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in 10:1 Hexane: 8: Use the image below to answer the following questions. The TLC plate was run gityl Acetate. (4 p...
Only need help with 5,6,7 and mechanism FTIR and NMR Spectra After completing a reaction and...
Only need help with 5,6,7
and mechanism
FTIR and NMR Spectra After completing a reaction and working up the products, it is still necessary to confirm that the correct product was formed. The most common tools used for this analysis are Fourier Transform Infrared (FTIR) and Nuclear Magnetic Resonance (NMR) spectroscopy. In the virtual laboratory, 'H and C NMR spectra are available. Details on interpreting FTIR and NMR spectra are found in your textbook. Your instructor may or may not...
please dont miss the questions 11-4: Aldol - 1 For this assignment, the target compound that...
please dont miss the questions
11-4: Aldol - 1 For this assignment, the target compound that you should synthesize is 2-ethyl-3-hydroxy-hexanal. This is a symmetric aldol reaction. Examine the product and determine which bond may be formed to link the two aldehydes. Keep in mind the mechanism and identify the nucleophile and the electrophile. Synthesis Procedures 1. Start Virtual ChemLab and select Aldol – 1 from the list of assignments on the whiteboard. After entering the synthesis laboratory, use the...
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...
1. Consider the three molecules below to answer the following questions. Circle TRUE or FALSE at...
1. Consider the three molecules below to answer the following questions. Circle TRUE or FALSE at the end of each question (0.5 points each). Molecule A Molecule C Molecule B A. The rate of EAS with Molecule B will be faster than the rate of EAS with Molecule A (assume MAJOR product formation). TRUE or FALSE B. Molecule C will undergo nitration to yield a meta-product that is the MAJOR product. TRUE or FALSE c. The rate of meta-product formation...
If you were to run this reaction on a 0.5 g acetaminophen, how much powdered potassium...
If you were to run this reaction on a 0.5 g acetaminophen, how
much powdered potassium carbonate would you use ? Show your
work
Alcohols and Ethers 185 14.3 THE WILLIAMSON ETHER SYNTHESIS: PREPARATION OF PHENACETIN FROM ACETAMINOPHEN One of the most common methods used to prepare ether Williamson ether synthesis. In this reaction, an alkoxide anion (RO) acts as a nucleophile in an S, 2 process, displacing a leaving group (X) from an electrophile (R-X). R-20 . RY ROR...
Use the following information to answer the next two questions Four histograms are displayed below. 2 0 1 2 345 67 89 10 0 2 45 6 789 10 123 4 5 6789 10 0 1 2 34 5 6 7 8 9 10 0 Match the description...
Use the following information to answer the next two questions Four histograms are displayed below. 2 0 1 2 345 67 89 10 0 2 45 6 789 10 123 4 5 6789 10 0 1 2 34 5 6 7 8 9 10 0 Match the description to the appropriate histogram. A distribution for the second to last digit of phone numbers sampled from students in a class (i.e., for the phone number 968-9667, the second to last digit...
Only need help with 5,6,7
and mechanism
FTIR and NMR Spectra After completing a reaction and working up the products, it is still necessary to confirm that the correct product was formed. The most common tools used for this analysis are Fourier Transform Infrared (FTIR) and Nuclear Magnetic Resonance (NMR) spectroscopy. In the virtual laboratory, 'H and C NMR spectra are available. Details on interpreting FTIR and NMR spectra are found in your textbook. Your instructor may or may not...
please dont miss the questions
11-4: Aldol - 1 For this assignment, the target compound that you should synthesize is 2-ethyl-3-hydroxy-hexanal. This is a symmetric aldol reaction. Examine the product and determine which bond may be formed to link the two aldehydes. Keep in mind the mechanism and identify the nucleophile and the electrophile. Synthesis Procedures 1. Start Virtual ChemLab and select Aldol – 1 from the list of assignments on the whiteboard. After entering the synthesis laboratory, use the...
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...
1. Consider the three molecules below to answer the following questions. Circle TRUE or FALSE at the end of each question (0.5 points each). Molecule A Molecule C Molecule B A. The rate of EAS with Molecule B will be faster than the rate of EAS with Molecule A (assume MAJOR product formation). TRUE or FALSE B. Molecule C will undergo nitration to yield a meta-product that is the MAJOR product. TRUE or FALSE c. The rate of meta-product formation...
If you were to run this reaction on a 0.5 g acetaminophen, how
much powdered potassium carbonate would you use ? Show your
work
Alcohols and Ethers 185 14.3 THE WILLIAMSON ETHER SYNTHESIS: PREPARATION OF PHENACETIN FROM ACETAMINOPHEN One of the most common methods used to prepare ether Williamson ether synthesis. In this reaction, an alkoxide anion (RO) acts as a nucleophile in an S, 2 process, displacing a leaving group (X) from an electrophile (R-X). R-20 . RY ROR...
Use the following information to answer the next two questions Four histograms are displayed below. 2 0 1 2 345 67 89 10 0 2 45 6 789 10 123 4 5 6789 10 0 1 2 34 5 6 7 8 9 10 0 Match the description to the appropriate histogram. A distribution for the second to last digit of phone numbers sampled from students in a class (i.e., for the phone number 968-9667, the second to last digit...
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