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HNMR --CNMR arbitrary intensity 200 100 100 100 120100 2 020 20 ppm MS Which compound...
HNMR arbitrary intensity - 220 2200 200 160 160 180 120 100 200 5 Which of the following molecules produces the spectra above? (1 pt)
3 of 8 arbitrary intensity Bogo Voz 6 ppm Which compound below gives the spectra above? uro in
2 ethyl levulinate, 1 CNMR is of compound 1 150 200 100 Ppm Using this spectrum and while envis ioni ng the IR spectra of compounds 1 and 2, set up a table that compares five diagnostic spectral observations that are consistent with compound 1 and inconsistent with compound 2, thus distinguishing them. You should focus on peak/band position as well as the presence/absence of peaks. 2 ethyl levulinate, 1 CNMR is of compound 1 150 200 100 Ppm Using...
need help on both question IHNMR cNmR * ms Which of the compounds below gives the spectra above? (1 pt) HNAR CNMR Which of the following molecules gives the spectra above? (1 ot)
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
Determine structure of unknown compound by deducing the formula and analyzing the spectra. Part C:S IR/HNMR/CNMR Unknown #93 MW=134 AMU / ring SOC-H dromul 5,311 - Overlapping Signals, 4 1,34 HEP-11-24 ppm 4 Signals 120-160 ppm 200 180 20-0-075 160 240 120 80 40 20 100 pon
HAMA (NMR ΓΙ' arbitrary intensity ' το ΤΤΤΤΤΤΤΙΤΙ το ppm IMS αδιά Which of the following molecules produces the spectra above? (1 pt)
Interpret the CNMR, HNMR and IR spectrum to determine the identity of the unknown compound. MP = -56 degrees C and BP = 131 degrees C 13C NMR 220 220 200 180 180 160 140 120 PPM 100 80 60 40 20 0 El-MS: 100.1 MP = -56 °C BP = 131 °C 1H NMR 2 4 3 8 PPM SciFinder® οοτ 001 οε 08 TRANSMITTANCE [%] 60 40 20 40ο 4000 38ο 3500 οοο 3000 εοο οοο 2500 2000...
arbitrary intensity L200 220200100100 1201002 Which compound below gives the spectra above? ML Å w
please can some one expalin how to get the molecular fomular and hnmr, cnmr Compound 8: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. 1) An MS was taken of compound 8 and the table is given below. Determine the molecular formula of 8 from the MS given below. relative m/z abundance 100 117 4.4 116 k) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule...