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  2. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon–carbon double bond. [1] The double bond may be internal or in the terminal position. Terminal alkenes are also known as α-olefins .

  3. 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.

  4. Alkylidene group - Wikipedia

    en.wikipedia.org/wiki/Alkylidene_group

    In organic chemistry, alkylidene is a general term for divalent functional groups of the form R 2 C=, where each R is an alkane or hydrogen. [1] They can be considered the functional group corresponding to mono- or disubstituted divalent carbenes (known as alkylidenes), [2] or as the result of removing two hydrogen atoms from the same carbon atom in an alkane.

  5. Category:Alkenes - Wikipedia

    en.wikipedia.org/wiki/Category:Alkenes

    Alkenes are hydrocarbons that have one or more double bonds between carbon atoms. Subcategories. This category has the following 11 subcategories, out of 11 total. A.

  6. Straight-chain terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Straight-chain_terminal_alkene

    Straight-chain terminal alkenes, also called linear alpha olefins (LAO) or normal alpha olefins (NAO), are alkenes (olefins) having a chemical formula C n H 2n, distinguished from other alkenes with a similar molecular formula by being terminal alkenes, in which the double bond occurs at the alpha (α-, 1-or primary) position, and by having a linear (unbranched) hydrocarbon chain.

  7. Pyramidal alkene - Wikipedia

    en.wikipedia.org/wiki/Pyramidal_alkene

    In one study, [3] the strained alkene 4.4 was synthesized with the highest pyramidalizion angles yet, 33.5° and 34.3°. This compound is the double Diels–Alder adduct of the diiodo cyclophane 4.1 and anthracene 4.3 by reaction in presence of potassium tert-butoxide in refluxing dibutyl ether through a di aryne intermediate 4.2 .

  8. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    The following is a list of straight-chain alkanes, the total number of isomers of each (including branched chains), and their common names, sorted by number of carbon atoms. [ 1 ] [ 2 ] Number of C atoms

  9. 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.