Search results
Results from the WOW.Com Content Network
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 hydride; methylethyl methane 5 3 3 C 5 H 12: n-pentane: amyl hydride; Skellysolve A 6 5 5 C 6 H 14: n-hexane: dipropyl; Gettysolve-B; hexyl ...
This page was last edited on 11 January 2025, at 01:38 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
However, the chain of carbon atoms may also be branched at one or more points. The number of possible isomers increases rapidly with the number of carbon atoms. For example, for acyclic alkanes: [3] C 1: methane only; C 2: ethane only; C 3: propane only; C 4: 2 isomers: butane and isobutane; C 5: 3 isomers: pentane, isopentane, and neopentane
The formula for acyclic saturated hydrocarbons (i.e., alkanes) is C n H 2n+2. [1]: 623 The most general form of saturated hydrocarbons, (whether linear or branched species, and whether with or without one or more rings) is C n H 2n+2(1-r), where r is the number of rings. Those with exactly one ring are the cycloalkanes.
Icosane (alternative spelling eicosane and eichosane [2]) is an alkane with the chemical formula C 20 H 42.It has 366,319 constitutional isomers.. n-Icosane (the straight-chain structural isomer of icosane) is the shortest compound found in paraffin waxes used to form candles.
Unsaturated compounds generally carry out typical addition reactions that are not possible with saturated compounds such as alkanes. A saturated organic compound has only single bonds between carbon atoms. An important class of saturated compounds are the alkanes. Many saturated compounds have functional groups, e.g., alcohols.
[citation needed] [8] The products produced in the reaction depend on the composition of the feed, the hydrocarbon-to-steam ratio, and on the cracking temperature and furnace residence time. Light hydrocarbon feeds such as ethane , LPGs or light naphtha give product streams rich in the lighter alkenes, including ethylene, propylene, and butadiene .
The naming of polycyclic alkanes such as bicyclic alkanes and spiro alkanes is more complex, with the base name indicating the number of carbons in the ring system, a prefix indicating the number of rings ( "bicyclo-" or "spiro-"), and a numeric prefix before that indicating the number of carbons in each part of each ring, exclusive of ...