Question:

Decreasing order of reactivity of hydrogen halide acids in the conversion of $ ROH\to RX $ is

Updated On: Jun 18, 2022
  • $ HCl>HBr>HI>HF $
  • $ HI>HBr>HCl>HF $
  • $ HF>HCl>HBr>HI $
  • $ HF>HBr>HI>HCl $
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The Correct Option is B

Solution and Explanation

Since the conversion of an alcohol to alkyl halide is an nucleophilic substitution reaction and the nucleophilicity (ie, tendency to donate an electron pair to the carbon atom) of the halide ions decreases in the order, $ I^{-}>Br^{-}>Cl^{-}>F^{-} $ , Thus, the order of reactivity of halogen acids decreases in order : $ HI > HBr > HCl > HF $ .
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Concepts Used:

Alcohols, Phenols, and Ethers

Alcohol is formed when a saturated carbon atom bonds to a hydroxyl (-OH) group. It is an organic compound that contains a hydroxyl functional group attached to a carbon atom.

Phenol is formed when the -OH group replaces the hydrogen atom in benzene. It is an organic compound in which a hydroxyl group directly attaches to an aromatic hydrocarbon.

Ether is formed when oxygen atom bonds to two alkyl or aryl groups. It is an organic compound that has an oxygen atom that is connected to two aryl and alkyl groups.

Read More: Alcohol, Phenol, and Ethers