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.
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
what is the chemical equation when phenol react with hydrochloric acid
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.
No they don't react together. but phenol is soluble in CHCl3.
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.
An iodoform reaction is the type of reaction when acetone reacts with triiodomethane.
Phenol does not react with carbonates because it is a weak acid and does not produce sufficient H⁺ ions to react with the carbonate ions (CO₃²⁻). In contrast, stronger acids like hydrochloric acid readily react with carbonates to produce carbon dioxide, water, and a salt. The equilibrium between phenol and its conjugate base (phenoxide ion) does not favor the release of H⁺ needed for the carbonate reaction. Thus, phenol remains unreactive towards carbonates under normal conditions.
Para amino phenol can react with hydrochloric acid to form para-aminophenol hydrochloride salt. This reaction involves the protonation of the amino group on the para amino phenol molecule by the hydrochloric acid.
Yes, phosphorus pentachloride (PCl5) can react with phenol. In this reaction, PCl5 can convert the hydroxyl group (-OH) of phenol into a chlorinated derivative, typically forming phenyl phosphate and releasing hydrogen chloride (HCl) as a byproduct. This reaction is part of a broader category of reactions where PCl5 acts as a chlorinating agent.