When 2,4-Dinitrochlorobenzene Is Treated with Sodium Hydroxide at 100°C Followed

question 19

Multiple Choice

When 2,4-dinitrochlorobenzene is treated with sodium hydroxide at 100°C followed by protonation ________.

• A) 2,4-dinitrophenol is formed via an addition-elimination nucleophilic aromatic substitution mechanism
• B) 2,4-dinitrophenol is formed via an elimination-addition nucleophilic aromatic substitution mechanism
• C) 3,5-dinitrophenol is formed via an elimination-addition nucleophilic aromatic substitution mechanism
• D) 3,5-dinitrophenol is formed via an electrophilic aromatic substitution mechanism
• E) 2,4-dinitrophenol is formed via an electrophilic aromatic substitution mechanism

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