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19H 7. Spectroscopy: (20 pts) The unknown compound A (C17H3403) gives the following 'H NMR and...
ITH 7. Spectroscopy: (20 pts) The unknown compound A (C17H3403) gives the following 'H NMR and IR spectra. Include degrees of unsaturation and show your work for partial credit. What is the structure of compound A? 6H 4H 2H 24 IH IH 24 24 24 24 IH Alle leden Willy ay 5 3 Ham 4000 3000 2000 1500 1000 500 Wavenumbers
2H 2n ZM 2H 9H 7. Spectroscopy: (20 pts) The unknown compound A (C17H3403) gives the following ‘H NMR and IR spectra. Include degrees of unsaturation and show your work for partial credit. What is the structure of compound A? 6H 4H 244 2ң IH IM TH A 3 5 4 2 1 WE Ann mm 4000 3000 2000 1000 500 1500 Wavenumbers
9H 7. Spectroscopy: (20 pts) The unknown compound A (C14H340) gives the following 'H NMR and IR spectra. Include degrees of unsaturation and show your work for partial credit. What is the structure of compound A? 6H 4H 2H 24 IH IH 2H 24 24 2H I IM 5 3 2 M m mm n 4000 3000 2000 1000 500 1500 Wavenumbers
9H 7. Spectroscopy: (20 pts) The unknown compound A (C17H340) gives the following 'H NMR and IR spectra. Include degrees of unsaturation and show your work for partial credit. What is the structure of compound A? 6H 4H 2H 24 IH IM 24 24 24 2H 1 IM 5 3 2 M m n 4000 3000 2000 1000 500 1500 Wavenumbers
The unknown compound A (C17H34O3) gives the following H NMR and
IR spectra. Include the degrees of unsaturation and show your work
for partial credit. What is the structure of compound A?
TH 7. Spectroscopy: (20 pts) The unknown compound A (C17H3403) gives the following 'H NMR and IR spectra. Include degrees of unsaturation and show your work for partial credit. What is the structure of compound A? 64 4H 24 2H IH IH 24 24 24 24 1H 정...
94 7. Spectroscopy: (20 pts) The unknown compound A (C17H3403) gives the following 'H NMR and IR spectra. Include degrees of unsaturation and show your work for partial credit. What is the structure of compound A? 6H 4H 2H 2H IH IH 24 24 24 24 1ң With the heat 5 4 دیا 2 M Lumm mm 4000 3000 2000 1000 500 1500 Wavenumbers 6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or...
organic chem help
What is the structure of the compound (C6H12O2) which gives the following IR and NMR spectra? NMR Data : 3.91(t, 2H), 1.89 (s, 3H), 1.45 (quintet, 2H), 1.23 (sextet, 2H), and 0.78 (t, 31 ) ppm. 4000 3000 2000 1500 сно но HEC 0
6. Spectroscopy. The molecular formula of an unknown organic compound is C8H1402. The IR, 1C-NMR and 'H-NMR spectra of this compound are shown on the next page. Answer the following questions about this compound. (a) What is the unsaturation number for this compound? (b) What functional group(s) does this compound contain? Indicate the specific evidence for your conclusion. (c) What can you conclude from the number of 13C-NMR signals? (d) What can you conclude from the H-NMR signal at 2.3...
Use the IR and NMR spectra to confirm the identity of
your final product. Identify all of the important peaks in the IR
spectrum. Assign all peaks in the NMR spectrum to their respective
hydrogen nuclei.
IR and 1H NMR of 9-Fluorenone: LOD TFRITTEN 9000 2000 LOOD MAVENUISERI 2 3 PPM 5 4H 8 2H2H 9 IR and 1H NMR of 9-Fluorenol: 100 TRANSMETTANCEI D 4000 3000 2000 1500 1000 500 HAVENUBIRII 1H 2H2H 2H 2H TH 9 5 3...
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...