Draw the enantiomer, if any, for each structure.
(g)
(h)

Chirality refers to the geometric property of a molecule that makes it non-superimposable on its mirror image. A chiral molecule typically has at least one carbon atom bonded to four different substituents, creating two distinct forms known as enantiomers. These enantiomers can exhibit different chemical behaviors, especially in biological systems.

Enantiomers are a pair of chiral molecules that are mirror images of each other. They have identical physical properties, such as melting and boiling points, but can differ significantly in their interactions with polarized light and biological systems. Understanding enantiomers is crucial in organic chemistry, particularly in drug design, where one enantiomer may be therapeutically active while the other is not.

Stereochemistry is the study of the spatial arrangement of atoms in molecules and how this affects their chemical behavior. It encompasses concepts such as chirality, enantiomers, and diastereomers. In organic chemistry, stereochemistry is essential for predicting the reactivity and properties of molecules, especially in reactions involving chiral centers.