C6H5OH + CH3Cl -----(AlCl3)-----> C6H5OHCH3 + HCl
phenol + chloromethane ----> 2-methylphenol
C6H5OHCH3 -----(alkaline KMnO4, then acidify with HCl)-----> C6H5OHCOOH
2-methylphenol -----> 2-hydroxybenzenecarboxylic acid
C6H5OHCOOH + (CH3CO)2O (ethanoic anhydride) -----(c.H2SO4 catalyst)-----> aspirin (C6H5OCOCH3COOH) + (ethanoic acid) CH3COOH
Phenol is converted to aspirin by adding carboxylic acid and esterifying the alcohol.
Aspirin (acetyl salycilic acid) is prepared from salycilic acid and acetic anhydride; salicylic acid is prepared from sodium phenoxide and carbon dioxide (Kolbe synthesis).
Some common drugs that contain an aromatic phenol group include aspirin, acetaminophen (paracetamol), ibuprofen, and diclofenac. These drugs are widely used as analgesics and anti-inflammatory agents.
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.
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).
Phenol is converted to aspirin by adding carboxylic acid and esterifying the alcohol.
Aspirin (acetyl salycilic acid) is prepared from salycilic acid and acetic anhydride; salicylic acid is prepared from sodium phenoxide and carbon dioxide (Kolbe synthesis).
you can say as it contain Phenol ring that is undergoes acetylation process to form -OCOCH3
yes using phenol, a compound that is derived from crude oil.
Some common drugs that contain an aromatic phenol group include aspirin, acetaminophen (paracetamol), ibuprofen, and diclofenac. These drugs are widely used as analgesics and anti-inflammatory agents.
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.
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.
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.
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.
Cumene can be converted to phenol through a two-step process. First, cumene is oxidized to cumene hydroperoxide using oxygen or air. Then, the cumene hydroperoxide undergoes acid-catalyzed cleavage to produce phenol and acetone.
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.
Convert the benzene into Phenol which is a good antiseptic material.