universidade de sÃo paulo - uspnequimed.iqsc.usp.br/files/2012/03/a31.pdf · march's advanced...
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![Page 1: UNIVERSIDADE DE SÃO PAULO - USPnequimed.iqsc.usp.br/files/2012/03/A31.pdf · MARCH'S ADVANCED ORGANIC CHEMISTRY REACTIONS, MECHANISMS, AND STRUCTURE FIFTH EDITION Michael B. Smith](https://reader033.vdocuments.mx/reader033/viewer/2022052408/5f07e5387e708231d41f4b6f/html5/thumbnails/1.jpg)
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UNIVERSIDADE DE SÃO PAULO - USP
Instituto de Química de São Carlos - IQSC
Grupo de Química Medicinal do IQSC/USP
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Nucleophilic Substitution MECHANISMS The SN2 Mechanism. The SN1 Mechanism Ion Pairs in the SN1 Mechanism Mixed SN1 and SN2 Mechanisms The Neighboring-Group Mechanism Neighboring-Group Participation by π and Bonds: Nonclassical Carbocations : Nucleophilic Substitution at an Allylic Carbon: Allylic Rearrangements Nucleophilic Substitution at an Aliphatic Trigonal Carbon: The Tetrahedral Mechanism REACTIVITY The Effect of Substrate Structure The Effect of the Attacking Nucleophile The Effect of the Leaving Group The Effect of the Reaction Medium Phase-Transfer Catalysis Ambident Nucleophiles: Regioselectivity Ambident Substrates REACTIONS
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Bibliography MARCH'S ADVANCED ORGANIC CHEMISTRY REACTIONS, MECHANISMS, AND STRUCTURE FIFTH EDITION Michael B. Smith Professor of Chemistry, University of Connecticut Jerry March Professor of Chemistry, Adelphi University
Advanced Organic Chemistry FOURTH EDITION Part A: Structure and Mechanisms FRANCIS A. CAREY and RICHARD J. SUNDBERG University of Virginia Charlottesville, Virginia
Eugene E. Kwan e David A. Evans Harvard University. 2010, 2006
Introduction to SN
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Representative Nucleophilic Substitution Reactions
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The SN2 Mechanism
Second-order kinetics
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Walden examples
Phillips, Kenyon, and co-workers.
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SN2
MO description of SN2 TS
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The SN1 Mechanism
First-order kinetics
Reaction energy profile for
nucleophilic substitution by the ionization SN 1 mechanism.
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Potential Energy Diagram Hammond Postulate
Solvent effects Solid line: polar solvent.
Dashed line: nonpolar solvent
(a) R–X → R+ + X−
Polar solvents increase the rate by
stabilization of the Rδ+- - -Xδ − TS.
(b) R–X+→R+ + X
Polar solvents decrease the rate because
stabilization of R- - δ +- -X TS is less than for
the more polar
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Ion pair
Detailed mechanism
Support to scheme
At 100 oC, kex/krac = 2.3
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ERG favors exchange
Isotopic scrambling with no racemization
Avoids a carbocation intermediate but requires a front-side displacement!
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Schematic relationship between reactants,
ion pairs, and products in substitution
proceeding through ion pairs.
The gradation from SN1 to SN 2 mechanisms
can be summarized in terms of the shape of the potential energy diagrams for the reactions
SN1limiting
mechanism SN2 limiting
mechanism SN2 intermediate
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Jencks: reaction energy profiles showing decreasing
carbocation stability in change from SN1(lim) to SN2(lim) mechanisms.
An example of a coupled displacement:
the “exploded” SN2 TS.
Second-order kinetics with a substantially ρ+
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Stereochemistry of Nucleophilic
Substitution Reactions
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Stereochemical, kinetic, and isotope effects
on solvolysis reactions of 1-phenylethyl chloride in several solvent systems
Structural and Solvation Effects on Reactivity Characteristics of Nucleophilicity
1. Strong solvation lowers the energy of an anionic nucleophile relative to
the TS, in which the charge is more diffuse, and results in an increased Ea.
