need molecular formula, compound name and assign at least 2 13C signals
need molecular formula, compound name and assign at least 2 13C signals 10 20 30 40...
28. A compound with the molecular formula of C3H.ON shows 1H NMR and 13C NMR as below. Give the most plausible structure in the box. 2H, 3 peaks 2H, 3 peaks 1H, 1 peak PPM 180 160 140 120 100 80 60 40 20 PPM
Which compound gives the following spectra?
For the 1H-NMR assign all signals. interpret mol peak and base peak
in the mass spectrum if a mole peak exists. Assign at least two 13C
signals. How does the IR spectrum support your finding?
Check 200 180 160 120 80 60 40 20 0 140 a 100 ppm s, 3H t, 3 H d. 2 a. 2 H d. 2H s, 1 H 1 10 9 8 7 6 4 3 2 1...
the compound. Trspectaldaa toanswer the following questions and deduce the structure of compound has molecular formula C1zH sCIO. 6H CDCI 2H 2H 2H 2H 1H TMS Expansion of peak near 128.5 ppm 2 peaks CDCI, TMS 200 190 180 170 160 150 140 130 120 110 100 90 80 70 60 50 40 30 20 100 a. (3 pts.) What is the DoU? b. (4 pts.) The mass spectrum shows a signal for M . at m/z : 210 (100%)...
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...
1) Which compound gives the following spectra? For the 'H-NMR assign all signals. Interpret base peak and mole peak in the mass spectrum if a mole peak exists. Assign at least two "C signals. How does the IR spectrum support your findings? (12 pts.) 100- Relative Intensity 0- 20 40 60 80 100 140 160 180 200 220 120 m/ 200 180 160 140 120 100 80 60 40 20 0 ppm t6H 9,4H 11H d, 2 H 9 8...
Find the compound. We do not have the molecular formula.
Sample 3 Mw# 124 100- 80 40 20- 10 20 30 4 50 60 70 80 90 100 110 120 m/ z 9023 84 1569 1272 84956 62 023 84 6 1004 8411+81 84 | 1207 841925 ธ, 196 52 11 10 ppm 200 180 160 140 120 100 80 60 40 20
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...
ty to whoever helps :,)
2. Determine the structure of a compound with molecular formula CHO and the following spectral data daudet Ho- 11 10 -o-H 1H NMR - - pom 200 180 160 340 120 100 ppm 80 60 40 20 13C NMR IR LY 2. Determine the structure of a compound with molecular formula C H200 and the following spectral data, doublet doublet 2H Sunglet 10 Ć -a 9 8 7 multis 11 10 - ppm
A compound with molecular formula C11H140 displays the following IR, H NMR and 13C NMR spectra. Propose a structure for this compound 180 20.200 160 0 120 100 06 60 40 20 PPM
10) Determine the structure of an unknown compound with a molecular formula of CuHz03. IR and NMRS are shown below: (10 points) 100 B0 mm 60 40 20 000 4000 RUM 2000 1500 Wavnumber 1000 3H 3H 2H2H 2H B 3 2 PPM 200 180 160 140 120 100 PPM 20 Draw a structure consistent with the above data and map the proton NMR signals to the structure you have drawn.