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・ 2,4-Dinitrophenol
・ 2,4-Dinitrophenylhydrazine
・ 2,4-Dinitrophenylmorphine
・ 2,4-Dinitrotoluene
・ 2,4-Dithiapentane
・ 2,4-DNP
・ 2,4-Xylidine
・ 2,5-Bis(hydroxymethyl)furan
・ 2,5-diamino-6-(ribosylamino)-4(3H)-pyrimidinone 5'-phosphate reductase
・ 2,5-Diamino-6-hydroxy-4-(5-phosphoribosylamino)pyrimidine
・ 2,5-Diaminotoluene
・ 2,5-diaminovalerate transaminase
・ 2,5-Dichloroaniline
・ 2,5-didehydrogluconate reductase
・ 2,5-Dihydrofuran
2,5-Dihydroxy-1,4-benzoquinone
・ 2,5-Dihydroxycinnamic acid
・ 2,5-dihydroxypyridine 5,6-dioxygenase
・ 2,5-diketocamphane 1,2-monooxygenase
・ 2,5-Diketopiperazine
・ 2,5-Dimethoxy-4-(2-fluoroethyl)amphetamine
・ 2,5-Dimethoxy-4-amylamphetamine
・ 2,5-Dimethoxy-4-bromoamphetamine
・ 2,5-Dimethoxy-4-butylamphetamine
・ 2,5-Dimethoxy-4-chloroamphetamine
・ 2,5-Dimethoxy-4-ethoxyamphetamine
・ 2,5-Dimethoxy-4-ethylamphetamine
・ 2,5-Dimethoxy-4-fluoroamphetamine
・ 2,5-Dimethoxy-4-iodoamphetamine
・ 2,5-Dimethoxy-4-isopropylamphetamine


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2,5-Dihydroxy-1,4-benzoquinone : ウィキペディア英語版
2,5-Dihydroxy-1,4-benzoquinone

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2,5-Dihydroxy-1,4-benzoquinone or 2,5-Dihydroxy-''para''-benzoquinone is an organic compound with formula , formally derived from 1,4-Benzoquinone by replacing two hydrogen atoms with hydroxyl (OH) groups. It is one of seven dihydroxybenzoquinone isomers.
The IUPAC name is 2,5-hydroxycyclohexa-2,5-diene-1,4-dione.
Like many alcohols, it behaves like an acid: it can cede two protons (pKal = 2.95, pKa2 = 4.87) to form the anion . 〔
Sahar I. Mostafa (), ''Complexes of 2,5-dihydroxy-1,4-benzoquinone and chloranilic acid with second and third row transition elements''. Journal Transition Metal Chemistry, volume 24, number 3, pages 306-310. .

==See also==

*Hydroxy-1,4-benzoquinone
*Tetrahydroxy-1,4-benzoquinone

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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