NMR: 2.82 shift (6H, singlet), 8.13 shift (4H, singlet)
IR: 1681 1/cm, no OH stretch

NMR:
2.82 shift (6H, singlet),---> two methyl groups (CH3)
8.13 shift (4H, singlet) ----> four identical hydrogens in the phenyl ring.
IR: 1681 1/cm, no OH stretch ---> carbonyl group (C=O)
NMR: 2.82 shift (6H, singlet), 8.13 shift (4H, singlet) IR: 1681 1/cm, no OH stretch
Identify the following compound C10H10O2 NMR: S 2.82 (6H,singlet); S 8.13 (4H, singlet) IR: 1681 cm^-1; no O-H stretch
Identify the following compound. C10H10O2: NMR: δ 2.82 (6H, s), δ 8.13 (4H, s) IR: 1681 cm–1, no O–H stretch
Identify the following compound. C10H10O2: NMR: δ 2.82 (6H, s), δ 8.13 (4H, s) IR: 1681 cm-1, no O-H stretch
Identify the following compound: C10H10O2: NMR: δ 2.82 (6 H, s), δ 8.13 (4 H, s) IR: 1681 cm-1, no O-H stretch
Chemical structure of C9H16O4 with H NMR 3.6 (6H, singlet) 2.2 (4H, singlet) 1.0 (6H, singlet)
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...
NMR & IR post lab question help!
NMR and IR 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppm IH The 'H NMR for the unknown C: 20 7.5 7.0 6.5 6.0 6.5 5.0 4.5 4.0 3.5 3.0 25 20 519 05 Proton peak Integration Chemical Shift (ppm) Neighbors (m) Splitting pattern (+1) report as singlet/doublettripletlets. C must be an aliphatic alcohol. There is a strong O-H stretch in the IR and zero degrees of unsaturation. The remaining structure...
Deduce the identity of the following compound from the IH NMR data given and IR data CA 1804: δ 3.9 (6H, singlet), 6.1 (2H, singlet) (ppm) IR: 3100 cm, 2950 cm, 1735 cm
NMR and IR The 'H NMR for the unknown C: O 70 70 20 85 60 15 20 30 30 25 20 10 % pom Proton peak Integration Chemical Shift (ppm) Neighbors (n) Splitting pattern (n+1) report as singlet/doublet/tripletete 12 3.4 C must be an aliphatic alcohol. There is a strong O-H stretch in the IR and zero degrees of unsaturation. The remaining structure is determined by 'H NMR. (e) Predicted Structure C (label hydrogens with letter for assignment below):...
2. Use the 'H NMR and IR data to determine the structure of the following compounds and name them. Compound A Molecular formula: CroH IR absorptions at N/A H NMR data: 1.3 (singlet, 9H), 7.0 to 7.5 (multiplet, 5H) ppm Compound B Molecular formula: CHO IR absorptions at 1H NMR data: 1735-1745, 1050 cm 0.93 (doublet, 6H), 1.52 (multiplet, 2H), 1.69 (multiplet, 1H), 2.04 (singlet, 3H), and 4.10 (triplet,2H) ppm Compound C Molecular ion: IR absorptions at 1710 cm 1H...