Quinine and quinidine are stereoisomers, meaning they have the same molecular formula but differ in the spatial arrangement of atoms. The specific area where they differ lies in their ability to rotate the plane of polarized light.
Explanation:
In conclusion, the fundamental way in which quinine and quinidine differ lies in how they interact with polarized light. Therefore, the correct answer is "Rotating the plane of polarized light."


Rancidity in the fixed oils generally show ‐
List I | List II | ||
|---|---|---|---|
| A | \(\Omega^{-1}\) | I | Specific conductance |
| B | \(∧\) | II | Electrical conductance |
| C | k | III | Specific resistance |
| D | \(\rho\) | IV | Equivalent conductance |
List I | List II | ||
|---|---|---|---|
| A | Constant heat (q = 0) | I | Isothermal |
| B | Reversible process at constant temperature (dT = 0) | II | Isometric |
| C | Constant volume (dV = 0) | III | Adiabatic |
| D | Constant pressure (dP = 0) | IV | Isobar |