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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. O o Br i 'N K DMF Step 1 Product KBr NaOH (xs) H₂O, heat NH₂ Step 2 Product

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. O o Br i 'N K DMF Step 1 Product KBr NaOH (xs) H₂O, heat NH₂ Step 2 Product

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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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. of Br i -=+ Step 1 NaOH (xs) Product H₂O, heat Draw the Step 1 product. Select Draw Templates More Ć C H DMF 0 N off O KBr Erase Q2 Q NH₂ 3 Ć Step 2 Product Draw the Step 2 product. Select Draw Templates More C H O Erase Q2 Q
Transcribed Image Text: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. of Br i -=+ Step 1 NaOH (xs) Product H₂O, heat Draw the Step 1 product. Select Draw Templates More Ć C H DMF 0 N off O KBr Erase Q2 Q NH₂ 3 Ć Step 2 Product Draw the Step 2 product. Select Draw Templates More C H O Erase Q2 Q
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