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Hint: You can use these hints to make this question easier for you (i) Formylation of phenols with chloroform is known as Reimer- Tiemann reaction. (ii) Kolbe process is a reaction that proceeds by heating sodium phenoxide with carbon dioxide.
Complete step by step answer:
Let’s discuss each reaction with proper mechanism -
Reimer-Tiemann reaction - The Reimer–Tiemann reaction is a chemical reaction used for the ortho-formylation of phenols; with the simplest example being the conversion of phenol to salicylaldehyde.
When phenols i.e. $C_6H_5OH$ is treated with $CHCl_3$ (chloroform) in the presence of NaOH (sodium hydroxide), an aldehyde group (-CHO) is introduced at the ortho position of benzene ring leading to the formation of o-hydroxybenzaldehyde (salicylaldehyde).
Kolbe’s reaction - Kolbe process or Kolbe–Schmitt reaction is a carboxylation chemical reaction that proceeds by heating sodium phenoxide with carbon dioxide under pressure, then treating the product with sulfuric acid.
The final product is an aromatic hydroxy acid which is also known as salicylic acid.
Therefore, we wrote the equation involved in the Reimer-Tiemann reaction and Kolbe’s reaction.
Additional information:
The Kolbe electrolysis involves the formation of symmetrical hydrocarbons through the coupling of radicals generated from carboxylic acid at an anode via electrolysis. This reaction is useful for the preparation of hydrocarbons.
Note: Here we observe that in the Reimer Tiemann reaction the ortho product is major.
Because the inductive effect dies with distance, so the ortho position will be more electron-rich as compared to the para position, and the incoming electrophile (carbene) will attack the ortho carbon. That's why ortho isomer is the major product.
Complete step by step answer:
Let’s discuss each reaction with proper mechanism -
Reimer-Tiemann reaction - The Reimer–Tiemann reaction is a chemical reaction used for the ortho-formylation of phenols; with the simplest example being the conversion of phenol to salicylaldehyde.
When phenols i.e. $C_6H_5OH$ is treated with $CHCl_3$ (chloroform) in the presence of NaOH (sodium hydroxide), an aldehyde group (-CHO) is introduced at the ortho position of benzene ring leading to the formation of o-hydroxybenzaldehyde (salicylaldehyde).
Kolbe’s reaction - Kolbe process or Kolbe–Schmitt reaction is a carboxylation chemical reaction that proceeds by heating sodium phenoxide with carbon dioxide under pressure, then treating the product with sulfuric acid.
The final product is an aromatic hydroxy acid which is also known as salicylic acid.
Therefore, we wrote the equation involved in the Reimer-Tiemann reaction and Kolbe’s reaction.
Additional information:
The Kolbe electrolysis involves the formation of symmetrical hydrocarbons through the coupling of radicals generated from carboxylic acid at an anode via electrolysis. This reaction is useful for the preparation of hydrocarbons.
Note: Here we observe that in the Reimer Tiemann reaction the ortho product is major.
Because the inductive effect dies with distance, so the ortho position will be more electron-rich as compared to the para position, and the incoming electrophile (carbene) will attack the ortho carbon. That's why ortho isomer is the major product.
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