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Provide a structure for the compound with molecular formula CoH100 and with the following spectroscopic data....
Get help answering Molecular Drawing questions Provide a structure for the compound with molecular formula CgH100...
Get help answering Molecular Drawing questions Provide a structure for the compound with molecular formula CgH100 and with the following spectroscopic data. IR: 1680 cm-1 iH NMR: 1.255 (triplet, 1-3H), 3.05 (quartet, 1-2H), 7-86(multiplet, 1-SH) Edit
Propose a structure for a compound with molecular formula C8H15ClO3 that fits the following spectroscopic data....
Propose a structure for a compound with molecular formula C8H15ClO3 that fits the following spectroscopic data. IR: 1780 cm-1, 1150 cm-1 1H NMR: 1.1δ (triplet, I=6), 1.9δ (quartet, I=2), 2.8δ (triplet, I=2), 3.4δ (quartet, I=4), 4.2δ (triplet, I=1) 13C NMR: 15, 31, 38, 57, 100, 173
Propose a structure for a compound with molecular formula C8H15ClO3 that fits the following spectroscopic data....
Propose a structure for a compound with molecular formula C8H15ClO3 that fits the following spectroscopic data. IR: 1780 cm-1, 1150 cm-1 1H NMR: 1.1δ (triplet, I=6), 1.9δ (quartet, I=2), 2.8δ (triplet, I=2), 3.4δ (quartet, I=4), 4.2δ (triplet, I=1) 13C NMR: 15, 31, 38, 57, 100, 173
Question 16 Propose a structure for a compound with molecular formula CgH15CIO3 that fits the following spectroscop...
Question 16 Propose a structure for a compound with molecular formula CgH15CIO3 that fits the following spectroscopic data, IR: 1780 cm 1, 1150 cm 1 1H NMR: 1.18 (triplet, 1-6), 1.98 (quartet, I=2), 2.88 (triplet, 1-2), 3.48 (quartet, I=4), 4.28 (triplet, 1=1) 13C NMR: 15, 31, 38, 57, 100, 173 Edit
The following spectroscopic data corresponds to an an unknown compound with the molecular formula C4H8O2. Deduce...
The following spectroscopic data corresponds to an an unknown compound with the molecular formula C4H8O2. Deduce and draw the structure of the compound that corresponds to the data 1H NMR: δ 4.07 (quartet, 2H), 1.97 (singlet, 3H), 1.18 (triplet, 3H) ppm. "C NMR: δ 170, 60, 20, 14 ppm.
2. Use the 'H NMR and IR data to determine the structure of the following compounds...
2. Use the 'H NMR and IR data to determine the structure of the following compounds and name them. Compound A Molecular formula: CroH IR absorptions at N/A H NMR data: 1.3 (singlet, 9H), 7.0 to 7.5 (multiplet, 5H) ppm Compound B Molecular formula: CHO IR absorptions at 1H NMR data: 1735-1745, 1050 cm 0.93 (doublet, 6H), 1.52 (multiplet, 2H), 1.69 (multiplet, 1H), 2.04 (singlet, 3H), and 4.10 (triplet,2H) ppm Compound C Molecular ion: IR absorptions at 1710 cm 1H...
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...
Name (PRINT): Provide a structure consistent with the following molecular formula and spectroscopic data. You will...
Name (PRINT): Provide a structure consistent with the following molecular formula and spectroscopic data. You will al a correct structure or partial credit for answers given below. Formula: CH.0 IR: 1700 cm (very strong) DE 1630 medium) Provide Structure a) 5 4 3 2 1 ppm (2 pts partial credit) Use the molecular formula to calculate the total number of n-bonds plus rings. (DU) for the molecule. DU = (2 pts partial credit) Use the IR data to indicate what...
The following spectroscopic data below corresponds to an unknown carbonyl compound with the molecular formula C8H12O....
