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  2. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Most people in developed countries have measureable baseline levels of benzene and other aromatic petroleum hydrocarbons in their blood. In the body, benzene is enzymatically converted to a series of oxidation products including muconic acid, phenylmercapturic acid, phenol, catechol, hydroquinone and 1,2,4-trihydroxybenzene. Most of these ...

  3. Hückel's rule - Wikipedia

    en.wikipedia.org/wiki/Hückel's_rule

    8 (cyclooctatetraenide anion), with ten π electrons obeys the 4n + 2 rule for n = 2 and is planar, while the 1,4-dimethyl derivative of the dication, with six π electrons, is also believed to be planar and aromatic. [8] The Cyclononatetraenide anion (C 9 H – 9) is the largest all-cis monocyclic annulene/annulenyl system that is planar and ...

  4. Hückel method - Wikipedia

    en.wikipedia.org/wiki/Hückel_method

    To summarize, we are assuming that: (1) the energy of an electron in an isolated C(2p z) orbital is =; (2) the energy of interaction between C(2p z) orbitals on adjacent carbons i and j (i.e., i and j are connected by a σ-bond) is =; (3) orbitals on carbons not joined in this way are assumed not to interact, so = for nonadjacent i and j; and ...

  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. Aromaticity - Wikipedia

    en.wikipedia.org/wiki/Aromaticity

    Two different resonance forms of benzene (top) combine to produce an average structure (bottom). In organic chemistry, aromaticity is a chemical property describing the way in which a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals exhibits a stabilization stronger than would be expected from conjugation alone.

  7. 1,2,4-Trimethylbenzene - Wikipedia

    en.wikipedia.org/wiki/1,2,4-Trimethylbenzene

    1,2,4-Trimethylbenzene, also known as pseudocumene, is an organic compound with the chemical formula C 6 H 3 (CH 3) 3. Classified as an aromatic hydrocarbon, it is a flammable colorless liquid with a strong odor. It is nearly insoluble in water but soluble in organic solvents.

  8. Mesitylene - Wikipedia

    en.wikipedia.org/wiki/Mesitylene

    The other two isomeric trimethylbenzenes are 1,2,4-trimethylbenzene (pseudocumene) and 1,2,3-trimethylbenzene (hemimellitene). All three compounds have the formula C 6 H 3 (CH 3) 3, which is commonly abbreviated C 6 H 3 Me 3. Mesitylene is a colorless liquid with sweet aromatic odor. It is a component of coal tar, which is its traditional source.

  9. Phenyl group - Wikipedia

    en.wikipedia.org/wiki/Phenyl_group

    Phenyl groups (like all aromatic compounds) have enhanced stability in comparison to equivalent bonding in aliphatic (non-aromatic) groups. This increased stability is due to the unique properties of aromatic molecular orbitals. [2] The bond lengths between carbon atoms in a phenyl group are approximately 1.4 Å. [6]