I need help with these questions please!
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I need help with these questions please!
1. Provide the product of the following reaction. Hint:...
Please provide a detailed ‘H-NMR and C-NMR analysis for both the reactant and product. For the ‘H-NMR analysis please i...
Please provide a detailed ‘H-NMR and C-NMR analysis for both the
reactant and product. For the ‘H-NMR analysis please include: 1) on
the reactant and product the types of protons and their peaks. 2)
splitting pattern
CH₂ Iz Reactant Product
Please provide a detailed ‘H-NMR and C-NMR analysis for both the reactant and product. For the ‘H-NMR analysis please i...
Please provide a detailed ‘H-NMR and C-NMR analysis for both
the reactant and product. For the ‘H-NMR analysis please
include:
1) on the reactant and product the types of protons and their
peaks.
2) splitting pattern
3) intergration ratio.
CHO Woolt Me or Reatant Meor Product
1. For each of the following structures, please fill in the missing information below or- Cl...
1. For each of the following structures, please fill in the missing information below or- Cl Molecular Formula:R_ Molecular Formula: DBE:_ DBE: 2. Given the reaction below, answer the following questions. Br HBr As the above reaction progresses to completion, what peak in the IR would you expect to disappear? Whereabout is the peak located in cm? a. b. Why does the M+1 peak NOT change from reactant to product? c. How many peaks (not the splitting pattern, just the...
please provide detailed explanation of solution for thumbs up 6. Reaction Coordinate Diagrams (10 points) (a)...
please
provide detailed explanation of solution for thumbs up
6. Reaction Coordinate Diagrams (10 points) (a) Sketch an accurate energy diagram that meets the following criteria (4 points) SM - OM Int - P SM - Int is endergonic and the slowest step. overall SM + P is exergonic. al Free Energy (G) Reaction Coordinate (b) Label the transitions states in your diagram (2 points) (c) Indicate AG. for the overall transformation (2 points) (d) Indicate E. for each step...
please explain your answer as i am a little slow For the following questions, provide the...
please explain your answer as i am a little slow
For the following questions, provide the following information, (1) If a molecular formula is provided, indicate the units of unsaturation in this molecule. (2) Label any important relevant peaks in the IR spectrum by indicating which type of bond it corresponds to (3) If the integration is not provided in the 'H NMR spectrum, determine the integration for each signal in this spectrum (4) Examine the mass spectrum carefully. If...
NMR IR Post-Lab Questions Name: Elizabeth Bean HWI. A student ran the following reaction 1 equiv....
NMR IR Post-Lab Questions Name: Elizabeth Bean HWI. A student ran the following reaction 1 equiv. Nah then MeBr HC A TLC or the reaction after workup indicated the presence of TWO spots. After running a column and separating the two compounds by TLC, the student found that the majority of the mass gave the following NMR and FT-IR data. Is the majority of the yield the desired product? Explain your answer. (HINT, compare the spreetra below with those of...
2. Examine the following Electrophilic Aromatic Substitution reaction. 1) Provide the number of 13C NMR signals...
2. Examine the following Electrophilic Aromatic Substitution reaction. 1) Provide the number of 13C NMR signals expected in both the reactant and the product. 2) Provide the carbocation intermediate that allowed the transformation to happen at that position. 3) This molecule is (ortho, meta, para) substituted (circle one). 4) Using resonance arrows show how that carbocation can be distributed (delocalized) to multiple locations on the arene ring system. 5) Predict a different structure that can form from this delocalization. FeBrg,...
hello i need some help with this. please provide details. 1) Which compound gives the following...
hello i need some help with this. please provide
details.
1) Which compound gives the following spectra? For the 'H-NMR assign all signals. Interpret mol peak and base peak in the mass spectrum if a mole peak exists. Assign at least two c signals. How does the IR spectrum support your findings? (12 pts.) Relative Intensity 20- 20 40 60 80 100 120 140 160 180 200 200 180 160 140 120 100 80 60 40 20 ppm t, 1H...
Please help (1-4 ) , thank youh ! Predict the product for the following reaction sequence....
Please help (1-4 ) , thank youh !