2. Because the SN 2 process is concerted, the strength of the partially formed
new bond is reflected in the TS.
3. A more electronegative atom binds its electrons more tightly than a less
electronegative one.
4. Polarizability describes the ease of distortion of the electron density of the
nucleophile.
5. A sterically congested nucleophile is less reactive than a less hindered one.
The trigonal bipyramidal geometry of the SN 2 transition state is sterically more
demanding than the tetrahedral reactant so steric interactions increase as the TS
is approached.
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Nucleophilic constant, n, defined by Swain and Scott
Effect of Solvation on Nucleophilicity In protic hydrogen-bonding solvents, anions are
subject to strong interactions with solvent.
Hard nucleophiles are more strongly solvated
by protic solvents than soft nucleophiles, and this
difference contributes to the greater nucleophilicity
of soft anions in such solvents.
Nucleophilic substitution reactions of anionic
nucleophiles usually occur more rapidly in polar
aprotic solvents than they do in protic
solvents, owing to the fact that anions are weakly solvated in such solvents
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Common polar aprotic solvents
But, in methanol, the relative reactivity order
N3 − > I− > CN−> Br− > Cl−
Becomes, in DMSO CN− > N3
− > Cl− > Br− > I−
The nucleophilicity of the solvent. The Winstein-Grunwald equation
Standard reactant l = 1.00; Standard solvent N = 0.00, for solvolysis of t-butyl chloride.
The scale has also been assigned for 2-adamantyl tosylate. Ethanol-water in the ratio 80:20 is taken as the standard solvent.
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Leaving group effects Relative Solvolysis Rates of 1-Phenylethyl Esters and Halides
Relative rates of solvolysis of 1-phenylethyl esters and
halides in 80% aqueous ethanol at 75 oC.
Ionization exhibits greater dependence on LG
Tosylate/Bromide Rate Ratios for Solvolysis of RX in 80% Ethanola
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Relative Reactivity of Leaving Groups in SN2 Substitution Reactions
A poor leaving group can be made more reactive by coordination to an electrophile.
It is endothermic by 16 kcal mol-1
N2 best LG
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Steric & strain effects Rate Constants for Nucleophilic Substitution of Primary Alkyl Bromides and Tosylates
A high CH3/H rate ratio is expected if nucleophilic participation is
weak and stabilization of the cationic nature of the TS is important.
In contrast to SN2 reactions, rates of reactions involving
TSs with cationic character increase with substitution.
Effects of conjugation
For example, allyl chloride is 33 times more reactive
than ethyl chloride toward iodide ion in acetone!
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α-Substituent Effect
Substituent Effects of α-EWG Substituents
Steric effects may be responsible for part of the observed acceleration.
Stabilizing π orbital TS
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Neighboring-Group Participation
The rates of solvolysis of the cis and trans isomers of 2-acetoxycyclohexyl p-toluenesulfonate differ by a factor of about 655!
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The π electrons of C=C can also become involved in SN
It is more reactive by a factor of about 1011 than
the saturated analog toward acetolysis
It reacts 107 times slower than the anti isomer.
Mechanism of Rearrangements of Carbocations
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The 2-butyl cation
The methyl-bridged ion is only slightly less stable.
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The 2-butyl to t-butyl rearrangement gives the following energy surface
A: H-bridged; B: methyl-bridged; C: Edge protonated methycyclopropane; D: classical secondary; E: classical primary; F: tertiary.
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The Norbornyl Cation Nonclassical Carbocations
The exo-brosylate is more reactive than the endo isomer by a factor of 350.
Racemic!
The plane of symmetry: intermediate explains racemic
product
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Nucleophilic Substitution at an Aliphatic Trigonal Carbon:
The Tetrahedral Mechanism
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Evidence
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Phase-Transfer Catalysis
1. Quaternary Ammonium or Phosphonium Salts.
2. Crown Ethers and Other Cryptands (no water needed)
Ambident Nucleophiles: Regioselectivity
1. Ions of the Type. —CO—C:-R—CO—
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Ambident Substrates
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Exercício do dia
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