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  2. Anthracene - Wikipedia

    en.wikipedia.org/wiki/Anthracene

    Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C 14 H 10, consisting of three fused benzene rings. It is a component of coal tar. Anthracene is used in the production of the red dye alizarin and other dyes. Anthracene is colorless but exhibits a blue (400–500 nm peak) fluorescence under ultraviolet radiation. [13]

  3. Polycyclic aromatic hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Polycyclic_aromatic...

    Therefore, in this molecule the outer rings have greater aromatic character whereas the central ring is less aromatic and therefore more reactive. [citation needed] In contrast, in anthracene the resonance structures have one sextet each, which can be at any of the three rings, and the aromaticity spreads out more evenly across the whole molecule.

  4. Clar's rule - Wikipedia

    en.wikipedia.org/wiki/Clar's_rule

    An aromatic π-sextet can be represented by a circle, as in the case of the anthracene molecule (below). Clar's rule states that for a benzenoid polycyclic aromatic hydrocarbon (i.e. one with only hexagonal rings), the resonance structure with the largest number of disjoint aromatic π-sextets is the most important to characterize its chemical ...

  5. List of benzo compounds - Wikipedia

    en.wikipedia.org/wiki/List_of_benzo_compounds

    Letters and numbers in the parent compound Structural formula of the benzocompound Benzocompound Anthracene: Benzo[a]anthracene: by adding four extra carbon atoms to the parent compound, the leftmost upper ring is formed. Phenanthrene: Benzo[b]fenanthrene: by adding four carbon atoms to the parent compound the right most ring is formed. Clearly ...

  6. Polycyclic compound - Wikipedia

    en.wikipedia.org/wiki/Polycyclic_compound

    In the field of organic chemistry, a polycyclic compound is an organic compound featuring several closed rings of atoms, primarily carbon. [1] These ring substructures include cycloalkanes , aromatics , and other ring types.

  7. Tetracene - Wikipedia

    en.wikipedia.org/wiki/Tetracene

    Tetracene, also called naphthacene, is a polycyclic aromatic hydrocarbon. It has the appearance of a pale orange powder. Tetracene is the four-ringed member of the series of acenes. Tetracene is a molecular organic semiconductor, used in organic field-effect transistors (OFETs) and organic light-emitting diodes (OLEDs).

  8. 11 Fast-Food Soups, Ranked Best to Worst - AOL

    www.aol.com/11-fast-food-soups-ranked-170000031.html

    4. Wendy’s Chili. Price: $2.69 cup / $3.59 bowl Let’s address the elephant in the room, because it’s a story so damning for Wendy’s that even today in 2024, it made me hesitate to order this.

  9. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    Heteroarenes are aromatic compounds, where at least one methine or vinylene (-C= or -CH=CH-) group is replaced by a heteroatom: oxygen, nitrogen, or sulfur. [3] Examples of non-benzene compounds with aromatic properties are furan, a heterocyclic compound with a five-membered ring that includes a single oxygen atom, and pyridine, a heterocyclic compound with a six-membered ring containing one ...