Yes Phenol will react with Primary amine
Example : It Replaces the Hydrogen in OH and Form amonia gas
Phenol + CH3NH2 gives anisol + amonia gas
By Ponniah
MTech Polymer science
CIPET
In the reaction between phenol and sodium metal, sodium donates an electron to the oxygen atom in the phenol molecule, forming a sodium phenoxide salt and hydrogen gas. This process is a type of redox reaction where the sodium is oxidized and the phenol is reduced.
In the reaction between phenol and sodium hydroxide, the phenol is deprotonated by the base, forming the phenolate ion. This reaction is an acid-base reaction where phenol acts as an acid and donates a proton to form water. The products of the reaction are the phenolate ion and water.
Phenol reacts with potassium permanganate in an acidic medium to form benzoquinone as the main product, along with small amounts of hydroquinone. This reaction is a redox reaction where phenol is oxidized to form benzoquinone.
The reaction between phenol and dilute nitric acid forms nitrophenol and water. The equation is: C6H5OH + HNO3 → C6H5NO3 + H2O
The reaction of phenol with Br2 proceeds through electrophilic aromatic substitution, where the bromine atom replaces a hydrogen atom on the benzene ring of phenol. This reaction is facilitated by the presence of the hydroxyl group on the phenol molecule, which activates the benzene ring towards electrophilic attack.
There is no reaction between phenol and sodium carbonate
reaction b/w phenol and zinc yield benzene by reduction.
In the reaction between phenol and sodium metal, sodium donates an electron to the oxygen atom in the phenol molecule, forming a sodium phenoxide salt and hydrogen gas. This process is a type of redox reaction where the sodium is oxidized and the phenol is reduced.
In the reaction between phenol and sodium hydroxide, the phenol is deprotonated by the base, forming the phenolate ion. This reaction is an acid-base reaction where phenol acts as an acid and donates a proton to form water. The products of the reaction are the phenolate ion and water.
The reaction between phenol and bromine water results in the substitution of a hydrogen atom on the benzene ring with a bromine atom. This forms bromophenol as the product. The reaction is a bromination reaction and the presence of phenol's hydroxyl group activates the benzene ring towards electrophilic substitution.
Phenol reacts with potassium permanganate in an acidic medium to form benzoquinone as the main product, along with small amounts of hydroquinone. This reaction is a redox reaction where phenol is oxidized to form benzoquinone.
The reaction between phenol and calcium hydroxide results in the formation of calcium phenolate and water. The chemical equation for this reaction is: C6H5OH (phenol) + Ca(OH)2 (calcium hydroxide) → Ca(C6H5O)2 (calcium phenolate) + H2O (water)
imidazole will form
the brawn colour is formed and this is due to the presece of the OH functional froup found in the phenol.
The hydroxyl group in phenol is an activating ortho/para director, but has some slight steric hindrance too ortho position substitution. Therefore, the predominant product of reaction between phenol and bromine will be 4-bromophenol, if reaction conditions are carefully controlled. With excess bromine, di- and tri-bromo phenols will be formed.
The reaction between phenol and dilute nitric acid forms nitrophenol and water. The equation is: C6H5OH + HNO3 → C6H5NO3 + H2O
There is no reaction when their molar ratio is around 1...but when phenol is present in excess it gives triphenylphosphate....