Consider the organic compound 2-butanol, which exists in two enantiomeric forms: R-2-butanol and S-2-butanol. Each of these forms has specific interactions with polarized light due to their chiral nature. When placed in a plane-polarized light field, R-2-butanol rotates the light in a clockwise direction whereas S-2-butanol rotates it counterclockwise.
Assuming you have a sample containing a racemic mixture of both enantiomers in equal amounts, how would you describe the optical activity of this mixture when analyzed under polarized light?