1. Chapter 8 Alkenes: Reactions and Synthesis

2.  Alkenes react with many electrophiles to give useful products by addition (often through special reagents) Diverse Reactions of Alkenes

3.  Alkenes are commonly made by  elimination of HX from alkyl halide (dehydrohalogenation)  Uses heat and KOH  elimination of H-OH from an alcohol (dehydration)  requires strong acids (sulfuric acid, 50 ºC) 8.1 Preparation of Alkenes: A Preview of Elimination Reactions

4.  Bromine and chlorine add to alkenes to give 1,2-dihaldes, an industrially important process  F 2 is too reactive and I 2 does not add  Cl 2 reacts as Cl + Cl -  Br 2 is similar 8.2 Addition of Halogens to Alkenes

5.  Addition is exclusively trans Addition of Br 2 to Cyclopentene

6.  Br + adds to an alkene producing a cyclic ion  Bromonium ion, bromine shares charge with carbon  Gives trans addition Mechanism of Bromine Addition

7.  Electrophilic addition of bromine to give a cation is followed by cyclization to give a bromonium ion.  This bromonium ion is a reactive electrophile and bromide ion is a good nucleophile. Bromonium Ion Mechanism

8.  This is formally the addition of HO-X to an alkene to give a 1,2-halo alcohol, called a halohydrin  The actual reagent is the dihalogen (Br 2 or Cl 2 ) in the presence of water. 8.3 Halohydrins from Alkenes: Addition of HO-X

9.  Br 2 forms bromonium ion, then water adds  Orientation toward stable C + species  Aromatic rings do not react Mechanism of Formation of a Bromohydrin

10.  Bromine is a difficult reagent to use for this reaction  N-Bromosuccinimide (NBS) produces bromine in organic solvents and is a safer source An Alternative to Bromine

11.  Hydration of an alkene is the addition of H-OH to give an alcohol  Acid catalysts are used in high temperature industrial processes: ethylene is converted to ethanol 8.4 Hydration of Alkenes: Addition of H 2 O by Acid Catalyst

12.  For laboratory-scale hydration of an alkene  Use mercuric acetate and water in THF followed by sodium borohydride  Markovnikov orientation – No carbocation rearrangement  via mercurinium ion 8.4 Hydration of Alkenes: Addition of H 2 O by Oxymercuration - Demercuration

13. 8.5 Hydration of Alkenes: Addition of H2O by Hydroboration-Oxidation  Borane (BH 3 ) is electron deficient  Borane adds to an alkene to give an organoborane

14.  Addition of H-BH 2 (from BH 3 -THF complex) to three alkenes gives a trialkylborane  Oxidation with alkaline hydrogen peroxide in water produces the alcohol derived from the alkene Hydroboration-Oxidation Forms an Alcohol from an Alkene

15.  Regiochemistry is opposite to Markovnikov orientation  OH is added to carbon with most H’s  H and OH add with syn stereochemistry, to the same face of the alkene (opposite of anti addition) Orientation in Hydration via Hydroboration

16.  Borane is a Lewis acid  Alkene is Lewis base  Transition state involves anionic development on B  The components of BH 3 are added across C=C  More stable carbocation is also consistent with steric preferences Mechanism of Hydroboration

17.  Addition of H-H across C=C  Reduction in general is addition of H 2 or its equivalent  Requires Pt or Pd as powders on carbon and H 2  Hydrogen is first adsorbed on catalyst  Reaction is heterogeneous (process is not in solution) 8.6 Reduction of Alkenes: Hydrogenation

18.  Selective for C=C. No reaction with C=O, C=N  Polyunsaturated liquid oils become solids  If one side is blocked, hydrogen adds to other Hydrogen Addition - Selectivity

19.  Heterogeneous – reaction between phases  Addition of H-H is syn Mechanism of Catalytic Hydrogenation

20.  Epoxidation results in a cyclic ether with an oxygen atom  Stereochemistry of addition is syn 8.7 Oxidation of Alkenes: Epoxidation and Hydroxylation

21.  Hydroxylation - converts to syn-diol  Osmium tetroxide, then sodium bisulfite  Via cyclic osmate di-ester Osmium Tetroxide Catalyzed Formation of Diols

22.  Ozone, O 3, adds to alkenes to form molozonide  Molozonideis converted to ozonide that may be reduced to obtain ketones and/or aldehydes 8.8 Oxidation of Alkenes: Cleavage to Carbonyl Compounds

23.  Used in determination of structure of an unknown alkene Examples of Ozonolysis of Alkenes

24.  Oxidizing reagents other than ozone also cleave alkenes  Potassium permanganate (KMnO 4 ) can produce carboxylic acids and carbon dioxide if H’s are present on C=C Permangate Oxidation of Alkenes

25.  Reaction of a 1,2-diol with periodic (per-iodic) acid, HIO 4, cleaves the diol into two carbonyl compounds  Sequence of diol formation with OsO 4 followed by diol cleavage is a good alternative to ozonolysis Cleavage of 1,2-diols

26.  The carbene functional group is “half of an alkene”  Carbenes are electronically neutral with six electrons in the outer shell  They add symmetrically across double bonds to form cyclopropanes 8.9 Addition of Carbenes to Alkenes: Cyclopropane Synthesis

27.  Base removes proton from chloroform  Stabilized carbanion remains  Unimolecular elimination of Cl - gives electron deficient species, dichlorocarbene Formation of Dichlorocarbene

28.  Addition of dichlorocarbene is stereospecific cis Reaction of Dichlorocarbene

29.  Equivalent of addition of CH 2 :  Reaction of diiodomethane with zinc-copper alloy produces a carbenoid species  Forms cyclopropanes by cycloaddition Simmons-Smith Reaction

30.  A polymer is a very large molecule consisting of repeating units of simpler molecules, formed by polymerization  Alkenes react with radical catalysts to undergo radical polymerization  Ethylene is polymerized to polyethylene, for example 8.10 Radical Additions to Alkenes: Chain-Growth Polymers

31.  Initiation - a few radicals are generated by the reaction of a molecule that readily forms radicals from a nonradical molecule  A bond is broken homolytically Free Radical Polymerization: Initiation

32.  Radical from initiation adds to alkene to generate alkene derived radical  This radical adds to another alkene, and so on many times Polymerization: Propagation

33.  Chain propagation ends when two radical chains combine  Not controlled specifically but affected by reactivity and concentration Polymerization: Termination

34.  Other alkenes give other common polymers Other Polymers

35.  Severe limitations to the usefulness of radical addition reactions in the lab  In contrast to electrophilic additions, reactive intermediate is not quenched so it reacts again and again uncontrollably 8.11 Biological Additions of Radicals to Alkenes

36.  Biological reactions different from in the laboratory  One substrate molecule at a time is present in the active site of an enzyme  Biological reactions are more controlled, more specific than other reactions Biological Reactions

37. Pathway of Biosynthesis of Prostaglandins

38. Let’s Work a Problem Which Reaction would one predict to be faster, addition of HBr to cyclohexene or to 1-methylcyclohexene?

39. Answer First, draw out both reactants with HBr. What we should realize at this point is that the formation of the intermediate that is more stabilized via carbocation formation is the one that will form product faster. At this point, we should see that the intermediate formed via the 3˚ intermediate from 1-methylcyclohexene (as opposed to the 2˚ carbocation intermediate in the case of cyclohexene) will proceed faster.