An unknown drug has a specific rotation of +82°. The commercial synthesis of this drug results in a mixture with an enantiomeric excess of 94 %.
i. Determine the absolute configuration of this drug.
ii. What is the percentage of each enantiomer in the commercial product?

i. The absolute configuration of this drug is 'R'.

ii. We can not determine the percentage of each enantiomer using the given data.

i. The absolute configuration of this drug is 'S'.

ii. (+) enantiomer = 94%, (-) enantiomer = 6%

i. The absolute configuration of this drug is 'R'.

ii. (+) enantiomer = 97%, (-) enantiomer = 3%

i. We can not determine the absolute configuration of this drug with the given data.

ii. (+) enantiomer = 97%, (-) enantiomer = 3%