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Hint: $ Diazomethane $ is a very reactive compound. It acts as a methylating agent. $ Diazomethane $ converts alcohol into ethers in the presence of ether. To solve this question remember the fact that $ Diazomethane $ is an alkylating agent therefore alkylates the phenol.
Complete answer:
$ Phenol $ is an aromatic organic compound which is a volatile compound. $ Phenol $ has a widespread use involving as a disinfectant, mouthwash, medicinal use like that in surgical antiseptics. $ Phenol $ are similar to alcohols but they form stronger hydrogen bonds that is why they are more soluble in water than are alcohols. $ Phenol $ was first mined from coal tar, but today it is manufactured on a large scale from petroleum. It is an important industrial product as a pioneer to various materials and useful compounds. $ Phenol $ and its chemical products are very important for the production of Bakelite, polycarbonates, detergents, nylon, epoxies, herbicides such as phenoxy herbicides.
$ Diazomethane $ is the simplest diazo compound. As mentioned in the hint $ Diazomethane $ converts alcohol into ethers. This is due to the fact that $ - C{H_2} $ group attaches to the alcohol group releasing molecular nitrogen.
$ Diazomethane $ when reacting with a $ Phenol $ acts as a base and abstracts a proton from phenol. This results in the formation of $ phenoxide $ ions. After this $ phenoxide $ ion acts as a nucleophile and under this nucleophilic attack $ Anisole $ ether is formed.
The reaction is shown below:
$ Anisole $ is formed in the reaction and nitrogen gas is liberated when $ Diazomethane $ reacts with . $ Phenol $ . This reaction takes place in the presence of $ Fluoroboric $ $ acid $ .
$ Anisole $ or $ methoxybenzene $ is an organic compound which is a colourless liquid. Its smell is reminiscent of anise seed. Due to this smell it is used in making perfumes, flavouring agents as well as solvent.
Note:
We not only use $ Fluoroboric $ $ acid $ to enhance the rate of reaction but also chemicals like $ Sodium{\text{ }}hydroxide $ which increases the rate of reaction. During such reactions, liberation of nitrogen always takes place.
Complete answer:
$ Phenol $ is an aromatic organic compound which is a volatile compound. $ Phenol $ has a widespread use involving as a disinfectant, mouthwash, medicinal use like that in surgical antiseptics. $ Phenol $ are similar to alcohols but they form stronger hydrogen bonds that is why they are more soluble in water than are alcohols. $ Phenol $ was first mined from coal tar, but today it is manufactured on a large scale from petroleum. It is an important industrial product as a pioneer to various materials and useful compounds. $ Phenol $ and its chemical products are very important for the production of Bakelite, polycarbonates, detergents, nylon, epoxies, herbicides such as phenoxy herbicides.
$ Diazomethane $ is the simplest diazo compound. As mentioned in the hint $ Diazomethane $ converts alcohol into ethers. This is due to the fact that $ - C{H_2} $ group attaches to the alcohol group releasing molecular nitrogen.
$ Diazomethane $ when reacting with a $ Phenol $ acts as a base and abstracts a proton from phenol. This results in the formation of $ phenoxide $ ions. After this $ phenoxide $ ion acts as a nucleophile and under this nucleophilic attack $ Anisole $ ether is formed.
The reaction is shown below:
$ Anisole $ is formed in the reaction and nitrogen gas is liberated when $ Diazomethane $ reacts with . $ Phenol $ . This reaction takes place in the presence of $ Fluoroboric $ $ acid $ .
$ Anisole $ or $ methoxybenzene $ is an organic compound which is a colourless liquid. Its smell is reminiscent of anise seed. Due to this smell it is used in making perfumes, flavouring agents as well as solvent.
Note:
We not only use $ Fluoroboric $ $ acid $ to enhance the rate of reaction but also chemicals like $ Sodium{\text{ }}hydroxide $ which increases the rate of reaction. During such reactions, liberation of nitrogen always takes place.
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