Reactivity Arenes

Benzene is resistant to addition reactions. Adding something new to the ring would require that some of the delocalized electrons form bonds with the substituent being added, resulting in a major loss of stability because the delocalization is broken. Instead, benzene primarily undergoes substitution reactions - replacing one or more of the hydrogen atoms with a new substituent, preserving the delocalized electrons as they were.

The reactivity of a compound like methylbenzene must be considered in two distinct parts:

For example, if you explore other pages in this section, you will find that alkyl groups attached to a benzene ring are oxidized by alkaline potassium manganate(VII) solution. This oxidation does not occur in the absence of the benzene ring. The tendency of the CH₃ group to "push" electrons away from itself also has an effect on the ring, making methylbenzene react more quickly than benzene itself. You will find this explored in other pages in this section as well.

مواضيع ذات صلة

مركبات الآزو متجانسة الحلقة Homocyclic azo compounds

تصنيف مركبات الآزو Classification of azo compound

أصباغ الآزو Azo Dye

تفاعلات الازدواج Reaction Coupling

أملاح الدايازونيوم الاروماتية      Aromtic Diazonium Salt    

أهمية الكواشف العضوية reagents Importance of organic

الثايوزبينات Thiazepines

الدايازبينات Diazepines

الاوكسازبينات Oxazepines

المركبات الحلقية غير المتجانسة Heterocyclic Compounds

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بعض مظاهر كيمياء الكلورامين-T