The MS, IR, HNMR, CNMR spectra (given in that order) are provided for each compound with...
The MS, IR, HNMR, CNMR spectra (given in that order) are provided for each compound with the given molecular formula. Calculate the unsaturation index and using the spectra, deduce the structure of the unknown molecule. For each method of analysis (IR, MS, NMR) provide all structural information gained from the spectra. Please show and explain work.
Thank you
Homework Answers
from the IR it is cear that there is a carboxylic acid is there because
broad peak at 3200 cm-1 and
shorp peak at 1720 cm-1 indicating
there is a -COOH functional group
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The MS, IR, HNMR, CNMR spectra (given in that order) are
provided for each compound with...
please write clearly so i can read everything. i would be writing on the graphs themselves...
please write clearly so i can read everything. i would be
writing on the graphs themselves so please write on the graphs
also. thank you!
10. The MS, IR, 1HNMR and 13CNMR spectra (given in that order) are provided for a compound with the given molecular formula. Calculate the unsaturation index and using the spectra, deduce the structure of the unknown molecule. For each method of analysis (IR, MS, NMR) provide all structural information gained from the spectra (Note: providing...
please can some one expalin how to get the molecular fomular and hnmr, cnmr Compound 8:...
please can some one expalin how to get the molecular fomular
and hnmr, cnmr
Compound 8: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. 1) An MS was taken of compound 8 and the table is given below. Determine the molecular formula of 8 from the MS given below. relative m/z abundance 100 117 4.4 116 k) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule...
Compound 2: Use the information provided below and the IR and NMR spectra on the next...
Compound 2: 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 2 and the table is given below. Determine the molecular formula of 2 from the MS given below relative abundance m/z 132 100 133 9.8 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 1H- and 13C-NMR spectra given below, determine...
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. m/z 166 relative abundance 100 10.9 4.5 167 168 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 'H- and 18C-NMR spectra given...
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...
Label the significant peaks in the IR and NMR spectra. When analyzing the signals in the 'HNMR, b...
Label the significant peaks in the IR and NMR spectra. When analyzing the signals in the 'HNMR, be sure to include all appropriate information. For example: 3H, singlet, 0 neighbors, and c (the letter referring to the corresponding unique type of hydrogens that were labeled in the structure). It is recommended to provide more analysis for each signal than what is described above, when necessary, such as labeling any coupling constants if any are provided For NMR label each peak...
for part a I need how to determine and draw the molecular formula part c and...
for
part a I need how to determine and draw the molecular formula part
c and d is for the hnmr nad cnmr
Compound 5: 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 5 and the table is given below. Determine the molecular formula of 5 from the MS given below. relative abundance 138 33.3 139 m/z 2.9 b) Calculate the...
FOR EACH DETERMINE (if applicable): • MS DATA • IR DATA • HNMR DATA • CNMR...
FOR EACH DETERMINE (if applicable):
• MS DATA
• IR DATA
• HNMR DATA
• CNMR DATA
• MOLECULAR FORMULA
• MOLAR MASS
• STRUCTURE AND EVIDENCE
Compound 56 is a high-boiling liquid (boiling point 229 C) that does not react with I, in aqueous base to give a yellow precipiale of CHI, (a negative iodoform test). The Mass, IR, and 'H NMR spectra, along with 1C NMR data, are given below. Analysis: Elemental C, 81.04; H, 8.16; O, 10.80....
Compound A displays the following MS, 'HNMR, and IR spectra. Compound A decolorizes a solution of...
q
is for quadruplet and t is for triplet
Compound A displays the following MS, 'HNMR, and IR spectra. Compound A decolorizes a solution of bromine in dichloromethane. Suggest a structure for Compound A consistent with all of the data given. Account for all of the numbered peaks in the MS, interpret each NMR signal, and identify each peak in the functional group region of the IR spectrum. 4. 100 80 20 10 30 50 60 70 100 A !...
Determine structure of unknown compound by deducing the formula and analyzing the spectra. Part C:S IR/HNMR/CNMR...
Determine structure of unknown compound by deducing the formula
and analyzing the spectra.
Part C:S IR/HNMR/CNMR Unknown #93 MW=134 AMU / ring SOC-H dromul 5,311 - Overlapping Signals, 4 1,34 HEP-11-24 ppm 4 Signals 120-160 ppm 200 180 20-0-075 160 240 120 80 40 20 100 pon
please write clearly so i can read everything. i would be
writing on the graphs themselves so please write on the graphs
also. thank you!
10. The MS, IR, 1HNMR and 13CNMR spectra (given in that order) are provided for a compound with the given molecular formula. Calculate the unsaturation index and using the spectra, deduce the structure of the unknown molecule. For each method of analysis (IR, MS, NMR) provide all structural information gained from the spectra (Note: providing...
please can some one expalin how to get the molecular fomular
and hnmr, cnmr
Compound 8: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. 1) An MS was taken of compound 8 and the table is given below. Determine the molecular formula of 8 from the MS given below. relative m/z abundance 100 117 4.4 116 k) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule...
Compound 2: 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 2 and the table is given below. Determine the molecular formula of 2 from the MS given below relative abundance m/z 132 100 133 9.8 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 1H- and 13C-NMR spectra given below, determine...
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. m/z 166 relative abundance 100 10.9 4.5 167 168 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 'H- and 18C-NMR spectra given...
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...
Label the significant peaks in the IR and NMR spectra. When analyzing the signals in the 'HNMR, be sure to include all appropriate information. For example: 3H, singlet, 0 neighbors, and c (the letter referring to the corresponding unique type of hydrogens that were labeled in the structure). It is recommended to provide more analysis for each signal than what is described above, when necessary, such as labeling any coupling constants if any are provided For NMR label each peak...
for
part a I need how to determine and draw the molecular formula part
c and d is for the hnmr nad cnmr
Compound 5: 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 5 and the table is given below. Determine the molecular formula of 5 from the MS given below. relative abundance 138 33.3 139 m/z 2.9 b) Calculate the...
FOR EACH DETERMINE (if applicable):
• MS DATA
• IR DATA
• HNMR DATA
• CNMR DATA
• MOLECULAR FORMULA
• MOLAR MASS
• STRUCTURE AND EVIDENCE
Compound 56 is a high-boiling liquid (boiling point 229 C) that does not react with I, in aqueous base to give a yellow precipiale of CHI, (a negative iodoform test). The Mass, IR, and 'H NMR spectra, along with 1C NMR data, are given below. Analysis: Elemental C, 81.04; H, 8.16; O, 10.80....
q
is for quadruplet and t is for triplet
Compound A displays the following MS, 'HNMR, and IR spectra. Compound A decolorizes a solution of bromine in dichloromethane. Suggest a structure for Compound A consistent with all of the data given. Account for all of the numbered peaks in the MS, interpret each NMR signal, and identify each peak in the functional group region of the IR spectrum. 4. 100 80 20 10 30 50 60 70 100 A !...
Determine structure of unknown compound by deducing the formula
and analyzing the spectra.
Part C:S IR/HNMR/CNMR Unknown #93 MW=134 AMU / ring SOC-H dromul 5,311 - Overlapping Signals, 4 1,34 HEP-11-24 ppm 4 Signals 120-160 ppm 200 180 20-0-075 160 240 120 80 40 20 100 pon
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