Linked from

The 17 pages that link to Naphthalene, each with the reason it gives.

• SublimationBroader topic: Its gradual loss from a solid illustrates sublimation at ordinary conditions.

• Coal tarBroader topic: Coal-tar fractions provided an early industrial source of naphthalene.

• Hückel's ruleBroader topic: Its ten π electrons meet the 4n + 2 criterion for the fused system.

• Polycyclic aromatic hydrocarbonBroader topic: It is the simplest PAH with two fused aromatic rings.

• Aromatic compoundBroader topic: Its fused rings illustrate aromaticity extending across a larger carbon framework.

• Aromatic hydrocarbonBroader topic: Naphthalene is a familiar fused-ring compound used in chemical manufacture.

• Benzo(a)pyreneBroader topic: Its simpler two-ring structure contrasts with benzo(a)pyrene's five fused rings.

• Fused ringBroader topic: It is the simplest familiar example of an aromatic fused-ring system.

• PhenanthreneBroader topic: It is a smaller fused-ring hydrocarbon in the same structural family.

• Degree of unsaturationBroader topic: Its seven degrees combine two rings with five formal double bonds.