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- 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.A'H NMR spectrum is shown for a molecule with the molecular formula of CeH9Br. Draw the structure that best fits this data.Chemistry H NMR AND C13NMR ??? IN 3 CI 5 A 20= B CI 7 9
- 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.Choose the molecule to which this IR spectrum corresponds.The number of unique carbons in a molecule will correspond to the number of signals in the ¹³C NMR spectrum. Identify the number of unique carbons in this structure. Br Br 1 4 7 +/- unique carbons 8 . 6 9 0 X C x 100 +
- 1. 4 4000 100 50 Identify the following compounds based on the spectra given. ff11 2 20 30 T 0 220 200 180 160 140 2008 CDS-00-094 KAVEMUNERI 40 1500 50 60 120 100 ppm 70 80 500 60 40 20 0Compound 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.Calculate the degree of unsaturation (DU) for a molecule with the formula of C₂H, O. 10