This experiment focuses on the concept of electrophilic aromatic substitution, which is a type of benzene reaction. This reaction consists usually of benzene and an electrophile. The role of the nucleophile is played by the double bond on the benzene ring. IT will react will the electrophile and this reaction will form a carbon cation intermediate. With additional reactions with a base, the electrophile fundamentally replaces the hydrogen of the benzene. Benzene is classified as one of the countless aromatic molecules, and this is just a plain benzene molecule. A different type of aromatic molecule will consist of different molecular structures, while the difference in their arrangement will give different properties. With regards to our lab, the aromatic samples hold a single distinct discrepancy. They all consist of different functional groups. As mentioned in previous lab reports, functional groups are the chemical components on an organic molecule. These particular components of the molecules institute the chemical properties of the molecule. Furthermore, the functional groups have fundamental role during the electrophilic aromatic substitution. It impinges on the reaction in two ways: the rate of the reaction and the directional control. In relation to this specific lab, we will zero in on the directional control of aromatic substances (nitration of bromobenzene).
The directional control of benzene is inclined by the functional groups and the dissimilarity in the functional groups will cause the electrophile of the aromatic substance to react in a specific manner. As on example, the reaction in our lab is a mono-substitution reaction. In simpler words, one electrophile group is substituted for a proton of the benzene ring. And because of the specificity of aromatic substances, the electrophile is capable of binding to certain areas of the ring. In the monos-substitution reaction, the electrophile has the potentiality to bind to three areas. With these...
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