You must initially convert it into benzene then heat it with Zn dust. And add CH3-Cl+anhydrous AlCl3 followed by hot concentrated KMnO4.
To convert phenol to 2,4,6-trinitrophenol (picric acid), you would first nitrate phenol by treating it with a mixture of nitric and sulfuric acids. This will lead to the substitution of hydrogen atoms on the phenol ring with nitro groups, resulting in the formation of the 2,4,6-trinitrophenol compound.
Phenol and carbolic acid are actually the same compound. "Carbolic acid" is an older, colloquial term for phenol.
Hydrochloric acid (HCl) is added to the solution during the estimation of phenol to convert phenol into its corresponding chloride salt, which is easier to separate and quantify. This reaction helps in the extraction and analysis of phenol from the sample.
To convert phenol to benzophenone, you can first react phenol with benzoyl chloride in the presence of a base, such as pyridine, to form an ester. Then, oxidize the ester using a strong oxidizing agent, like chromic acid or potassium permanganate, to obtain benzophenone.
Yes, phenol is considered a weak acid.
Phenol is converted to aspirin by adding carboxylic acid and esterifying the alcohol.
To convert phenol to 2,4,6-trinitrophenol (picric acid), you would first nitrate phenol by treating it with a mixture of nitric and sulfuric acids. This will lead to the substitution of hydrogen atoms on the phenol ring with nitro groups, resulting in the formation of the 2,4,6-trinitrophenol compound.
React aniline with HCl/NaNO2 (diazotisation) followed by reaction with KOH to give phenol. Nitration of phenol with fuming nitric acid gives picric acid (or trinitrophenol).
Anisole can be converted into phenol by using a strong aqueous acid, such as hydrochloric acid, in the presence of water and heat. The acidic conditions will cleave the methoxy group (–OCH3) from the benzene ring, resulting in the formation of phenol. This reaction is known as hydrolysis of an ether.
Phenol and carbolic acid are actually the same compound. "Carbolic acid" is an older, colloquial term for phenol.
Hydrochloric acid (HCl) is added to the solution during the estimation of phenol to convert phenol into its corresponding chloride salt, which is easier to separate and quantify. This reaction helps in the extraction and analysis of phenol from the sample.
To convert phenol to benzophenone, you can first react phenol with benzoyl chloride in the presence of a base, such as pyridine, to form an ester. Then, oxidize the ester using a strong oxidizing agent, like chromic acid or potassium permanganate, to obtain benzophenone.
Yes, phenol is considered a weak acid.
The derivative of Phenol is Carbolic acid.
The equation for the oxidation of carbolic acid, also known as phenol, is C6H5OH + 3O2 -> C6H4O2 + 3H2O. Oxygen is used as the oxidizing agent to convert phenol into benzoquinone and water.
Phenol red is yellow at an acid pH.
I'd do it this way. Use Dow's Process (NaOH) to convert chlorobenzene to phenol. Now, use nitrating mixture to get both o and p- nitrophenol. Fractional distillation should give you what you finally need.