Question
Question: Phenyl cyanide on reduction with \(Na/{C_2}{H_5}OH\) yields: A.\({C_6}{H_5}C{H_2}N{H_2}\) B.\({C...
Phenyl cyanide on reduction with Na/C2H5OH yields:
A.C6H5CH2NH2
B.C6H5NHCH3
C.
D.C6H5NH2
Solution
When phenyl cyanide C6H5CN is reacted with sodium ethanol Na/C2H5OH a simple reduction reaction occurs in which cyanide (−CN) is reduced. So, we should know about the basic reduction reaction of cyanides.
Complete step by step answer:
First, we will understand the basics of a reaction. The given question says that phenyl cyanide which is also known as benzonitrile cyanides are used to be termed as nitriles undergo a reduction in the presence of sodium ethanol Na/C2H5OH which acts as a reducing agent in the reaction. So, we can represent the following reaction using proper symbols and representations as given below.
C6H5CNNa/C2H5OHC6H5CH2NH2
From the above reduction reaction, we can observe that phenyl cyanide also known as benzonitrile is a reactant and is represented as C6H5CN. Now when phenyl cyanide undergoes a reduction in the presence of sodium ethanol which is represented as Na/C2H5OH. Due to the presence of sodium ethanol, the cyanide attached with the benzene ring is reduced to a primary aromatic amine. The final product of the reduction reaction is benzylamine which is a primary aromatic amine and the chemical formula is C6H5CH2NH2. So, we can conclude that Phenyl cyanide on reduction with Na/C2H5OH yields benzylamine C6H5CH2NH2.
Therefore, the correct option is (A).
Additional information:
Here we will discuss some basic preparation of amines. One of the most basic preparations of primary aromatic amine is the reaction of ammonia with an alkyl halide. The primary amine can also be obtained using Gabriel phthalimide synthesis.
Note:
Phenyl cyanide or benzonitrile is a colorless liquid with an almond-like odor. Generally, it is used as the specialty solvent and for the production of other chemicals. In Na/C2H5OH sodium, the metal reacts easily to give off bubbles of hydrogen gas.