Amino Products - Organic Chemistry
Card 0 of 8
A secondary alkyl halide is treated with 
, then 
, then acid. The final product is .
A secondary alkyl halide is treated with
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The 
group replaces the halogen as the halogen is a better leaving group. Lithium aluminum hydride is a strong reducing agent. It takes nitrogen-nitrogen bonds and allows for nitrogen hydrogen bonds to be formed instead. A primary nitrogen is bonded to two hydrogens and one R group. After reduction, a primary amine is formed.
The
What product would be obtained for the acid catalyzed reaction shown above?
What product would be obtained for the acid catalyzed reaction shown above?
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The reaction given is for the nucleophilic addition of a secondary amine to a ketone. Below is the mechanism for this acid catalyzed reaction:
The protonation of the hydroxyl group makes it a better leaving group.
The reaction given is for the nucleophilic addition of a secondary amine to a ketone. Below is the mechanism for this acid catalyzed reaction:
The protonation of the hydroxyl group makes it a better leaving group.
A secondary alkyl halide is treated with , then , then acid. The final product is .
A secondary alkyl halide is treated with
Tap to see back →
The group replaces the halogen as the halogen is a better leaving group. Lithium aluminum hydride is a strong reducing agent. It takes nitrogen-nitrogen bonds and allows for nitrogen hydrogen bonds to be formed instead. A primary nitrogen is bonded to two hydrogens and one R group. After reduction, a primary amine is formed.
The
What product would be obtained for the acid catalyzed reaction shown above?
What product would be obtained for the acid catalyzed reaction shown above?
Tap to see back →
The reaction given is for the nucleophilic addition of a secondary amine to a ketone. Below is the mechanism for this acid catalyzed reaction:
The protonation of the hydroxyl group makes it a better leaving group.
The reaction given is for the nucleophilic addition of a secondary amine to a ketone. Below is the mechanism for this acid catalyzed reaction:
The protonation of the hydroxyl group makes it a better leaving group.
A secondary alkyl halide is treated with , then , then acid. The final product is .
A secondary alkyl halide is treated with
Tap to see back →
The group replaces the halogen as the halogen is a better leaving group. Lithium aluminum hydride is a strong reducing agent. It takes nitrogen-nitrogen bonds and allows for nitrogen hydrogen bonds to be formed instead. A primary nitrogen is bonded to two hydrogens and one R group. After reduction, a primary amine is formed.
The
What product would be obtained for the acid catalyzed reaction shown above?
What product would be obtained for the acid catalyzed reaction shown above?
Tap to see back →
The reaction given is for the nucleophilic addition of a secondary amine to a ketone. Below is the mechanism for this acid catalyzed reaction:
The protonation of the hydroxyl group makes it a better leaving group.
The reaction given is for the nucleophilic addition of a secondary amine to a ketone. Below is the mechanism for this acid catalyzed reaction:
The protonation of the hydroxyl group makes it a better leaving group.
A secondary alkyl halide is treated with , then , then acid. The final product is .
A secondary alkyl halide is treated with
Tap to see back →
The group replaces the halogen as the halogen is a better leaving group. Lithium aluminum hydride is a strong reducing agent. It takes nitrogen-nitrogen bonds and allows for nitrogen hydrogen bonds to be formed instead. A primary nitrogen is bonded to two hydrogens and one R group. After reduction, a primary amine is formed.
The
What product would be obtained for the acid catalyzed reaction shown above?
What product would be obtained for the acid catalyzed reaction shown above?
Tap to see back →
The reaction given is for the nucleophilic addition of a secondary amine to a ketone. Below is the mechanism for this acid catalyzed reaction:
The protonation of the hydroxyl group makes it a better leaving group.
The reaction given is for the nucleophilic addition of a secondary amine to a ketone. Below is the mechanism for this acid catalyzed reaction:
The protonation of the hydroxyl group makes it a better leaving group.