Identify the structure of a compound with the molecular formula C9H100 that exhibits the following 'H NMR spectrum: 10 Proton NMR L 10.2 9 8 7 54.1 6 Integration Values Triplet Triplet LO 5 4 3 2 ppm 2. 22.3
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- 3-Bromo-1-phenyl-1-propene shows a complex NMR spectrum in which the vinylic proton at C2 is coupled with both the C1 vinylic proton (J = 16 Hz) and the C3 methylene protons (J = 8 Hz). Draw a tree diagram for the C2 proton signal, and account for the fact that a five-line multiplet is observed.A compound has the molecular formula: C4H8O2 and gives the following C-13 NMR spectrum. Provide the most likely functional groups for each signal. nmrsim presentation 1 1 C:Bruken Topspin3.5pl7 examdata -170.7658 150 100 d 170.8 (O CH3) ; 60.4 (OCH2); 20.8, 14.1 (2 x C=0) 8170.8 (0 CH₂); 60.4 (OCH₂); 20.8, 14.1 (2 x CH3). 8 170.8 (CH3); 60.4 (C-0); 20.8, 14.1 (2 x OCH₂) 8170.8 (C=0); 60.4 (OCH₂); 20.8, 14.1 (2 x CH3). 8170.8 (C) ; 60.4 (O CH2); 20.8, 14.1 (2 x O CH3) -60.4293 50 -20.7902 -14.1385 [ppm] [+]What is the structure of the compound in the following ¹H-NMR spectrum with the molecular formula C9H10O₂? Relative integration is shown. HO₂C CO₂H CO₂H CHO CO₂H PPM 2
- Can you help me determine the structure of the compound represented in this spectrum?How could 1H NMR spectroscopy be used to distinguish betweencompounds X and Y?Identify the structure of a compound with the molecular formula C9H100 that exhibits the following 1H NMR spectrum. Proton NMR 10 L 10.2 о 8 7 6 5 3 2 ppm L 54.1 Integration Values 21.1 22.3 مند H H