11. (20 points) The 1H NMR, 13C NMR, Mass Spectra and IR spectra for a mystery compound with the formula C5H12O are shown below. Please draw the structure for the compound in the box below. Note: The numbers on top of the 1H NMR peaks are the number of protons associated with that peak. A chart for 1H NMR, IR and 13C NMR spectra shift values are on the following pages.
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11. (20 points) The 1H NMR, 13C NMR, Mass Spectra and IR spectra for a mystery...
IL (20 points) The 'H NMR, "C NMR, Mass Spectra and IR spectra for a mystery compound with the formula CsH20 are shown below. Please draw the structure for the compound in the box below. Note: The numbers on top of the 'H NMR peaks are the number of protons associated with that peak. A chart for 'H NMR, IR and C NMR spectra shift values are on the following pages. FTIR 13C NMR Zoom Out 'H NMR Zoom Out...
Assign as many peaks as possible in the IR, 1H NMR, and 13C NMR spectra. The spectra are for triphenylmethanol.
On the attached image are 1H NMR, 13C NMR, and IR spectra of a compound with the formula C4H8O. 1H NMR signal at 1.2 is caused by 3 hydrogens, the sigbal at 2.1 is caused by 3 hydrogens, and the signal at 2.5 is caused by 2 hydrogens. Identify the compound. CH 1110 9 8 7 6?4 Problem 6. 'H NMR spectrum of compound HsO Problem 6. 13C NMR spectrum of compound C4HsO 200 180 160 140 120 100 80...
Please interpret the NMR spectra and fill out the chart: Peak Chemical Shift (δ) Multiplicity† H‡ Peak Chemical Shift (δ) Multiplicity† H‡ 1. 7. 2. 8. 3. 9. 4. 10. 5. 11. 6. 12. Common Name: IUPAC Name CAS No.: Zoom Out ALDR CH Solvent: ВР: MP: 1.00 0.80 0.70 0.60 0.40 0.20 0.10 7.0 6.0 5.0 4.0 3.0 2.0 1.0
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...
I need help identifying a compound based on the spectra. The compound contains an aromatic ring. The spectra are attached. I would appreciate an accurate description.The 1H NMR, 13C NMR, mass and IR spectra of compound with a molecular formula (C9H11NO2) are given below. Use the given spectroscopic data to provide rational interpretation (motivation) of all the spectral data to determine the structure of this compound.
What information can we gather from these three spectra (IR, H NMR, 13C NMR) to correctly identify the unknown compound? What is the identity of my unknown? Please explain how we get there and from what information we do so. I understand that I must initially use the rule of 13. IR Spectrum: H NMR Spectrum: 13C NMR spectra: OOT 08 TRANSMITTANCE [%] 09 0+ 4000 3500 3000 2500 2000 WAVENUMBER [cm-1] 15:00 10:00 500 1H NMR 2 3 12.10ģ...
A compound with molecular formula C11H140 displays the following IR, 1H NMR and 13C NMR spectra. Propose a structure for this compound. Ppin 220.200.180.160.140 120 PPM 100 80 60 40 20
Using IR spectrum and 1H and 13C NMR spectra to figure out what the unknown compound is C: 63.15 H: 5.30 7.0 6.5 4,5 4.0 MW 152.149 12. Ola C
This chart shows the different spectra of an unknown organic compound. Explain the different peaks in its 1H-NMR, 13C-NMR and mass spectra as shown. PLEASE, ANSWER CORRECT. WILL GIVE ? 13 CIDENT