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🧪 Chemistry  ·  Haloalkanes & Haloarenes  ·  NEET & JEE

The optical rotation of a racemic mixture is:

Answer: 0° (optically inactive).

  • A +180°, indicating a single pure dextrorotatory enantiomer is present
  • B -180°, indicating a single pure levorotatory enantiomer is present
  • C 0° (optically inactive)
  • D A variable value that changes randomly each time it is measured

Correct answer: C. 0° (optically inactive)

Explanation: A racemic mixture contains equal amounts of (+) and (-) enantiomers; their rotations exactly cancel, giving zero net optical rotation.

SN2: one stepNu-CX-backside attackNuC+ X-Inversion of configuration(Walden inversion)SN1: two stepsCX-slow: leaving group exits+CcarbocationNu-Planar intermediate givesracemisation (both faces attacked)

SN2 proceeds in a single step with backside attack and inversion of configuration, while SN1 forms a planar carbocation intermediate first, leading to racemisation.

Concept context

Study carbon-halogen compounds: how they are made, how they react via SN1/SN2 and elimination, their stereochemistry, and their environmental impact.

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