NCH, Starting with the Claison reaction of ethyl acetate and itself. Use any other reactants with 3 or fewer carbons. он a. Describe the major functional group(s) present in your molecule imine, hydroxyl group b. Based on the starting material allowance, map substructure building blocks onto your target molecule. c. Describe logical "disconnections" that could be used to connect the pieces you have circled d. Arrange your retrosynthetic pieces into a logical order for taking your molecule apart.
NCH, Starting with the Claison reaction of ethyl acetate and itself. Use any other reactants with 3 or fewer carbons. он a. Describe the major functional group(s) present in your molecule imine, hydroxyl group b. Based on the starting material allowance, map substructure building blocks onto your target molecule. c. Describe logical "disconnections" that could be used to connect the pieces you have circled d. Arrange your retrosynthetic pieces into a logical order for taking your molecule apart.
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter20: Acidity And Pka Of Phenols
Section: Chapter Questions
Problem 11E
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![STRUCTURE BELOW USED FOR ALL PARTS
NCH,
Starting with the Claison reaction of ethyl
acetate and itself. Use any other reactants
with 3 or fewer carbons.
он
a. Describe the major functional group(s) present in your molecule
imine, hydroxyl group
b. Based on the starting material allowance, map substructure building blocks onto
your target molecule.
c. Describe logical "disconnections" that could be used to connect the pieces you
have circled
d. Arrange your retrosynthetic pieces into a logical order for taking your molecule
apart.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F9a4df0a2-8398-47c1-9cf4-c51acae36dfd%2F3153dde7-1416-40b1-b1bb-53249d1e9af3%2Fo7pq1dt_processed.png&w=3840&q=75)
Transcribed Image Text:STRUCTURE BELOW USED FOR ALL PARTS
NCH,
Starting with the Claison reaction of ethyl
acetate and itself. Use any other reactants
with 3 or fewer carbons.
он
a. Describe the major functional group(s) present in your molecule
imine, hydroxyl group
b. Based on the starting material allowance, map substructure building blocks onto
your target molecule.
c. Describe logical "disconnections" that could be used to connect the pieces you
have circled
d. Arrange your retrosynthetic pieces into a logical order for taking your molecule
apart.
![N-CH3
DBH3: THF
2) H20z-NOOH
N-CH3
Hz NCH3
HO
NaDEFi
H200
D NaOE t,
Br
2) H308](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F9a4df0a2-8398-47c1-9cf4-c51acae36dfd%2F3153dde7-1416-40b1-b1bb-53249d1e9af3%2Fhe79757_processed.jpeg&w=3840&q=75)
Transcribed Image Text:N-CH3
DBH3: THF
2) H20z-NOOH
N-CH3
Hz NCH3
HO
NaDEFi
H200
D NaOE t,
Br
2) H308
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