tutorial/theory for chemical shifts and descriptions of peak splitting. NMR There are 4 NMR problems. For...

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tutorial/theory for chemical shifts and descriptions of peak splitting. NMR 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 degrees of unsaturation, and assign as many peaks as you can to your predicted structure. Problem #1: CSH100 (Assign hydrogens in your structure with the same labels used in the NMR spectra) 100- 50 4000 3000 2000 Wavenumber (cm") 500 1500 1000 singlet, 3H (d) triplet, 2H (c) sextet, 2H (b) triplet, 3H (a) lla PPM 12 % Transmittance tutorial/theory for chemical shifts and descriptions of peak splitting. NMR 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 degrees of unsaturation, and assign as many peaks as you can to your predicted structure. Problem #1: CSH100 (Assign hydrogens in your structure with the same labels used in the NMR spectra) 100- 50 4000 3000 2000 Wavenumber (cm") 500 1500 1000 singlet, 3H (d) triplet, 2H (c) sextet, 2H (b) triplet, 3H (a) lla PPM 12 % Transmittance tutorial/theory for chemical shifts and descriptions of peak splitting. NMR 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 degrees of unsaturation, and assign as many peaks as you can to your predicted structure. Problem #1: CSH100 (Assign hydrogens in your structure with the same labels used in the NMR spectra) 100- 50 4000 3000 2000 Wavenumber (cm") 500 1500 1000 singlet, 3H (d) triplet, 2H (c) sextet, 2H (b) triplet, 3H (a) lla PPM 12 % Transmittance tutorial/theory for chemical shifts and descriptions of peak splitting. NMR 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 degrees of unsaturation, and assign as many peaks as you can to your predicted structure. Problem #1: CSH100 (Assign hydrogens in your structure with the same labels used in the NMR spectra) 100- 50 4000 3000 2000 Wavenumber (cm") 500 1500 1000 singlet, 3H (d) triplet, 2H (c) sextet, 2H (b) triplet, 3H (a) lla PPM 12 % Transmittance tutorial/theory for chemical shifts and descriptions of peak splitting. NMR 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 degrees of unsaturation, and assign as many peaks as you can to your predicted structure. Problem #1: CSH100 (Assign hydrogens in your structure with the same labels used in the NMR spectra) 100- 50 4000 3000 2000 Wavenumber (cm") 500 1500 1000 singlet, 3H (d) triplet, 2H (c) sextet, 2H (b) triplet, 3H (a) lla PPM 12 % Transmittance tutorial/theory for chemical shifts and descriptions of peak splitting. NMR 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 degrees of unsaturation, and assign as many peaks as you can to your predicted structure. Problem #1: CSH100 (Assign hydrogens in your structure with the same labels used in the NMR spectra) 100- 50 4000 3000 2000 Wavenumber (cm") 500 1500 1000 singlet, 3H (d) triplet, 2H (c) sextet, 2H (b) triplet, 3H (a) lla PPM 12 % Transmittance

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C HIO O2 clegree of unsatturahion In IR 2C2 H5 a 200 um in... View the full answer