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The alkanes have two main commercial sources: petroleum (crude oil) and natural gas. An alkyl group is an alkane-based molecular fragment that bears one open valence for bonding. They are generally abbreviated with the symbol for any organyl group , R, although Alk is sometimes used to specifically symbolize an alkyl group (as opposed to an ...
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 hydride; methylethyl methane 5 3 3 C 5 H 12: n-pentane: amyl hydride; Skellysolve A 6 5 5 C 6 H ...
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 2 n +2(1- r ) , where r is the number of rings.
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Natural gas burning on a gas stove Burning of natural gas coming out of the ground. Natural gas (also called fossil gas, methane gas, or simply gas) is a naturally occurring mixture of gaseous hydrocarbons consisting primarily of methane (95%) [1] in addition to various smaller amounts of other higher alkanes.
Butane (/ ˈ b juː t eɪ n /) is an alkane with the formula C 4 H 10. Butane exists as two isomers, n-butane with connectivity CH 3 CH 2 CH 2 CH 3 and iso-butane with the formula (CH 3) 3 CH. Both isomers are highly flammable, colorless, easily liquefied gases that quickly vaporize at room temperature and pressure. Butanes are a trace ...
Higher alkanes are naturally present in crude oil and can be obtained via fractional distillation.Saturated fatty acids decarboxylate to higher alkanes. Long olefins can be hydrogenated to yield higher alkanes. n-alkanes can be isolated via the formation of urea clathrates.They can also be synthesized through Kolbe electrolysis or other coupling reactions like the Wurtz reaction.
In petrochemistry, petroleum geology and organic chemistry, cracking is the process whereby complex organic molecules such as kerogens or long-chain hydrocarbons are broken down into simpler molecules such as light hydrocarbons, by the breaking of carbon–carbon bonds in the precursors.