o-xylene, m-xylene, and p-xylene are structural isomers.
o-xylene, m-xylene, and p-xylene are examples of aromatic isomers, also known as ortho-, meta-, and para-xylene, respectively. These isomers are classified as aromatic because they are part of a family of compounds known as aromatic hydrocarbons, which contain a ring of six carbon atoms bonded to each other in a specific way.
o-xylene, m-xylene, and p-xylene are also examples of structural isomers. Structural isomers are compounds that have the same molecular formula but differ in the arrangement of their atoms. In the case of o-xylene, m-xylene, and p-xylene, the atoms are arranged differently around the ring of six carbon atoms.
o-xylene, m-xylene, and p-xylene are not optical isomers, which are also known as enantiomers. Optical isomers are compounds that are mirror images of each other but are not superimposable. Optical isomers are important in medicinal chemistry because they can have different biological properties even though they have the same molecular formula and structure.
o-xylene, m-xylene, and p-xylene are also not geometric isomers. Geometric isomers are compounds that have the same molecular formula and the same arrangement of atoms, but differ in the orientation of their atoms or groups of atoms in space. Geometric isomers are often found in compounds with cis-trans double bonds or ring structures.