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Q: How anisole is prepared from phenol?
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Give a simple procedure to convert anisole into phenol?

in the presence of con.h2so4 anisole will convert into phenol and hi


Why phenol is more reactive than anisol?

Because the -OH group present in phenol is more ring activating than -OCH3 group in anisole.


What product form when anisole react with HI?

Phenol, though additional iodide salt is sometimes needed.


What is the color of phenol formaldehyde resin after it is prepared?

Phenol Formaldehyde Resin in liquid phase appear as rides brown.


What is Alkyl phenol ethoxlate?

Surfactants that are prepared by reaction of ethylene oxide with the appropriate alkyl phenol. These surfactants are cheap to produce but suffer from biodegradability and potential toxicity.


Role of phenol in DNA isolation?

Purification of the DNA sample. Phenol is carbolic acid and is used to dissolve proteins and other cellular debris associated with the DNA being prepared for analysis.


Why doesn't Anisole form peroxide easily?

anisole does not form peroxides easily as the oxygen atom is strongly bonded to the benzene ring .


How will you convert phenol into aspirin?

Aspirin (acetyl salycilic acid) is prepared from salycilic acid and acetic anhydride; salicylic acid is prepared from sodium phenoxide and carbon dioxide (Kolbe synthesis).


What is an anisole?

An anisole is a type of aromatic compound that has a methoxy group (-OCH3) attached to a benzene ring. It is often used as a solvent in various chemical reactions and as a starting material for the synthesis of other compounds. Anisole has a sweet, pleasant odor and is a colorless liquid at room temperature.


What is the atomic number for Anisole?

Anisole is a compound, not an element and so it does not have an atomic number. It is composed of carbon, hydrogen, and oxygen which have the atomic numbers 6,1, and 8 respectively.


Structure of phenol?

phenol


Which is more acidic phenol or para-chloro phenol?

Phenol. Anisole doesn't have any acidic protons.