By drawing the structures of the methoxybenzene and benzoic acid we explain which products will be formed as a result of the reaction with nitronium ion in the electrophilic aromatic substitution reaction.
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By drawing the structures of the methoxybenzene and benzoic acid we explain which products will be formed as a result of the reaction with nitronium ion in the electrophilic
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- Draw the structure of methoxybenzene and explain which product will be formed as a result of the reaction with nitronium ion in electrophilic aromatic displacement reaction.Draw the structure of benzoic acid and explain which product will be formed as a result of the reaction with the nitronium ion in the electrophilic aromatic displacement reaction.Draw the benzoic acid structure and explain which products will be formed as a result of the reaction with the nitronium ion in the electrophilic aromatic displacement reaction.
- In electrophilic aromatic substitution reaction by drawing the structures of the compounds given below Explain which products will be formed as a result of the reaction with the nitronium ion.a)Methoxybenzeneb)Benzoic acidExplain which products will be formed as a result of the reaction with the nitronium ion in the electrophilic aromatic displacement reaction by drawing the structures of the compounds given below. methoxybenzene, benzoic acidUsing the concept of resonance, explain why the nitro group deactivates electrophilic aromatic substitution reactions, but facilitates nucleophilic aromatic substitution reactions.
- Which of the two aromatic rings of phenyl benzoate would undergo nitration? What is the structure of the product?Based on your knowledge of reactivity of substituted aromatic compounds, what do you hypothesize will be the major product of the competitive nitration reaction (methyl benzoate)?p-Fluoronitrobenzene is more reactive toward hydroxide ion than is p-chloronitrobenzene. What does this tell you about the rate-determining step for nucleophilic aromatic substitution?
- In an electrophilic aromatic substitution, the substitution pattern on the product is determine by the directing nature of the substituents on the ring. What controls the substitution pattern in a nucleophilic aromatic substitution reaction?Investigate the mechanism and reaction condition via which carbon side chains can be introduced into an aromatic ring via an electrophilic aromatic substitution process?For the following reaction scheme, identify by drawing the reagents b and d and the intermediate c that are formed in the synthesis of benzoic acid.