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  2. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Benzene is an organic chemical compound with the molecular formula C 6 H 6. The benzene molecule is composed of six carbon atoms joined in a planar hexagonal ring with one hydrogen atom attached to each. Because it contains only carbon and hydrogen atoms, benzene is classed as a hydrocarbon.

  3. Degree of unsaturation - Wikipedia

    en.wikipedia.org/wiki/Degree_of_unsaturation

    For hydrocarbons, the DBE (or IHD) tells us the number of rings and/or extra bonds in a non-saturated structure, which equals the number of hydrogen pairs that are required to make the structure saturated, simply because joining two elements to form a ring or adding one extra bond (e.g., a single bond changed to a double bond) in a structure reduces the need for two H's.

  4. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    Benzoic acid occurs naturally in many plants [9] and serves as an intermediate in the biosynthesis of many secondary metabolites. Salts of benzoic acid are used as food preservatives . Benzoic acid is an important precursor for the industrial synthesis of many other organic substances.

  5. 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 ...

  6. Prismane - Wikipedia

    en.wikipedia.org/wiki/Prismane

    Prismane is far less stable than benzene. The carbon (and hydrogen) atoms of the prismane molecule are arranged in the shape of a six-atom triangular prism—this compound is the parent and simplest member of the prismanes class of molecules. Albert Ladenburg proposed this structure for the compound now known as benzene. [2]

  7. Transfer hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Transfer_hydrogenation

    It uses hydrogen donor compounds such as formic acid, isopropanol or dihydroanthracene, dehydrogenating them to CO 2, acetone, or anthracene respectively. [1] Often, the donor molecules also function as solvents for the reaction. A large scale application of transfer hydrogenation is coal liquefaction using "donor solvents" such as tetralin. [2 ...

  8. Indiana plastics fire spewed toxic chemicals, EPA tests find ...

    www.aol.com/news/indiana-plastics-fire-spewed...

    Indiana plastics fire spewed toxic chemicals, EPA tests find, including benzene and hydrogen cyanide Selina Guevara and Aria Bendix and David K. Li Updated April 14, 2023 at 8:03 PM

  9. Hydrogen compounds - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_compounds

    [2] [3] Hydrogen also forms compounds with less electronegative elements, such as metals and metalloids, where it takes on a partial negative charge. These compounds are often known as hydrides. [4] Water contains two hydrogen atoms covalently bonded to one oxygen atom, [5] and is one of the most well-studied compounds. [6]