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  2. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    In organic chemistry, the cycloalkanes (also called naphthenes, but distinct from naphthalene) are the monocyclic saturated hydrocarbons. [1] In other words, a cycloalkane consists only of hydrogen and carbon atoms arranged in a structure containing a single ring (possibly with side chains ), and all of the carbon-carbon bonds are single .

  3. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

    C 5 H 10 is the molecular formula of 13 hydrocarbon isomers (represented by their CAS numbers on the chart). They can be divided into cycloalkanes and alkenes . Cycloalkanes

  4. Mass spectral interpretation - Wikipedia

    en.wikipedia.org/wiki/Mass_spectral_interpretation

    Cycloalkanes have relatively intense molecular ion peaks (two bonds have to break). Alkene fragmentation peaks are often most significant mode. Loss of “CH 2 CH 2 “ (= 28) is common, if present. However, for the substituted cycloalkanes, they prefer to form the cycloalkyl cations by cleavage at the branched points. [11]

  5. Cyclopropane - Wikipedia

    en.wikipedia.org/wiki/Cyclopropane

    Cyclopropane is the cycloalkane with the molecular formula (CH 2) 3, consisting of three methylene groups (CH 2) linked to each other to form a triangular ring.The small size of the ring creates substantial ring strain in the structure.

  6. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    Cyclohexane is the most stable of the cycloalkanes, due to the stability of adapting to its chair conformer. [4] This conformer stability allows cyclohexane to be used as a standard in lab analyses. More specifically, cyclohexane is used as a standard for pharmaceutical reference in solvent analysis of pharmaceutical compounds and raw materials.

  7. Cyclodecane - Wikipedia

    en.wikipedia.org/wiki/Cyclodecane

    Print/export Download as PDF; Printable version; In other projects Wikimedia Commons; ... Cyclodecane is a cycloalkane with the chemical formula C 10 H 20. References

  8. Ring strain - Wikipedia

    en.wikipedia.org/wiki/Ring_strain

    In alkanes, optimum overlap of atomic orbitals is achieved at 109.5°. The most common cyclic compounds have five or six carbons in their ring. [6] Adolf von Baeyer received a Nobel Prize in 1905 for the discovery of the Baeyer strain theory, which was an explanation of the relative stabilities of cyclic molecules in 1885.

  9. Housane - Wikipedia

    en.wikipedia.org/wiki/Housane

    Housane or bicyclo[2.1.0]pentane is a saturated cycloalkane with the formula C 5 H 8. It is a colorless, volatile liquid at room temperature. It is a colorless, volatile liquid at room temperature. It was named "housane" because of its shape, which resembles a simple drawing of a house.