1 / 88

Preview of Chapter 7 Alkyl Halides and Nucleophilic substitution

Preview of Chapter 7 Alkyl Halides and Nucleophilic substitution. Alkyl Halides : R-X properties and reactions, preparation Substitution reaction mechanism S N 1 v.s. S N 2 - Properties and Selectivity. Assignment for the March 27 th Class. What is Hammond postulation?

zorion
Download Presentation

Preview of Chapter 7 Alkyl Halides and Nucleophilic substitution

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Preview of Chapter 7 Alkyl Halides and Nucleophilic substitution • Alkyl Halides : R-X • properties and reactions, preparation • Substitution reaction • mechanism • SN1 v.s. SN2 • - Properties and Selectivity

  2. Assignment for the March 27th Class. • What is Hammond postulation? • 2. What is the product and stereochemical outcome • of the reaction of (S)-2-bromobutane with -OH • a) through SN1 mechanism? • b) through SN2 mechanism? Your answers should be submitted to your TA On Thursday.

  3. Chapter 7 AlkylHalides and Nucleophilic Substitution

  4. Alkyl Halides and Nucleophilic Substitution Introduction to Alkyl Halides • Alkyl halides : organic molecules containing a halogen atom bonded to an sp3 hybridized carbon atom. • Alkyl halides are classified as primary (1°), secondary (2°), or tertiary (3°), depending on the number of carbons bonded to the carbon with the halogen atom. • The single most important factor that determines the reactivity of alkyl haide.

  5. Alkyl Halides and Nucleophilic Substitution Introduction to Alkyl Halides • Allylic halides : X bonded to the carbon atom adjacent to a C—C double bond. • Benzylic halides have X bonded to the carbon atom adjacent to a benzene ring.

  6. Alkyl Halides and Nucleophilic Substitution Introduction to Alkyl Halides • Vinyl halideshave a halogen atom (X) bonded to a C—C double bond. • Aryl halideshave a halogen atom bonded to a benzene ring.

  7. Alkyl Halides and Nucleophilic Substitution Nomenclature F: fluoro Cl: chloro Br: bromo I: iodo

  8. Alkyl Halides and Nucleophilic Substitution Nomenclature • Common names are often used for simple alkylhalides. chloroethane 2-iodo-2-methylpropane

  9. Alkyl Halides Physical Properties • weak polar molecules • dipole-dipole interactions • incapable of intermolecular hydrogen bonding.

  10. Alkyl Halides Physical Properties

  11. Alkyl Halides Interesting Alkyl Halides

  12. Alkyl Halides Interesting Alkyl Halides DichloroDiphenylTrichloroethane

  13. The Polar Carbon-Halogen Bond

  14. Alkyl Halides and Nucleophilic Substitution General Features of Nucleophilic Substitution • Three components are necessary in any substitution reaction. Lewis base Lewis acid

  15. Alkyl Halides and Nucleophilic Substitution General Features of Nucleophilic Substitution • Since the identity of the counterion is usually inconsequential, it is often omitted from the chemical equation. • When a neutral nucleophile is used, the substitution product bears a positive charge.

  16. Alkyl Halides and Nucleophilic Substitution General Features of Nucleophilic Substitution • when the substitution product bears a positive charge and also contains a proton bonded to O or N, • the initially formed substitution product readily loses a proton in a BrØnsted-Lowry acid-base reaction, forming a neutral product. • To draw any nucleophilic substitution product: • Find the sp3 hybridized carbon with the leaving group. • Identify the nucleophile, the species with a lone pair or  bond. • Substitute the nucleophile for the leaving group and assign charges (if necessary) to any atom that is involved in bond breaking or bond formation.

  17. Alkyl Halides and Nucleophilic Substitution The Leaving Group • For example, H2O is a better leaving group than HO¯ because H2O is a weaker base. • The more stable the leaving group X:¯, the better able it is to accept (accommodate) an electron pair.

  18. The Leaving Group • There are periodic trends in leaving group ability: Equilibrium will favor products of nucleophilic substitution when the leaving group is a weaker base than the in-coming nucleophile.

  19. Alkyl Halides and Nucleophilic Substitution The Leaving Group

  20. Alkyl Halides and Nucleophilic Substitution The Leaving Group

  21. Alkyl Halides and Nucleophilic Substitution The Leaving Group 21

  22. Alkyl Halides and Nucleophilic Substitution The Nucleophile • Nucleophiles v.s. bases • structurally similar: both have a lone pair or a  bond. They differ in what they attack.

  23. Alkyl Halides and Nucleophilic Substitution The Nucleophile • Basicity : a measure of how readily an atom donates its electron pair to a proton. It is characterized by an equilibrium constant, Ka in an acid-base reaction, making it a thermodynamic property. • Nucleophilicity: a measure of how readily an atom donates its electron pair to other atoms. It is characterized by a rate constant, k, making it a kinetic property.

  24. Alkyl Halides and Nucleophilic Substitution The Nucleophile • Nucleophilicity parallels basicity in three instances: • For two nucleophiles with the same nucleophilic atom, the stronger base is the stronger nucleophile. • The relative nucleophilicity of HO¯ and CH3COO¯, two oxygen nucleophiles, is determined by comparing the pKa values of their conjugate acids (H2O = 15.7, and CH3COOH = 4.8). HO¯ is a stronger base and stronger nucleophile than CH3COO¯. • 2. A negatively charged nucleophile is always a stronger nucleophile than its conjugate acid. • HO¯ is a stronger base and stronger nucleophile than H2O. • 3. Right-to-left-across a row of the periodic table, nucleophilicity increases as basicity increases:

  25. Alkyl Halides and Nucleophilic Substitution The Nucleophile – steric factor • Nucleophilicity does not parallel basicity when steric hindrance becomes important. • Steric hindrance : a decrease in reactivity resulting from the presence of bulky groups at the site of a reaction. • Steric hindrance decreases nucleophilicity but not basicity. • Sterically hindered bases that are poor nucleophiles are called nonnucleophilic bases.

