FACTOID # 29: Qataris have lots and lots of gas.
 
 Home   Encyclopedia   Statistics   Countries A-Z   Flags   Maps   Education   Forum   FAQ   About 
 
WHAT'S NEW
RECENT ARTICLES
More Recent Articles »
 

SEARCH ALL

FACTS & STATISTICS    Advanced view

Search encyclopedia, statistics and forums:

 

 

(* = Graphable)

 

 


Encyclopedia > Electrophilic substitution reaction

An electrophilic aromatic substitution is a chemical reaction in which a hydrogen atom of an aromatic ring is replaced by an electrophile. When the electrophile approaches the aromatic ring, the electrons are displaced. The structure gets charged due to electromeric/mesomeric effect. This leads to the formation of a pi-complex. Formation of a complex is followed by the formation of Sigma Complex. The Sigma Complex is stable due to resonance taking place.


The Attacking Groups can be classified as:

  1. Activating Groups

Five membered heterocyclic compounds

These compounds undergo aromatic electrophilic substitution reactions under much milder conditions.


  Results from FactBites:
 
JEE Syllabus : IIT JEE Syllabus (1806 words)
Preparation, properties and reactions of alkanes: Homologous series, physical properties of alkanes (melting points, boiling points and density); Combustion and halogenation of alkanes; Preparation of alkanes by Wurtz reaction and decarboxylation reactions.
Reactions of benzene: Structure and aromaticity; Electrophilic substitution reactions: halogenation, nitration, sulphonation, Friedel-Crafts alkylation and acylation; Effect of o-, m- and p-directing groups in monosubstituted benzenes.
Phenols: Acidity, electrophilic substitution reactions (halogenation, nitration and sulphonation); Reimer-Tieman reaction, Kolbe reaction.
Aromatic Reactivity (2788 words)
A demonstration of bromine substitution and addition reactions is helpful at this point, and a virtual demonstration may be initiated by clicking here.
This activation or deactivation of the benzene ring toward electrophilic substitution may be correlated with the electron donating or electron withdrawing influence of the substituents, as measured by molecular dipole moments.
A practical concern in the use of electrophilic aromatic substitution reactions in synthesis is the separation of isomer mixtures.
  More results at FactBites »


 

COMMENTARY     


Share your thoughts, questions and commentary here
Your name
Your comments
Please enter the 5-letter protection code

Want to know more?
Search encyclopedia, statistics and forums:

 


Lesson Plans | Student Area | Student FAQ | Reviews | Press Releases |  Feeds | Contact
The Wikipedia article included on this page is licensed under the GFDL.
Images may be subject to relevant owners' copyright.
All other elements are (c) copyright NationMaster.com 2003-5. All Rights Reserved.
Usage implies agreement with terms.