Based on the absolute configuration of (S)-butan-2-ol, what can you say about the direction it rotates plane-polarized light?

Using a 1.0-cm polarimeter cell and a solution prepared by dissolving 2.54 g of glucose in 1 L of H₂O, the specific rotation of d-glucose was calculated to be +52.7° at 20 °C using the sodium D line as the source of light. What was the observed rotation of the solution?
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Key Concepts
Specific Rotation
Observed Rotation
Concentration Calculation
A student wanted to measure the specific rotation of the following propionate derivative (density = 1.12 g/ml).
A sample of the pure compound was placed in a 10.0-cm polarimeter tube, and using the sodium D line, the observed rotation at 20°C was determined to be +46.6° . What is the specific rotation of the propionate derivative?
Imagine a sample that is enriched in the R enantiomer. If the % ee of the sample is 83%,
(a) what percent of the mixture is racemic?
(b) What is the ratio of R to S?
(S)-Propranolol, a drug used for the treatment of anxiety, has a specific rotation of -25.5° . Attempting to prepare it in enantiopure form, a chemist produced a compound that gave a specific rotation of -18.3° . What is the ratio of (S)- to (R)-propranolol produced by the chemist?
(R)-Selegiline, a monoamine oxidase (MAO) inactivator, was approved by the FDA in 1989 for the treatment of Parkinson's disease. In pure form, it has a specific rotation, [α]²⁰D = - 11.0°. What is the expected specific rotation of a mixture containing 64% S and 36% R?
Cholesterol (50 mg) was dissolved in 10 mL of chloroform and placed in a 1.0-cm polarimeter cell. This solution produced an observed rotation (using the sodium D line at 20°C ) of - 1.58° . What is the specific rotation of cholesterol?
