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Table 15-1, p. 612

Table 15-1, p. 612. Common Names of Carboxylic Acids. Table 15.1. Common Names of Dicarboxylic Acids. Table 15.1. p. 614. Table 15-2, p. 615. p. 615. Fig. 15-1, p. 616. p. 616. p. 618. p. 618. Electrophilic Aromatic Substitution. Fig. 9-16, p. 338.

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Table 15-1, p. 612

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  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. Table 15-2, p. 615

  6. p. 615

  7. Fig. 15-1, p. 616

  8. p. 616

  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. CrO3, H3O+ • b. K2Cr2O7, H2SO4 • Oxidation of 1 alcohols: p. 620

  14. Preparation of Carboxylic Acids : Review • 2. Oxidation of aldehydes: • a. KMnO4 • b. CrO3, H3O+ • c. K2Cr2O7, H2SO4 (Jones) • Oxidation of 1 alcohols: p. 620

  15. Preparation of Carboxylic Acids : Review • 3. Oxidative cleavage (of double bonds): • a. KMnO4 • b. O3, H2O2 • Oxidation of 1 alcohols: p. 620

  16. Preparation of Carboxylic Acids : Review • 3. Oxidative cleavage a- to arene: • a. KMnO4 • b. CrO3, H3O+ • Oxidation of 1 alcohols: Methyl, 1° , 2°

  17. Fig. 15-4, p. 627

  18. p. 628

  19. Fig. 15-5, p. 628

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