Interaction | Reaction | Process     Data Page

The amine base abstracts a proton to form a stabilised carbanion which then spontaneously fragments. This step is rate limiting.
  +  
(CH3)3N
         
  +  
[CN]–
  +  
[(CH3)3NH]+
Reactant Page Go To Go To
1-Phenyl-1,1,2,2-tetracyanoethane     Reactions Using    Reactions Forming
Trimethylamine     Reactions Using    Reactions Forming
Phenyl tricyanoethene     Reactions Using    Reactions Forming
Cyanide ion     Reactions Using    Reactions Forming
Trimethylammonium ion     Reactions Using    Reactions Forming

Interaction, Reaction, Process defined as:
Decomplexation or Fragmentation
Elimination
Elimination: First Order Carbanion Mechanism
Eliminations 2: The E1, E1cb, E2, and Ei Mechanisms

© Mark R. Leach 1999 –

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