What can you tell me about the following proton NMR? The following is benzocaine
8 LSE. 8 96E, t PZE" z091 196L 996L 8 O'E
2 2 9LET 2 SZET 8 8 8
Homework Answers
Add Answer to:
What can you tell me about the following proton NMR? The following is benzocaine 0 9.0 8.0 7.0 6.0 5.0 4.0 3.0 2.0 X: parts per Million: Proton 8 LSE. 8 96E, t PZE" z091 196L 996L 8 O'E 2 2 9...
9.0 4.0 4.9 5.0 4.9 7.0 5.8 6.0 7.2 HH 58 10 11 Figure 1 3.0...
9.0 4.0 4.9 5.0 4.9 7.0 5.8 6.0 7.2 HH 58 10 11 Figure 1 3.0 0 9.0 2.0 10.0 1.0 Figure 2 1.0 1.0 2.0 7.6 9.3 2.0 9.4 7.04.2 8.0 7. 2 9. 0 6.2 10.0 4.0 HHHH Figure 3 9.0 Figure 4 10.0 8.4 Answer the following questions about the relationships between pairs of variables and the values of r, the sample correlation coeffic may be the correct answer for more than one question. the m, n...
х у V 1.0 7.6 1.0 1.0 2.0 8.7 11 2.0 2.0 3.0 7.3 3.0 3.0...
х у V 1.0 7.6 1.0 1.0 2.0 8.7 11 2.0 2.0 3.0 7.3 3.0 3.0 4.0 5.8 11 10- 9- 8 7-1 6 5- 4+ 3+ 2 4.0 4.0 11 10 9+ 8+ 71 6+ 5+ 4+ 3+ 2+ 1. X 5.0 8.2 5.0 5.0 6.0 4.9 6.0 6.0 X 7.0 4.5 7.0 7.0 8.0 7.2. 8.0 8.0 0 1 2 3 4 5 6 7 8 9 10 11 7 8 9 10 11 9.0 5.9 9.0 9.0...
Hello.. could you please help me label the peaks on H NMR and 13C spectra. The...
Hello.. could you please help me label the peaks on H NMR and
13C spectra. The compound is
4-Methyl-2,6-bis(4-methylbenzylidene)cyclohexanone.
Thank you!
I had to determine the product based off ketone and aldehyde
reactants. The product could be incorrect. I was only given NMR and
13C spectra to determine reactants and product. Sorry for
confusion! Thanks
Unknown D-4 HH JEOL 21.65 4.0 Azor C Ć-H. - B . T& solvent H tueleton 3.0 Data ammat od ri . DIE Dion ste...
Below are pictures of my HNMR and CNMR for salenH2. I have already assigned some of...
Below are pictures of my HNMR and CNMR for salenH2. I have already
assigned some of the protons and carbons myself, but I am having
trouble with the rest. As far as I know, there are 8 unique carbons
and 7 unique hydrogens. The carbons are numbered and the hydrogens
are lettered. I have included a labeled picture of the compound on
each page.
CNMR overall:
CNMR zoomed:
HNMR overall:
HNMR zoomed:
Thanks!
(thousandths) 0 2.0 4.0 6.0 8.0 10.0...
(I) Let's start with very simple data table 1.0 2.0 3.0 4.0 5.0 6.0 -1 ±...
(I) Let's start with very simple data table 1.0 2.0 3.0 4.0 5.0 6.0 -1 ± 1.8 4±2.0 9+ 1.0 14 + 0.8 19 s 0.8 24 + 1.2 2% 1.8 34 ± 2.0 7.0 8.0 9.0 1. Plot a graph of y vs. X on a piece of graph paper 2. Is it a straight line? Draw the best-fit line. 3. Compute the slope and y-intercept for this line. Write the equation for y in terms of x using...
The following slides contain 1H and 13C-NMR spectra as well as GC/MS spectra for compound 2...
The following slides contain 1H and 13C-NMR spectra as well as
GC/MS spectra for compound 2 shown below. After analyzing the
spectra, assign all proton and carbon NMR signals using the
numbering given on the structure. Additionally, present your data
in table form including chemical shift, integration, coupling
pattern, and coupling constants (where possible). For mass spectral
data, justify key fragmentations (those which are starred*) by
proposing fragment structures.
5 96337 03828 047734 739073 23444 14703 3 8 9 2...
Evaluate and investigate the following IR Spectrum and 1H NMR Spectrum. Identify the most important peaks and correlate the results as much as you can from the obtained product in the multi-step synth...
