Draw the predicted 1H and 13C NMR Spectra of the following
compound: (where R1= Ph, R2=CH3)
Note: There will be two diastereomers. Be sure to include this in the predicted spectra, and explain how to differentiate the two using the spectra.
Draw the predicted 1H and 13C NMR Spectra of the following compound: (where R1= Ph, R2=CH3)...
Draw the structure of the compound identified by the following
simulated 1H and 13C NMR spectra. The molecular formula of the
compound is C10H12O. (Blue numbers next to the lines in the 1H NMR
spectra indicate the integration values.)
13C and 1H NMR spectra of a compound,
C10H14, are displayed below. What is the
structure of the compound? Explain.
Note: This same question was
asked here:
http://www.chegg.com/homework-help/questions-and-answers/13c-1h-nmr-spectra-compound-c10h14-displayed--structure-compound-explain-please-explain-q3820429
As pointed out, the structure is C10H14
and the answered offered had 11 carbons.
11. (20 points) The 1H NMR, 13C NMR, Mass Spectra and IR spectra
for a mystery compound with the formula C5H12O are shown below.
Please draw the structure for the compound in the box below. Note:
The numbers on top of the 1H NMR peaks are the number of protons
associated with that peak. A chart for 1H NMR, IR and 13C NMR
spectra shift values are on the following pages.
nts) The 'H NMR, "C NMR, Mass Spectra and...
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.
A compound with molecular formula C11H140 displays the following IR, 1H NMR and 13C NMR spectra. Propose a structure for this compound. Ppin 220.200.180.160.140 120 PPM 100 80 60 40 20
How many 1H NMR signals would the following compound show in its NMR spectra? (CH3)2CHCH2CH3
This chart shows the different spectra of an unknown organic
compound. Explain the different peaks in its 1H-NMR, 13C-NMR and
mass spectra as shown.
PLEASE, ANSWER CORRECT. WILL GIVE ?
13 CIDENT
Using IR spectrum and 1H and 13C NMR spectra to figure out
what the unknown compound is
C: 63.15 H: 5.30 7.0 6.5 4,5 4.0 MW 152.149 12. Ola C
Create OscerSkotch Answer 6 Th e 1H-NMR and 13C-NMR spectra of an unknown compound s (formula CoMzo) are shown below. Draw the structure of B. The total integration of the peaks at around 7 ppm is 4. The integration of the peak at around 2 ppm is 6 ppm 200 180 160 140 120 100 060 4020
What is the name of the compound? and draw the structure
1H NMR spectra - Double click to zoom out, SHIFT + double click to zoom out by step, SHIFT + drag to move spectrum Q82" C4H100 (ppm) Download all — predicted Spectrum