[PDF] 1 Chapter 11: Nucleophilic Substitution and Elimination Walden





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CHM 2520 Chimie organique II

mécanismes organiques (années 20 et 30). – principes importants: • nucléophile électrophile. • effet inductif



Substitution nucléophile et ?-élimination

LES TROIS GRANDS TYPES DE REACTIONS RENCONTREES DANS CE COURS DE CHIMIE ORGANIQUE. SN1 versus SN2 en fonction des variations structurales .



6. Réactions délimination

respectivement E1 et E2. mécanismes : on a donc compétition entre la SN1 et la E1. ... TABLEAU COMPARATIF DES MÉCANISMES SN1 E1



MÉCANISMES RÉACTIONNELS EN CHIMIE ORGANIQUE

Justifier le choix d'un mécanisme limite SN 1 ou SN 2 E1 ou E2 ; C/ Critère de choix entre mécanismes de type SN1 et de type SN2?





ue1 – chimie paris xii - fiche n°8 substitutions nucléophiles

Compétition entre SN1 et SN2 ?? . Exemples de SN2 (à connaître) . ... Plus le carbocation formé est stable plus la réaction de SN1 est rapide ?. E1. E2.



Exercices Complémentaires - Chapitre 7

type d'élimination (E1 ou E2) ? s'agira d'une SN1 via un carbocation : ... SN2. Et. CN. Me. H. + Cl. Réaction 2: Obtention d'un racémique : SN1 (B faux).



LES REACTIONS EN CHIMIE ORGANIQUE

? Mécanisme E1 . ? Mécanisme E2. Page 16. LES REACTIONS EN CHIMIE ORGANIQUE. V- REACTIVITE DES 



1 Chapter 11: Nucleophilic Substitution and Elimination Walden

mol•sec. Nucleophilic Substitution comes in two reaction types: SN2. SN1 Vinyl and aryl halides do not react in nucleophilc substitution reactions.



Cours de Chimie Organique I

Substitution nucléophile SN1 et SN2 ; substitution radicalire ; substitution électrophile



SN2 SN1 E2 & E1: Substitution and Elimination Reactions

SN2 SN1 E2 & E1: Substitution and Elimination Reactions l Nucleophilic Substitution Reactions - SN2 Reaction: •Reaction is: o Stereospecific (Walden Inversion of configuration) o Concerted - all bonds form and break at same time o Bimolecular - rate depends on concentration of both nucleophile and substrate •Substrate:



Practice Problems on SN1 SN2 E1 & E2 - Answers

2 For each of the chemical substitution reactions below identify the major products and whether the reaction is likely an S N1 or S N2 Br ethanol-water Br Cl 3 For each of the following compounds provide appropriate reactants and solvent systems to synthesize them by a substitution reaction

What is the relationship between SN1 and E1?

Under such neutral condition, S N 1 and E1 usually occur together for secondary substrates, and increasing the reaction temperature favors E1 over SN1.

Which pathway is used in SN2 reaction?

Since primary substrates are very good candidates for SN2 reaction, so SN2 is the predominant pathway when good nucleophile is used. The only exception is that when big bulky base/nucleophile is used, E2 becomes the major reaction.

How to predict E2 and E1 reactions?

You can also go over the stereoselectivity and stereospecificity of the E2 and E1 reactions. The reactivity of the substrate (alkyl halide), the effect of the solvent, and temperature should also be taken into consideration. 1. Predict the mechanism as SN1, SN2, E1 or E2 and draw the major organic product formed in each reaction.

Is tBuOH a SN1 reaction?

No base = S N 1/S N 2. Leaving group: OTf is a dynamite leaving group. Awesome LG = S N 1. Solvent: tBuOH is a polar protic solvent = S N 1. All of the factors point to an S N 1 reaction, therefore I feel comfortable saying it is an SN1 reaction.

