3b. Analysis of FTIR, NMR Mass spectrum for Organic Unknown Compound. Below is the FTIR, 1H-NMR,...
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
The 1H- and 13C-NMR spectra for an unknown compound with molecular formula C6H1202 are shown below. Deduce a structural formula for this compound.
The 1H-NMR and 13C-NMR spectra of an unknown compound (formula C8H10) are shown below. Draw the structure of the unknown compound. The total integration of the peaks at around 7 ppm is 4. The integration of the peak at around 2 ppm is 6. 7 6 5 4 3 ppm TTTTTTTTTTTTTTTT 200 180 160 140 120 100 80 60 40 20 0 pom CH3 Create OscerSketch Answer 8 Incorrect: Answer has an incorrect structure.
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...
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 Submit your answer for Quiz 3 at: https://uglabs.cbc.osu.edu/cgi-test/organic/spec-quiz.pl Mass Spectrum (not shown): [M-206 (100%) m/z...
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. nts) The 'H NMR, "C NMR, Mass Spectra and...
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
5. The 1H-NMR, 13C-NMR and MS spectrums of an unknown compound are shown below. The molecular formula of the compound is C7H14O. What is the structure of the unknown? 5. The H-NMR, 13C-NMR and MS spectrums of an unknown compound are shown below. The molecular formula of the compound is C,H4O. What is the structure of the unknown? 2 Hs, sexnet 2 Hs, triplet Organic Chemistry 2 Homework due February 14, 2019 Mass Percent 15.0 26.0 27.0 2B.0 29,0 39.0...
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.
Create OscerSkotch Answer 6 Th e 1H-NMR and 13C-NMR spectra of an unknown compound s (formula CoMzo) are shown below. Draw the structure of B. The total integration of the peaks at around 7 ppm is 4. The integration of the peak at around 2 ppm is 6 ppm 200 180 160 140 120 100 060 4020