A compound with molecular formula C_9 H_10 O_2 displays the following^1HNMR spectrum. Propose a structure for...
Propose a structure for a compound of molecular formula C_7 H_14 O_2 with an IR absorption at 1740 cm^-1 and the following^1 H NMR data:
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure for this compound in the box at the bottom of the page. Peak assignments written on the spectra may be worth partial credit. (5 marks) r IR Spectrum liquid film) 1735 1717 4000 3000 1200 800 2000 1600 V (cm) 13C NMR Spectrum (100 MHz, CDCI, solution) DEPT CHI Chit Cht solvent proton decoupled 100 no Sloml proton decoupled 200 160 120 80 40...
Deduce the structure of the compound with molecular formula C5H10O. Deduce the structure of a compound with molecular formula C_3 H_10 O that exhibits the following IR, H^2 NMR, and C^13 NMR spectra. Data from the mass spectrum are also provided.
A compound with a molecular formula C5H10O has the following 1H NMR spectrum. Provide a structure that is consistent with this spectrum. 3. A compound with a molecular formula CsHioO has the following 'H NMR spectrum. pound with a molecular formula CsHioO has the following H NMR Propose a structure for this compound. PPM
Propose a structure for the compound that has the following data: Molecular formula: C9H10O2 13C NMR ? 26.1, 55.3, 113.7, 130.4, 130.5, 163.5, 196.4 ppm. Propose a structure for the compound that has the following data: Molecular formula: CgH0O2 13C NMR δ 26.1, 55.3, 113.7, 130.4, 130.5, 163.5, 196.4 pprm CH2 CH2-OH 80 706050 4 3020e ati H NMR spectrum shown above. 3.0 1.0 University of Machiga
Propose a molecular formula for a compound that has one degree of unsaturation and a mass spectrum that displays a molecular ion signal at m/z = 86.
Predict the major product for the following reaction. A carboxylic acid with molecular formula C_5 H_19 O_2 is treated with thionyl chloride to give compound A. Compound A has only one signal in its^1HNMR spectrum. Draw the structure of the product that is formed when compound A is treated with excess ammonia. Provide the reagents necessary to carry out the following conversion.
6. The 1H NMR spectrum for a compound with molecular formula C7H1402 is given below. Propose a structure for this compound and LABEL the protons on your structure to match the appropriate 'H NMR peak. (1 pt) C7H1402 1.12 0.55 1.08 3.2 1.6 PPM
8) Propose a structure for the following compound based on its molecular formula (C4H2O2) and its IR spectrum 25 2.6 2.7 2.8 2.9 3.5 4 45 9 10 11 12 13 14 15 16 4000 3800 36000 3400 3200 3000 2800 2600 2400 2200 2000 1400 1200 1000 1800 1600 Wavenumber(cm) 9) Propose a structure for the following compound based on its molecular formula (C6H120) and its IR spectrum wavelength (um) 25 26 2.7 2.8 2. 9 3 5 4...
A compound with molecular formula C H140, displays the following IR, 1 H NMR and SC NMR spectra. Propose a structure for this compound, ppm 180 160 140 120 10080604620 PPM