Acetyl chloride cannot be obtained by treating acetic acid with:
A.\[{\rm{CHC}}{{\rm{l}}_{\rm{3}}}\]
​B.\[{\rm{PC}}{{\rm{l}}_{\rm{3}}}\]
​C.\[{\rm{PC}}{{\rm{l}}_5}\]
​D.\[{\rm{SOC}}{{\rm{l}}_{\rm{2}}}\]

Hint: Acetyl chloride is an acyl chloride originating from acetic acid.
It has no colour and is a volatile liquid.

Complete Step by Step Solution:

Acetyl chloride relates to the category of organic compounds called acid halides.
Acid halides are the compounds in which the -OH group of the carboxylic acid is replaced by a halide like chlorine, bromine, fluorine and iodine.
Acetyl chloride has the chemical formula\[{\rm{C}}{{\rm{H}}_{\rm{3}}}{\rm{COCl}}\].
One of the methods of preparation of acetyl chloride is the treatment of acetic acid with compounds containing chlorine atoms.

A. \[{\rm{CHC}}{{\rm{l}}_{\rm{3}}}\]
When chloroform is treated with acetic acid, acetyl chloride is not formed as a product.
So, A is correct.

B. \[{\rm{PC}}{{\rm{l}}_{\rm{3}}}\]
This is phosphorus trichloride.
When phosphorus trichloride is treated with acetic acid, acetyl chloride is formed as the product.
Phosphorous acid is formed as the side product.
The reaction occurs as follows:

Image: Reaction of phosphorus trichloride with acetic acid.
So, B is incorrect.

​C. \[{\rm{PC}}{{\rm{l}}_5}\]
This is phosphorus pentachloride.
When phosphorus pentachloride is treated with acetic acid, acetyl chloride is formed as the product.
Phosphorus oxychloride and hydrochloric acid are formed as side products.
The reaction occurs as follows:


Image: the reaction of phosphorus pentachloride with acetic acid.

​D.\[{\rm{SOC}}{{\rm{l}}_{\rm{2}}}\]
This is thionyl chloride.
When thionyl chloride is treated with acetic acid, acetyl chloride is formed as the product.
Sulfur dioxide and hydrochloric acid are formed as side products.
This reaction is preferred over other methods of conversion due to the by-products in these reactions being gases escaping leaving the acetyl chloride in an almost pure state.
The reaction occurs as follows:

Image: the reaction of thionyl chloride with acetic acid.

So, option A is correct.

Note: While attempting the question, one must know about the structures of every given option. The oxidation of benzyl chloride out of the given options will yield benzoic acid. Oxidation of chlorophenol, chlorotoluene, and chlorobenzene will yield benzene diols, chlorobenzoic acid, and ortho-substituted oxy-chlorobenzene respectively.