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.
The compound is 1,2-diethylbenzene. Interpretation of 1H and 13C NMR spectra is given below.
(1) 1HNMR:
13CNMR:
13C and 1H NMR spectra of a compound, C10H14, are displayed below. What is the structure...
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...
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.)
I need help identifying a compound based on the spectra. The compound contains an aromatic ring. The spectra are attached. I would appreciate an accurate description.The 1H NMR, 13C NMR, mass and IR spectra of compound with a molecular formula (C9H11NO2) are given below. Use the given spectroscopic data to provide rational interpretation (motivation) of all the spectral data to determine the structure of this compound.
What is the structure of unknown compound based on 1H and 13C
NMR and IR Spectra
BRUKER 3500 3000 2500 2000 Wavenumber cm-1 1500 1000 500 C1OPUS 65)MEASIGB Product 20 GB Product 2 Instrument type and / or accessony 01/03/2018 Page 1/1
On the attached image are 1H NMR, 13C NMR, and IR
spectra of a compound with the formula C4H8O. 1H NMR signal at 1.2
is caused by 3 hydrogens, the sigbal at 2.1 is caused by 3
hydrogens, and the signal at 2.5 is caused by 2 hydrogens. Identify
the compound.
CH 1110 9 8 7 6?4 Problem 6. 'H NMR spectrum of compound HsO Problem 6. 13C NMR spectrum of compound C4HsO 200 180 160 140 120 100 80...
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
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.
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.
RY OEt R
The 1H- and 13C-NMR spectra for an unknown compound with molecular formula C6H1202 are shown below. Deduce a structural formula for this compound.
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