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・ 1-Fluoro-2,4-dinitrobenzene
・ 1-Heptacosanol
・ 1-Heptanol
・ 1-Hexacosanol
・ 1-Hexanol
・ 1-Hexene
・ 1-Hexene (data page)
・ 1-hydroxy-2-naphthoate 1,2-dioxygenase
・ 1-hydroxy-2-naphthoate hydroxylase
・ 1-Hydroxy-7-azabenzotriazole
・ 1-Hydroxycarotenoid 3,4-desaturase
・ 1-Hydroxyphenanthrene
・ 1-Hydroxypyrene
・ 1-Ichi
・ 1,4-Cycloheptadiene
1,4-Cyclohexadiene
・ 1,4-Cyclohexanedione
・ 1,4-Diamino-2,3-dihydroanthraquinone
・ 1,4-Diazepine
・ 1,4-Dibromobenzene
・ 1,4-Dichloro-2-nitrobenzene
・ 1,4-Dichlorobenzene
・ 1,4-Dichlorobut-2-ene
・ 1,4-dihydroxy-2-naphthoate polyprenyltransferase
・ 1,4-dihydroxy-2-naphthoyl-CoA hydrolase
・ 1,4-Dihydroxyanthraquinone
・ 1,4-Dimethoxybenzene
・ 1,4-Dioxane
・ 1,4-Dioxene
・ 1,4-Dioxin


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1,4-Cyclohexadiene : ウィキペディア英語版
1,4-Cyclohexadiene

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1,4-Cyclohexadiene is an organic compound with the formula C6H8. It is a colourless, flammable liquid that is of academic interest as a prototype of a large class of related compounds called terpenoids, an examples being γ-terpinene. An isomer exists of this compound, 1,3-cyclohexadiene.
==Synthesis and reactions==
In the laboratory, substituted 1,4-cyclohexadienes are synthesized by Birch reduction of related aromatic compounds using an alkali metal and a proton donor such as ammonia. In this way, over reduction to the fully saturated ring is avoided.

1,4-Cyclohexadiene and its derivatives are easily aromatized, the driving force being the formation of an aromatic ring. The conversion to an aromatic system may be performed in the laboratory using an alkene such as styrene, along with a hydrogen transfer agent such as palladium metal supported on charcoal.

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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