Please help me and answer all 5 questions.
1. What is the name of the reaction?
2. Identify the number of unique carbons and protons in each of the starting materials and in the product
3. Predict the product of the reaction.
4. Illustrate the mechanism of the reaction based on notes or book as a reference. You can use the structures from the book/notes instead of your assigned compounds, especially if your starting materials are complicated.
5. Give advice on how to predict the product correctly (do you have a short cut or another method?; what do you notice now that you’ve been asked this question. It is ok if you do not see one- it is also ok to communicate with members of your group to come up with something together).
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Please help me and answer all 5 questions.
1. What is the name of the reaction?...
solve and answer all 5 questions please 1. What is the name of the reaction? 2....
solve and answer all 5 questions please
1. What is the name of the reaction? 2. Identify the number of unique carbons and protons in each of the starting materials and in the product 3. Predict the product of the reaction. 4. Illustrate the mechanism of the reaction based on notes or book as a reference. You can use the structures from the book/notes instead of your assigned compounds, especially if your starting materials are complicated. 5. Give advice on...
please help solve all 1. What is the name of the reaction? 2. Identify the number...
please help solve all
1. What is the name of the reaction? 2. Identify the number of unique carbons and protons in each of the starting materials and in the product 3. Predict the product of the reaction. 4. Illustrate the mechanism of the reaction 5. Give advice on how to predict the product correctly (do you have a short cut or another method? or 1. Phli 2. H,0*
Could you do both questions? Thank you in advance! 2. For the reaction below: a. Predict...
Could you do both questions?
Thank you in advance!
2. For the reaction below: a. Predict the most stable product(s) and draw the mechanism OK + E b. Redraw the product(s) below and label all the non-equivalent carbons. How many signals would you expect to see in the 13C NMR of the product? Predict the chemical shifts of each carbon below. c. Redraw the product(s) below and label all the non-equivalent hydrogens. How many signals would you expect to see...
Please help with these questions, there may be more than 1 correct answer! The final product...
Please help with these questions, there may be more than 1
correct answer!
The final product in equation (ii) is P. How many unique protons are there in P? он CH 3 СНз O 5 0 6 0 8 Which statements correctly describe the relationship between unique protons in a molecule and peaks in the molecule's 1H NMR spectrum? Check all that apply The number of 1H NMR peaks is exactly equal to the number of unique protons. The number...
QUESTION 29 0.5 points Save Answer For problems 29-33, answer the questions about the 2-step reaction...
QUESTION 29 0.5 points Save Answer For problems 29-33, answer the questions about the 2-step reaction sequence shown below ?? 3Intermediate Reaction 4 Br Reaction Product Z Number the carbons in your starting material. Identify those same carbons in your final product and number them accordingly. What new bond do you know you have to form? a. C-N O b. C-O Of. C-C
I cannot find similar questions in the book nor the powerpoints. please help. 10. (5 pts)...
I cannot find similar questions in the book nor the
powerpoints. please help.
10. (5 pts) Write a mechanism to account for this aqueous acid-catalyzed reaction. Do not add any other reactants besides water, acid, and the starting material shown. (Hint: you may find it helpful to write one or more of the hydrogens on the ring in your mechanism) он 11. (5 pts) Predict the product of this reaction. Add no other reactants 200°C We were unable to transcribe...
This is for the Grignard Reaction laboratory. Please help me answer this question, much appreciated. 1....
This is for the Grignard Reaction laboratory. Please help me answer this question, much appreciated. 1. If a student performing Laboratory with Grignard reaction accidently used acetone as the reaction solvent instead of diethyl ether, what would the major organic product(s) be? Draw the structure of the product(s) (no mechanism necessary). b. What was the purpose of adding magnesium sulfate in this experiment? c. Grignard reagents react with both aldehyde and ketone functional groups. How do you predict the reaction...
I need help with questions 5, 6, & 7. The FTIR and NMR is provided. I...
I need help with questions 5,
6, & 7. The FTIR and NMR is provided. I also need help creating
a reaction mechanism using the following:
Starting material: methyl acetate.
Solvent: diethyl ether
Reagent: sodium methoxide
Product: methyl acetoacetate
THANK YOU!!!!!
11-8: Claisen Condensation - 1 For this assignment, the target compound that you should synthesize is methyl acetoacetate.This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep...
I need help with these questions please! 1. Provide the product of the following reaction. Hint:...
I need help with these questions please!
