The direct chemical fluorination of benzene is highly violent and unpredictable. What specialized na β Amines Chemistry Question
Question
The direct chemical fluorination of benzene is highly violent and unpredictable. What specialized named reaction utilizes a diazonium intermediate to successfully synthesize fluorobenzene in a highly controlled manner?
Answer: C
π‘ Solution & Explanation
The Baltz-Schiemann reaction precisely utilizes benzene diazonium chloride. It is first treated with cold fluoroboric acid ($HBF_4$) to precipitate the highly stable diazonium fluoroborate salt. This specific salt is then carefully isolated and strongly heated until it physically decomposes into fluorobenzene, expelling $BF_3$ and $N_2$ gas.
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