Title: Table 15-1, p. 612
1Table 15-1, p. 612
2Common Names of Carboxylic Acids
Table 15.1
3Common Names of Dicarboxylic Acids
Table 15.1
4p. 614
5p. 615
6Fig. 15-1, p. 616
7p. 616
8Table 15-2, p. 615
9p. 618
10p. 618
11(No Transcript)
12Electrophilic Aromatic Substitution
Fig. 9-16, p. 338
13pKas of Substituted Benzoic Acids
Lower pKa
Higher pKa
Fig. 9-16, p. 338
14Preparation of Carboxylic Acids Review
- Oxidation of 1? alcohols
- a.
- b.
p. 620
15a
Preparation of Carboxylic Acids Review
- Oxidation of 1? alcohols
- a. CrO3, H2SO4
- b. K2Cr2O7, H3O
- Oxidation of 1? alcohols
p. 620
16Preparation of Carboxylic Acids Review
2. Oxidation of aldehydes a. b.
p. 620
17Preparation of Carboxylic Acids Review
2. Oxidation of aldehydes a. CrO3, H2SO4 b.
K2Cr2O7, H3O
p. 620
18Preparation of Carboxylic Acids Review
3. Oxidative cleavage a. of aryl benzenes (sect
9.10) b. carbon-carbon double bonds
i. ii.
p. 620
19Preparation of Carboxylic Acids Review
3. Oxidative cleavage a. of aryl benzenes (sect
9.10) KMnO4 b. carbon-carbon double
bonds i. ii.
p. 620
20Preparation 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.
p. 620
21Preparation 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
p. 620
22Preparation 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
p. 620
23Preparation of Carboxylic Acids
- Oxidative Cleavage
- a. O3, H2O2
2. Reduction of Carbon Dioxide a. Examples b.
Mechanism c. Limitations
p. 620
24Preparation of Carboxylic Acids
- 3. Hydrolysis of Nitriles
- Examples
- Limitations
- Mechanisms
- Acid catalyzed
- Base catalyzed
p. 620
25Preparation of Nitriles
- From Alkyl Halides
- 2. From Amides
p. 620
26Reactions of Nitriles with Reducing Agents
- Lithium Aluminum Hydride
- 2. Grignard Reagents
p. 620
27Fig. 15-4, p. 627
28p. 628
29Fig. 15-5, p. 628
30End