1. 6-1 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Introduction to Organic Chemistry 2 ed William H. Brown

2. 6-2 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reactions of Alkenes Chapter 6

3. 6-3 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Characteristic Reactions

4. 6-4 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Characteristic Reactions

5. 6-5 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Characteristic Reactions

6. 6-6 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reaction Mechanisms A reaction mechanism describes how a reaction occurs which bonds are broken and which new ones are formed the order in which bond-breaking and bond-forming steps take place the role of the catalyst (if any is present) the energy of the entire system during the reaction

7. 6-7 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. PE Diagrams Potential energy (PE) diagram: a graph showing the changes in energy that occur during a chemical reaction Reaction coordinate: a measure of the change in position of atoms during a reaction

8. 6-8 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. PE Diagrams

9. 6-9 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. PE Diagrams Heat of reaction,  H: the difference in potential energy between reactants and products exothermic: products are lower in energy than reactants; heat is released endothermic: products are higher in energy than reactants; heat is absorbed Transition state: an energy maximum on a PE diagram represents an unstable species of maximum PE formed during the course of a reaction

10. 6-10 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Activation Energy Activation Energy, E a : the difference in potential energy between reactants and the transition state determines the rate of reaction if activation energy is large, only a few molecular collisions occur with sufficient energy to reach the transition state, and the reaction is slow if activation energy is small, many collisions generate sufficient energy to reach the transition state, and the reaction is fast

11. 6-11 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Developing a Mechanism Design experiments to reveal details of a particular chemical reaction Propose a set or sets of steps that might account for the overall transformation A mechanism becomes established when it is shown to be consistent with every test that can be devised This does mean that the mechanism is correct, only that it is the best explanation we are able to devise

12. 6-12 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Why Mechanisms? A framework within which to organize descriptive chemistry The intellectual satisfaction derived from constructing models that accurately reflect the behavior of chemical systems A tool with which to search for new information and new understanding

13. 6-13 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Electrophilic Additions Hydrohalogenation using HCl, HBr, HI Hydration using H 2 O, H 2 SO 4 Halogenation using Cl 2, Br 2

14. 6-14 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Addition of HX Carried out with pure reagents or in a polar solvent such as acetic acid Addition is regioselective Regioselective reaction: a reaction in which one direction of bond-forming or bond-breaking occurs in preference to all other directions

15. 6-15 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Addition of HX Addition is regioselective Markovnikov’s ruleMarkovnikov’s rule: in the addition of HX or H 2 O to an alkene, H adds to the carbon of the double bond that has the greater number of hydrogens bonded to it

16. 6-16 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. HCl + 2-Butene A two-step mechanism Step 1: formation of sec-butyl cation, a 2° carbocation intermediate

17. 6-17 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. HCl + 2-Butene Step 2: reaction of the sec-butyl cation with chloride ion

18. 6-18 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Carbocations CarbocationCarbocation: a species containing a positively charged carbon Carbocations are classified as 1°, 2°, or 3° depending on the number of carbons bonded to the carbon bearing the positive charge electrophiles; that is, they are “electron-lovers”

19. 6-19 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Carbocation Structure Bond angles about the positively charged carbon are 120° Carbon uses sp 2 hybrid orbitals to form sigma bonds to the three attached groups The unhybridized 2p orbital lies perpendicular to the sigma bond framework and contains no electrons

20. 6-20 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Carbocation Stability A 3° carbocation is more stable (requires a lower activation energy for its formation) than a 2° carbocation A 2° carbocation is, in turn, more stable (requires a lower activation energy for its formation) than a 1° carbocation 1° and methyl cations is so unstable that they are rarely if ever observed in solution

21. 6-21 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Carbocation Stability Relative stability

22. 6-22 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Carbocation Stability Carbocations are stabilized by the electron- withdrawing inductive effect of the positively- charged carbon according to molecular orbital calculations:

23. 6-23 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Addition of H 2 O Addition of water is called hydration Acid-catalyzed hydration of an alkene is regioselective - hydrogen adds to the less substituted carbon of the double bond

24. 6-24 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Addition of H 2 O Step 1: proton transfer from solvent to the alkene

25. 6-25 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Addition of H 2 O Step 2: reaction of the carbocation intermediate with H 2 O to form an oxonium ion Step 3: proton transfer to solvent

26. 6-26 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Addition of Cl 2 and Br 2 Carried out with either the pure reagents or in an inert solvent such as CCl 4 or CH 2 Cl 2

27. 6-27 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Addition of Cl 2 and Br 2 Addition is stereoselective Stereoselective reactionStereoselective reaction: a reaction in which one stereoisomer is formed or destroyed in preference to all others than might be formed or destroyed

28. 6-28 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Addition of Cl 2 and Br 2 Addition involves a two-step mechanism Step 1: formation of a bridged bromonium ion intermediate

29. 6-29 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Addition of Cl 2 and Br 2 Step 2: Attack of halide ion from the opposite side of the three-membered ring

30. 6-30 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Addition of Cl 2 and Br 2 For a cyclohexene, anti coplanar addition corresponds to trans-diaxial addition

31. 6-31 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Oxidation/Reduction Oxidation: the loss of electrons Reduction: the gain of electrons Recognize using a balanced half-reaction write a half-reaction showing one reactant and its product(s) complete a material balance. Use H 2 O and H + in acid solution; use H 2 O and OH - in basic solution complete a charge balance using electrons, e -

32. 6-32 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Oxidation with OsO 4 Oxidation by OsO 4 converts an alkene to a glycol, a compound with -OH groups on two adjacent carbons oxidation is syn stereoselective

33. 6-33 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Oxidation with OsO 4 Intermediate is a cyclic osmic ester containing a five-membered ring

34. 6-34 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reduction of Alkenes Most alkenes react with H 2 in the presence of a transition metal catalyst to give alkanes commonly used catalysts are Pt, Pd, Ru, and Ni The process is called catalytic reduction or, alternatively, catalytic hydrogenation

35. 6-35 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reduction of Alkenes the most common pattern is syn stereoselectivity

36. 6-36 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reduction of Alkenes Mechanism of catalytic hydrogenation H 2 is absorbed on the metal surface with formation of metal-hydrogen bonds the alkene is also absorbed with formation of metal- carbon bonds a hydrogen atom is transferred to the alkene forming one new C-H bond a second hydrogen atom is transferred forming the second C-H bond

37. 6-37 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reaction Stereochemistry Consider the addition of bromine to 2-butene? three stereoisomers are possible for 2,3- dibromobutane; one pair of enantiomers

38. 6-38 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reaction Stereochemistry how many stereoisomers are formed in the addition of bromine to cis-2-butene?

39. 6-39 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reaction Stereochemistry Consider the oxidation of 2-butene by OsO 4 three stereoisomers are possible for 2,3-butanediol; one pair of enantiomers and one meso compound which are formed in this oxidation?

40. 6-40 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reaction Stereochemistry syn hydroxylation of cis-2-butene produces only the meso compound

41. 6-41 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reaction Stereochemistry Enantiomerically pure products can never be formed from achiral starting materials and achiral reagents An enantiomerically pure product can be generated in a reaction if at least one of the reactants is enantiomerically pure, or if the reaction is carried out in an achiral environment

42. 6-42 6 Copyright © 2000 by John Wiley & Sons, Inc. All rights reserved. Reactions of Alkenes End Chapter 6