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Part 3 - Question 4 Molecular Formula: C.H.O. a) Degree of unsaturation (show calculation and circle...
For part B also calculate degree of unsaturation and use the MS and 13CNMR spectra...
For part B also calculate degree of
unsaturation and use the MS and 13CNMR spectra to identify the
molecule. Label the graphs with the information gained.
9. Identify the compound with give molecular formula that gives the IR and 'H NMR spectra shown. Label the IR peaks with the type of functional group. Draw the structure of the compound and label the signals on the structure using letters (a, b, c, etc.) then label the signals on the 'H...
1. For the molecular formula CHINO, please provide the degrees of unsaturation (DOU) and the structure....
1. For the molecular formula CHINO, please provide the degrees of unsaturation (DOU) and the structure. Draw and label your proposed structure for both your proton NMR table and the carbon NMR table. Please provide a table for the proton NMR that includes the signal label, chemical shift, multiplicity and the integration. For the Carbon NMR please provide a table that includes the signal label and the chemical shift. (10) CNMR 200 180 160 140 120 80 40 20 100...
For the molecular formula C9H11NO, please provide the degrees of unsaturation (DoU) and the structure. Draw...
For the molecular formula C9H11NO, please provide the degrees of
unsaturation (DoU) and the structure. Draw and label your proposed
structure for both your proton NMR table and the carbon NMR table.
Please provide a table for the proton NMR that includes the signal
label, chemical shift, multiplicity and the integration. For the
Carbon NMR please provide a table that includes the signal label
and the chemical shift
CNMR 200 180 160 140 120 80 60 40 100 PPM 20...
5) Draw 3 isomers with the molecular formula C6H14 that do NOT contain a stereocenter Below...
5) Draw 3 isomers with the molecular formula C6H14 that do NOT contain a stereocenter Below each molecule, indicate: (i) the degrees of unsaturation (2), (ii) number of signals in the C-NMR spectrum, and (iii) number of signals in the 'H-NMR spectrum. Be sure to properly label awarded. For example you could format your answers below each structure 13 or credit will not be
1. For the molecular formula C9H1NO, please provide the degrees of unsaturation (DoU) and the structure....
1. For the molecular formula C9H1NO, please provide the degrees of unsaturation (DoU) and the structure. Draw and label your proposed structure for both your proton NMR table and the carbon NMR table. Please provide a table for the proton NMR that includes the signal label, chemical shift, multiplicity and the integration. For the Carbon NMR please provide a table that includes the signal label and the chemical shift. (10) CNMR 200 180 160 140 120 100 PPM 80 60...
CHE 310 Homework #9 Due WED NOV 20 3. Given the 'H NMR spectrum below and a molecular formula of C.H.O. provide a s...
CHE 310 Homework #9 Due WED NOV 20 3. Given the 'H NMR spectrum below and a molecular formula of C.H.O. provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 3300 cm (broad) (5 pts.) 3H, d 24.9 2H,m 1H, bs 1H, PPM 4. In the space below, draw a 'H NMR spectrum for each of the following molecules. Note that only one of these will be graded but...
A compound with molecular formula C7H160 displays the following IR and 'H-NMR spectra. The 13C NMR...
A compound with molecular formula C7H160 displays the following IR and 'H-NMR spectra. The 13C NMR data suggest that there is some symmetry within the molecule. a) Calculate the degrees of unsaturation (DU) for the compound in the space provided below. DU = b) Identify and label the two indicated peaks in the IR spectrum in the boxes provided. Identify and label ALL peaks in the 'H NMR spectrum below. The numbers given on the 'H NMR are integration values...
A compound with molecular formula C7H160 displays the following IR and 'H-NMR spectra. The 13C NMR...
A compound with molecular formula C7H160 displays the following IR and 'H-NMR spectra. The 13C NMR data suggest that there is some symmetry within the molecule. a) Calculate the degrees of unsaturation (DU) for the compound in the space provided below. DU = b) Identify and label the two indicated peaks in the IR spectrum in the boxes provided. Identify and label ALL peaks in the 'H NMR spectrum below. The numbers given on the 'H NMR are integration values...
A compound with molecular formula C7H160 displays the following IR and 'H-NMR spectra. The 13C NMR data suggest that th...
A compound with molecular formula C7H160 displays the following IR and 'H-NMR spectra. The 13C NMR data suggest that there is some symmetry within the molecule. a) Calculate the degrees of unsaturation (DU) for the compound in the space provided below. DU = b) Identify and label the two indicated peaks in the IR spectrum in the boxes provided. Identify and label ALL peaks in the 'H NMR spectrum below. The numbers given on the 'H NMR are integration values...
