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  2. Allenes - Wikipedia

    en.wikipedia.org/wiki/Allenes

    In organic chemistry, allenes are organic compounds in which one carbon atom has double bonds with each of its two adjacent carbon atoms (R 2 C=C=CR 2, where R is H or some organyl group). [1] Allenes are classified as cumulated dienes. The parent compound of this class is propadiene (H 2 C=C=CH 2), which is itself also called allene.

  3. Propadiene - Wikipedia

    en.wikipedia.org/wiki/Propadiene

    Propadiene (/ p r oʊ p ə ˈ d aɪ iː n /) or allene (/ ˈ æ l iː n /) is the organic compound with the formula H 2 C=C=CH 2. It is the simplest allene, i.e. a compound with two adjacent carbon double bonds. [3] As a constituent of MAPP gas, it has been used as a fuel for specialized welding.

  4. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    Number of C atoms Number of isomers [3] [4] Number of isomers including stereoisomers [3] [5] Molecular Formula Name of straight chain Synonyms 1 1 1 CH 4: methane: methyl hydride; natural gas 2 1 1 C 2 H 6: ethane: dimethyl; ethyl hydride; methyl methane 3 1 1 C 3 H 8: propane: dimethyl methane; propyl hydride 4 2 2 C 4 H 10: n-butane: butyl ...

  5. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    Each carbon atom of the double bond uses its three sp 2 hybrid orbitals to form sigma bonds to three atoms (the other carbon atom and two hydrogen atoms). The unhybridized 2p atomic orbitals, which lie perpendicular to the plane created by the axes of the three sp 2 hybrid orbitals, combine to form the pi bond.

  6. Carbones - Wikipedia

    en.wikipedia.org/wiki/Carbones

    The structure of carbodicarbenes greatly resembles that of carbodiphosphoranes. [4] Computational data for a N-methyl-substituted carbodicarbene predicted a carbon-carbon bond with a length only marginally longer than a C=C bond in a typical allene at 1.358 Å (compared with 1.308 Å for allene), but with a significantly bent bond angle of 131.8° (compared to 180° for a standard linear ...

  7. 1-Phosphaallenes - Wikipedia

    en.wikipedia.org/wiki/1-phosphaallenes

    The first example of a stable heteroalkene E=C or E=E' (E, E' = P) containing a heavy group 15 element was reported in 1982 by Yoshifuji. [1] [2] After the realization of heavier heteroalkenes, the field of organometallic chemistry began exploring the idea of heteroallenes E=C=E' and E=C=C=E', in which one or more carbon atom of an allene is substituted by a heavier atom.

  8. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    In two of the isomers, the three carbon atoms are connected in an open chain, but in one of them (propadiene or allene; I) the carbons are connected by two double bonds, while in the other (propyne or methylacetylene; II) they are connected by a single bond and a triple bond.

  9. 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.