Optical Isomerism: The Chirality of Molecules and Their Unique Optical Activity

What is optical isomerism a result of?

Chirality in molecules with a single chiral centre

Optical isomerism is a result of the chirality of a molecule. Chiral molecules are non-superimposable mirror images of each other and are characterized by having at least one stereogenic center, which is an atom that is attached to four different substituents. This creates two possible versions of the molecule that are mirror images of each other and cannot be superimposed on each other. These two versions of the molecule are called enantiomers. Enantiomers have identical physical and chemical properties except for their effect on plane-polarized light. This property is called optical activity and arises because each enantiomer rotates plane-polarized light in a different direction. Therefore, optical isomerism is a result of the chirality of a molecule and is the existence of enantiomers that have different optical activities.

More Answers:

The Stability Difference between cis and trans Isomers of Decalin: Trans-Cis Isomerism Rule in Cyclic Compounds
Cis-Decalin: Properties, Reactivity, and Applications in Organic Synthesis and Industrial Chemistry
Stereochemistry: Absolute vs. Relative Stereochemistry Explained

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