Deduce the final structure consistent to the 1H-NMR data.
C10H12O2
2.0ppm(singlet, 3H), 2.9 ppm (triplet, 2H), 4.3 ppm (triplet, 2H)7.3 ppm (singlet, 5H)
Deduce the final structure consistent to the 1H-NMR data. C10H12O2 2.0ppm(singlet, 3H), 2.9 ppm (triplet, 2H), 4.3 ppm (...
Deduce the final structure consistent to the 1H-NMR data. C10H12O2 1.2 ppm (triplet, 3H), 3.5 ppm (singlet, 2H), 4.1 ppm (quartet, 2H), 7.1 ppm (singlet, 5H)
Deduce the final structure consistent to the 1H-NMR data. C9H10O2 2.1 ppm (singlet, 3H), 4.3 ppm (singlet, 2H), 7.3 ppm (singlet, 5H)
Deduce the final structure consistent to the 1H-NMR data. C5H9BrO2 1.2 ppm (triplet, 3H), 2.9 ppm (triplet, 2H), 3.5 ppm (triplet, 2H), 4.0 ppm (quartet, 2H)
Deduce the final structure consistent to the 1H-NMR data. C4H8O2 1.2 ppm (triplet, 3H), 2.3 ppm (quartet, 2H), 3.6 ppm (singlet, 3H)
C9H12 13C NMR 7 peaks 1H NMR δ 1.13 (triplet, 3H); δ 1.71 (multiplet, 2H); δ 2.64 (triplet, 2H); δ 7.34 (multiplet, 5H) Degree of Unsaturation _______ Draw the structure of your compound and indicate the ppm of each of the H’s. 2. C5H10O2 13C NMR 5 peaks 1H NMR δ 0.93 (triplet, 3H); δ 1.70 (multiplet, 2H); δ 2.25 (triplet, 2H); δ 3.59 (singlet, 3H) Degree of Unsaturation _______ Draw the structure of your compound and indicate the ppm...
just the circled ones only 8.10 Suggest structures consistent with the following 'H NMR data: a. Сно triplet (1.0 ppm, 3H) singlet (2.1 ppm, 3H) quartet (2.4 ppm, 2H) b. С Н.о, triplet (1.2 ppm, 3H) singlet (2.1 ppm, 3H) quartet (4.1 ppm, 2H) усно singlet (2.4 ppm, 3H) multiplet (7.5 ppm, 5H) singlet (1.6 ppm, 6H) singlet (3.1 ppm, 2H) multiplet (7.3 ppm, 5H) 1. Сно, triplet (1.2 ppm, 3H) singlet (2.4 ppm, 3H quartet (4.2 ppm, 2H) ....
Deduce the identity of the following compound from the 1H NMR data given. C8H100:8 3.4 (3H, singlet), 4.5 (2H, singlet), 7.2 (5H, apparent singlet) (ppm) A) PhCOCH3, B) PhCH2OCH3 C) (CH3)3CCH2CHO D) PHCH2CH3 ОА OB Ос
H NMR: 7.0d (4H, broad singlet); 2.85 o (1H, septet); 2.28 (3H, singlet); 1.20 0(6H doublet) R: 825 cm What is the structure of a hydrocarbon that shows a molecular ion at m/z- 182 in the mass spectrum and has the following 1H NMR spectrum? 7.20, singlet, 5H- 2.9 d, singlet, 2H H NMR: 7.0d (4H, broad singlet); 2.85 o (1H, septet); 2.28 (3H, singlet); 1.20 0(6H doublet) R: 825 cm What is the structure of a hydrocarbon that shows...
Draw the structure that would be responsible or the following spectra: 5. CH.0;septet (1H), singlet (3H), doublet (6H) 11 10 8 7 6 4 3 2 1 0 5 ppm 6. C1H1402, multiplet (5H), singlet (2H), triplet (2H), multiplet (2H), triplet (3H) E 11 10 9 2 ppm
Which structure is consistent with the following proton NMR data: 1.2 (3H, triplet, J = 8Hz), 3.7 (2H, quartet, J = 8Hz), 4.1 (2H, singlet) 11.1 (1H, singlet) CH,CH3 OCH, or OOOO co What is the product of this reaction sequence? 1. NaOEt 2. PhCH,Br 3. H2O*, Heat ОН Question 19 (1 point) Which of the following can be prepared by acetoacetic ester synthesis? 04 only O1 only O3 and 4 only O2 and 3 only