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ethylene
(redirected from Ethylenes)

   Also found in: Medical, Wikipedia, Hutchinson 0.01 sec.
ethylene (ĕth`əlēn') or ethene (ĕth`ēn), H2C=CH2, a gaseous unsaturated hydrocarbon. It is the simplest alkene alkene (ăl`kēn), any of a group of aliphatic hydrocarbons whose molecules contain one or more carbon-carbon double bonds (see
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. Ethylene is colorless, has a faint odor, and has a slightly sweet taste; it melts at −169.4°C; and boils at −103.8°C;. Because of the presence of the double bond in its molecule, ethylene is very reactive. It burns in air with a luminous flame and forms explosive mixtures with pure oxygen. It combines directly with the halogens, e.g., with chlorine to form 1,2-dichloroethane. With hydrogen it forms ethane. Ethylene may be prepared by the dehydration of ethanol with sulfuric acid at about 180°C;. It is prepared commercially from natural gas and petroleum, e.g., by cracking and fractional distillation. Ethylene has many uses. It is important in the synthesis of many chemicals. It is used in making polyethylene and saran, in the manufacture of ethanol and ethylene oxide, and as an anesthetic. Ethylene was called olefiant gas by early chemists.

ethylene

Simplest olefin (CH2CH2), a colourless, flammable gas with a sweetish taste and odour. The petrochemical having the highest volume, it occurs in petroleum and natural gas but is usually produced by heating higher hydrocarbons (usually ethane and ethane-propane mixtures). Ethylene is polymerized to polyethylene either at high pressures and temperatures or by catalysis. It reacts with numerous other chemicals to produce ethanol, solvents, gasoline additives, antifreeze, detergents, and various plastics. In plants, ethylene is a hormone that inhibits growth and promotes leaf fall and fruit ripening.


ethylene
a colourless flammable gaseous alkene with a sweet odour, obtained from petroleum and natural gas and used in the manufacture of polythene and many other chemicals. Formula: CH2:CH2

ethylene [′eth·ə‚lēn]
(organic chemistry)
C2H4A colorless, flammable gas, boiling at -102.7°C; used as an agricultural chemical, in medicine, and for the manufacture of organic chemicals and polyethylene. Also known as ethene; olefiant gas.


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Comonomer diads and triads are rare, and comonomer tends to be isolated between ethylenes and very well distributed along the ethylene chain.
In Dow's ethylene/styrene copolymer, for example, ethylene units can attach in any order either to other ethylenes or to styrene monomer units, while styrene units are "hindered," meaning they can only link tail-to-tail to another styrene.
 
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