The reaction of benzene diazonium fluoroborate with aqueous sodium nitrite in the presence of copper leads to the formation of nitrobenzene. This reaction is a typical example of the Sandmeyer reaction, where a diazonium salt undergoes a substitution reaction in the presence of copper and sodium nitrite, forming a nitro group on the benzene ring.
The correct option is (E) : nitrobenzene
The reaction involves benzene diazonium fluoroborate (\(C_6H_5N_2BF_4\)) reacting with aqueous sodium nitrite (NaNO2) solution in the presence of copper.
This is a variation of the Sandmeyer reaction. The diazonium salt is converted to a nitro group (\(-NO_2\)). The reaction proceeds as follows:
\(C_6H_5N_2BF_4 + NaNO_2 \xrightarrow{Cu} C_6H_5NO_2 + N_2 + NaBF_4\)
Benzene diazonium fluoroborate reacts with sodium nitrite in the presence of copper to form nitrobenzene.
Therefore, the answer is nitrobenzene.
Which of the following amines does not give foul smell of isocyanide on heating with chloroform and ethanolic KOH ?
Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.