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  2. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    The simplest alkene, ethylene (C 2 H 4) (or "ethene" in the IUPAC nomenclature) is the organic compound produced on the largest scale industrially. [5] Aromatic compounds are often drawn as cyclic alkenes, however their structure and properties are sufficiently distinct that they are not classified as alkenes or olefins. [3]

  3. Saturated and unsaturated compounds - Wikipedia

    en.wikipedia.org/wiki/Saturated_and_unsaturated...

    alkene (unsaturated) vs alkane (saturated) alkyne (unsaturated) vs alkane (saturated) arene (unsaturated) vs cycloalkane (saturated) For organic compounds containing heteroatoms (other than C and H), the list of unsaturated groups is long but some common types are:

  4. Terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Terminal_alkene

    There are two types of alpha-olefins, branched and linear (or normal). The chemical properties of branched alpha-olefins with a branch at either the second (vinylidene) or the third carbon number are significantly different from the properties of linear alpha-olefins and those with branches on the fourth carbon number and further from the start of the chain.

  5. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    This is because the bond angle for an alkene, C-C=C, is 122°, while the bond angle for an alkane, C-C-C, is 112°. When these carbons form a small ring, the alkene which has a larger bond angle will have to compress more than the alkane causing more bond angle strain. [4] Cycloalkenes have a lower melting point than cycloalkanes of the same size.

  6. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    There are several functional groups that contain an alkene such as vinyl group, allyl group, or acrylic group. Hydrocarbons may form charged structures: positively charged carbocations or negative carbanions. Carbocations are often named -um. Examples are tropylium and triphenylmethyl cations and the cyclopentadienyl anion.

  7. Alkenyl peroxides - Wikipedia

    en.wikipedia.org/wiki/Alkenyl_peroxides

    The radicals formed from alkenyl peroxides can be utilized in organic radical reactions. For example, they can mediate hydrogen atom abstraction reactions and thus lead to the functionalization of C-H bonds, [7] or they can be used to introduce ketone residues by addition of the alkenyloxyl radicals to alkenes. [8] [9] [10]

  8. 1-Butene - Wikipedia

    en.wikipedia.org/wiki/1-Butene

    1-Butene (IUPAC name: But-1-ene, also known as 1-butylene) is the organic compound with the formula CH 3 CH 2 CH=CH 2.It is a colorless gas. But-1-ene is an alkene easily condensed to give a colorless liquid.

  9. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_bond

    Double bonds occur most commonly between two carbon atoms, for example in alkenes. Many double bonds exist between two different elements: for example, in a carbonyl group between a carbon atom and an oxygen atom. Other common double bonds are found in azo compounds (N=N), imines (C=N), and sulfoxides (S=O).