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  2. C3H6O - Wikipedia

    en.wikipedia.org/wiki/C3H6O

    The molecular formula C 3 H 6 O may refer to: . Chemistry portal; Alcohols. Allyl alcohol or 2-propen-1-ol, CH 2 =CH-CH 2 OH, CAS number 107-18-6; cyclopropanol or cyclopropyl alcohol, cyclo (-CH 2-CH 2-HOHC-), CAS number 16545-68-9

  3. 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 ...

  4. File:C3H6O isomers.svg - Wikipedia

    en.wikipedia.org/wiki/File:C3H6O_isomers.svg

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  5. Isobutane - Wikipedia

    en.wikipedia.org/wiki/Isobutane

    Since the longest continuous chain in isobutane contains only three carbon atoms, the preferred IUPAC name is 2-methylpropane but the locant (2-) is typically omitted in general nomenclature as redundant; C2 is the only position on a propane chain where a methyl substituent can be located without altering the main chain and forming the ...

  6. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    In another major industrial process, cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [24] 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid, used to make nylon.

  7. Butane - Wikipedia

    en.wikipedia.org/wiki/Butane

    Butane exists as two isomers, n-butane with connectivity CH 3 CH 2 CH 2 CH 3 and iso-butane with the formula (CH 3) 3 CH. Both isomers are highly flammable, colorless, easily liquefied gases that quickly vaporize at room temperature and pressure. Butanes are a trace components of natural gases (NG gases).

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  9. Cycloisomerization - Wikipedia

    en.wikipedia.org/wiki/Cycloisomerization

    Enyne cycloisomerization, an alkyne variant of the Alder-ene reaction (figure 5), is an intramolecular rearrangement of 1,n–enynes to give the corresponding cyclic isomer. Although the rearrangement may occur under thermal conditions, the scope of the thermal rearrangement is limited due to the requirement of high temperatures, thus ...