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
- There are four esters with molecular formula C4H8O2. How can they be distinguished by 1H NMR?Determine the structure of an alcohol with molecular formula C6H14O that exhibits the ff DEPT 135 NMR SpectrumAn organic compound with molecular formula C4H8O2 has the following nmr values. Propose the structure of the compound? Shift (ppm) Area 4.13 2.05 quartet 2.02 3.04 singlet 1.15 3.00 triplet
- According to this H NMR spectrum, identify the structure of the compound. the only additional information given is the molecular weight is 240.3 14 72 7.0 8 (ppm) 6.8 6.4 3.0 2.5 2.0 6 tppm)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