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9H 7. Spectroscopy: (20 pts) The unknown compound A (C14H340) gives the following 'H NMR and...
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
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
19H 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 24 2H IH IM 2H 2H 2M 2H TH 5 4 3 2 1 LA w min 4000 3000 2000 1000 500 1500 Wavenumbers
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
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...
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...
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
an Formula = = C11H2202 1644 2M 27 24 ІН M s 4 3 2 hanya 4000 3000 2000 1000 500 1500 Wavenumbers Look at the given spectra and formula. How many degrees of unsaturation are there in the molecule? What kind of bond does the IR peak at 1720 cm*1 represent? A (single, double, triple) bond between (elements) and What is the region between 1500-500 cm-1 called? Looking only at the information in the spectra: Is there a ketone...
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...
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...