arbitrary intensity L200 220200100100 1201002 Which compound below gives the spectra above? ML Å w
3 of 8 arbitrary intensity Bogo Voz 6 ppm Which compound below gives the spectra above? uro in
arbitrary intensity Which of the following molecules produces the spectra above?
HNMR --CNMR arbitrary intensity 200 100 100 100 120100 2 020 20 ppm MS Which compound below gives the spectra above? (1 pt)
m Relative Intensity - Which compound gives rise to the MS below? HN 58 100 N.N-dimethylethylamine 80 60 20 TE 65 70 75 10 15 20 25 30 35 40 45 50 55 60 MacBook Air 4 SEE.. % & 2 3 4 5 7 R T Y U O W fab m Relative Intensity - Which compound gives rise to the MS below? HN 58 100 N.N-dimethylethylamine 80 60 20 TE 65 70 75 10 15 20 25 30...
HAMA (NMR ΓΙ' arbitrary intensity ' το ΤΤΤΤΤΤΤΙΤΙ το ppm IMS αδιά Which of the following molecules produces the spectra above? (1 pt)
HNMR arbitrary intensity - 220 2200 200 160 160 180 120 100 200 5 Which of the following molecules produces the spectra above? (1 pt)
Determine the structure of the C4H8O2 compound that gives the following spectra. Determine the structure of the C4H8O2 compound that gives the following spectra.
please help... ignore the written work 1) Which compound gives the following spectra? For the 'H-NMR assign all signals. Interpret mol peak and base 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.) s, 4 H s, 3 H t, 3 H q, 2h s, 1 H 2 1 6 5 4 7 8 11 10 ppm esce 100- 80 40 20 150...
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...
The unknown compound A (C17H34O3) gives the following H NMR and IR spectra. Include the degrees of unsaturation and show your work for partial credit. What is the structure of compound A? TH 7. Spectroscopy: (20 pts) The unknown compound A (C17H3403) gives the following 'H NMR and IR spectra. Include degrees of unsaturation and show your work for partial credit. What is the structure of compound A? 64 4H 24 2H IH IH 24 24 24 24 1H 정...