3 (Spts) If you needed te distinguish each of the compounds in the following pairs (...
pls help. thank you so much. WOT 3. Propose structures for compounds that fit the following 1 NMR. a. C.H,C: 81.60 (doublet, 3H), 2.15 (multiplet, 28), 3.72 triplet, 211), 47, 18) b. C.H.Br: 81.1 (doublet, 6H), 1.9 (multiplet, 1H), and 3 A (doublet, 24) c. C-H140:8 0.9 (triplet, 6H), 1.6 (sextet, 4H), and 2.4 (triplet, 4H) d. CsH1002: 8 1.2 (doublet, 6H), 2.0 (singlet, 3H) and 5.0 (septet, 1H)
Predict the proton NMR of compound 5, 5-(2-(diethylammonio)-5-oxocyclopent-3-en-1-yl)-2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-olate, by labeling each inequivalent hydrogen with a letter and creating a table with each inequivalent hydrogen in a separate row in the below table. Proton Label Chemical Shift (ppm) Integral (e.g., 1H,2H, 3H…6H) Coupling (e.g., singlet, doublet, triplet) PLEASE fill out table when answering. Proton Label Chemical Shift (ppm) Integral (e.g., 1H, 2H, 3H...6H) Coupling (e.g., singlet, doublet, triplet)
Identify each compound in the following questions and make assignments in the 1H NMR a) First spectra: Compound 1, 1H NMR given, and has a strong absorbance in the IR at 1715 cm-1 b) Second spectra: Compound 2, a carboxylic acid of formula C8H6O3Cl2 with 1H NMR given c) Third spectra: Compound 3 with molecular formula of C6H9ClO2, with 1H NMR given (the four signal from highest to lowest chemical shift are quartet, quartet, double, and triplet) d) Compound 4,...
s and give the m 0~시 2. How could you distinguish the following pairs of isomeric compounds using IR and MS? For some pairs- one of these spectral techniques may be different enough to distinguish the compounds. and (b) and 3. Analyne the IR and MS spectra below to predict a possible structure for each compound. Label the major peaks or (a) C,110 1500 1000 (b) CsHro 3000 2000 1500 1000 m/z ollowing problem is to ys ar wwight of...
practice quiz 1. (3 pts) For each of the following compounds, indicate whether the two protons shown are homotopic, enantiotopic, or diastereotopic. 2. (8 pts) Indicate the number of signals each of the following compounds would show in their 'Hand C NMR spectra: OME 'H__ _ H__ __ H__ __ H__ "C 3. (10 pts) For each of the following compounds, determine the multiplicity of each signal in the H NMR spectrum: la xiu ood ex gx x x 4....
Thanks! On each the following IR spectra, circle and indicate the most important stretching signal from the following choices:N-H, O-H, CEN, CEO, C-O, Top, IR spectrum of Compound 18a: C14H1402 Bottom, IR Spectrum of Compound 18b: C3H120. write your answer on the corresponding square provided (2.5 pts each, 5 pts total) mar 2000 6 18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of...
Questions 1. Given the H NMR spectrum and molec- ular formula for each of the following compounds, deduce the structure of the compound, estimate the chemical shifts of all its protons using the parameters in Tables 22.3–22.5, and assign the NMR sig- nals to their respective protons. (a) C.H,,Cl; 1H NMR (CDC12): 8 3.33 (2H, s); 1.10 (9H, s) (b) C-H,,0,; 1H NMR (CDC12): 8 3.88 (1H, s); 2.25 (3H, s); 1.40 (6H, s) (C) CH,,0,; 1H NMR (CDC1,): 8...