Coordination complexes exhibit geometrical isomerism when distinct ligands adopt varied spatial orientations around the central metal atom. For instance, in the complex [Co(NH\textsubscript{3})\textsubscript{4}Cl\textsubscript{2}]\textsuperscript{+}, the two chloride ligands can be positioned either adjacently (cis) or opposite each other (trans), leading to geometrical isomerism.