This document discusses aromatic compounds and Hückel's rule for aromaticity. It explains that aromatic compounds are cyclic, planar and have (4n+2) π electrons, allowing for resonance delocalization that contributes to the compounds' stability. This delocalization leads to intermediate bond lengths and shielding/deshielding patterns in NMR. Anti-aromatic compounds follow the same criteria but have 4n π electrons, making them less stable due to their paramagnetic ring currents. Examples are provided to illustrate aromatic and anti-aromatic systems based on the number of π electrons.