1 Chapter 11: Nucleophilic Substitution and Elimination

Walden Inversion

OOH OH HO O (S)-(-) Malic acid [a] D = -2.3 ° PCl 5 OCl OH HO O Ag 2 O, H 2 O OOH OH HO O (R)-(+) Malic acid [a] D = +2.3 ° PCl 5 Ag 2 O, H 2 O OCl OH HO O (+)-2-Chlorosuccinic acid (-)-2-Chlorosuccinic acid The displacement of a leaving group in a nucleophilic substitution reaction has a defined stereochemistry

Stereochemistry of nucleophilic substitution

p-toluenesulfonate ester (tosylate): converts an alcohol into a leaving group; tosylate are excellent leaving groups. abbreviates as Tos CX Nu: CNu + X

X= Cl, Br, I

COH S O O Cl CH 3 COS O O CH 3 tosylate COS O O CH 3 Nu: CNu S O O O CH 3 2 The nucleophilic substitution reaction "inverts" the Stereochemistry of the carbon (electrophile)- Walden inversion O H

Tos-Cl

pyridine O H H Tos [a] D = +33.0 H 3 CO O H O OCH 3 [a] D = +31.1[a] D = -7.06 + TosO HO H O H [a] D = -33.2

Tos-Cl

pyridine H O Tos [a] D = -31.0 H 3 CO O O H OCH 3 HO TosO [a] D = -7.0

Kinetics of nucleophilic substitution

Reaction rate: how fast (or slow) reactants are converted into product (kinetics) Reaction rates are dependent upon the concentration of the reactants. (reactions rely on molecular collisions)

Consider:

At a given temperature:

If [OH

] is doubled, then the reaction rate may be doubled

If [CH

3 -Br] is doubled, then the reaction rate may be doubled A linear dependence of rate on the concentration of two reactants is called a second-order reaction (molecularity) CBr H H H HO _ CHO H H H Br _ 3 CBr H H H HO _ CHO H H H Br _ Reaction rates (kinetic) can be expressed mathematically: reaction rate = disappearance of reactants (or appearance of products)

For the disappearance of reactants:

rate = k [CH 3

Br] [OH

[CH 3

Br] = CH

3

Br concentration

[OH ] = OH concentration k= constant (rate constant) For the reaction above, product formation involves a collision between both reactants, thus the rate of the reaction is dependent upon the concentration of both. L mol•sec Nucleophilic Substitution comes in two reaction types: S N

2 S

N 1

S= substitutionS= substitution

N= nucleophilicN= nucleophilic

2= biomolecular1= unimolecular

rate = k [R-X] [Nu:]rate = k [R-X] 4 The S N

2 Reaction: Mechanism

Steric effects in the S

N

2 reaction:

• For an S N

2 reaction, the nucleophile approaches the electrophilic

carbon at an angle of 180 ° from the leaving group (backside attack) • the rate of the S N

2 reaction decrease as the steric hindrance

(substitution) of the electrophile increases. 5 CH 3 C CH 3 CH 3 BrCH 3 C CH 3 CH 3 CH 2 Br CH 3 C CH 3 H BrCH CH 3 H BrCH H H Br tertiaryneopentyl secondary primarymethyl realtive reactivity << 1150040,0002,000,000

Increasing reactivity in the S

N

2 reaction

Vinyl and aryl halides do not react in nucleophilc substitution reactions X R 1 R 2 R 3 + Nu: R 1 NuR 2 R 3 X X + Nu: X Nu X R 1 R 2 R 3 + (CH 3 2 CuLi CH 3 R 1 R 2 R 3

From Chapter 10:

NOT a nucleophilc

substitution reaction

The nature of the nucleophile in the S

N

2 Reaction:

The measure of nucleophilicity is imprecise.

Anionic

Neutral

Nu: + R-X Nu-R + X: _ _ Nu: + R-X Nu-R + X: _

Nu + H

3

C-Br Nu-CH

3 + Br

Nu = H

2

O relative reactivity= 1

CH 3 CO 2 500
NH 3 700
Cl 1,000 HO

16,000

CH 3 O

25,000

I

100,000

N≡C

125,000

HS

125,000

6

Nucleophiles are Lewis bases

Nucleophilicity roughly parallels basicity when comparing nucleophiles that have the same attacking atom

Nu: CH

3 O HO CH 3 CO 2 H 2 O relative reactivity: 25,000 16,000 500 1 pKa of the conj. acid: 15.5 15.7 4.7 -1.7 Nucleophilicity usually increases going down a column of the periodic chart. Thus, sulfur nucleophiles are more reactive than oxygen nucleophiles. I > Br > Cl Negatively charges nucleophiles are usually more reactive than neutral nucleophiles.

The role of the leaving group in S

N

2 reactions:

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