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4. An unknown organic compound has a molecular formula C10H140. The NMR spectra is summarized below....
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...
The 1H- and 13C-NMR spectra for an unknown compound with molecular formula C6H1202 are shown below. Deduce a structural formula for this compound.
2. (12 pt) Unknown compound has a molecular formula of CH.0. The proton NMR spectra presented below. Identify substructures (explain why) and draw your final solution in the space provided CH 3,482 H
The IR and proton NIR spectra of an unknown organic compound, with the molecular formula CaHioO, are shown be Assign the most informative IR peaks, assign the NMR signals, and determine the structure of the unknown. 1Combined IR NMMR probiem ategral valos Dr. Joel Slade Laboratory Exam I March 7, 2019
The H-and 1c-NMR spectra for an unknown compound with molecular formula CH1402 are shown below. Deduce a structural formula for this compound H-NMR 13C-NMR 171.15 63.12 37.31 25.05 22,45 21.06 0.92 (d, 6H) 1.52 (m, 2H) 1.70 (m, 1H 2.09 (s, 3H) 4.10 (t, 2H) .You do not have to consider stercochemistry You do not have to explicitly draw H atoms Do not include lone pairs in your answer. They will not be considered in the grading
Need help with number 1. Thanks. An unknown compound has the molecular formula C_5H_10O_2. Its^1H NMR spectrum is shown below (integral values are shown below each peak). Its IR spectrum shows a strong peak at 1740 cm^-1. Determine its structure and assign all peaks on the NMR spectrum.^1H NMR (300 MHz, in CDCl_3) An unknown compound has the molecular formula C_9H_10O. Its^1H NMR is shown below (integral values are shown next to each peak). Its IR spectrum shows a strong...
Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 1H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a “zoom-in” on an important part of the spectrum. Unknown number: 2111 Callam/Paul Chemistry 2540 Spectroscopy Unknown - 25 points Information: Each spectra below...
The spectra of an unknown organic compound A having the molecular formula C1oH1o0 are shown below. Elucidate the structure of the compound. Show your work. (8 pts; no partial credits) 500 1500 Wave numbers 4000 3000 2000 1000 130 125 200 150 δ(ppm) 100 50 0 7A 6.8 76 14 12 10 3.2 16.1 3.3 6 (pom) 9.8 Draw your structure in this box
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...