翻訳と辞書 Words near each other ・ 1,3-Dipolar cycloaddition ・ 1,3-dipole ・ 1,3-Dithietane ・ 1,3-Indandione ・ 1,3-Propane sultone ・ 1,3-Propanediol ・ 1,3-propanediol dehydrogenase ・ 1,3-Propanedithiol ・ 1,3-Thiazepine ・ 1,4,2-Dithiazole ・ 1,4,6-Androstatriene-3,17-dione ・ 1,4,7-Triazacyclononane ・ 1,4,7-Trithiacyclononane ・ 1,4-a-glucan 6-a-glucosyltransferase ・ 1,4-Benzodioxine ・ 1,4-Benzoquinone ・ 1,4-beta-D-xylan synthase ・ 1,4-Butanediol ・ 1,4-Butynediol ・ 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 Dictionary Lists mini英和辞書 mini和英辞書 Webster 1913 Latin-English FOLDOC Wikipedia English ウィキペディア

翻訳と辞書　辞書検索 [ 開発暫定版 ] スポンサード リンク 1,4-Benzoquinone ： ウィキペディア英語版 1,4-Benzoquinone |Section2= |Section7= |Section8= }} 1,4-Benzoquinone, commonly known as ''para''-quinone, is a chemical compound with the formula C6H4O2. In a pure state, it forms bright-yellow crystals with a characteristic irritating odor, resembling that of chlorine, bleach, and hot plastic. This six-membered ring compound is the oxidized derivative of 1,4-hydroquinone. The molecule is multifunctional: it exhibits properties of a ketone, forming an oxime; an oxidant, forming the dihydroxy derivative; and an alkene, undergoing addition reactions, especially those typical for α,β-unsaturated ketones. 1,4-Benzoquinone is sensitive toward both strong mineral acids and alkali, which cause condensation and decomposition of the compound. ==Preparation== 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「1,4-Benzoquinone」の詳細全文を読む スポンサード リンク 翻訳と辞書 : 翻訳のためのインターネットリソース Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.