In the Gabriel synthesis of primary amines, N-potassiophthalimide is used as a source of the nitrogen atom. Complete the synthesis reactions by drawing the missing structures. Ignore inorganic counterions. NH₂ of DMF Step 1 Product NaOH (xs) H₂O, heat Step 2 Product Br KBr

In the Gabriel synthesis of primary amines, N-potassiophthalimide is used as a source of the nitrogen atom. Complete the synthesis reactions by drawing the missing structures. Ignore inorganic counterions. NH₂ of DMF Step 1 Product NaOH (xs) H₂O, heat Step 2 Product Br KBr

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter19: Enolate Anions And Enamines

Section19.9: Crossed Enolate Reactions Using Lda

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Question

In the Gabriel synthesis of primary amines, N-potassiophthalimide is used as a source of the nitrogen atom. Complete the
synthesis reactions by drawing the missing structures. Ignore inorganic counterions.
NH₂
DMF
Step 1
Product
NaOH (xs)
H₂O, heat
+
Step 2
Product
Br
KBr
Draw the Step 1 product.
Draw the Step 2 product.
0
a
0
Incorrect
Incorrect
0
0
OH
OH

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