Complete the mechanism of the reaction between benzaldehyde and dimethylamine in acid followed by introduction of a hydride reducing agent. Add any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows. Note that the use of a generic base B : represents another amine in solution that acts as a shuttle for the added acid. Step 1: Add curved arrows. Step 2: Complete the structure of the

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter19: Eas: Electrophilic Aromatic Substitution
Section: Chapter Questions
Problem 25E
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Step 3: A series of proton transfer steps results in the
Step 4: Complete the structure of the expected
hydroxyamine. The curved arrows are drawn for you.
intermediate, and add curved arrows.
Select Draw Rings More
Erase
H
N
B
B-H
proton
transfer
H
:OH
: в
steps
hydride
added
Step 5: Complete the structure of the expected
Step 6: Complete the structure of the final product.
Lintermediate and add curved arrows
Transcribed Image Text:Step 3: A series of proton transfer steps results in the Step 4: Complete the structure of the expected hydroxyamine. The curved arrows are drawn for you. intermediate, and add curved arrows. Select Draw Rings More Erase H N B B-H proton transfer H :OH : в steps hydride added Step 5: Complete the structure of the expected Step 6: Complete the structure of the final product. Lintermediate and add curved arrows
Complete the mechanism of the reaction between benzaldehyde and dimethylamine in acid followed by introduction of a
hydride reducing agent. Add any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows. Note that
the use of a generic base B : represents another amine in solution that acts as a shuttle for the added acid.
Step 1: Add curved arrows.
Step 2: Complete the structure of the
expected intermediate.
Select Draw Rings More
Erase
Select
Draw
Rings
More
Erase
H
N
B
H
N
B
:0:
:N -
H
N -
H
Transcribed Image Text:Complete the mechanism of the reaction between benzaldehyde and dimethylamine in acid followed by introduction of a hydride reducing agent. Add any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows. Note that the use of a generic base B : represents another amine in solution that acts as a shuttle for the added acid. Step 1: Add curved arrows. Step 2: Complete the structure of the expected intermediate. Select Draw Rings More Erase Select Draw Rings More Erase H N B H N B :0: :N - H N - H
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