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Nucleophilic Aromatic Substitution - Aryl Halides: Electron Withdrawing Groups Ortho or para To The Site of

Nucleophilic aromatic substitution reactions involve an aromatic halide reacting with a nucleophile to replace the halide. [1] Electron withdrawing groups ortho or para to the site of attack activate the aryl halide by stabilizing the intermediate carbanion. [2] In the absence of such groups, the reaction occurs through an elimination/addition mechanism rather than SN1 or SN2, forming the unstable intermediate benzyne. [3] Experimental evidence shows this leads to a 50:50 mixture of products, distinguishing it from the carbanion mechanism.

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Ananda Vijayasarathy
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73 views4 pages

Nucleophilic Aromatic Substitution - Aryl Halides: Electron Withdrawing Groups Ortho or para To The Site of

Nucleophilic aromatic substitution reactions involve an aromatic halide reacting with a nucleophile to replace the halide. [1] Electron withdrawing groups ortho or para to the site of attack activate the aryl halide by stabilizing the intermediate carbanion. [2] In the absence of such groups, the reaction occurs through an elimination/addition mechanism rather than SN1 or SN2, forming the unstable intermediate benzyne. [3] Experimental evidence shows this leads to a 50:50 mixture of products, distinguishing it from the carbanion mechanism.

Uploaded by

Ananda Vijayasarathy
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Nucleophilic Aromatic Substitution — Aryl Halides

Ar-X + :Nu > Ar-Nu + :X

Electron withdrawing groups ortho or para to the site of


attack activate the aryl halide toward nucleophilic
substitution —
Cl OH Cl OH

aq. NaOH aq. NaOH


350o 160o

NO2 NO2

Cl OH Cl OH
NO2 NO2 NO2 NO2 NO2 NO2
aq. Na2CO3 H2O
130o warm

NO2 NO2 NO2 NO2

These nucleophilic substitutions do not take place by SN1


or SN2 mechanisms ---
Cl SN1 leads to
X + Cl
-
unstable phenyl
S N 1 O N
O2N 2
sp2 orbital, carbocation.
unstable carbocation

Cl SN2 requires
X HO + Cl
-
backside attack:
O2N - SN2 O2N bad geometry!
HO


A more feasible mechanism –
addition-elimination also known as SNAr —

A Carbanion

Cl
OH
O
N
major
O
contributor
OH

Cl Cl Cl
Cl
OH OH OH
slow
O2N O N O N O N
O O O

Cl OH
OH fast + Cl
Etc.
O2N O 2N

It turns out that this mechanism does NOT operate in the


absence of powerful electron withdrawing groups ortho
and/or para to the site of nucleophilic attack. Electron
withdrawing groups stabilize the carbanion intermediate
and the transition state leading to it; when they are not
present the Meisenheimer carbanion does not form.


In the absence of electron withdrawing groups o/p to the
site of nucleophilic attack reaction takes place by an
elimination/addition sequence; this only happens with
strong bases or vigorous conditions —
Cl Cl + Cl

H OH + H 2O benzyne

H + OH
H OH
OH
OH OH

Benzyne is a reactive, unstable 


intermediate. The 6 aromatic π  

π

electrons have been shown as a 


circle here to emphasize that the 
new π bond is not part of the 
  

 
aromatic system, but is at right π
   



angles to it and lies in the plane
of the carbon atoms. This π bond is highly reactive,
having been formed from the not-so-parallel joining of two
sp2 (not p) orbitals.

Benzyne may form in a two-step process, as shown


above, or the hydrogen and halogen may depart
simultaneously, as in an E2 elimination.


Experimental evidence for elimination/addition in the
absence of electron withdrawing groups o/p to nucleophilic
attack —
$  
"# "# "#
! ! !  
  %




Elimination/addition leads to the 50:50 mixture as shown


below; the carbanion mechanism would lead only to the
first product.
     

     

     
 
  
  

        
  
 

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