HNMR arbitrary intensity - 220 2200 200 160 160 180 120 100 200 5 Which of...

Question

Question

Answer 1

Answer #1

Aromatic protons HNMR OH group ECNMR 0.8 .06 arbitrary intensity Aromatic carbons .. No aliphatic carbons 94 m/z O-H and C-H

Answer 2

Similar Homework Help Questions

HNMR --CNMR arbitrary intensity 200 100 100 100 120100 2 020 20 ppm MS Which compound...

HNMR --CNMR arbitrary intensity 200 100 100 100 120100 2 020 20 ppm MS Which compound below gives the spectra above? (1 pt)
7 12 o 10.5 9.0 7.5 6.0 15 180 160 200 240 220 140 120 100...

7 12 o 10.5 9.0 7.5 6.0 15 180 160 200 240 220 140 120 100 40 20 Ppm Propose a compound that would furnish all of the above spectra. arbitrary intensity 90
HAMA (NMR ΓΙ' arbitrary intensity ' το ΤΤΤΤΤΤΤΙΤΙ το ppm IMS αδιά Which of the following...

HAMA (NMR ΓΙ' arbitrary intensity ' το ΤΤΤΤΤΤΤΙΤΙ το ppm IMS αδιά Which of the following molecules produces the spectra above? (1 pt)

arbitrary intensity Which of the following molecules produces the spectra above?

arbitrary intensity Which of the following molecules produces the spectra above?
Which compound corresponds to the 13C NMR spectrum below? 240 220 200 180 160 140 100...

Which compound corresponds to the 13C NMR spectrum below? 240 220 200 180 160 140 100 80 50 120 PPM 40 20 0 to in OH A B с D E OA OB What is the product in the following reaction sequence? Br 1. NaN, 2. Hz (excess). Pdic NH NH2 B С D E OA OB Ос OD OE Identify which of the following molecules corresponds to the MS data below. tot Le ОН А D E F 100...
identifying the unknown using IR, HNMR CNMR and Mass spectrums Unknown H407 100- 18-N-9500 Relative Intensity...

identifying the unknown using IR, HNMR CNMR and Mass spectrums Unknown H407 100- 18-N-9500 Relative Intensity 160 180 200 220 Order 20 40 60 80 100 120 140 m/z Unknown H407 mm NREUTHER Unknown H407 d. 3H 1 Зн m, 3H d. 1H m, 2H m, 2H m, 1Η br. s, 1H 10 8 PPM Unknown H407 20 0 80 60 4 0 100 120 140 180 160

The compound is dibenzalacetone MS 100 - MS-NW-6013 Relative Intensity 20 40 60 80 160 180 200 220 240 100 120 14...

The compound is dibenzalacetone MS 100 - MS-NW-6013 Relative Intensity 20 40 60 80 160 180 200 220 240 100 120 140 m/z Peak data 1) (%BP) m/z m/z 50.0 51. 01 76.0 77.0 78.0 89.0 91.0 102.0 103.0 104.0 115,0 5.7 18.1 5.4 48.7 5.5 5.1 26.6 13.0 61.6 9.5 5.8 129.0 131.0 132.0 156.0 157.0 191.0 205. 01 206.0 233.0 234.0 235.0 (a) (%BP) 7.3 42.7 $4.8 10.3 4.1 9.0 15.3 8.4 68.6 100.0 18.1 Report only the...
need help on quetion 6 & 7 6 HAMK 1 CNMR 240 220 200 180 140...

need help on quetion 6 & 7 6 HAMK 1 CNMR 240 220 200 180 140 160 120 100 60 40 20 ppm IR MS 404 3000 2000 Propose a compound for that would furnish all of the above spectra. (1 pt) go zo arbitrary intensty 7 H NMK 12.0 10.5 9.0 7.5 6.0 4.5 3.0 15 C NMR 240 220 160 200 180 140 120 100 Ppm IR tóo Propose a compound that would furnish all of the above...
draw the structure of the NMR and caculate degrees of unsaturation C11H1203. 220 200 180 160...

draw the structure of the NMR and caculate degrees of unsaturation C11H1203. 220 200 180 160 140 120 PPM 100 60 46 26 0 多く 3fis itts, iHS z4t,244 PPM

how many non-aromatic carbons and where 200 180 160 140 120 100 80 6040 200 ppm

how many non-aromatic carbons and where 200 180 160 140 120 100 80 6040 200 ppm