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Use a sheet of paper to answer the following question. Take a picture of your answers...
Complete Assignment M 2.10.6 Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment. There are several isomeric alcohols and ethers of molecular formula C5H120. Two of these exhibit the following 'H-NMR spectra. Propose a structure for each of the isomers. Isomer A: 5 = 0.92 (t, 7.8 Hz, 3 H), 1.20 (s, 6H), 1.49 (q, 7.8 Hz, 2H), 1.85 (s, 1H) ppm Isomer B: 5 = 1.19 (s,...
1. Propose structure formulas for each isomer of C7H140 in the boxes below based on the attached H-NMR and 18C-NMR spectra. C,H40 Isomer 1 C,Hl40 Isomer 2 CH4 Isomer 3 C,H40 ISOMER 1 1H NMR 9H 2H 3H 3 220 200 180 160 140 120 100 8060 40 0 PPM CjH40 ISOMER 2 1H NMR 6H ЗН 300 2H PPM 13C NMFR 220 20 180 160140 120 1008604020 0) PPM C7H140 ISOMER 3 1H NMR зн зн зн 2H 2H...
There are seven isomers of C4H10O. Draw line diagrams of the seven isomers and then match each isomer with the following H-NMR data. NOTE: s = singlet, d = doublet, t = triplet, m = multiplet i , 0.95 (t, 3H); 1.52 (m, 2H); 3.30 (s, 3H); 3.40 (t, 2H) ii , 1.15 (s, 1H); 1.29 (s, 9H) iii. , 1.20 (t, 3H); 3.45 (quartet, 2H) iv. , 0.90 (d, 6H); 1.78 (m, 1H); 2.45 (s, 1H); 3.30 (d, 2H)...
Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment. Compound 1 has molecular formula C6H12. It shows three signals in the 1H-NMR spectrum, one at 0.96 ppm, one at 2.03 ppm, and one at 5.33 ppm. The relative integrals of these three signals are 3, 2, and 1, respectively. Compound 2 has molecular formula C7H15Br. It shows two signals in the 1H-NMR spectrum, one at 1.08 ppm and...
Use a sheet of paper to answer the following question: Take a picture of your answers and attach to this assignment. Compound 1 has molecular formula CH 12. It shows three signals in the TH-NMR spectrum, one at 0.96 ppm, one at 2.03 ppm, and one at 5.33 ppm. The relative integrals of these three signals are 3, 2, and 1, respectively. Compound 2 has molecular formula CH1Br. It shows two signals in the 'H-NMR spectrum, one at 1.08 ppm...
2. Consider the protons labeled H., H., H., of the compound shown below. Each of these protons are chemically different and are split by at least one other type of proton. coupling constants are shown below. HA HOHC C= "Hc JAB = 15.1 Hz JBC = 6.4 Hz Draw the splitting tree for each proton, H., Ho, and H. 3. Propose a structure for the following compounds piven the spectra and molecula formula. Briefly describe how each spectrum supports your...
Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment The 'H-NMR spectrum of 1-bromopropane shows three signals and the 'H-NMR spectrum of 2- bromopropane shows two signals. Draw these two molecules and determine the relative integrals of each signal.
use both spectra to determine the exact structure of the compound and put your final answer in the box with formula pul youl tmllal answer in the box under the 'H NMR Compound 29 3H 2H 1H 3 PPM 7 Please put your final answer in the box under the 'H NMR. Compound 29 20 40 140 120 100 8060 PPM 180 200 pul youl tmllal answer in the box under the 'H NMR Compound 29 3H 2H 1H 3...
c) Using your answers to question 5 and 6a, what percent of the mixture obtained in reaction 1 is the ortho isomer? d) What percent of the mixture obtained in reaction 1 is the meta isomer? e) What percent of the mixture obtained in reaction 1 is the para isomer? f) Could we have used Mass Spectrometry after the GC analysis (GC-MS) to identify which peak on the GC was which isomer? Why or why not? g) Could we have...
Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment Draw an isomer of dibromocyclopropane that has (a) one proton environment; (b) two proton environments; (c) three proton environments.