Evaluate and investigate the
following IR Spectrum and 1H
NMR Spectrum. Identify the most important
peaks and correlate the results as much
as you can from the obtained product in the multi-step
synthesis of ethyl acetoacetate. This is Product
C from this multi-step synthesis where Product
B was identified as in the figure below and as such,
identify what product can be obtained after the synthesis
from the spectra provided. Use the template below in analysing the
spectra.
Figure 1...
Present Value of $1 Periods 1.0% 3.0% 3.75% 4.0% 4.25% 5.0% 6.0% 7.0% 0.99010 0.98030 0.97059...
Present Value of $1 Periods 1.0% 3.0% 3.75% 4.0% 4.25% 5.0% 6.0% 7.0% 0.99010 0.98030 0.97059 0.96098 0.95147 0.94205 0.93272 0.92348 0.91434 0.90529 Present Value of $1 Periods 1.0% 2.0% 0.98039 0.96117 0.94232 0.92385 0.90573 0.88797 0.87056 0.85349 0.83676 0.82035 0.97087 0.94260 0.91514 0.88849 0.86261 0.83748 0.81309 0.78941 0.76642 0.74409 0.96386 0.92902 0.89544 0.86307 0.83188 0.80181 0.77283 0.74490 0.71797 0.69202 0.96154 0.92456 0.88900 0.85480 0.82193 0.79031 0.75992 0.73069 0.70259 0.67556 0.95923 0.92013 0.88262 0.84663 0.81212 0.77901 0.74725 0.71679 0.68757 0.65954...
Can someone help with the analysis of this NMR spectrum for the synthesis of benzyl methyl...
Can someone help with the analysis of this NMR spectrum for the
synthesis of benzyl methyl ether. (Benzyl chloride, diethyl ether
and then added sodium methoxide to produce benzyl methyl
ether)?
What I have so far is:
4 different protons:
3 x 1H on the benzene ring, doublet
2 x 1H on benzene ring, either side of O, doublet
2H on Carbon beside O, quartet
3H on end of alkene with O, triplet
I don't understand where they match up...
draw structure of C8H10 and C8H8O2 based on the 1HNMR AND 13C-NMR shown in the pictures...
draw structure of C8H10 and C8H8O2 based on the 1HNMR AND 13C-NMR
shown in the pictures provided.
any tips of steps will help! thank you!
please scroll for all lictures!
C-NMR data given. D ons: Solve the structures for C8H10 and C8H8O2 using only the molecular formula and 'H- and R data given. DO NOT WORK IN GROUPS. You may ask your TA for minor assistance. You may use your tab manual (pages 31-39). Please write your final structures in...
9.0 4.0 4.9 5.0 4.9 7.0 5.8 6.0 7.2 HH 58 10 11 Figure 1 3.0 0 9.0 2.0 10.0 1.0 Figure 2 1.0 1.0 2.0 7.6 9.3 2.0 9.4 7.04.2 8.0 7. 2 9. 0 6.2 10.0 4.0 HHHH Figure 3 9.0 Figure 4 10.0 8.4 Answer the following questions about the relationships between pairs of variables and the values of r, the sample correlation coeffic may be the correct answer for more than one question. the m, n...
х у V 1.0 7.6 1.0 1.0 2.0 8.7 11 2.0 2.0 3.0 7.3 3.0 3.0 4.0 5.8 11 10- 9- 8 7-1 6 5- 4+ 3+ 2 4.0 4.0 11 10 9+ 8+ 71 6+ 5+ 4+ 3+ 2+ 1. X 5.0 8.2 5.0 5.0 6.0 4.9 6.0 6.0 X 7.0 4.5 7.0 7.0 8.0 7.2. 8.0 8.0 0 1 2 3 4 5 6 7 8 9 10 11 7 8 9 10 11 9.0 5.9 9.0 9.0...
Hello.. could you please help me label the peaks on H NMR and
13C spectra. The compound is
4-Methyl-2,6-bis(4-methylbenzylidene)cyclohexanone.
Thank you!
I had to determine the product based off ketone and aldehyde
reactants. The product could be incorrect. I was only given NMR and
13C spectra to determine reactants and product. Sorry for
confusion! Thanks
Unknown D-4 HH JEOL 21.65 4.0 Azor C Ć-H. - B . T& solvent H tueleton 3.0 Data ammat od ri . DIE Dion ste...
Below are pictures of my HNMR and CNMR for salenH2. I have already
assigned some of the protons and carbons myself, but I am having
trouble with the rest. As far as I know, there are 8 unique carbons
and 7 unique hydrogens. The carbons are numbered and the hydrogens
are lettered. I have included a labeled picture of the compound on
each page.
CNMR overall:
CNMR zoomed:
HNMR overall:
HNMR zoomed:
Thanks!
(thousandths) 0 2.0 4.0 6.0 8.0 10.0...
