"1":"data":"Benzonitrile is prepared by the reaction of r nchlorobenzene with potassium cyanide. ","imageType":"-1","image":"-1","2":"data":"Cyanide (CN-) is a strong nucleophile.","imageType":"-1","image":"-1"

Question

"1":"data":"Benzonitrile is prepared by the reaction of r nchlorobenzene with potassium cyanide. ","imageType":"-1","image":"-1","2":"data":"Cyanide (CN-) is a strong nucleophile.","imageType":"-1","image":"-1" (A)  (B)  (C)  (D)

Tardigrade Admin · Accepted Answer

Statement I is incorrect, aryl halides do not undergo nucleophilic substitution reaction with ease. Cyanide ion (CN-) is a strong nucleophile.

Q. {"1":{"data":"Benzonitrile is prepared by the reaction of
\r\nchlorobenzene with potassium cyanide.
","imageType":"-1","image":"-1"},"2":{"data":"Cyanide $(C N^{-})$ is a strong nucleophile.","imageType":"-1","image":"-1"}}

Statement I is incorrect, aryl halides do not undergo
nucleophilic substitution reaction with ease. Cyanide ion $(C N^{-})$
is a strong nucleophile.

Q. {"1":{"data":"Benzonitrile is prepared by the reaction of \r\nchlorobenzene with potassium cyanide. ","imageType":"-1","image":"-1"},"2":{"data":"Cyanide (CN−) is a strong nucleophile.","imageType":"-1","image":"-1"}}

Statement I is incorrect, aryl halides do not undergo nucleophilic substitution reaction with ease. Cyanide ion (CN−) is a strong nucleophile.

Q. {"1":{"data":"Benzonitrile is prepared by the reaction of
\r\nchlorobenzene with potassium cyanide.
","imageType":"-1","image":"-1"},"2":{"data":"Cyanide $(C N^{-})$ is a strong nucleophile.","imageType":"-1","image":"-1"}}

Statement I is incorrect, aryl halides do not undergo
nucleophilic substitution reaction with ease. Cyanide ion $(C N^{-})$
is a strong nucleophile.