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Nitrating Acetanilide and Methyl benzoate: Electrophilic Aromatic Substitution

Essay specific features

 

Issue:

Science

 

Written by:

Michael D

 

Date added:

February 23, 2016

 

Level:

University

 

Grade:

A

 

No of pages / words:

12 / 3275

 

Was viewed:

1232 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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General issues of this essay:
Economic effects on U.S. economy of removing all import restraints Resonance teen depression resulting in alcoholism Electrophilic Aromatic Iodination of Vanillin methyl orange Do Electrons Really Exist? Removing the Slave Mentality and Oppression through Violence Chapter 28: Nitration of Methyl Benzoate Electrons to Quarks Electrons Electrophilic addition electrons methyl bromide Nitrating Acetanilide and Methyl benzoate: Electrophilic Aromatic Substitution sodium benzoate food preservative
 

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