  26. Alkyl Halides and Nucleophilic Substitution The Nucleophile – solvent effect • If the salt NaBr is used as a source of the nucleophile Br¯ in H2O, the Na+ cations are solvated by ion-dipole interactions with H2O molecules, and the Br¯ anions are solvated by strong hydrogen bonding interactions.

  27. Alkyl Halides and Nucleophilic Substitution The Nucleophile – solvent effect • protic solvents : compounds with OH or NH bond • In polar protic solvents, nucleophilicity increases down a column of the periodic table as the size of the anion increases. This is the opposite of basicity. • polar protic solvents

  28. Alkyl Halides and Nucleophilic Substitution The Nucleophile – solvent effect • Polar aprotic solvents also exhibit dipole—dipole interactions, but they have no O—H or N—H bonds. Thus, they are incapable of hydrogen bonding.

  29. Alkyl Halides and Nucleophilic Substitution The Nucleophile – solvent effect • Polar aprotic solvents solvate cations by ion—dipole interactions. • Anions are not well solvated because the solvent cannot hydrogen bond to them. These anions are said to be “naked”.

  30. Alkyl Halides and Nucleophilic Substitution • In polar aprotic solvents, nucleophilicity parallels basicity, and the stronger base is the stronger nucleophile. • Because basicity decreases as size increases down a column, nucleophilicity decreases as well. example CH3CH2CH2CH2-Br + N3-CH3CH2CH2CH2N3 + Br- Solvent CH3OH H2O DMSO DMF CH3CN HMPA Rel. rate 1 7 1300 2800 5000 2x105

  31. Alkyl Halides and Nucleophilic Substitution The Nucleophile

  32. Alkyl Halides and Nucleophilic Substitution Mechanisms of Nucleophilic Substitution In a nucleophilic substitution: Possible mechanisms [1] Bond making and bond breaking occur at the same time. In this scenario, the mechanism is comprised of one step. In such a bimolecular reaction, the rate depends upon the concentration of both reactants, that is, the rate equation is second order.

  33. Alkyl Halides and Nucleophilic Substitution Mechanisms of Nucleophilic Substitution [2] Bond breaking occurs before bond making. In this scenario, the mechanism has two steps and a carbocation is formed as an intermediate. Because the first step is rate-determining, the rate depends on the concentration of RX only; that is, the rate equation is first order.

  34. Alkyl Halides and Nucleophilic Substitution Mechanisms of Nucleophilic Substitution [3] Bond making occurs before bond breaking. This mechanism has an inherent problem. The intermediate generated in the first step has 10 electrons around carbon, violating the octet rule. Because two other mechanistic possibilities do not violate a fundamental rule, this last possibility can be disregarded.

  35. Alkyl Halides and Nucleophilic Substitution Mechanisms of Nucleophilic Substitution Kinetic data show that the rate of reaction [1] depends on the concentration of both reactants, which suggests a bimolecular reaction with a one-step mechanism. SN2 (substitution nucleophilic bimolecular) mechanism.

  36. Alkyl Halides and Nucleophilic Substitution Mechanisms of Nucleophilic Substitution Kinetic data show that the rate of reaction [2] depends on the concentration of only the alkyl halide. This suggests a two-step mechanism in which the rate-determining step involves the alkyl halide only. SN1 (substitution nucleophilic unimolecular) mechanism.

  37. Alkyl Halides and Nucleophilic Substitution SN2 Mechanism Kinetics Rate = k[CH3Br][CH3COO-] one step mechanism

  38. Alkyl Halides and Nucleophilic Substitution SN2 Mechanism backside attack

  39. Alkyl Halides and Nucleophilic Substitution SN2 Mechanism -- stereochemistry Frontside attack : Nu approaches from the same side as the leaving group Backside attack : Nu approaches from the opposite side as the leaving group

  40. Alkyl Halides and Nucleophilic Substitution SN2 Mechanism -- stereochemistry • All SN2 reactions proceed with backside attack of the nucleophile, resulting in inversion of configuration at a stereogenic center. 41

  41. Alkyl Halides and Nucleophilic Substitution SN2 Mechanism -- stereochemistry R S R S

  42. Alkyl Halides and Nucleophilic Substitution SN2 Mechanism -- stereochemistry 43

  43. Alkyl Halides and Nucleophilic Substitution Influence of Identity of R group on SN2 reactions • Methyl and 1° alkyl halides undergo SN2 reactions with ease. • 2° Alkyl halides react more slowly. • 3° Alkyl halides do not undergo SN2 reactions. • This order of reactivity can be explained by steric effects. Steric hindrance caused by bulky R groups makes nucleophilic attack from the backside more difficult, slowing the reaction rate.

  44. Alkyl Halides and Nucleophilic Substitution Influence of Identity of R group on SN2 reactions Substrate (CH3)3CBr (CH3)3CCH2Br (CH3)2CHBr CH3CH2Br CH3Br 3o hindered 1o 2o 1o methyl (neopentyl) Rel. rate <1 1 500 4 x 104 2 x 106

  45. Alkyl Halides and Nucleophilic Substitution Influence of Identity of R group on SN2 reactions

  46. Alkyl Halides and Nucleophilic Substitution

  47. Alkyl Halides and Nucleophilic Substitution Application: Useful SN2 Reactions

  48. Alkyl Halides and Nucleophilic Substitution Application: Useful SN2 Reactions SN2 reaction in Nature Nucleophilic substitution reactions are important in biological systems as well. methylation

More Related