An enantiomerically pure acid is treated with a racemic mixture of an alcohol having one chiral carbon. The ester formed will be

  • A
    $A$ racemic mixture
  • B
    $A$ pure enantiomer
  • C
    $A$ meso compound
  • D
    $A$ mixture of diastereomers

Explore More

Similar Questions

What is necessary for an organic molecule to exhibit optical activity?

The given structures are related as:

In which property do $d$ and $l$ isomers differ?

Total possible stereoisomers from the given compound $CH_3-CH=CH-CH(OH)-CH(OH)-CH_3$ will be:

The number of optical isomers of lactic acid is

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo