Which dedicated named reaction strictly safely converts benzene diazonium chloride cleanly into high β Haloalkanes and Haloarenes Chemistry Question
Question
Which dedicated named reaction strictly safely converts benzene diazonium chloride cleanly into highly stable fluorobenzene using fluoroboric acid ($HBF_4$)?
Answer: B
π‘ Solution & Explanation
The Balz-Schiemann reaction involves precipitating benzene diazonium fluoroborate ($Ph-N_2^+BF_4^-$). Gently heating this dried, stable salt chemically safely liberates $N_2$ and $BF_3$, yielding pure fluorobenzene.
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