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
Correct Answer:

Verified
Correct Answer:
Verified
Q14: Provide the major organic product of the
Q15: Provide the major organic product of the
Q16: Provide the major organic product of the
Q17: Name the major organic product which results
Q18: In electrophilic aromatic substitution reactions the hydroxyl
Q20: Which of the following species is attacked
Q21: Provide the major organic product of the
Q22: In electrophilic aromatic substitution reactions, a cyano
Q23: Show what reagents are needed to complete
Q24: Provide the major organic product of the