1. Chapter 11 Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations

2. Alkyl Halides React with Nucleophiles and Bases
Alkyl halides are polarized at the carbon-halide bond, making the carbon electrophilic
Nucleophiles will replace the halide in C-X bonds of many alkyl halides (reaction as Lewis base)
Nucleophiles that are Brønsted bases produce elimination

3. Why this Chapter?
Nucleophilic substitution, base induced elimination are among most widely occurring and versatile reaction types in organic chemistry
Reactions will be examined closely to see:
How they occur
What their characteristics are
How they can be used

4. 11.1 The Discovery of Nucleophilic Substitution Reactions
In 1896, Walden showed that (-)-malic acid could be converted to (+)-malic acid by a series of chemical steps with achiral reagents
This established that optical rotation was directly related to chirality and that it changes with chemical alteration
Reaction of (-)-malic acid with PCl5 gives (+)-chlorosuccinic acid
Further reaction with wet silver oxide gives (+)-malic acid
The reaction series starting with (+) malic acid gives (-) acid

5. Reactions of the Walden Inversion

6. Significance of the Walden Inversion
The reactions alter the array at the chirality center
The reactions involve substitution at that center
Therefore, nucleophilic substitution can invert the configuration at a chirality center
The presence of carboxyl groups in malic acid led to some dispute as to the nature of the reactions in Walden’s cycle

7. Kenyon and Phillips reaction demonstrating Walden’s inversion - Video
1) SN2 Nucleophilic Substitution Kenyon and Phillips reaction demonstrating Walden’s discovery. START 8:12 END 18:08

8. 11.2 The SN2 Reaction Reaction is with inversion at reacting center
Follows second order reaction kinetics
Ingold nomenclature to describe characteristic step:
S=substitution
N (subscript) = nucleophilic
2 = both nucleophile and substrate in characteristic step (bimolecular)

9. Kinetics of Nucleophilic Substitution
Rate (V) is change in concentration with time
Depends on concentration(s), temperature, inherent nature of reaction (barrier on energy surface)
A rate law describes relationship between the concentration of reactants and conversion to products
A rate constant (k) is the proportionality factor between concentration and rate
Example: for S converting to P
V = d[S]/dt = k [S]

10. Reaction Kinetics The study of rates of reactions is called kinetics
Rates decrease as concentrations decrease but the rate constant does not
Rate units: [concentration]/time such as mol/(L x s)
The rate law is a result of the mechanism
The order of a reaction is sum of the exponents of the concentrations in the rate law – the example is second order

11. SN2 Process
The reaction involves a transition state in which both reactants are together

12. SN2 Transition State
The transition state of an SN2 reaction has a roughly planar arrangement of the carbon atom and the remaining three groups

13. SN2 - Video
1) SN2 Reactions

14. Sn2 Stereochemistry - Video

15. 11.3 Characteristics of the SN2 Reaction
Sensitive to steric effects
Methyl halides are most reactive
Primary are next most reactive
Secondary might react
Tertiary are unreactive by this path
No reaction at C=C (vinyl halides)

16. Reactant and Transition State Energy Levels Affect Rate
Higher reactant energy level (red curve) = faster reaction (smaller G‡).
Higher transition state energy level (red curve) = slower reaction (larger G‡).

17. Steric Effects on SN2 Reactions
The carbon atom in (a) bromomethane is readily accessible
resulting in a fast SN2 reaction. The carbon atoms in (b) bromoethane (primary), (c) 2-bromopropane (secondary), and (d) 2-bromo-2-methylpropane (tertiary) are successively more hindered, resulting in successively slower SN2 reactions.

18. Order of Reactivity in SN2
The more alkyl groups connected to the reacting carbon, the slower the reaction

19. Steric Effects on SN2 Reactions - Video
1) Steric Hindrance

20. The Nucleophile Neutral or negatively charged Lewis base
Reaction increases coordination at nucleophile
Neutral nucleophile acquires positive charge
Anionic nucleophile becomes neutral
See Table 11-1 for an illustrative list

21. Relative Reactivity of Nucleophiles
Depends on reaction and conditions
More basic nucleophiles react faster
Better nucleophiles are lower in a column of the periodic table
Anions are usually more reactive than neutrals

22. The Leaving Group
A good leaving group reduces the barrier to a reaction
Stable anions that are weak bases are usually excellent leaving groups and can delocalize charge

23. Poor Leaving Groups
If a group is very basic or very small, it prevents reaction
Alkyl fluorides, alcohols, ethers, and amines do not typically undergo SN2 reactions.

24. The Solvent
Solvents that can donate hydrogen bonds (-OH or –NH) slow SN2 reactions by associating with reactants
Energy is required to break interactions between reactant and solvent
Polar aprotic solvents (no NH, OH, SH) form weaker interactions with substrate and permit faster reaction

25. The Nucleophile - Videos
1) [SN1] & [SN2] Structure-Reactivity: The Nucleophile
2) Nucleophilicity (Nucleophile Strength)
2) Nucleophilicity vs. Basicity

26. 11.4 The SN1 Reaction
Tertiary alkyl halides react rapidly in protic solvents by a mechanism that involves departure of the leaving group prior to addition of the nucleophile
Called an SN1 reaction – occurs in two distinct steps while SN2 occurs with both events in same step
If nucleophile is present in reasonable concentration (or it is the solvent), then ionization is the slowest step

27. SN1 Energy Diagram Rate-determining step is formation of carbocation
V = k[RX]
Rate-determining step is formation of carbocation

28. Rate-Limiting Step
The overall rate of a reaction is controlled by the rate of the slowest step
The rate depends on the concentration of the species and the rate constant of the step
The highest energy transition state point on the diagram is that for the rate determining step (which is not always the highest barrier)

