What is the name or structure of unknown compound related to
below NMR and IR? Don't say this question needs more information
please. It is the question. It has full and complete
information.
What is the name or structure of unknown compound related to below NMR and IR? Don't...
4. Determine the structure of an unknown compound whose mass, IR, and 'H-NMR spectra are shown below.. MS 100 43 71 Structure of the unknown compound 50 114 0 40 60 80 100 120 m/z IR H-NMR δ (ppm) 0
Accordng to this IR and NMR, what is the complete structure of
the unknown compound present?
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...
6. An unknown compound, CsH10O2, gives the NMR and IR shown below. Propose a structure. wavelength (m) 9 10 11 12 13 14 15 16 100 80 60 40 20 ol 4000 3500 3000 2500 1400 1200 1000 800 2000 1800 1600 wavenumber(cm) 600 SOHE 5.5.6 7.11 70 690 200 156 LA 1.6 10 8 (ppm)
What could be the name of unknown compound that has below IR
and NMR?
Sat Nov 09 09 18 25 2019 (GMT-05:00) 85 Sat Nov 09 09 18 25 2019 (GMT 500) 05 EDOC 740 10 2000 4000 Wavnumbers (cm-1) 588) Y (54090) X600 1.0000 8.1610 8.1481 0.4966 1.0024 NNNNNN (ppm) 30 [rell
Compound 2: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. a) An MS was taken of compound 2 and the table is given below. Determine the molecular formula of 2 from the MS given below relative abundance m/z 132 100 133 9.8 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 1H- and 13C-NMR spectra given below, determine...
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.
The H-NMR spectrum of an unknown compound (formula CaHgO2) is shown below. Draw the structure of the unknown compound. Question 5 4 1 6 5 8 10 11 Ppm The 13C-NMR spectrum of an unknown compound (formula CgH180) is shown below. Its 1H-NMR spectrum only shows one singlet at 1.2 ppm. Draw the structure of this unknown compound. uestion 2 220 200 160 140 120 PPM 100 80 240 180 60 40 20 Create OscerSketch Answer 2 What would be...
7. Consider the IR, 'H-NMR and C-NMR spectra of the compound with MF:C,H, 0. 4 pts Identify the structure of the unknown compound. MF C7H140 MW 114 $C 73.6 SH 12.4 Mass Spec. D m/ sbund. 27 35 relativ 114 11 Popyright © 1994 1.0 PPM 3.0 Proton NMA TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 200 180 160 140 Carbon 13 NMR T 120 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 100 80 60 40 20 PPM O en og and 8. Consider the IR, 'H-NMR and C-NMR spectra of the...
Must know the unknowns name and structure.
NAME IR & 13C NMR Unknown Your mission is to determine the structure of your unknown from the molecular formula, IR and 'SC NMR spectra. Assign all of your 3C NMR absorptions. You want to know which resonances correspond to which parts of the product's structure. The best way to do this is to draw a picture of the molecule right on the NMR spectrum then label each C on the molecule with...