A compound with molecular formula C H160 displays the following IR and 'H-NMR spectra. The 13C...
A compound with molecular formula C H160 displays the following IR and 'H-NMR spectra. The 13C NMR data suggest that there is some symmetry within the molecule. a) Calculate the degrees of unsaturation (DU) for the compound in the space provided below. DU = b) Identify and label the two indicated peaks in the IR spectrum in the boxes provided. Identify and label ALL peaks in the 'H NMR spectrum below. The numbers given on the 'H NMR are integration...
For part B also calculate degree of
unsaturation and use the MS and 13CNMR spectra to identify the
molecule. Label the graphs with the information gained.
9. Identify the compound with give molecular formula that gives the IR and 'H NMR spectra shown. Label the IR peaks with the type of functional group. Draw the structure of the compound and label the signals on the structure using letters (a, b, c, etc.) then label the signals on the 'H...
1. For the molecular formula CHINO, please provide the degrees of unsaturation (DOU) and the structure. Draw and label your proposed structure for both your proton NMR table and the carbon NMR table. Please provide a table for the proton NMR that includes the signal label, chemical shift, multiplicity and the integration. For the Carbon NMR please provide a table that includes the signal label and the chemical shift. (10) CNMR 200 180 160 140 120 80 40 20 100...
For the molecular formula C9H11NO, please provide the degrees of
unsaturation (DoU) and the structure. Draw and label your proposed
structure for both your proton NMR table and the carbon NMR table.
Please provide a table for the proton NMR that includes the signal
label, chemical shift, multiplicity and the integration. For the
Carbon NMR please provide a table that includes the signal label
and the chemical shift
CNMR 200 180 160 140 120 80 60 40 100 PPM 20...
5) Draw 3 isomers with the molecular formula C6H14 that do NOT contain a stereocenter Below each molecule, indicate: (i) the degrees of unsaturation (2), (ii) number of signals in the C-NMR spectrum, and (iii) number of signals in the 'H-NMR spectrum. Be sure to properly label awarded. For example you could format your answers below each structure 13 or credit will not be
1. For the molecular formula C9H1NO, please provide the degrees of unsaturation (DoU) and the structure. Draw and label your proposed structure for both your proton NMR table and the carbon NMR table. Please provide a table for the proton NMR that includes the signal label, chemical shift, multiplicity and the integration. For the Carbon NMR please provide a table that includes the signal label and the chemical shift. (10) CNMR 200 180 160 140 120 100 PPM 80 60...
CHE 310 Homework #9 Due WED NOV 20 3. Given the 'H NMR spectrum below and a molecular formula of C.H.O. provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 3300 cm (broad) (5 pts.) 3H, d 24.9 2H,m 1H, bs 1H, PPM 4. In the space below, draw a 'H NMR spectrum for each of the following molecules. Note that only one of these will be graded but...
A compound with molecular formula C7H160 displays the following IR and 'H-NMR spectra. The 13C NMR data suggest that there is some symmetry within the molecule. a) Calculate the degrees of unsaturation (DU) for the compound in the space provided below. DU = b) Identify and label the two indicated peaks in the IR spectrum in the boxes provided. Identify and label ALL peaks in the 'H NMR spectrum below. The numbers given on the 'H NMR are integration values...
A compound with molecular formula C7H160 displays the following IR and 'H-NMR spectra. The 13C NMR data suggest that there is some symmetry within the molecule. a) Calculate the degrees of unsaturation (DU) for the compound in the space provided below. DU = b) Identify and label the two indicated peaks in the IR spectrum in the boxes provided. Identify and label ALL peaks in the 'H NMR spectrum below. The numbers given on the 'H NMR are integration values...
A compound with molecular formula C7H160 displays the following IR and 'H-NMR spectra. The 13C NMR data suggest that there is some symmetry within the molecule. a) Calculate the degrees of unsaturation (DU) for the compound in the space provided below. DU = b) Identify and label the two indicated peaks in the IR spectrum in the boxes provided. Identify and label ALL peaks in the 'H NMR spectrum below. The numbers given on the 'H NMR are integration values...
A compound with molecular formula C H160 displays the following IR and 'H-NMR spectra. The 13C NMR data suggest that there is some symmetry within the molecule. a) Calculate the degrees of unsaturation (DU) for the compound in the space provided below. DU = b) Identify and label the two indicated peaks in the IR spectrum in the boxes provided. Identify and label ALL peaks in the 'H NMR spectrum below. The numbers given on the 'H NMR are integration...
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