propose a structure for each problem and label the protons in HNMR corresponding to the structure...
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...
Based on the IR and NMR spectra, determine the structure of each of the following compounds A) The compound with the formula CHN Based on the IR and NMR spectra, determine the structure of each of the following compounds A) The compound with the formula CHN LLLLLLL B) The compound with the formula C,H03 11 10 We were unable to transcribe this imageD) The compound with the formula C, H, NO4 Te 200 180 160 E) The compound with the...
Identify each carbon and H HNMR and CNMR bands with letters to the corresponding part on the structure provided. IH, singlete multi, I H multi, 2 H multi, 2 H 10 0 PPM 2 señales 140 100 PPM 120 40 20 200 180 160 80 0 60 140
please show all work and label each graph with necessaey peaks *Road next Chapter hope & Lee chce DOUSWH - 10 - 2 2 Noring story student was converting cyclohexanol to cyclohexyl bromide by using one equivalent of um bromide in a large excess of concentrated sulfuric acid. The major product she recovered was 967 m .compound of formula CHao that gave the following spectra: 1PC NMR not cyclohexyl bromide, but a comp u t er 70 180 160 140...
1. label all spectra in IR 2. figure out structure. label a,b,c,d, etc in structure and corresponding letter on all peaks in HMNR and CNMR 3. show all calculations IR/HNMR/CNMR MW=122: 124 AMU 1:1 11 10 200 150 160 140 120 100 ppm 100 0
For the following unknown, annotate the corresponding spetras and determine the molecular formula and lewis structure. Unknown # s IR/HNMR/CNMR 1 MW= 88 AMU AVENUE S, 3 T, 1, 2] Broads, Ppm 200 160 140 180 120 80 40 60 20 ó 100 rpm
Label the spectra and propose a structure for the compound. Compound IR Spectrum Olquid fim 1740 4000 3000 2000 1800 1200 800 100 Mass Spectrum yood M = 150/152 (15) CH40, CI 240 280 40 80 120 160 mle 200 13C NMR Spectrum (500 MG, COO, solo DEPT CH CH.CH selvon proton decoupled 200 160 120 80 40 0 (ppm) 'H NMR Spectrum (200 ML. COCI, solution) 10 9 8 7 6 5 4 3 2 1 (ppm)
Label the spectra and propose a structure for the compound. Compound 5 IR Spectrum Olquid fim 1740 4000 3000 20 ,1600 1200 300 100% Mass Spectrum M = 150/152 (15) CH,40, CI 240 280 40 80 120 160 200 13C NMR Spectrum (500 M , CDC, son DEPT CH CH CH selvon proton decoupled 200 160 120 80 40 0 8 (ppm) 'H NMR Spectrum (200 MH. COCI, solution 10 9 8 7 6 5 4 3 2 (ppm)
c13h9No3 mw=227 please provide hnmr structure and label corresponding hnmr spec a,b,c etc Problem 42 - 1H NMR spectrum (CDCl3, 500 MHz) 2H 2H 2H 2H 1H Click on the highlighted area to zoom. Click again to zoom back out.
Label the spectra and propose a structure for the compound. The IR spectra are listed in the translation. Compound 2 R Spectrum Medisch 3400 1720 4000 3000 1600 vomi) 1200 183 Mass Spectrum So base UV Spectrum mas 253 nm 109,9€ 2.6) homas 250 nm 109,96 2.7) ho mar 284 m 109,0 2.5) M -220N) CH2O| 280 40 80 120 160 200 240 13C NMR Spectrum (100 . CDC, DEPT CH CH CH protondeco 200 160 1 20 80 400...