Direct fluorination of benzene is highly violent. What specialized named reaction utilizes a diazoni β Amines Chemistry Question
Question
Direct fluorination of benzene is highly violent. What specialized named reaction utilizes a diazonium intermediate to successfully synthesize fluorobenzene?
Answer: C
π‘ Solution & Explanation
The Baltz-Schiemann reaction treats benzene diazonium chloride with cold fluoroboric acid ($HBF_4$) to precipitate the diazonium fluoroborate salt. This salt is then heated until it physically decomposes into fluorobenzene, expelling $BF_3$ and $N_2$.
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