1 / 30

Carboxylic Acids: Preparation and Reactions

This article provides an overview of the preparation of carboxylic acids through oxidation of alcohols, aldehydes, and oxidative cleavage. It also discusses the hydrolysis of nitriles and reactions of nitriles with reducing agents.

nweaver
Télécharger la présentation

Carboxylic Acids: Preparation and Reactions

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Table 15-1, p. 612

  2. Common Names of Carboxylic Acids Table 15.1

  3. Common Names of Dicarboxylic Acids Table 15.1

  4. p. 614

  5. p. 615

  6. Fig. 15-1, p. 616

  7. p. 616

  8. Table 15-2, p. 615

  9. p. 618

  10. p. 618

  11. Electrophilic Aromatic Substitution Fig. 9-16, p. 338

  12. pKa’s of Substituted Benzoic Acids Lower pKa Higher pKa Fig. 9-16, p. 338

  13. Preparation of Carboxylic Acids : Review • Oxidation of 1 alcohols: • a. • b. p. 620

  14. a Preparation of Carboxylic Acids : Review • Oxidation of 1 alcohols: • a. CrO3, H2SO4 • b. K2Cr2O7, H3O+ • Oxidation of 1 alcohols: p. 620

  15. Preparation of Carboxylic Acids : Review • 2. Oxidation of aldehydes: • a. • b. • Oxidation of 1 alcohols: p. 620

  16. Preparation of Carboxylic Acids : Review • 2. Oxidation of aldehydes: • a. CrO3, H2SO4 • b. K2Cr2O7, H3O+ • Oxidation of 1 alcohols: p. 620

  17. Preparation of Carboxylic Acids : Review • 3. Oxidative cleavage • a.of aryl benzenes (sect 9.10): • b.carbon-carbon double bonds : • i. • ii. Methyl, 1° , 2° p. 620

  18. Preparation of Carboxylic Acids : Review • 3. Oxidative cleavage • a.of aryl benzenes (sect 9.10): KMnO4 • b.carbon-carbon double bonds : • i. • ii. Methyl, 1° , 2° p. 620

  19. Preparation of Carboxylic Acids : Review • 3. Oxidative cleavage • a.of aryl benzenes (sect 9.10): KMnO4 • b.carbon-carbon double bonds : • i. (sect 8.8) KMnO4 • ii. Methyl, 1° , 2° p. 620

  20. Preparation of Carboxylic Acids : Review • 3. Oxidative cleavage • a.of aryl benzenes (sect 9.10): KMnO4 • b.carbon-carbon double bonds : • i. (sect 8.8) KMnO4 • ii. O3, H2O2 Methyl, 1° , 2° p. 620

  21. Preparation of Carboxylic Acids : Review • 3. Oxidative cleavage • a.of aryl benzenes (sect 9.10): KMnO4 • b.carbon-carbon double bonds : • i. (sect 8.8) KMnO4 • ii. O3, H2O2 Methyl, 1° , 2° p. 620

  22. Preparation of Carboxylic Acids : • Oxidative Cleavage: • a. O3, H2O2 • 2. Reduction of Carbon Dioxide: • a. Examples • b. Mechanism • c. Limitations p. 620

  23. Preparation of Carboxylic Acids : • 3. Hydrolysis of Nitriles • Examples • Limitations • Mechanisms • Acid catalyzed • Base catalyzed p. 620

  24. Preparation of Nitriles • From Alkyl Halides • 2. From Amides p. 620

  25. Reactions of Nitriles with Reducing Agents • Lithium Aluminum Hydride • 2. Grignard Reagents p. 620

  26. Fig. 15-4, p. 627

  27. p. 628

  28. Fig. 15-5, p. 628

  29. End

More Related