enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Benzene is a natural constituent of petroleum and is one of the elementary petrochemicals. Due to the cyclic continuous pi bonds between the carbon atoms, benzene is classed as an aromatic hydrocarbon. Benzene is a colorless and highly flammable liquid with a sweet smell, and is partially responsible for the aroma of gasoline.

  3. Dewar benzene - Wikipedia

    en.wikipedia.org/wiki/Dewar_benzene

    Dewar benzene (also spelled dewarbenzene) or bicyclo[2.2.0]hexa-2,5-diene is a bicyclic isomer of benzene with the molecular formula C 6 H 6. The compound is named after James Dewar who included this structure in a list of possible C 6 H 6 structures in 1869. [ 1 ]

  4. Benzene (data page) - Wikipedia

    en.wikipedia.org/wiki/Benzene_(data_page)

    *** Benzene is a carcinogen (cancer-causing agent). *** Very flammable. The pure material, and any solutions containing it, constitute a fire risk. Safe handling: Benzene should NOT be used at all unless no safer alternatives are available. If benzene must be used in an experiment, it should be handled at all stages in a fume cupboard.

  5. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    Line bond structure of benzene [5] Electron flow through p orbitals showing the aromatic nature of benzene [5] Benzene, C 6 H 6, is the least complex aromatic hydrocarbon, and it was the first one defined as such. [6] Its bonding nature was first recognized independently by Joseph Loschmidt and August Kekulé in the 19th century. [6]

  6. Molecular orbital theory - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_theory

    All carbon–carbon bonds in benzene are chemically equivalent. In MO theory this is a direct consequence of the fact that the three molecular π orbitals combine and evenly spread the extra six electrons over six carbon atoms. Structure of benzene. In molecules such as methane, CH

  7. Clar's rule - Wikipedia

    en.wikipedia.org/wiki/Clar's_rule

    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 and physical properties. Such a resonance structure is called a Clar structure. In other words, a ...

  8. 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]

  9. Claus' benzene - Wikipedia

    en.wikipedia.org/wiki/Claus'_benzene

    Claus' benzene (C 6 H 6) is a hypothetical hydrocarbon and an isomer of benzene. [1] It was proposed by Adolf Karl Ludwig Claus in 1867 [ 2 ] as a possible structure for benzene at a time when the structure of benzene was still being debated.