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Beckmann's Rearrangement
Lesson 16 of 18 • 13 upvotes • 11:43mins
Ankita Chowdhury
This lesson covers Beckmann's rearrangement, through which oximes are converted to secondary amides. This lesson also covers the synthesis of primary amines from the Beckmann's rearrangement product.
Amines: Reaction Mechanisms
18 lessons • 2h 47m
1
Gabriel Phthalimide Synthesis - 1
4:11mins
2
Gabriel Phthalimide Synthesis - 2
11:42mins
3
Questions for Practice
8:14mins
4
Carbylamine Test
6:39mins
5
Questions on Carbylamine Test - 1
10:58mins
6
Questions on Carbylamine Test - 2
7:18mins
7
Hoffmann's Bromamide Reaction
7:44mins
8
Hoffman's Bromamide Reaction: Detailed Mechanism
12:24mins
9
Hoffmann's Bromamide Reaction: Questions
12:08mins
10
Schmidt Reaction: Primary Amine Synthesis
7:24mins
11
Schmidt Reaction: Detailed Reaction Mechanism
7:48mins
12
Curtious Reaction: Detailed Mechanism-Acidic Medium
10:53mins
13
Curtious Reaction: Basic medium reaction mechanism
7:18mins
14
Lossen's Reaction: Detailed Mechanism-Acidic Medium
12:06mins
15
Lossen's Reaction: Detailed Mechanism-Basic Medium
11:18mins
16
Beckmann's Rearrangement
11:43mins
17
Beckmann's Rearrangement Questions with Shortcut
9:28mins
18
SNAE Reaction Mechanism
8:01mins
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