H NMR Spectrum:
For each signal:
1.) Identify its environment
2.) Identify its spin-spin coupling (identify how many protons are 3 bonds away, causing the coupling)
3.) Identify its integration value
Why is the peak at 6.3 ppm broadened?
Explain why there are 2 doublets in the aromatic region, but 4 aromatic protons on benzocaine
Why is the quartet at ~4.3 ppm so far downfield compared to the triplet at ~ 1.3 ppm?
What is the purpose of using sulfuric acid in this reaction?
PLEASE HELP! THANK YOU
Homework Answers
Add Answer to:
H NMR Spectrum: For each signal: 1.) Identify its environment 2.) Identify its spin-spin coupling...
b) Which area of the spectrum did you focus on and which key piece of information...
b) Which area of the spectrum did you focus on and which
key piece of information (chemical shift, integration, or splitting
pattern) helped you decide which spectrum belonged to which isomer?
Please explain your responses.
Reaction 1: Nitration HNO3 NO2 + + H2SO4, H20 NO2 toluene NO2 ortho meta para Spectrum For Peak A on GC For Peak B on GC For Peak Con GC Isomer Ortho Nitro Toluene Para Nitro Toluene Meta Nitro Toluene Proton NMR Spectrum for Peak...
b) Which area of the spectrum did you focus on and which key piece of information...
b) Which area of the spectrum did you focus on and which key
piece of information (chemical shift, integration, or splitting
pattern) helped you decide which spectrum belonged to which isomer?
Please explain your responses.
Reaction 1: Nitration HNO3 NO2 + + H2SO4, H20 NO2 toluene NO2 ortho meta para Spectrum For Peak A on GC For Peak B on GC For Peak Con GC Isomer Ortho Nitro Toluene Para Nitro Toluene Meta Nitro Toluene Proton NMR Spectrum for Peak...
Identify each compound in the following questions and make assignments in the 1H NMR a) First...
Identify each compound in the following questions and make
assignments in the 1H NMR
a) First spectra: Compound 1, 1H NMR given, and has a strong
absorbance in the IR at 1715 cm-1
b) Second spectra: Compound 2, a carboxylic acid of formula
C8H6O3Cl2 with 1H NMR given
c) Third spectra: Compound 3 with molecular formula of
C6H9ClO2, with 1H NMR given (the four signal from highest to lowest
chemical shift are quartet, quartet, double, and triplet)
d) Compound 4,...
1. Provide the structure of the compound illustrated in the below H-NMR spectrum. Label the sets...
1. Provide the structure of the compound illustrated in the
below H-NMR spectrum. Label the sets of unequivalent hydrogens in
your structure. The formula for the structure is
C6H10O2.
2. What is the complex splitting pattern for He?
3. Draw the complex splitting pattern for He and
label the coupling constants (J).
4. Why is He more downfield than He?
Include drawings to support your answer.
1н 1H 2H ЗН Зн PPM
practice quiz (15 pts) Draw the structures of the compounds that produce each of the following...
practice quiz
(15 pts) Draw the structures of the compounds that produce each of the following 'H NMR spectra and label the protons in the structures with their corresponding signals in the spectra (a, b, c, etc.): 7. сHhao Зн triplet 2H quartet 2H Зн multiplet multiplet d c b 2 0 11 10 4 CH40 6H doublet 1H septet b a 11 10 8 6 4 1 CaHBr Note: the two signals at 6 ppm are really doublets, but...
(4 pts) Factoring in the spin-spin coupling, draw the expected NMR spectrum of the methyl protons...
(4 pts) Factoring in the spin-spin coupling, draw the expected NMR spectrum of the methyl protons (H* and H) of the propane molecule in this sample. Assume that the coupling constant (J) of the proton H* or H' by Hy is 0.01 ppm. Label each peak with its chemical shift value and specify their relative peak area. d.
Part A The 1H NMR spectrum of a compound which has the molecular formula c4Hao is...
Part A The 1H NMR spectrum of a compound which has the molecular formula c4Hao is shown below. Identify the compound. See pages 22-24 of the Chapter 13 notes. 6.45 ppm dd, J 18, 10 Hz, 1H 4.18 ppm dd, J 18, 2 Hz, 1 3.95 ppm dd, J 10, 2 Hz, 1 3.75 ppm quartet, 2H 1.30 ppm triplet, 3H
yuLLIUI The IR and 'H-NMR spectrum of a compound with molecular formula 102 is provided below....
yuLLIUI The IR and 'H-NMR spectrum of a compound with molecular formula 102 is provided below. What is its unsaturation number identify the key functional groups from the IR spectrum and explicitly state which stretches (with wavenumber) were used to identify them. Name or provide the condensed structure of a compound that will give rise to the above data (15 pts.) IR H-NMR-doublet - 79 ppm-2H, doublet - 7.3 ppm - 2H. quartet - 2.7 ppm - 2 triplet -1.2...
c) Using your answers to question 5 and 6a, what percent of the mixture obtained in...
c) Using your answers to question 5 and 6a, what percent of the
mixture obtained in reaction 1 is the ortho isomer?
d) What percent of the mixture obtained in reaction 1 is the
meta isomer?
e) What percent of the mixture obtained in reaction 1 is the
para isomer?
f) Could we have used Mass Spectrometry after the GC analysis
(GC-MS) to identify which peak on the GC was which isomer? Why or
why not?
g) Could we have...
