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Nitrating Acetanilide and Methyl benzoate: Electrophilic Aromatic Substitution
Essay specific features
Written by:
Michael D
Date added:
February 23, 2016
Level:
University
Grade:
A
No of pages / words:
12 / 3275
Was viewed:
1288 times
Rating of current essay:
Essay content:
Crystallization was used to purify the product. The melting point was used to determine its purity and the regiochemistry of the products. The methyl benzoate reaction product, methyl nitrobenzoate, was determined to be meta-substituted and the acetanilide reaction product, nitroacetanilide, was determined to be para-substituted...
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This reaction allows for the introduction of other functional groups onto the aromatic ring. The electrophile attacks the aromatic ring at the aliphatic position removing two electrons destabilizing the aromatic ring, but creating a resonance-stabilized carbocation called a sigma complex (arenium ion)...
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