Phenols do not react with HX (hydrogen halides) because the oxygen atom in the phenol molecule is more electronegative than the hydrogen atom attached to the halogen in HX. This leads to stabilization of the phenol ring structure through resonance, making it less favorable for the hydrogen halide to protonate the phenol.
When phenol reacts with ammonium sulfite in the presence of ammonia, the result is the formation of a salt called ammonium phenoxide. This reaction involves the replacement of the hydrogen in the phenol with the ammonium cation from the ammonium sulfite.
When iodoform reacts with phenol, the iodoform is reduced to triiodomethane and phenol is oxidized to benzoquinone. The reaction results in the formation of a white precipitate of triiodomethane.
Phenol reacts with concentrated sulfuric acid to form the sulfonated product, and then with concentrated nitric acid to form picric acid (2,4,6-trinitrophenol).
Yes, phenol is soluble in sodium hydroxide due to the formation of the water-soluble sodium phenolate salt. Phenol reacts with sodium hydroxide to form sodium phenolate and water.
When phenol reacts with concentrated nitric acid (HNO3) in the presence of sulfuric acid (H2SO4), a mixture of products is formed, including picric acid (2,4,6-trinitrophenol) and water. This reaction is known as nitration of phenol and is used to synthesize picric acid, which is a yellow, explosive compound.
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
When phenol reacts with ammonium sulfite in the presence of ammonia, the result is the formation of a salt called ammonium phenoxide. This reaction involves the replacement of the hydrogen in the phenol with the ammonium cation from the ammonium sulfite.
When iodoform reacts with phenol, the iodoform is reduced to triiodomethane and phenol is oxidized to benzoquinone. The reaction results in the formation of a white precipitate of triiodomethane.
Hinsberg reagent is used for amines.
Phenol reacts with concentrated sulfuric acid to form the sulfonated product, and then with concentrated nitric acid to form picric acid (2,4,6-trinitrophenol).
Phenol reacts with bromine water to form 2,4,6-tribromophenol in the presence of a catalyst. The word equation for this reaction is: Phenol + Bromine water → 2,4,6-tribromophenol.
Yes, phenol is soluble in sodium hydroxide due to the formation of the water-soluble sodium phenolate salt. Phenol reacts with sodium hydroxide to form sodium phenolate and water.
Phenol reacts with phosphorus pentachloride to form chlorobenzene and phosphoric acid as byproduct. The reaction involves substitution of the hydroxyl group in phenol with a chlorine atom.
When phenol reacts with concentrated nitric acid (HNO3) in the presence of sulfuric acid (H2SO4), a mixture of products is formed, including picric acid (2,4,6-trinitrophenol) and water. This reaction is known as nitration of phenol and is used to synthesize picric acid, which is a yellow, explosive compound.
When anisole reacts with HI (hydroiodic acid), it forms iodobenzene and phenol as products.
In the phenol sulfuric acid test, glucose reacts with phenol and sulfuric acid to form a colored product. The color change is due to the formation of furfural, which reacts with the sulfuric acid to produce a colored compound. This color change is used to detect the presence of glucose in a sample.
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.