1 carboxylic acid derivatives. 2 phosphate nomenclature

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1

Carboxylic Acid Derivatives

2

Phosphate Nomenclature

3

Nucleophilic Substitution Rxn’s

4

Sterics

5

Electronics (polarization)

Sulfer is more polarizable than oxygen, thus a better leaving group

Why acetic anhydride then? Resonance (stabilization of L.G.)

6

7

8

Isotope Labeling

• How do we really know how these mechanisms work?

9

10

DCC most commonly used for the synthesis of peptides (proteins)

11

LAH reduction forms an alcohol

Aluminum plays an important role in the mechanism

12

13

Sterics Role in Alcoholysis

14

Grignard attack of Acid Chlorides

Will get two additions, can’t control single vs. double addition

15

Gilman Reagent – Can Isolate the Ketone

Example:

16

17

Synthesis of Aspirin

18

Preparation of Tylenol

19

Interesting Ester Examples

20

Ester Synthesis

21

22

Base Catalyzed Hydrolysis

23

Acid Catalyzed Hydrolysis

24

Synthesis of Amides

25

Base Catalyzed Hydrolysis

26

What should you expect in Biochemistry?

27

LAH reduction of Amides

28

29

Step Growth Polymers

30

31

Biodegradable Polymers

32

33

NMR of Ethyl Acetate

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