemDoodle A compound, C3H100, exhibits IR absorption at 1730 cm-1. Its carbon NMR shifts and substitution, determined by DEPT, are given below. 13C NMR: 822.6 (3), 23.6 (1),...
In this NMR handout, you will get practice interpreting NMR spectra. Refer to the NMR tutorial/theory for chemical shifts and descriptions of peak splitting. There are 4 NMR problems. For each problem, you have been given the chemical formula as well as the IR and NMR spectra. Draw the structure for each unknown compound and provide sufficient reasoning as to why you think it has that structure. To get full credit, determine the structure of the unknown compound, calculate the...
Question 3) Propose a structure consistent with the following spectral data for a compound C H..0, IR 3100 (broad, strong). 1710 (strong) cm '; 'H NMR: 1.05 (triplet, 3H), 2.40 (triplet: 2H), 3.46 (quartet, 2H), 3.61 (triplet, 2H), 12.01 (broad singlet, IH) (10 points)
formula is C4H10O
1. Fill in the table below. (7 pts.) Peak letter Chemical shift Splitting pattern Integration # Type of H that made the peak (i.e CH) 2. Calculate the degree of unsaturation for your compound. (3 pts.) 3. Predict a structure for your unknown compound. (5 pts.) 4. Label the hydrogens in your structure with the letter of the NMR peak with which they correspond. (5pts.) 5. Explain how you arrived at your predicted structure. For example, "The...
Compound 3: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. a) An MS was taken of compound 3 and the table is given below. Determine the molecular formula of 3 from the MS given below. . relative abundance m/z 152 100 153 9.7 154 4.5 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 'H- and 13C-NMR spectra...
if you can explain to me step by step how to come up with the
answer.
Versic Part 8 (15 Points Total) An unknown compound was found to have the molecular formula C.HCIO using high resolution mass spectrometry (m/z = 149.9680). An Infrared spectrum of this compound includes an absorbance at 1715 cm 1H NMR, TMS = Oppm 3H Зн 1H, quartet PPM (3 Points) How many units of unsaturation are in this unknown compound? (2 Points) What functional group...
Spectroscopy Problems For each problem, you must: 1) Calculate the degree of unsaturation. 2) Assign the principal IR absorption bands above 1500 cm-1 3) Draw the structure of the compound 4) Label the protons on your structure with letters and assign them to peaks on the NMR spectrum (see the example below). в OHD 3.5- 3. 2.5 1.0 PPM 0.5 Each problem contains the formula of the compound, the IR spectrum (with axes in cm vs. % transmission), and the...
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)...
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