Question
Question: Which of the following reagents cannot be used to prepare an alkyl halide? A. \(NaCl\) B. \(HCl ...
Which of the following reagents cannot be used to prepare an alkyl halide?
A. NaCl
B. HCl+ZnCl2
C. SOCl2
D. PCl5
Solution
In organic chemistry, the term "reagent" denotes a chemical ingredient (a compound or mixture, typically of inorganic or small organic molecules) introduced to cause the desired transformation of an organic substance.
Complete step by step answer:
The mixture of HCl and ZnCl2 is called the Lucas Reagent.
HCl+ZnCl2 is used in the Groove's process for the preparation of alkyl halides from alcohols.
The reaction can be written as:
It is also used to distinguish primary, secondary and tertiary alcohols.
The reaction can be accomplished in the presence of only HCl in the same way, although often ZnCl2 which is a Lewis acid is added to help compensate for the lower nucleophilicity of chloride ion.
The most common methods for converting 10 and 20 alcohols to the corresponding chloro and bromo alkanes (i.e. replacement of the hydroxyl group) are treatments with thionyl chloride and phosphorus tribromide, respectively.
Hence we can say Thionyl chloride, SOCl2 is also used as a reagent to convert alcohols into alkyl chlorides.
R−OHSOCl2 RX+HCl+SO2
The reaction of alcohols R−OH with PCl5 and PCl3 yields an alkyl halide R−Cl.
WithPCl5, the reaction is quite simple leading to the formation of R−Cl and POCl3.
Hence options (B), (C) and (D) can be eliminated.
And NaCl cannot be used for the preparation of alkyl chlorides from alcohols.
Hence option (A) will be considered as a correct option.
Note: Lucas' reagent is a solution of anhydrous zinc chloride in concentrated hydrochloric acid. This solution is used to classify alcohols of low molecular weight. The reaction is a substitution in which the chloride replaces a hydroxyl group.