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  2. 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 was named "housane" because of its shape, which resembles a simple drawing of a house. Structurally, the molecule consists of cyclopropane fused to cyclobutane.

  3. 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 .

  4. Cyclodecane - Wikipedia

    en.wikipedia.org/wiki/Cyclodecane

    3D model . Interactive image ... 282 to 283 K) Boiling point: 201 °C (394 °F; 474 K) Hazards Flash point: ... Cyclodecane is a cycloalkane with the chemical formula ...

  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. Category:Cycloalkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Cycloalkanes

    Cycloalkanes are hydrocarbons that form one or more rings. See also. Category:Cycloalkenes; Subcategories. This category has the following 6 subcategories, out of 6 ...

  7. Prelog strain - Wikipedia

    en.wikipedia.org/wiki/Prelog_strain

    Molecular mechanics calculations of strain energy differences ΔSI between a sp 2 and sp 3 state in cycloalkanes show linear correlations with rates (as ⁡) of many reactions involving the transition between sp 2 and sp 3 states, such as ketone reduction, alcohol oxidation or nucleophilic substitution, the contribution of transannular strain ...

  8. Cyclooctane - Wikipedia

    en.wikipedia.org/wiki/Cyclooctane

    Hendrickson noted that "cyclooctane is unquestionably the conformationally most complex cycloalkane owing to the existence of many conformers of comparable energy". The boat-chair conformation (below) is the most stable form. [4] This conformation was confirmed by Allinger and co-workers. [5] The crown conformation (below) [6] is slightly less ...

  9. Cyclohexadecane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexadecane

    319 °c (606 °f; 592 k) Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references