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・ Cyclopis
・ Cycloplane C-1
・ Cycloplegia
・ Cyclopogon
・ Cyclopogon cranichoides
・ Cyclopogon elatus
・ Cyclopogon elegans
・ Cyclopoida
・ Cycloponympha
・ Cycloponympha hermione
・ Cycloponympha julia
・ Cycloponympha perspicua
・ Cycloprionus
・ Cycloprop-2-ene carboxylic acid
・ Cyclopropanation
Cyclopropane
・ Cyclopropane fatty acid
・ Cyclopropane-fatty-acyl-phospholipid synthase
・ Cyclopropanetrione
・ Cyclopropanol
・ Cyclopropanone
・ Cyclopropatriene
・ Cyclopropene
・ Cyclopropenone
・ Cyclopropenylidene
・ Cyclopropyl cyanide
・ Cyclopropyl group
・ Cyclopropylmescaline
・ Cycloprora
・ Cycloprorodes


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Cyclopropane : ウィキペディア英語版
Cyclopropane

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Cyclopropane is a cycloalkane molecule with the molecular formula C3H6, consisting of three carbon atoms linked to each other to form a ring, with each carbon atom bearing two hydrogen atoms resulting in D3h molecular symmetry. Cyclopropane and propene have the same molecular formula but have different structures, making them structural isomers.
Cyclopropane is an anaesthetic when inhaled. In modern anaesthetic practice, it has been superseded by other agents, due to its extreme reactivity under normal conditions: when the gas is mixed with oxygen, there is a significant risk of explosion.
==History==
Cyclopropane was discovered in 1881 by August Freund, who also proposed the correct structure for the new substance in his first paper. Freund treated 1,3-dibromopropane with sodium, causing an intramolecular Wurtz reaction leading directly to cyclopropane. The yield of the reaction was improved by Gustavson in 1887 with the use of zinc instead of sodium. Cyclopropane had no commercial application until Henderson and Lucas discovered its anaesthetic properties in 1929; industrial production had begun by 1936.

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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