1. Provide the product of the following reaction. Hint: Pay attenti and product, label unique Hs and provide expected integration and splitting pattem wing reaction. Hint: Pay attention to the functional groups! For both the reactant OH 1. Li, pentane Br 2. H*, H,0 HNMR Prediction - Reactant C3H30 HNMR Prediction - Product 2. Provide the reactant of the following reaction. How could you use IR spectroscopy to determine if the reaction was...
I need help with questions 5, 6, & 7. The FTIR and NMR is provided. I...
I need help with questions 5, 6, & 7. The FTIR and NMR is
provided. I also need help creating a reaction mechanism using the
following:
Starting material: 1,7-Dimethyl-heptanedioate
Solvent: Diethyl ether
Reagent: sodium methoxide
Product: 3-oxo-cyclohexane carboxylic acid methyl ester
THANK YOU!!!!!
Ö 11-11: Dieckmann Reaction For this assignment, the target compound that you should synthesize is 2-oxo-cyclohexane carboxylic acid methyl ester.This is an intramolecular carbonyl addition variation. Examine the product and determine which ester is the nucleophile and...
solve and answer all 5 questions please
1. What is the name of the reaction? 2. Identify the number of unique carbons and protons in each of the starting materials and in the product 3. Predict the product of the reaction. 4. Illustrate the mechanism of the reaction based on notes or book as a reference. You can use the structures from the book/notes instead of your assigned compounds, especially if your starting materials are complicated. 5. Give advice on...
please help solve all
1. What is the name of the reaction? 2. Identify the number of unique carbons and protons in each of the starting materials and in the product 3. Predict the product of the reaction. 4. Illustrate the mechanism of the reaction 5. Give advice on how to predict the product correctly (do you have a short cut or another method? or 1. Phli 2. H,0*
Could you do both questions?
Thank you in advance!
2. For the reaction below: a. Predict the most stable product(s) and draw the mechanism OK + E b. Redraw the product(s) below and label all the non-equivalent carbons. How many signals would you expect to see in the 13C NMR of the product? Predict the chemical shifts of each carbon below. c. Redraw the product(s) below and label all the non-equivalent hydrogens. How many signals would you expect to see...
Please help with these questions, there may be more than 1
correct answer!
The final product in equation (ii) is P. How many unique protons are there in P? он CH 3 СНз O 5 0 6 0 8 Which statements correctly describe the relationship between unique protons in a molecule and peaks in the molecule's 1H NMR spectrum? Check all that apply The number of 1H NMR peaks is exactly equal to the number of unique protons. The number...
QUESTION 29 0.5 points Save Answer For problems 29-33, answer the questions about the 2-step reaction sequence shown below ?? 3Intermediate Reaction 4 Br Reaction Product Z Number the carbons in your starting material. Identify those same carbons in your final product and number them accordingly. What new bond do you know you have to form? a. C-N O b. C-O Of. C-C
I cannot find similar questions in the book nor the
powerpoints. please help.
10. (5 pts) Write a mechanism to account for this aqueous acid-catalyzed reaction. Do not add any other reactants besides water, acid, and the starting material shown. (Hint: you may find it helpful to write one or more of the hydrogens on the ring in your mechanism) он 11. (5 pts) Predict the product of this reaction. Add no other reactants 200°C We were unable to transcribe...
I need help with questions 5,
6, & 7. The FTIR and NMR is provided. I also need help creating
a reaction mechanism using the following:
Starting material: methyl acetate.
Solvent: diethyl ether
Reagent: sodium methoxide
Product: methyl acetoacetate
THANK YOU!!!!!
11-8: Claisen Condensation - 1 For this assignment, the target compound that you should synthesize is methyl acetoacetate.This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep...
I need help with these questions please!
1. Provide the product of the following reaction. Hint: Pay attenti and product, label unique Hs and provide expected integration and splitting pattem wing reaction. Hint: Pay attention to the functional groups! For both the reactant OH 1. Li, pentane Br 2. H*, H,0 HNMR Prediction - Reactant C3H30 HNMR Prediction - Product 2. Provide the reactant of the following reaction. How could you use IR spectroscopy to determine if the reaction was...
I need help with questions 5, 6, & 7. The FTIR and NMR is
provided. I also need help creating a reaction mechanism using the
following:
Starting material: 1,7-Dimethyl-heptanedioate
Solvent: Diethyl ether
Reagent: sodium methoxide
Product: 3-oxo-cyclohexane carboxylic acid methyl ester
THANK YOU!!!!!
Ö 11-11: Dieckmann Reaction For this assignment, the target compound that you should synthesize is 2-oxo-cyclohexane carboxylic acid methyl ester.This is an intramolecular carbonyl addition variation. Examine the product and determine which ester is the nucleophile and...
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