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- Geminal_diol abstract "A geminal diol (or gem-diol for short) is any organic compound having two hydroxyl functional groups (-OH) bound to the same carbon atom.The simplest geminal diol is methanediol CH4O2 or H2C(OH)2. Other examples are dihydroxymalonic acid HOOC-C(OH)2-COOH and decahydroxycyclopentane (C(OH)2)5.Geminal diols are a subclass of the diols, which in turn are a special class of alcohols. The two hydroxyls in a geminal diol are easily converted to a carbonyl or keto group C=O by loss of one water molecule, thus turning the diol into a ketone. Conversely, ketones tend to combine with water to form the corresponding geminal diols. The equilibrium in water solution may be shifted towards either compound; for example, the equilibrium constant for the conversion of acetone (H3C)2C=O to propane-2,2-diol (H3C)2C(OH)2 is about 10−3, while that of formaldehyde H2C=O to methanediol H2C(OH)2 is 10+3, and that of hexafluoroacetone (F3C)2C=O to hexafluoropropane-2,2-diol (F3C)2C(OH)2 is about 10+6. In some cases, such as decahydroxycyclopentane and dodecahydroxycyclohexane, the geminal diol is stable while the ketone is not.".
- Geminal_diol thumbnail Ketone-hydrate-2D-skeletal.png?width=300.
- Geminal_diol wikiPageID "2475208".
- Geminal_diol wikiPageLength "2211".
- Geminal_diol wikiPageOutDegree "26".
- Geminal_diol wikiPageRevisionID "608054309".
- Geminal_diol wikiPageWikiLink Acetone.
- Geminal_diol wikiPageWikiLink Alcohol.
- Geminal_diol wikiPageWikiLink Carbon.
- Geminal_diol wikiPageWikiLink Carbonyl.
- Geminal_diol wikiPageWikiLink Category:Diols.
- Geminal_diol wikiPageWikiLink Covalent_bond.
- Geminal_diol wikiPageWikiLink Decahydroxycyclopentane.
- Geminal_diol wikiPageWikiLink Dihydroxymalonic_acid.
- Geminal_diol wikiPageWikiLink Diol.
- Geminal_diol wikiPageWikiLink Dodecahydroxycyclohexane.
- Geminal_diol wikiPageWikiLink Equilibrium_constant.
- Geminal_diol wikiPageWikiLink Formaldehyde.
- Geminal_diol wikiPageWikiLink Functional_group.
- Geminal_diol wikiPageWikiLink Functional_groups.
- Geminal_diol wikiPageWikiLink Geminal.
- Geminal_diol wikiPageWikiLink Hexafluoroacetone.
- Geminal_diol wikiPageWikiLink Hexafluoropropane-2,2-diol.
- Geminal_diol wikiPageWikiLink Hydrogen.
- Geminal_diol wikiPageWikiLink Hydroxyl.
- Geminal_diol wikiPageWikiLink Ketone.
- Geminal_diol wikiPageWikiLink Methanediol.
- Geminal_diol wikiPageWikiLink Organic_compound.
- Geminal_diol wikiPageWikiLink Oxygen.
- Geminal_diol wikiPageWikiLink Propane-2,2-diol.
- Geminal_diol wikiPageWikiLink Vicinal_(chemistry).
- Geminal_diol wikiPageWikiLink File:Ketone-hydrate-2D-skeletal.png.
- Geminal_diol wikiPageWikiLinkText "Geminal diol".
- Geminal_diol wikiPageWikiLinkText "geminal diol".
- Geminal_diol hasPhotoCollection Geminal_diol.
- Geminal_diol wikiPageUsesTemplate Template:Reflist.
- Geminal_diol subject Category:Diols.
- Geminal_diol hypernym O.
- Geminal_diol type Person.
- Geminal_diol type Alcohol.
- Geminal_diol type Polyol.
- Geminal_diol comment "A geminal diol (or gem-diol for short) is any organic compound having two hydroxyl functional groups (-OH) bound to the same carbon atom.The simplest geminal diol is methanediol CH4O2 or H2C(OH)2. Other examples are dihydroxymalonic acid HOOC-C(OH)2-COOH and decahydroxycyclopentane (C(OH)2)5.Geminal diols are a subclass of the diols, which in turn are a special class of alcohols.".
- Geminal_diol label "Geminal diol".
- Geminal_diol sameAs Diol_géminal.
- Geminal_diol sameAs Diole_geminalne.
- Geminal_diol sameAs m.09g9zqm.
- Geminal_diol sameAs Geminal_diol.
- Geminal_diol sameAs Q3028705.
- Geminal_diol sameAs Q3028705.
- Geminal_diol wasDerivedFrom Geminal_diol?oldid=608054309.
- Geminal_diol depiction Ketone-hydrate-2D-skeletal.png.
- Geminal_diol isPrimaryTopicOf Geminal_diol.