Quantrex Quantrex AcademyJEE · NEET · NDA PYQs with solutions Open app
NEETChemistryAlcohols Phenols and Ethers

In Kolbe’s reaction, instead of phenol, phenoxide ion is treated with carbon dioxide. Why?

Options

  1. APhenoxide ion is more readily available and stable than phenol.
  2. BPhenoxide ion is a stronger base and can deprotonate phenol to form the nucleophilic species.
  3. CIn phenoxide ion, the ability to give a lone pair of electrons to the benzene ring is more in comparison to ph
  4. DPhenoxide ion is less stable and reacts more readily with carbon dioxide to form the desired product.

Correct answer

C. In phenoxide ion, the ability to give a lone pair of electrons to the benzene ring is more in comparison to ph

Step-by-step solution

Correct Option is : (C) In phenoxide ion, the ability to give a lone pair of electrons to the benzene ring is more in comparison to phenols. Therefore.the reactivity of phenoxide ion towards electrophilic substitution reaction is more in comparison to phenols.Thus, phenoxide ion being a stronger nucleophile reacts easily with CO 2 , (weak electrophile) than phenols in Kolbe's reaction.

Practice Alcohols Phenols and Ethers on Quantrex Academy →

More from Alcohols Phenols and Ethers

Identify the product formed when ethyl alcohol reacts with H ₂ SO ₄ at 443 K. 2026Identify the product obtained when phenol reacts with bromine in presence of CS ₂ 2026Which is the Lucas reagent among following? 2026Identify the type of the following reaction? 2026Identify the compounds formed when anisole is heated with concentrated HI. 2026Identify the product of Kolbe's reaction from following. 2026Identify the product formed when the mixture of Phenol and Hydrogen is passed over nickel catalyst at 433 K. 2026Which of the following compounds is found in Indian gooseberry? 2026 Full Alcohols Phenols and Ethers list All NEET PYQs