40) Deduce the structure of the compound whose spectral data is shown below. 7 NO OH...
40) 7. Based on the spectral data shown, determine the structure of this compound. Draw the structure in the box so no 200 130 120 /z m Two 2H triplets Actually 3 peaks
40 7. Based on the spectral data shown, determine the structure of this compound. Draw the estructure of this compound. Draw the structure in the box 20 mz Two 2 triplets Actually 3 peaks
Draw the structure in the box 40) 7. Based on the spectral data shown, determine the structure of this compound. eo 60 20 1000 1500 200 po00 2000 40 20 140 160 40 120 180 60 100 m/z SH 2H Two 2H triplets Actually 3 peaks 140 160 12o 100
no it doesnt 40) 7. Based on the spectral data shown, determine the structure of this compound. Draw the structure in the box oto mz Two 2H triplets Actually 3 peaks Totho 100 bebas
Elucidate the structure of the compound that is described by the spectral data shown below. Place your structure in the box to the left. For partial credit place your pieces and constraints in the respective other box.
13C NMR 1. Propose a structure for the compound CsH12, with the following 13C NMR spectral data. 160 140 120 80 60 40 20 0 200 180 CDS-00-748 100 ppm 2. Propose a structure for the compound CaH;Br, with the following C NMR spectral data. 200 180 160 140 120 80 60 40 100 ppm 20 0 3. Propose a structure for the compound C H2O2, with the following "'C NMR spectral data. 200 180 160 140 120 30600 T...
4 (10 pts) 7. Determine the structure of compound C, whose NMR is shown below. The formula for C is CH,CI. The IR has a band at 2950 cm. Assign the NMR signals to the structure you are proposing (i.e. label your hydrogens). Alkene Compound C GHA 2HE 2WE 2HD IRC 0.14 0.15 0.07 0.15 0.43 PPM
4. Determine the structure of an unknown compound whose mass, IR, and 'H-NMR spectra are shown below.. MS 100 43 71 Structure of the unknown compound 50 114 0 40 60 80 100 120 m/z IR H-NMR δ (ppm) 0
Deduce the following structure of the compound given their IR, H1 NMR, 13C NMR spectra, and assign IR functional group absorptions and assign the structure's protons and carbons to their respective spectral resonances. Compound 6 1756 IR Spectrum uid Sm) 15820 4000 3000 2000 1600 1200 800 V (cm) 100 55 Mass Spectrum 71 80 70 60 No significant UV M158 (1%) absorption above 220 nm C&H140s 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz,...
1.Identify the compound whose spectral data are shown. 2. Describe the coupling observed and show the splitting diagram for each hydrogen. 3. Determine the value of each coupling constants. 4. Label and assign each 1 H and 13 C signal to your answer. 100 3 % of Base Peak 90 80 100 120 m/z 5 SA % Transmittance --1689 -3047 --14197 --1273 -957 E9EE- -702 3000 1000 4000 'H NMR 300 MHz 2000 Wavenumber (cm-1) 2720 2700 Hz 2600 2580...