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USING THE SPECTRUMS IDENTIFY THE UNKNOWN COMPOUND Unknown Organic Compound - All Spectra C-NMR 100- 30...
The spectra of an unknown organic compound A having the molecular formula C1oH1o0 are shown below. Elucidate the structure of the compound. Show your work. (8 pts; no partial credits) 500 1500 Wave numbers 4000 3000 2000 1000 130 125 200 150 δ(ppm) 100 50 0 7A 6.8 76 14 12 10 3.2 16.1 3.3 6 (pom) 9.8 Draw your structure in this box
10) Identify the unknown compound with the formula C&H O using the following 'H NMR,"C NMR, and IR spectra. Label all peaks used to make your identification as appropriate. Draw the structure of the unknown compound in the box provided. Answer (structure) deguer of insulation 200 180 160 140 120 100 ppm 30 0 40 20 0
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.
what the the unknown compund for the NMR? NMR Unknown 77 percorso CH co CH C3 nmr 200 180 160 140 120 80 60 40 20 0 100 pom 1.0 R-H + saturated alkane) Hô - og 3.5 a overall it's Hi nmr RICH 1. 80 CH2 2nH 11 10 9 8 7 ppm UCH H pois ce Biccolopettromagadde deset Wood c ocoot Spackup 100- Relative Intensity M+ -> 124 II gimol 100 125 50 m/z
91T Q9) Identify the unknown aromatic compound using the following spectra. Use the 'H NMR splitting in the aromatic region to determine the substitution pattern on the aromatic ring. Label and assign all relevant peaks on the IR and NMR spectra. For the Mass Spectrum, label the molecular ion peak, base peak, and any halogen isotopes, along with any mass losses (change in m/z between peaks) that are helpful in determining your structure. ortho meta arbitrary units 140 160 180...
identify the unknown from the given spectra "H-NMR multiplet, 10H triplet, 6H N PPM 13 C-NMR 35 30 25 20 15 10 PPM IR LOD TRATTEET 3000 2000 1500 1000 50 BRYNNERE Mass Spec. 100 80 60 Relative Intensity 40 м 20- 0 ti LO 20 30 40 50 60 70 80 90 100 m/z
6. Spectroscopy. The molecular formula of an unknown organic compound is C8H1402. The IR, 1C-NMR and 'H-NMR spectra of this compound are shown on the next page. Answer the following questions about this compound. (a) What is the unsaturation number for this compound? (b) What functional group(s) does this compound contain? Indicate the specific evidence for your conclusion. (c) What can you conclude from the number of 13C-NMR signals? (d) What can you conclude from the H-NMR signal at 2.3...
5. The 1H-NMR, 13C-NMR and MS spectrums of an unknown compound are shown below. The molecular formula of the compound is C7H14O. What is the structure of the unknown? 5. The H-NMR, 13C-NMR and MS spectrums of an unknown compound are shown below. The molecular formula of the compound is C,H4O. What is the structure of the unknown? 2 Hs, sexnet 2 Hs, triplet Organic Chemistry 2 Homework due February 14, 2019 Mass Percent 15.0 26.0 27.0 2B.0 29,0 39.0...
I need to identify this unknown using this NMR spectra The chemical formula is c7h14o2 moli than socia ng 0 a hal ding molet rativit site. cooper endent 80 70 60 50 40 30 20 10 0 10 20 30 40-50-60 260 250 240 230 220 210 200 190 180 170 160 150 140 150 120 110 100 90 OCH 10000 10 10 20 20 240 200210000 We were unable to transcribe this image
NMR How to use this information to help determine my unknown compound 100 - M- 0656 Relative Intensity 100 75 m/z Unknown F 200 180 160 140 120 80 60 40 20 0 100 ppm Unknown F HSP-00-108 ppm Unknown F