Cyanide ion acts as an ambident nucleophile. From which end it acts as a stronger nucleophile in medium?

Question

Cyanide ion acts as an ambident nucleophile. From which end it acts as a stronger nucleophile in medium? (A) It acts as a stronger nucleophile from carbon end (B) It acts as a stronger nucleophile from nitrogen end (C) It depends on the nature of alkyl halide (D) It has same strength from both the ends

Tardigrade Admin · Accepted Answer

It acts as a stronger nucleophile from the carbon end because it will lead to the formation of C -C bond which is more stable than C -N bond.

Q. Cyanide ion acts as an ambident nucleophile. From which end it acts as a stronger nucleophile in medium?

It acts as a stronger nucleophile from carbon end

It acts as a stronger nucleophile from nitrogen end

It depends on the nature of alkyl halide

It has same strength from both the ends

It acts as a stronger nucleophile from the carbon end because it will lead to the formation of $C - C$ bond which is more stable than $C - N$ bond.

Q. Cyanide ion acts as an ambident nucleophile. From which end it acts as a stronger nucleophile in medium?

It acts as a stronger nucleophile from carbon end

It acts as a stronger nucleophile from nitrogen end

It depends on the nature of alkyl halide

It has same strength from both the ends

It acts as a stronger nucleophile from the carbon end because it will lead to the formation of C−C bond which is more stable than C−N bond.

It acts as a stronger nucleophile from the carbon end because it will lead to the formation of $C - C$ bond which is more stable than $C - N$ bond.