Please Print Your Name Part II. Bonus Question Deduce the identity of the following compound from...
Deduce the identity of the following compound from the spectral data given. C_4H_8O_2:^1H NMR, delta 1.23 (3H, triplet), 2.00 (3H, singlet), 4.02 (2H, quartet) (ppm); IR, 2980, 1740 cm^-1.
The following spectroscopic data corresponds to an an unknown compound with the molecular formula C4H8O2. Deduce and draw the structure of the compound that corresponds to the data 1H NMR: δ 4.07 (quartet, 2H), 1.97 (singlet, 3H), 1.18 (triplet, 3H) ppm. "C NMR: δ 170, 60, 20, 14 ppm.
Part B 1) Deduce the identity of the following compound. Molecular formula C5H 100: lH NMR. δ 1.04 (6H, doublet), 2.10 (3H, singlet. 2.6 ( IH, septet) Page10 (ppm): IR, 2980, 1710 cm-1
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
Question 3) Propose a structure consistent with the following spectral data for a compound C H..0, IR 3100 (broad, strong). 1710 (strong) cm '; 'H NMR: 1.05 (triplet, 3H), 2.40 (triplet: 2H), 3.46 (quartet, 2H), 3.61 (triplet, 2H), 12.01 (broad singlet, IH) (10 points)
Please provide solutions for #8-#14. Thank you!
is not a property of ethers which makes them good solvents in organic reactions? A) They have rela B) They dissolve a wide range of nonpolar substances C) They dissolve a wide range of po D) They are normally unreactive toward strong bases. E) They are nonhydroxylic. e avely high boiling points for their molecular weights lar substances 9) Deduce the identity of the following compound from the spectral data given. C4Hgo2: 1H...
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
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...
The following problem is similar to question 3, except the molecular formala is not provided. Yea lecular weight of the molecule and clues from the IR to igare out the molecular formula and structur oawill have to use the tructure of the molecule 3000 2000 1500 1000 S. Propose a structure for a compound, with molecular formula CH N that fits the following spectroscopic data: IR: 3400 cm 'H NMR: 0.9 δ (triplet, 6H), 1.1 δ (singlet i H, exchanges...
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...