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  2. C6H10 - Wikipedia

    en.wikipedia.org/wiki/C6H10

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  3. Hexene - Wikipedia

    en.wikipedia.org/wiki/Hexene

    In organic chemistry, hexene is a hydrocarbon with the chemical formula C 6 H 12.The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the "-ene" suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond.

  4. C6H10O - Wikipedia

    en.wikipedia.org/wiki/C6H10O

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  5. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    Functional isomers are structural isomers which have different functional groups, resulting in significantly different chemical and physical properties. [ 11 ] An example is the pair propanal H 3 C–CH 2 –C(=O)-H and acetone H 3 C–C(=O)–CH 3 : the first has a –C(=O)H functional group, which makes it an aldehyde , whereas the second has ...

  6. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    Isomers do not necessarily share similar chemical or physical properties. Two main forms of isomerism are structural (or constitutional) isomerism, in which bonds between the atoms differ; and stereoisomerism (or spatial isomerism), in which the bonds are the same but the relative positions of the atoms differ. Isomeric relationships form a ...

  7. C6H10O3 - Wikipedia

    en.wikipedia.org/wiki/C6H10O3

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  8. Hexose - Wikipedia

    en.wikipedia.org/wiki/Hexose

    Of these D-isomers, all except D-altrose occur in living organisms, but only three are common: D-glucose, D-galactose, and D-mannose. The L -isomers are generally absent in living organisms; however, L -altrose has been isolated from strains of the bacterium Butyrivibrio fibrisolvens .

  9. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    The most stable trans-isomers of 10 ring or greater cycloalkenes exhibit 4 irregularities from standard geometric norms. The first irregularity is twisted planes of substituents along the C=C. Using C=C as the stable axis, 2 substituents of 1 carbon can be visualized on the same plane, equally applied to the other carbon.