Predict the product for the following reaction sequence. Aspartame is an artificial sweetence used in equal and diet soft drinks. Predict the product(s) for the following reaction Provide the stepwise synthesis for the following compound starting with cycloneptene and using the Dieckmann cyclization. Provide the structure of the reactant (x) necessary to carry out the following conversion
please help ): Part A Provide the major organic product of the following reaction. Br 1....
please help ):
Part A Provide the major organic product of the following reaction. Br 1. Mg 2. CO2 3. H30 НАС Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), At 1 * H: 120 EXP CONT. ? H + C N -
Please provide a detailed ‘H-NMR and C-NMR analysis for both the
reactant and product. For the ‘H-NMR analysis please include: 1) on
the reactant and product the types of protons and their peaks. 2)
splitting pattern
CH₂ Iz Reactant Product
Please provide a detailed ‘H-NMR and C-NMR analysis for both
the reactant and product. For the ‘H-NMR analysis please
include:
1) on the reactant and product the types of protons and their
peaks.
2) splitting pattern
3) intergration ratio.
CHO Woolt Me or Reatant Meor Product
1. For each of the following structures, please fill in the missing information below or- Cl Molecular Formula:R_ Molecular Formula: DBE:_ DBE: 2. Given the reaction below, answer the following questions. Br HBr As the above reaction progresses to completion, what peak in the IR would you expect to disappear? Whereabout is the peak located in cm? a. b. Why does the M+1 peak NOT change from reactant to product? c. How many peaks (not the splitting pattern, just the...
please
provide detailed explanation of solution for thumbs up
6. Reaction Coordinate Diagrams (10 points) (a) Sketch an accurate energy diagram that meets the following criteria (4 points) SM - OM Int - P SM - Int is endergonic and the slowest step. overall SM + P is exergonic. al Free Energy (G) Reaction Coordinate (b) Label the transitions states in your diagram (2 points) (c) Indicate AG. for the overall transformation (2 points) (d) Indicate E. for each step...
please explain your answer as i am a little slow
For the following questions, provide the following information, (1) If a molecular formula is provided, indicate the units of unsaturation in this molecule. (2) Label any important relevant peaks in the IR spectrum by indicating which type of bond it corresponds to (3) If the integration is not provided in the 'H NMR spectrum, determine the integration for each signal in this spectrum (4) Examine the mass spectrum carefully. If...
NMR IR Post-Lab Questions Name: Elizabeth Bean HWI. A student ran the following reaction 1 equiv. Nah then MeBr HC A TLC or the reaction after workup indicated the presence of TWO spots. After running a column and separating the two compounds by TLC, the student found that the majority of the mass gave the following NMR and FT-IR data. Is the majority of the yield the desired product? Explain your answer. (HINT, compare the spreetra below with those of...
2. Examine the following Electrophilic Aromatic Substitution reaction. 1) Provide the number of 13C NMR signals expected in both the reactant and the product. 2) Provide the carbocation intermediate that allowed the transformation to happen at that position. 3) This molecule is (ortho, meta, para) substituted (circle one). 4) Using resonance arrows show how that carbocation can be distributed (delocalized) to multiple locations on the arene ring system. 5) Predict a different structure that can form from this delocalization. FeBrg,...
hello i need some help with this. please provide
details.
1) Which compound gives the following spectra? For the 'H-NMR assign all signals. Interpret mol peak and base peak in the mass spectrum if a mole peak exists. Assign at least two c signals. How does the IR spectrum support your findings? (12 pts.) Relative Intensity 20- 20 40 60 80 100 120 140 160 180 200 200 180 160 140 120 100 80 60 40 20 ppm t, 1H...
Please help (1-4 ) , thank youh !
Predict the product for the following reaction sequence. Aspartame is an artificial sweetence used in equal and diet soft drinks. Predict the product(s) for the following reaction Provide the stepwise synthesis for the following compound starting with cycloneptene and using the Dieckmann cyclization. Provide the structure of the reactant (x) necessary to carry out the following conversion
please help ):
Part A Provide the major organic product of the following reaction. Br 1. Mg 2. CO2 3. H30 НАС Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), At 1 * H: 120 EXP CONT. ? H + C N -
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