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・ 2-Arachidonoylglycerol
・ 2-Arachidonyl glyceryl ether
・ 2-Azetidinone
・ 2-Benzylpiperidine
・ 2-bit
・ 2-bridge knot
・ 2-Bromo-1-chloropropane
・ 2-Bromo-4,5-methylenedioxyamphetamine
・ 2-Bromo-LSD
・ 2-Bromobutane
・ 2-Bromobutyric acid
・ 2-Bromohexane
・ 2-Bromomescaline
・ 2-Bromopropane
・ 2-Butanol
2-Butene
・ 2-Butoxyethanol
・ 2-Butoxyethanol acetate
・ 2-Butyne
・ 2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase
・ 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase
・ 2-C-Methyl-D-erythritol-2,4-cyclopyrophosphate
・ 2-C-Methylerythritol 4-phosphate
・ 2-Carbomethoxytropinone
・ 2-Carboxy-D-arabinitol-1-phosphatase
・ 2-category
・ 2-chloro-4-carboxymethylenebut-2-en-1,4-olide isomerase
・ 2-Chloro-9,10-bis(phenylethynyl)anthracene
・ 2-Chloro-9,10-diphenylanthracene
・ 2-Chloro-m-cresol


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2-Butene : ウィキペディア英語版
2-Butene

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2-Butene is an acyclic alkene with four carbon atoms. It is the simplest alkene exhibiting ''cis''/''trans''-isomerism (also known as (''E''/''Z'')-isomerism); that is, it exists as two geometric isomers ''cis''-2-butene ((''Z'')-2-butene) and ''trans''-2-butene ((''E'')-2-butene).
It is a petrochemical, produced by the catalytic cracking of crude oil or the dimerization of ethylene. Its main uses are in the production of gasoline (petrol) and butadiene,〔.〕 although some 2-butene is also used to produce the solvent butanone via hydration to 2-butanol followed by oxidation.
The two isomers are extremely difficult to separate by distillation because of the proximity of their boiling points (~4 °C for ''cis'' and ~1 °C for ''trans''〔(Chemical Safety Information from Intergovernmental Organizations )〕). However, separation is unnecessary in most industrial settings, as both isomers behave similarly in most of the desired reactions. A typical industrial 2-butene mixture is 70% (''Z'')-2-butene (''cis''-isomer) and 30% (''E'')-2-butene (''trans''-isomer). Butane and 1-butene are common impurities, present at 1% or more in industrial mixtures, which also contain smaller amounts of isobutene, butadiene and butyne.〔
==References==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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