need help drawing the structures for each
need help drawing the structures for each For each pair of spectra, first calculate the THD...
Analzye the following spectra, and propose a structure for each. The bottom set of 3 spectra are DEPT spectra, top: CH only, middle: CH, CH3 up, CH2 down, bottom: normal BB decoupled spectrum. Explain your assignments . Analyze means determine integrals, draw splitting trees, determine carbon type (C, vs CH vs CH2 vs CH3 and structural environment. Use ChemDraw to check your proposed structure (include output), Problem C 7.5 7.0 .5 6.05.55.0 4.5 4.03.5 3.0 2.5 ppm 31 ppm 140...
You are provided with the molecular formula for each compound. calculate the unsaturation index for each problem. -u2C+2+N-X-H For IR, determine the functional groups present and annotate the absorbances that confirm the functional group (including finger print region absorbances). 2 . For 1H NMR, label each signal (a, b, c,.... starting from the right (0.0 PPM). Draw the structure of the compound in the spectra and annotate. 13C NMR spectra is provided for information. Annotation of the 13C NMR is...
please help 3. Identify and Assign the structures for Eugenol and Acetyleugenol for the follow spectra Ppa 160.B 151.04 138.93 130.23 137.14 122.56 120.63 116.05 112.82 55.68 40.07 20.40 200 180 160 140 120 80 60 40 20 0 100 ppm Рpm 146.60 144.03 137.91 131.94 121.26 115.49 114.46 111.28 55.84 39.92 TTTT 200 180 160 140 120 80 60 40 20 0 100 ppm
determine the structure of the compound and label the peaks on spectra left to right compound 3: C.H. 'H NMR integration, right to left: 1:6 11 10 9 ppm 140120 1000 left to right sound 3: CsH14. 'H NMR integration, right to left: 1:6 Compound 3: CH. CC 11 7 10 9 8 Cửa - Chº ppm RECH/ /R₂ CH2 200 180 160 140 120 80 60 40 20 0 100 pom
dedude the structure of the organic compound that would provide the following spectra CHsoOz 1.00 6.00 3.00 0 pp 6 140 120 100 PPM 80 60 40 20 160 180 eace www CHsoOz 1.00 6.00 3.00 0 pp 6 140 120 100 PPM 80 60 40 20 160 180 eace www
Part A: Make sure to write the labelled molecule structure on each 'HNMR and CNMR. Unknown #73: Annotate and assign the NMR Spectra of 5-chloro-2-pentanone: I m, 3H CH-CH2-CH2-CH - CH, m 3H m2H 11 10 9 8 7 6 5 1 HSP-00-414 ppm 10-09 Ci 6 b CH CH₂ CH₂ 1 1 CH₂ à el 1 СЕ О 60 40 200 200 180 160 140 120 100 30 ppm CDS-04-000
2. Consider the protons labeled H., H., H., of the compound shown below. Each of these protons are chemically different and are split by at least one other type of proton. coupling constants are shown below. HA HOHC C= "Hc JAB = 15.1 Hz JBC = 6.4 Hz Draw the splitting tree for each proton, H., Ho, and H. 3. Propose a structure for the following compounds piven the spectra and molecula formula. Briefly describe how each spectrum supports your...
The 1H-NMR and 13C-NMR spectra of an unknown compound (formula C8H10) are shown below. Draw the structure of the unknown compound. The total integration of the peaks at around 7 ppm is 4. The integration of the peak at around 2 ppm is 6. 7 6 5 4 3 ppm TTTTTTTTTTTTTTTT 200 180 160 140 120 100 80 60 40 20 0 pom CH3 Create OscerSketch Answer 8 Incorrect: Answer has an incorrect structure.
problem 4.05 please 1-3. There are two sets of spectra attached. For each provide a structure and assign the peaks by labeling the structures and listing the peaks in the tables provided. 208 Label H NMR 6 Label C NMR 6 4.05 Label H NMR 8 Label C NMR 8 Problem 4.05 Given the spectroscopic data below (Proton, Carbon, gHSQC, gCOSY, and gHMBC), provide the structure of the molecule. (HR-MS: 238.1358 amu), {'H, 'H) Nuclear Overhauser effect correlation was observed...
5. (8 Pts) Using the following spectra, draw a possible structure for C5H19NO2- DOU= Expected Structure 6H, d 1H,d 2H, s 1H, S 1H,m 12 10 8 6 4 2 0 PPM 180 160 140 120 80 60 40 20 100 PPM