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
Yes, the reaction between phenol and a primary amine is possible. It typically involves the formation of an amide and water as a byproduct. This reaction is known as amide formation.
The reaction between a phenol and a primary amine is possible. It is used in the fabrication of robust multilayer films.
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 color change in the reaction between ferric chloride and phenol occurs due to the formation of a complex between the two compounds. This complex has a different absorption spectrum compared to the individual compounds, resulting in a visible color change.
There is no reaction between phenol and sodium carbonate
The reaction between zinc and phenol can be represented by the following equation: Zn(s) + 2C6H5OH(l) → Zn(C6H5O)2(s) + H2(g)
In the reaction between sulphamic acid and sodium hydroxide in paracetamol estimation, sulphamic acid reacts with paracetamol to form a colorless solution. The addition of sodium hydroxide then helps to break down the paracetamol into its constituent components, allowing for accurate estimation of the amount present in the solution.
it cant decolourise
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.
Phenols are soluble in sodium hydroxide due to the formation of sodium phenoxide salt when they react with sodium hydroxide. This salt is polar and soluble in polar solvents like water. The phenoxide ion formed can hydrogen bond with water molecules, further enhancing its solubility.
Calcium hydroxide, a base, will reaction with phenol, a weak acid in a neutralization reaction to give a salt (calcium phenoxide (Ca(PhO-)2) and water.
imidazole will form
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 Leuckart-Wallach reaction, phenol is converted into aniline through the reduction of the nitro group, followed by acid hydrolysis.
the brawn colour is formed and this is due to the presece of the OH functional froup found in the phenol.
There is no reaction when their molar ratio is around 1...but when phenol is present in excess it gives triphenylphosphate....