The triiodomethane (iodoform) reaction of phenol involves the conversion of phenol to iodoform in the presence of iodine and sodium hydroxide. The reaction proceeds through oxidation of phenol to benzoic acid, followed by further oxidation and degradation to iodoform. This reaction is commonly used as a test for the presence of a methyl group attached to a phenolic compound.
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
Phenol is not dissolved in a sodium hydroxide solution; having the characteristics of a weak acid phenol react with NaOH.
A positive Lucas test on phenol would indicate that phenol is a strong enough acid to react with Lucas reagent (a mixture of concentrated hydrochloric acid and zinc chloride) to form a cloudy solution or a precipitate. This reaction distinguishes phenol from other alcohols that do not react with the Lucas reagent.
reaction b/w phenol and zinc yield benzene by reduction.
Yes
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.
The triiodomethane (iodoform) reaction of phenol involves the conversion of phenol to iodoform in the presence of iodine and sodium hydroxide. The reaction proceeds through oxidation of phenol to benzoic acid, followed by further oxidation and degradation to iodoform. This reaction is commonly used as a test for the presence of a methyl group attached to a phenolic compound.
what is the chemical equation when phenol react with hydrochloric acid
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
Phenol is not dissolved in a sodium hydroxide solution; having the characteristics of a weak acid phenol react with NaOH.
No, sodium bicarbonate will not react with phenol red. Phenol red is a pH indicator that changes color based on pH levels, while sodium bicarbonate is a salt commonly used as an antacid.
Phenol + 3Br2 = 2,4,6-tribromophenol + 3HBr Everything you need to know :) http://www.chemguide.co.uk/organicprops/phenol/ring.html
There is no reaction between phenol and sodium carbonate
No they don't react together. but phenol is soluble in CHCl3.
The reaction between phenol and dilute nitric acid forms nitrophenol and water. The equation is: C6H5OH + HNO3 → C6H5NO3 + H2O
A positive Lucas test on phenol would indicate that phenol is a strong enough acid to react with Lucas reagent (a mixture of concentrated hydrochloric acid and zinc chloride) to form a cloudy solution or a precipitate. This reaction distinguishes phenol from other alcohols that do not react with the Lucas reagent.