Question
Question: The Compound A on treatment with Na gives B, and with \({\text{PC}}{{\text{l}}_{\text{5}}}\) gives C...
The Compound A on treatment with Na gives B, and with PCl5 gives C. B and C react together to give diethyl ether. A, B and C are in the order.
A.C2H5Cl , C2H6 , C2H5OH
B.C2H5OH , C2H6 , C2H5Cl
C.C2H5OH ,C2H5ONa , C2H5Cl
D.C2H5OH ,C2H5Cl , C2H5ONa
Solution
To solve this question the knowledge of alcohol is required. Any alcohol would react with alkali metals to form salt of the form (ROM) where R is the alkyl group, O is Oxygen of alcohol and M is the alkali metal. This salt when it reacts with PCl5 , the (−ONa) group is replaced by the chloride group.
Complete step by step answer:
The reaction given in the question is Williamson synthesis reaction. In the reaction, an alcohol reacts with an alkali metal to form a salt. The reaction goes as follows:
ROH+Na→RONa
As the R group given in the question is C2H5 , the reaction will be:
C2H5OH+Na→C2H5ONa
When an alcohol reacts with PCl5 , the alcohol group is replaced by halide and it forms an alkyl halide. The reaction goes as follows:
C2H5OH+PCl5→C2H5Cl
The sodium salt of the ethyl alcohol and ethyl chloride reacts together to form diethyl ether.
Thus, A is C2H5OH , B is C2H5ONa and C is C2H5Cl .
Hence, the correct option is option C.
Note:
Alcohols react with sodium metal or other alkali metals due to the difference in electronegativities between the alkyl group and Oxygen atom to form alkoxides, releasing Hydrogen in the process.
The alkoxide ion is a very good nucleophile and reacts easily with chlorinating agents like PCl5 to form alkyl halide and this reaction is used in different organic transformations.
In the Williamson ether synthesis, an alkoxide, which is a nucleophile, reacts with an alkyl halide by an SN2 substitution reaction to form the ether.