(I) Let's start with very simple data table 1.0 2.0 3.0 4.0 5.0 6.0 -1 ± 1.8 4±2.0 9+ 1.0 14 + 0.8 19 s 0.8 24 + 1.2 2% 1.8 34 ± 2.0 7.0 8.0 9.0 1. Plot a graph of y vs. X on a piece of graph paper 2. Is it a straight line? Draw the best-fit line. 3. Compute the slope and y-intercept for this line. Write the equation for y in terms of x using...
The following slides contain 1H and 13C-NMR spectra as well as
GC/MS spectra for compound 2 shown below. After analyzing the
spectra, assign all proton and carbon NMR signals using the
numbering given on the structure. Additionally, present your data
in table form including chemical shift, integration, coupling
pattern, and coupling constants (where possible). For mass spectral
data, justify key fragmentations (those which are starred*) by
proposing fragment structures.
5 96337 03828 047734 739073 23444 14703 3 8 9 2...
Evaluate and investigate the
following IR Spectrum and 1H
NMR Spectrum. Identify the most important
peaks and correlate the results as much
as you can from the obtained product in the multi-step
synthesis of ethyl acetoacetate. This is Product
C from this multi-step synthesis where Product
B was identified as in the figure below and as such,
identify what product can be obtained after the synthesis
from the spectra provided. Use the template below in analysing the
spectra.
Figure 1...
Present Value of $1 Periods 1.0% 3.0% 3.75% 4.0% 4.25% 5.0% 6.0% 7.0% 0.99010 0.98030 0.97059 0.96098 0.95147 0.94205 0.93272 0.92348 0.91434 0.90529 Present Value of $1 Periods 1.0% 2.0% 0.98039 0.96117 0.94232 0.92385 0.90573 0.88797 0.87056 0.85349 0.83676 0.82035 0.97087 0.94260 0.91514 0.88849 0.86261 0.83748 0.81309 0.78941 0.76642 0.74409 0.96386 0.92902 0.89544 0.86307 0.83188 0.80181 0.77283 0.74490 0.71797 0.69202 0.96154 0.92456 0.88900 0.85480 0.82193 0.79031 0.75992 0.73069 0.70259 0.67556 0.95923 0.92013 0.88262 0.84663 0.81212 0.77901 0.74725 0.71679 0.68757 0.65954...
Can someone help with the analysis of this NMR spectrum for the
synthesis of benzyl methyl ether. (Benzyl chloride, diethyl ether
and then added sodium methoxide to produce benzyl methyl
ether)?
What I have so far is:
4 different protons:
3 x 1H on the benzene ring, doublet
2 x 1H on benzene ring, either side of O, doublet
2H on Carbon beside O, quartet
3H on end of alkene with O, triplet
I don't understand where they match up...
draw structure of C8H10 and C8H8O2 based on the 1HNMR AND 13C-NMR
shown in the pictures provided.
any tips of steps will help! thank you!
please scroll for all lictures!
C-NMR data given. D ons: Solve the structures for C8H10 and C8H8O2 using only the molecular formula and 'H- and R data given. DO NOT WORK IN GROUPS. You may ask your TA for minor assistance. You may use your tab manual (pages 31-39). Please write your final structures in...
Most questions answered within 3 hours.
-
Oxidative phosphorylation is achieved through chemiosmotic
coupling, which turns chemical energy into osmotic potential energy
that...
asked 1 hour ago -
Hollywood Shoes would like to maintain their cash account at a
minimum level of $64,000, but...
asked 1 hour ago -
Proteins CtrA-P, DnaA, and GcrA behave similarly to what
molecule in the Eukaryotic Cell Cycle?
asked 1 hour ago -
TRUE OR FALSE
In case of a competitive tender procedure, in the request for
quotation, the...
asked 1 hour ago -
I am a little behind please provide some explanation, will
provide thumbs up.
This question considers...
asked 1 hour ago -
Let say the utility function as U(X,Y) = lnX + Y. Show that the
marginal rate...
asked 1 hour ago -
A current of I=8.0A is flowing in a typical extension cord of
length L=3.00m. The cord...
asked 2 hours ago -
1. When balancing the equation H2SO4 (aq) + NaOH (aq) →
Na2SO4(aq) + H2O(aq), would you...
asked 2 hours ago -
Provide a definition of “classification hierarchy” and
illustrate your definition with an example of how and...
asked 2 hours ago -
1. Describe the four main green solvents. Provide one example of
the use of each solvent....
asked 2 hours ago -
International ethics focus on:
1) exploitation of labor
2)corruption
3) environmental impact
4) none of the...
asked 2 hours ago -
Costing Models You work for XYZ trucking and your boss has asked
you to figure out...
asked 2 hours ago