2. Reaction Stereochemistry

3. A regioselective reaction: preferential formation of one constitutional isomer A stereoselective reaction: preferential formation of a stereoisomer

4. http://ep.llnl.gov/msds/orgchem/Chem226/stereo1.html Stereoselectivity vs. Sterospecificity Chiral Acids-Bases Diastereomers

5. A stereospecific reaction: each stereoisomeric reactant produces a different stereoisomeric product or a different set of products All stereospecific reactions are stereoselective Not all stereoselective reactions are stereospecific

6. Many reactions convert achiral reactants to chiral products. If all of the components of the starting state (reactants, catalysts, solvents, etc.) are achiral, any chiral products that will be formed are racemic mixtures. "Optically inactive starting materials can't give optically active products." In order for a substance to be optically active, it must be chiral and one enantiomer must be present in greater amounts than the other.

8. Stereochemistry of Electrophilic Addition Reactions of Alkenes Can you determine the absolute configuration of the product?

9. Addition reactions that form one asymmetric carbon: How much of each isomer forms? 50:

11. Many biochemical reactions convert an achiral reactant to a single enantiomer of a chiral product Reactions in living systems are catalyzed by enzymes, which are enantiomerically homogeneous. "Optically inactive starting materials can't give optically active products." The enzyme (catalyst), which is chiral and optically active, is part of the reacting system, so such reactions don't violate the generalization that "Optically inactive starting materials can't give optically active products."

12. Example fumarase H2OH2OH2OH2O C C HO 2 C H CO 2 H H C OHH HO 2 C HO 2 CCH 2 Fumaric acid (S)-(–)-Malic acid Achiral Single enantiomer Lactic acid: Chem 226 Web pages http://ep.llnl.gov/msds/orgchem/Chem226/stereo1.html

13. Addition reactions that form an additional asymmetric carbon

14. A radical reaction intermediate Addition reactions that form two asymmetric carbons

15. Stereochemistry of Hydrogen Addition (Syn Addition)

16. What is the optical yield for the reaction? What is the optical yield for the reaction? Will the physical properties of the products be the same? Will the physical properties of the products be the same? + CH 3 H H 68% 32% A stereoselective reaction CH 3 CH 2 H CH 3 H H H2H2H2H2Pt No, diastereomers have different physical properties. 36%= Pure - Racemic

17. Stereochemistry of Hydroboration– Oxidation Syn addition, that is from the same side: either top or bottom. What is the distribution and relationship of the products? Enantiomers or Diastereomers? 50:50 Enantiomers

18. Addition reactions that form a bromonium ion (anti addition)

20. Stereochemistry Vocabulary pro-R-hydrogen pro-S-hydrogen Enantiotopic hydrogens have the same chemical reactivity and cannot be distinguished by achiral agents, but they are NOT chemically equivalent toward chiral reagents (Most relevant in biochemistry/physiology.)

21. Diastereotopic hydrogens do not have the same reactivity with achiral reagents

23. Applying the Principle: Resolution of Enantiomers Separation of a racemic mixture into its two enantiomeric forms.

24. Resolution of a Racemic Mixture (R)-acid (S)-acid enantiomers (S)-base (R,S)-salt(S,S)-salt diastereomers (R,S)-salt(S,S)-salt HCl (S)-baseH + + (R)-acid (S)-baseH + + (S)-acid

25. enantiomers C(+)C(+)C(-)C(-) Strategy

26. enantiomers C(+)C(+)C(-)C(-) 2P(+) C(+) C(+)P(+) C(-) C(-)P(+) diastereomers Strategy

27. enantiomers C(+)C(+)C(-)C(-) 2P(+) C(+) C(+)P(+) C(-) C(-)P(+) diastereomers C(+) C(+)P(+) C(-) C(-)P(+) Strategy

28. enantiomers C(+)C(+)C(-)C(-) 2P(+) C(+) C(+)P(+) C(-) C(-)P(+) diastereomers C(+) C(+)P(+) C(-) C(-)P(+) P(+) C(+)C(+) C(-)C(-) Strategy

29. http://ep.llnl.gov/msds/orgchem/Chem226/stereo1.html Resolving Racemic Mixtures Chiral Acids-Bases Diastereomers