Organic Chemistry
SearchMicro-courses:21
01:18
1. Reactivity of Enols
01:23
2. Reactivity of Enolate Ions
01:19
3. Types of Enols and Enolates
01:15
4. Enolate Mechanism Conventions
01:33
5. Regioselective Formation of Enolates
01:12
6. Stereochemical Effects of Enolization
01:21
7. Acid-Catalyzed α-Halogenation of Aldehydes and Ketones
00:51
8. Base-Promoted α-Halogenation of Aldehydes and Ketones
01:28
9. Multiple Halogenation of Methyl Ketones: Haloform Reaction
01:14
10. α-Halogenation of Carboxylic Acid Derivatives: Overview
01:15
11. α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
01:17
12. Reactions of α-Halocarbonyl Compounds: Nucleophilic Substitution
01:19
13. Nitrosation of Enols
01:10
14. C–C Bond Formation: Aldol Condensation Overview
01:08
15. Base-Catalyzed Aldol Addition Reaction
01:15
16. Acid-Catalyzed Aldol Addition Reaction
01:14
17. Dehydration of Aldols to Enals: Base-Catalyzed Aldol Condensation
00:43
18. Dehydration of Aldols to Enones: Acid-Catalyzed Aldol Condensation
01:18
19. Intramolecular Aldol Reaction
00:57
20. C–C Bond Cleavage: Retro-Aldol Reaction
01:04
21. Crossed Aldol Reactions: Overview
01:14
22. Crossed Aldol Reaction Using Weak Bases
01:01
23. Ketones with Nonenolizable Aromatic Aldehydes: Claisen–Schmidt Condens...
00:56
24. Crossed Aldol Reaction Using Strong Bases: Directed Aldol Reaction
01:27
25. Aldol Condensation with β-Diesters: Knoevenagel Condensation
01:24
26. Esters to β-Ketoesters: Claisen Condensation Overview
01:08
27. Esters to β-Ketoesters: Claisen Condensation Mechanism
01:33
28. Aldol Condensation vs Claisen Condensation
01:13
29. Intramolecular Claisen Condensation of Dicarboxylic Esters: Dieckmann ...
01:18
30. β-Dicarbonyl Compounds via Crossed Claisen Condensations
01:10
31. α-Alkylation of Ketones via Enolate Ions
01:10
32. Factors Affecting α-Alkylation of Ketones: Choice of Base
01:07
33. Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
01:14
34. Alkylation of β-Diester Enolates: Malonic Ester Synthesis
01:09
35. Conjugate Addition to α,β-Unsaturated Carbonyl Compounds
01:27
36. Conjugate Addition (1,4-Addition) vs Direct Addition (1,2-Addition)
01:08
37. Conjugate Addition of Enolates: Michael Addition
01:27
38. Cyclohexenones via Michael Addition and Aldol Condensation: The Robins...
01:26
39. Synthesis of α-Substituted Carbonyl Compounds: The Stork Enamine React...
01:25