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- How many unique 13C NMR and 1H NMR signals exist in the spectrum for the compound: 1,3-dibromobenzene?1Compound 1 has molecular formula C7H16. It shows three signals in the 1H-NMR spectrum, one at 0.85 ppm, one at 1.02 ppm, and one at 1.62 ppm. The relative integrals of these three signals are 6, 1, and 1, respectively. Compound 2 has molecular formula C7H14. It shows three signals in the 1H-NMR spectrum, one at 0.98 ppm, one at 1.36 ppm, and one at 1.55 ppm. The relative integrals of these three signals are 3, 2, and 2, respectively. Propose structures for compounds 1 and 2, explaining how you reach your conclusion.How many signals would you expect to find in the 'H NMR spectrum of the following compound? H3C O. CH3 H,C CH3 O 7 O 8 0 6 O 5
- How many signals would you expect to find in the 'H NMR spectrum of each given compound? Part 1 of 2 Part 2 of 2 H H OH OHHow many signals would you expect to see in the 1H NMR spectrum of each of the five compounds with molecular formula C6H14?Compound 1 has molecular formula C7H16. It shows three signals in the 1H-NMR spectrum, one at 0.85 ppm, one at 1.02 ppm, and one at 1.62 ppm. The relative integrals of these three signals are 6, 1, and 1, respectively. Compound 2 has molecular formula C7H14. It shows three signals in the 1H-NMR spectrum, one at 0.98 ppm, one at 1.36 ppm, and one at 1.55 ppm. The relative integrals of these three signals are 3, 2, and 2, respectively. Propose structures for compounds 1 and 2, explaining how you reach your conclusion.
- Which of the protons in the following molecule appear at the highest 8-value in the ¹H NMR spectrum? Explain your reasoning. H₂ iii iv H CH3 i y HC1. How many unique proton (¹H) and carbon (13C) NMR signals would you expect for the following compounds? NH₂ "NH₂ علا yokHow many signals would you expect to find in the H NMR spectrum of each given compound? Part 1 of 2 Part 2 of 2 X X Ś Ś
- 1. How many proton signals would you expect to see in the ¹H-NMR spectrum of the following molecule? For each of the proton signals, predict the splitting pattern, assuming that you can see only 3-bond splitting.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 one at 1.59 ppm. The relative integrals of these two signals are 3 and 2, respectively. Propose structures for compounds 1 and 2, explaining how you reach your conclusion.How many non-equivalent signals would you expect in the ¹H NMR spectrum of the compound shown below? 07 O 5 O 4 O 6 3 لا