Draw the structure of any organic compound that contains eight carbons, but only has six distinct...
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 4 Da- U6)+20 IR Spectrum Oquid fim) 1760 800 1200 2000 1600 3000 4000 v (cm) Mass Spectrum 100 43 No significant UV absorption above 220 nm M146 (1% ) 87 20 CH1004 280 40 80 120 m/e 160 200 240 13C NMR Spectrum (1000 MHz,...
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,...
2. Draw the structure of the major organic product that is formed from the following reaction. Draw this structure in the box at the bottom of the next page. Then use letters to label all the sets of chemically equivalent carbons in this structure. The broadband proton-decoupled 13C NMR spectrum of the product is shown below. DEPT 90 and DEPT 135 data are included in the table on the following page. Use this spectroscopic data to make clear assignments of...
NMR IR CAN YOU PLEASE ANSWER AS SOON AS POSSIBLE THANK YOU PLEASE EXPLAIN IT IN DETAIL THANK YOU Experimental Data Only report the IR absorptions that provide diagnosis for the major functional groups. Copies of your spectra will be included in your lab report with this information written on the spectra. However, the information should also be included in the body of the report in a text format similar to the example given below IR cm1: 1735 (C-o); MS:...