We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
Propose structures for the following isomeric alcohols that give the 13C NMR spectra below. Assign the carbons to their respective peaks.1d page 2.jpg1d page 3.jpg1d page 1.jpg09 13C shift chart 304.pdf
2. Determine the full structure of an unknown compound with spectral data from MS, H-1, and C-13 NMR. 12 10 H-1 NMR Relative Intensity MS m/z Two peaks overlapped 1.60 340 120 3600 20 C-13 NMR
q is for quadruplet and t is for triplet Compound A displays the following MS, 'HNMR, and IR spectra. Compound A decolorizes a solution of bromine in dichloromethane. Suggest a structure for Compound A consistent with all of the data given. Account for all of the numbered peaks in the MS, interpret each NMR signal, and identify each peak in the functional group region of the IR spectrum. 4. 100 80 20 10 30 50 60 70 100 A !...
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...
Propose the structure of a monosubstituted geminal alkene that fits the following NMR spectrum.4-3.jpg
Propose the structure of a disubstituted geminal alkene that fits the following NMR spectrum.4-4.jpg
4. Determine the structure for the compound that has the following MS, IR and 'H-NMR spectra and explain the reason. (7pts) 100 MS 60 40- m/z IR 400 P00T н R- H-NMR 1.1 1.0 ppm 3 H 16 1.5 ppm .. 2.0 1,9 ppm H (CHa) Si 1 2 H 2 H 22 2.1 ppm w ppm (6) Reat ve htensity 4. Determine the structure for the compound that has the following MS, IR and 'H-NMR spectra and explain the...
How many 1H NMR signals do each of the planar cyclic compounds display?3-1.jpg
3. Find the structure of a compound given the MS, IR, and NMR data below. When you have the solution, use it to determine the correct multiplicity of the signal at 5.1 ppm and explain the coupling pattern. A correct answer with no explanation will receive no credit. MASS 951 FL 100 128 1107 677 r69 r45 50 557 811 130 120 100 110 90 80 70 60 50 mt IR 100 50 2000 Wavenumber (cm-1) 1000 3000 4000 'H...
The MS, IR, HNMR, CNMR spectra (given in that order) are provided for each compound with the given molecular formula. Calculate the unsaturation index and using the spectra, deduce the structure of the unknown molecule. For each method of analysis (IR, MS, NMR) provide all structural information gained from the spectra. Please show and explain work. Thank you