The following spectroscopic data below corresponds to an unknown carbonyl compound with the molecular formula C8H12O. Deduce and draw the structure of the compound that corresponds to the data. The letter \"m\" refers to an uninterpretable multiplet in the spectra. 1H NMR: δ 0.94 (t, 3H), 1.48 (sextet, 2H), 2.21 (q, 2H), 5.8-7.1 (m, 4H), and 9.56 (d, 1H) ppm. 13C NMR: δ 13.6, 21.9, 35.2, 129.0, 135.2, 146.7, 152.5, 193.2 ppm.
The following spectroscopic data below corresponds to an unknown carbonyl compound with the molecular formula C_8H_12O....
The following spectroscopic data below corresponds to an unknown carbonyl compound with the molecular formula C_8H_12O. Deduce and draw the structure of the compound that corresponds to the data. The letter "m" refers to an uninterpretable multiplet in the spectra. ^1H NMR: delta 0.94 (t, 3H), 1.48 (sextet, 2H), 2.21 (q, 2H), 5.8-7.1 (m, 4H), and 9.56 (d, 1H) ppm. ^13 C NMR: delta 13.6, 21.9, 35.2, 129.0, 135.2. 146.7, 152.5, 193.2 ppm.
Get help answering Molecular Drawing questions Provide a structure for the compound with molecular formula CgH100 and with the following spectroscopic data. IR: 1680 cm-1 iH NMR: 1.255 (triplet, 1-3H), 3.05 (quartet, 1-2H), 7-86(multiplet, 1-SH) Edit
Question 16 Propose a structure for a compound with molecular formula CgH15CIO3 that fits the following spectroscopic data, IR: 1780 cm 1, 1150 cm 1 1H NMR: 1.18 (triplet, 1-6), 1.98 (quartet, I=2), 2.88 (triplet, 1-2), 3.48 (quartet, I=4), 4.28 (triplet, 1=1) 13C NMR: 15, 31, 38, 57, 100, 173 Edit
The following spectroscopic data corresponds to an an unknown compound with the molecular formula C4H8O2. Deduce and draw the structure of the compound that corresponds to the data 1H NMR: δ 4.07 (quartet, 2H), 1.97 (singlet, 3H), 1.18 (triplet, 3H) ppm. "C NMR: δ 170, 60, 20, 14 ppm.
2. Use the 'H NMR and IR data to determine the structure of the following compounds and name them. Compound A Molecular formula: CroH IR absorptions at N/A H NMR data: 1.3 (singlet, 9H), 7.0 to 7.5 (multiplet, 5H) ppm Compound B Molecular formula: CHO IR absorptions at 1H NMR data: 1735-1745, 1050 cm 0.93 (doublet, 6H), 1.52 (multiplet, 2H), 1.69 (multiplet, 1H), 2.04 (singlet, 3H), and 4.10 (triplet,2H) ppm Compound C Molecular ion: IR absorptions at 1710 cm 1H...
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...
Name (PRINT): Provide a structure consistent with the following molecular formula and spectroscopic data. You will al a correct structure or partial credit for answers given below. Formula: CH.0 IR: 1700 cm (very strong) DE 1630 medium) Provide Structure a) 5 4 3 2 1 ppm (2 pts partial credit) Use the molecular formula to calculate the total number of n-bonds plus rings. (DU) for the molecule. DU = (2 pts partial credit) Use the IR data to indicate what...
The following spectroscopic data below corresponds to an unknown carbonyl compound with the molecular formula C_8H_12O. Deduce and draw the structure of the compound that corresponds to the data. The letter "m" refers to an uninterpretable multiplet in the spectra. ^1H NMR: delta 0.94 (t, 3H), 1.48 (sextet, 2H), 2.21 (q, 2H), 5.8-7.1 (m, 4H), and 9.56 (d, 1H) ppm. ^13 C NMR: delta 13.6, 21.9, 35.2, 129.0, 135.2. 146.7, 152.5, 193.2 ppm.
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