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  1. Dienes, Conjugation and Aromatic Compounds
  2. Reactions with Benzene
  3. Hydrogenation of Benzene
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1,2-Dienes
Conjugated Systems
Diels-Alder Reaction
Aromatic Compounds
Reactions with Benzene
Birch Reduction of Benzene
Hydrogenation of Benzene
Diels-Alder with Aromatic Molecules
Deuterium Substitution of Benzene
Sulfonation of Benzene
Nitration of Benzene
Halogenation of Benzene
Friedel-Crafts Alkylation
Friedel-Crafts Alkylation Example
Friedel-Crafts Acylation
Formation of Benzenediazonium Chloride
Reactions with Benzenediazonium Chloride
Electrophilic Substitution of Pyrrole and Pyridine
Ortho, Meta and Para Substitution
Ortho-Para Substitution Example
Meta Substitution Example
Inductive Effects in Electrophilic Substitution
Nucleophilic Addition of Benzene
Nucleophilic Addition to Benzene Example
Synthesis Reactions with Benzene (1)
Synthesis Reactions with Benzene (2)

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Hydrogenation of Benzene

Content Provider AK Lectures
Description Although hydrogenation of benzene does take place, it only takes place under conditions of either high temperature or high pressure and in the presence of a very active catalyst. This is because benzene is stabilized by the delocalization of electron density around its six carbons and is said to be aromatic. As a result of its high activation energy, the reaction will not take place at a considerable rate under normal conditions and that is why a high energy condition (high temperature) must be used for the reaction to actually take place. Although the reaction is exothermic, it is not nearly as exothermic as it should be. This is once again due to the fact that benzene is aromatic.
Language English
Access Restriction Open
Subject Keyword Organic Chemistry delocalization catalyst carbons activation energy pressure presence hydrogenation
Content Type Video
Educational Role Teacher Student
Educational Use Self Learning Lecture Reading
Resource Type Video Lecture
Education Level Under Graduate
Subject Organic chemistry
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