Using the data in the chart, which of the following would be a correct analysis?
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Prontosil is a compound produced by the coupled reaction of an aryldiazonium ion and an aromatic compound.
<h3>What are diazonium compounds?</h3>
These are organic compounds in which there are ionic interactions between the azo group (-N₂⁺) and an anion X⁻.
The general structure is RN₂⁺X⁻.
- R is the lateral chain that might be an aromatic ring, among other options.
- N₂⁺ is the azo group
- X⁻ is the anion
The azo group characterizes as being unstable and reactive. This property is because one of the N atoms has a positive charge.
-N⁺≡ N
<h3>What is the coupling reaction of aryldiazonium compounds?</h3>Aryldiazonium salt reactions can occur in two ways,
- Substitution reactions
- Coupling reactions
Coupling reactions are the aromatic electrophilic substitution, where the aryldiazonium ion acts as an electrophile for an activated aromatic compound to attack it.
The coupling reaction occurs at the azo group level.
In the exposed example,
- the benzene ring with sulfur bonded to oxygen atoms is the coupling component
- the benzene ring with NH₂ and the azo group is the diazonium ion
In the attached files you will find the drawings.
You can learn more about diazonium compounds at
The following reaction gives a product with the molecular formula C₄H₈O₂. The diagram of the structure of the product can be seen in the image attached below.
The reaction between C₂H₂(ONa)₂ and C₂H₄Br results in the formation of the product C₄H₈O₂ and 2NaBr.
This reaction undergoes an SN₂ mechanism since there is no stable carbocation formed. In the reaction -O⁻Na⁺ attacks the ortho position in C₂H₄Br to form C₄H₈O₂.
In SN₂ mechanism is a nucleophilic substitution reaction where one bond is formed while another one is broken simultaneously.
The mechanism for the reaction can be seen in the image attached below.
Learn more about nucleophilic substitution reaction here:
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