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 reduced to benzene when it is distilled with zinc dust or its vapour is passed over granules of zinc at 400°C.
Freidel Crafts acylation of benzene with acetyl chloride in presence of AlCl3 gives acetophenone
Williamson ether synthesis
in a laberatory.
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).
in the presence of con.h2so4 anisole will convert into phenol and hi
Aspirin paracetamol morphine ibuprofen
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
in the presence of con.h2so4 anisole will convert into phenol and hi
Aspirin paracetamol morphine ibuprofen
yes using phenol, a compound that is derived from crude oil.
very easy, a single step reaction. When phenol is heated with Concentrated Nitric acid 2,4.6-trinitrophenol (Picric acid) is produced.
Convert the benzene into Phenol which is a good antiseptic material.
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.
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).
You must initially convert it into benzene then heat it with Zn dust. And add CH3-Cl+anhydrous AlCl3 followed by hot concentrated KMnO4.
Simple phenolic resins are condensation polymers formed from phenol and formaldehyde. Therefore, they contain only the elements found in phenol and formaldehyde: carbon, hydrogen, and oxygen. The characteristic bond for a cured phenolic resin is a methylene group, derived from a formaldehyde molecule, joining two aromatic rings derived from two phenol molecules. A wide variety of structural formulas are possible, because resins can be made from a variety of ratios between phenol and formaldehyde.