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Numerous organic compounds have other common names, often originating in historical source material thereof. The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid.
Pentane is an organic compound with the formula C 5 H 12 —that is, an alkane with five carbon atoms. The term may refer to any of three structural isomers, or to a mixture of them: in the IUPAC nomenclature, however, pentane means exclusively the n-pentane isomer, in which case pentanes refers to a mixture of them; the other two are called isopentane (methylbutane) and neopentane ...
2-Methylpentane, trivially known as isohexane, is a branched-chain alkane with the molecular formula C 6 H 14. It is a structural isomer of hexane composed of a methyl group bonded to the second carbon atom in a pentane chain.
The longest possible main alkane chain is used; therefore 3-ethyl-4-methylhexane instead of 2,3-diethylpentane, even though these describe equivalent structures. The di-, tri- etc. prefixes are ignored for the purpose of alphabetical ordering of side chains (e.g. 3-ethyl-2,4-dimethylpentane, not 2,4-dimethyl-3-ethylpentane).
These long chain compounds have surprising electronic properties - high electrical conductivity, for example - arising from sigma delocalization of the electrons in the chain. [9] Even silicon–silicon pi bonds are possible. However, these bonds are less stable than the carbon analogues. Disilane and longer silanes are quite reactive compared ...
2,2-Dimethylpentane can form a clathrate hydrate with helper gas molecules. The type of clathrate formed is called "clathrate H". 2,2-Dimethylpentane was the first compound for which the structure was determined. The clathrate has 34 molecules of water per molecule, and also has xenon and hydrogen sulfide as helper molecules.
The prototypical example of antiaromaticity, cyclobutadiene, is the subject of debate, with some scientists arguing that antiaromaticity is not a major factor contributing to its destabilization. [2] Cyclooctatetraene appears at first glance to be antiaromatic, but is an excellent example of a molecule adopting a non-planar geometry to avoid ...
It is of similar structure to the isomeric 2-methylpentane, which has the methyl group located on the second carbon of the pentane chain. As of early 1990s, it was present in American [3] and European [4] gasoline in small amounts, and by 2011 its share in US gas varied between 1.5 and 6% [5] It has close research and motor octane numbers of 74 ...