29. Stereochemistry of SN1 Reaction
The planar intermediate leads to loss of chirality
A free carbocation is achiral
Product is racemic or has some inversion

30. SN1 in Reality
Carbocation is biased to react on side opposite leaving group
Suggests reaction occurs with carbocation loosely associated with leaving group during nucleophilic addition
Alternative that SN2 is also occurring is unlikely

31. Effects of Ion Pair Formation
If leaving group remains associated, then product has more inversion than retention
Product is only partially racemic with more inversion than retention
Associated carbocation and leaving group is an ion pair

32. The SN1 Reaction - Video
1) SN1 Reactions: Introduction to SN1 reactions

33. 11.5 Characteristics of the SN1 Reaction
Substrate
Tertiary alkyl halide is most reactive by this mechanism
Controlled by stability of carbocation
Remember Hammond postulate,”Any factor that stabilizes a high-energy intermediate stabilizes transition state leading to that intermediate”

34. Allylic and Benzylic Halides
Allylic and benzylic intermediates stabilized by delocalization of charge
Primary allylic and benzylic are also more reactive in the SN2 mechanism

35. Effect of Leaving Group on SN1
Critically dependent on leaving group
Reactivity: the larger halides ions are better leaving groups
In acid, OH of an alcohol is protonated and leaving group is H2O, which is still less reactive than halide
p-Toluenesulfonate (TosO-) is excellent leaving group

36. Nucleophiles in SN1
Since nucleophilic addition occurs after formation of carbocation, reaction rate is not normally affected by nature or concentration of nucleophile

37. Solvent in SN1
Stabilizing carbocation also stabilizes associated transition state and controls rate
Solvent effects in the SN1 reaction are due largely to stabilization or destabilization of the transition state

38. Polar Solvents Promote Ionization
Polar, protic and unreactive Lewis base solvents facilitate formation of R+
Solvent polarity is measured as dielectric polarization (P)
Nonpolar solvents have low P
Polar solvents have high P values

39. The Solvent Effects on Sn1 and Sn2 Reactions - Video

40. 11.6 Biological Substitution Reactions
SN1 and SN2 reactions are well known in biological chemistry
Unlike what happens in the laboratory, substrate in biological substitutions is often organodiphosphate rather than an alkyl halide

41. 11.7 Elimination Reactions of Alkyl Halides: Zaitsev’s Rule
Elimination is an alternative pathway to substitution
Opposite of addition
Generates an alkene
Can compete with substitution and decrease yield, especially for SN1 processes

42. Zaitsev’s Rule for Elimination Reactions
In the elimination of HX from an alkyl halide, the more highly substituted alkene product predominates

43. Mechanisms of Elimination Reactions
Ingold nomenclature: E – “elimination”
E1: X- leaves first to generate a carbocation
a base abstracts a proton from the carbocation
E2: Concerted transfer of a proton to a base and departure of leaving group

44. Zaitsev’s Rule for Elimination Reactions - Video
1) Zaitsev's Rule: Zaitsev's Rule for E2 and E1 reactions

45. 11.8 The E2 Reaction and the Deuterium Isotope Effect
A proton is transferred to base as leaving group begins to depart
Transition state combines leaving of X and transfer of H
Product alkene forms stereospecifically

46. Geometry of Elimination – E2
allows orbital overlap and minimizes steric interactions

47. E2 Stereochemistry
Overlap of the developing  orbital in the transition state requires periplanar geometry, anti arrangement

48. Predicting Product E2 is stereospecific
Meso-1,2-dibromo-1,2-diphenylethane with base gives cis 1,2-diphenyl
RR or SS 1,2-dibromo-1,2-diphenylethane gives trans 1,2-diphenyl

49. The E2 Reaction - Video 1) E2 Reactions: E2 Elimination Reactions
2) E2 Elimination: regioselectivity

50. 11.9 The E2 Reaction and Cyclohexene Formation
Abstracted proton and leaving group should align trans-diaxial to be anti periplanar (app) in approaching transition state
Equatorial groups are not in proper alignment

51. 11.10 The E1 and E1cB Reactions Competes with SN1 and E2 at 3° centers
V = k [RX], same as SN1

52. Comparing E1 and E2 Strong base is needed for E2 but not for E1
E2 is stereospecific, E1 is not
E1 gives Zaitsev orientation

53. E1cB (conjugate Base) Reaction
Takes place through a carbanion intermediate

54. E1Reaction - Video 1) E1 Reactions: E1 Elimination Reactions
2) E1 Elimination: regioselectivity and stereoselectivity

55. Stepwise Elimination Mechanisms: Review E1 and E1cb - Video

56. 11.11 Biological Elimination Reactions
All three elimination reactions occur in biological pathways
E1cB very common
Typical example occurs during biosynthesis of fats when 3-hydroxybutyryl thioester is dehydrated to corresponding thioester

57. 11.12 Summary of Reactivity: SN1, SN2, E1, E1cB, E2
Alkyl halides undergo different reactions in competition, depending on the reacting molecule and the conditions
Based on patterns, we can predict likely outcomes

58. Summary of Reactivity: SN1, SN2, E1, E2 - Video
1) Comparing E2 E1 Sn2 Sn1 Reactions
2) E2 E1 Sn2 Sn1 Reactions Example 2
3) E2 E1 Sn2 Sn1 Reactions Example 3

59. Let’s Work a Problem
Tell whether the following reaction will be SN1, SN2, E1, E1cB, or E2?

60. Answer
Let’s examine the reactant. butylBr is a 1˚ halide, the nucleophile (NaN3) is nonbasic, and the product is a SUBSTITUTION. This means that SN2 is the likely mechanism to produce the azide.