5. Using the GC mentioned in question 4 and the values listed on the chromatogram for...
5. Using the GC mentioned in question 4 and the values listed on the chromatogram for the height and width (at half height) of each peak, calculate the percent composition for each product (A, B and C). Be sure to show your work. (8 points) 6. The products corresponding to each peak on the GC are the ortho, meta, and para isomers of the nitrated product shown in the scheme for reaction 1. These isomers were isolated, and a proton...
b) Which area of the spectrum did you focus on and which
key piece of information (chemical shift, integration, or splitting
pattern) helped you decide which spectrum belonged to which isomer?
Please explain your responses.
Reaction 1: Nitration HNO3 NO2 + + H2SO4, H20 NO2 toluene NO2 ortho meta para Spectrum For Peak A on GC For Peak B on GC For Peak Con GC Isomer Ortho Nitro Toluene Para Nitro Toluene Meta Nitro Toluene Proton NMR Spectrum for Peak...
b) Which area of the spectrum did you focus on and which key
piece of information (chemical shift, integration, or splitting
pattern) helped you decide which spectrum belonged to which isomer?
Please explain your responses.
Reaction 1: Nitration HNO3 NO2 + + H2SO4, H20 NO2 toluene NO2 ortho meta para Spectrum For Peak A on GC For Peak B on GC For Peak Con GC Isomer Ortho Nitro Toluene Para Nitro Toluene Meta Nitro Toluene Proton NMR Spectrum for Peak...
Identify each compound in the following questions and make
assignments in the 1H NMR
a) First spectra: Compound 1, 1H NMR given, and has a strong
absorbance in the IR at 1715 cm-1
b) Second spectra: Compound 2, a carboxylic acid of formula
C8H6O3Cl2 with 1H NMR given
c) Third spectra: Compound 3 with molecular formula of
C6H9ClO2, with 1H NMR given (the four signal from highest to lowest
chemical shift are quartet, quartet, double, and triplet)
d) Compound 4,...
1. Provide the structure of the compound illustrated in the
below H-NMR spectrum. Label the sets of unequivalent hydrogens in
your structure. The formula for the structure is
C6H10O2.
2. What is the complex splitting pattern for He?
3. Draw the complex splitting pattern for He and
label the coupling constants (J).
4. Why is He more downfield than He?
Include drawings to support your answer.
1н 1H 2H ЗН Зн PPM
practice quiz
(15 pts) Draw the structures of the compounds that produce each of the following 'H NMR spectra and label the protons in the structures with their corresponding signals in the spectra (a, b, c, etc.): 7. сHhao Зн triplet 2H quartet 2H Зн multiplet multiplet d c b 2 0 11 10 4 CH40 6H doublet 1H septet b a 11 10 8 6 4 1 CaHBr Note: the two signals at 6 ppm are really doublets, but...
(4 pts) Factoring in the spin-spin coupling, draw the expected NMR spectrum of the methyl protons (H* and H) of the propane molecule in this sample. Assume that the coupling constant (J) of the proton H* or H' by Hy is 0.01 ppm. Label each peak with its chemical shift value and specify their relative peak area. d.
Part A The 1H NMR spectrum of a compound which has the molecular formula c4Hao is shown below. Identify the compound. See pages 22-24 of the Chapter 13 notes. 6.45 ppm dd, J 18, 10 Hz, 1H 4.18 ppm dd, J 18, 2 Hz, 1 3.95 ppm dd, J 10, 2 Hz, 1 3.75 ppm quartet, 2H 1.30 ppm triplet, 3H
yuLLIUI The IR and 'H-NMR spectrum of a compound with molecular formula 102 is provided below. What is its unsaturation number identify the key functional groups from the IR spectrum and explicitly state which stretches (with wavenumber) were used to identify them. Name or provide the condensed structure of a compound that will give rise to the above data (15 pts.) IR H-NMR-doublet - 79 ppm-2H, doublet - 7.3 ppm - 2H. quartet - 2.7 ppm - 2 triplet -1.2...
c) Using your answers to question 5 and 6a, what percent of the
mixture obtained in reaction 1 is the ortho isomer?
d) What percent of the mixture obtained in reaction 1 is the
meta isomer?
e) What percent of the mixture obtained in reaction 1 is the
para isomer?
f) Could we have used Mass Spectrometry after the GC analysis
(GC-MS) to identify which peak on the GC was which isomer? Why or
why not?
g) Could we have...
5. Using the GC mentioned in question 4 and the values listed on the chromatogram for the height and width (at half height) of each peak, calculate the percent composition for each product (A, B and C). Be sure to show your work. (8 points) 6. The products corresponding to each peak on the GC are the ortho, meta, and para isomers of the nitrated product shown in the scheme for reaction 1. These isomers were isolated, and a proton...
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