2. For cach of the following sets of data, provide the correct ester structure and correlate...
a) Provide the structure that is consistent with the data below. C7H14O2 IR (cm-1): 2950, 1750 1H NMR (d): 2.3 (2H, q), 1.0 (3H, t), 0.9 (9H, s) b) Deduce the identity of the compound from the data provided. C10H14O: IR (cm-1): 3200-3500 (broad), 3050, 2950, 1610 1H NMR(δ): 1.0 (s, 6H), 2.0 (s, 3H), 2.8 (broad s, 1H), 7.3 (d, 2H), 7.6 (d, 2H) c) An unknown compound, C3H5Cl3, gave the following proton NMR...
2. An organic compound E has the molecular formula C12Hi7NO gives spectroscopic data as follow: a) IR (KBR Disc): Amux 3296, 1642 cm b) 'H NMR (CDCl) : 6 0.93 (, 3H); 1.48 (d, 3H); 1.66 (sextet, 2HD) 2.15 (G, 2H); 5.14 (q, 1H):5.74 (broad, s, exchange with D20, 1H); 7.42-7.23 (m, 5H) i3C NMR (CDCl;) : δ 13.7 (q); 19.1 (t); 21.7 (q); 38.8 (t); 48.5 (d); 126.1 (d): 127.3 (d); 128.6 (d); 143.0 (s); 172.0 (s) c) d)...
Provide the most likely chemical structure that corresponds to each set of spectral data 2. Formula: C6H120 IR: 2960 cm-- (strong), 2874 cm 2 (medium), 1716 cm2 (strong, sharp) "H NMR: 2H, doublet (2.312 ppm); 1H, multiplet (2.133 ppm); 3H, singlet (2.123 ppm); 6H, doublet (0.926 ppm) 13C NMR: 208 ppm, 53 ppm, 30 ppm, 24 ppm, 22 ppm 3. Formula: C4H100 IR: 3339 cm (broad, strong), 2957 cm (strong), 2874 cm (medium) "H NMR: 6H, doublet (0.9 ppm); 1H,...
Please, correct answer. I will give ? 2. Two compounds having same molecular formula C8H1402 show the following 'H NMR and 13C NMR spectral data: Compound (A). 'H NMR: 0.96 (t, 3H), 1.33 - 1.57 (m, 4H), 1.93 (s, 3H), 4.15 (t, 2H), 5.58 (d, 1H), 6.15 (d, 1H) "C NMR: 13.7(9), 18.4(q), 19.3(t), 32.2(t), 66.8(t), 122.9(t), 138.0(s), 165.0(s) Compound (B). 'H NMR: 1.01 (d, 6H), 1.93 (s, 3H), 2.43 (m, 1H), 4.11 (d, 2H), 5.58 (d, 1H), 6.15 (d,...
2. Given the 'H NMR spectrum below and a molecular formula of CsH60, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1710 cm (5 pts.) 6H, 1H, S 2H, d 1H, m NH PPM CHE 310 Homework 9 Due WED NOV 20 3. Given the 'H NMR spectrum below and a molecular formula of CH..0. provide a structure. Note you must assign all of the signals in the...
For the foowing 1H NMR spectra, choose the correct structure. d, 6H 3H, m 11. septet 2H, m 12 11 10 9 8 7 6 5 obl foro yo ok olar For the folowing 1H NMR spectre choose the correct structure. 2H s 3H. 2H, 2. m Hm oplom
1. Given the 'H NMR spectrum below and a molecular formula of CH20, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1600-1650 cm' (multiple peaks) (5 pts.) 3H, S 3H. t 2H, d 2H, d 2H, PPM 2. Given the 'H NMR spectrum below and a molecular formula of CH.0, provide a structure. Note you must assign all of the signals in the spectrum below to receive full...
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...
Determine the structure of the compound with chemical formula C8H11N using the following 1H-NMR data: S(6H), 3.06 δ T(1H), 6.79 δ D(2H), 6.94 δ T(2H), 7.27 δ (S = singlet, D = doublet, T = triplet, Q = quartet)
3. Given the 'H NMR spectrum below and a molecular formula of C.HO. provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 3300 cm' (broad) (5 pts.) 3H, d 3H, 2H, t 2H, 2H, m 1H, bs 1H, m PPM