What happens when chlorobenzene react with NaNH2?

When chlorobenzene is treated with NaNH2 in liquid ammonia at 196K, aniline is formed.

Which of the following on treatment with NaNH2 in liquid NH3 gives M anisidine?

Nucleophilic substitution in the pressence of a strong base like NaNH2 takes place through elimination-addition or benzyne mechanism as explained below. In this reaction both o-and m-bromonaisole give the same benzyne intermediate which on the addition of NH3 gives m-anisidine.

What is the role of NaNH2?

What it’s used for: NaNH2 is a strong base. As a strong base, NaNH2 will deprotonate alkynes, alcohols, and a host of other functional groups with acidic protons such as esters and ketones. As a base, it’s often used in situations where a strong, small base is required.

Which of the following compound react with NaNH2?

The correct option is: a C2H2Explanation:Alkynes react with strong bases like NaNH2 to form sodium acetylide derivative known as acetylides.

What happens when quinoline is treated with NaNH2?

Quinoline undergoes nucleophilic substitution on heating with NaNH2 to give.

What compound is carbolic acid?

Phenol
Phenol (also called carbolic acid) is an aromatic organic compound with the molecular formula C6H5OH.

Can be prepared by reacting aniline with?

Aniline can be prepared by the reaction of chlorobenzene with $$Na{NH}_{2}/Liq.

Is NaNH2 a reducing agent?

Sodium amide is a strong reducing agent which removes the halide atoms and generates an alkyne. Complete Step by step answer: We know that Sodium amide ($NaN{H_2}$) is a strong base and is used for deprotonation of weak acids and also for elimination reactions.

What is the chemical name of NaNH2?

SODIUM AMIDE
Sodium amide