Question:

The correct IUPAC names of the compounds X and Y given below are respectively

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In IUPAC nomenclature: \[ -OH \] has higher priority than alkyl or phenyl substituents. Therefore numbering must always give the hydroxyl group the lowest possible locant.
Updated On: Jun 17, 2026
  • 3-Methyl-4-ethylheptane ; 1-Phenylbutan-2-ol
  • 4-Ethyl-3-Methylheptane ; 1-Phenylbutan-2-ol
  • 3-(sec-butyl)-hexane ; 2-Hydroxy-1-phenylbutane
  • 3-Methyl-4-Ethylheptane ; 2-Hydroxybutylbenzene
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The Correct Option is B

Solution and Explanation

Concept: IUPAC nomenclature requires:

• Identification of the longest carbon chain

• Assignment of lowest possible locants

• Alphabetical ordering of substituents

• Priority-based naming of functional groups

Step 1: Naming compound X. The longest continuous chain contains: \[ 7 \text{ carbon atoms} \] Therefore the parent hydrocarbon is: Heptane Substituents present are: Ethyl and Methyl Numbering from the appropriate end gives: \[ 4\text{-Ethyl} \] and \[ 3\text{-Methyl} \] According to alphabetical order: \[ \boxed{4\text{-Ethyl-3-Methylheptane}} \]

Step 2: Naming compound Y. The principal functional group is: \[ -OH \] Hence alcohol receives suffix priority. The longest chain containing the hydroxyl group consists of four carbons. Parent chain: Butan-2-ol Phenyl substituent occurs at carbon-1. Therefore: \[ \boxed{1\text{-Phenylbutan-2-ol}} \]

Step 3: Check the options. Only option (B) contains both correct names.

Step 4: Final conclusion. \[ \boxed{\text{Option (B)}} \]
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