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- Alkoxide abstract "An alkoxide is the conjugate base of an alcohol and therefore consists of an organic group bonded to a negatively charged oxygen atom. They can be written as RO−, where R is the organic substituent. Alkoxides are strong bases and, when R is not bulky, good nucleophiles and good ligands. Alkoxides, although generally not stable in protic solvents such as water, occur widely as intermediates in various reactions, including the Williamson ether synthesis. Transition metal alkoxides are widely used for coatings and as catalysts.Enolates are unsaturated alkoxides derived by deprotonation of a C-H bond adjacent to a ketone or aldehyde. The nucleophilic center for simple alkoxides is located on the oxygen, whereas the nucleophilic site on enolates is delocalized onto both carbon and oxygen sites.Phenoxides are close relatives of the alkoxides, in which the alkyl group is replaced by a derivative of benzene. Phenol is more acidic than a typical alcohol; thus, phenoxides are correspondingly less basic and less nucleophilic than alkoxides. They are, however, often easier to handle, and yield derivatives that are more crystalline than those of the alkoxides.".
- Alkoxide thumbnail Alkoxide_General_Formulae_V.1.png?width=300.
- Alkoxide wikiPageID "485854".
- Alkoxide wikiPageRevisionID "597741121".
- Alkoxide hasPhotoCollection Alkoxide.
- Alkoxide subject Category:Alkoxides.
- Alkoxide subject Category:Bases.
- Alkoxide subject Category:Coordination_chemistry.
- Alkoxide subject Category:Functional_groups.
- Alkoxide type Abstraction100002137.
- Alkoxide type Bases.
- Alkoxide type Footing113790912.
- Alkoxide type Foundation113790712.
- Alkoxide type FunctionalGroups.
- Alkoxide type Group100031264.
- Alkoxide type Relation100031921.
- Alkoxide comment "An alkoxide is the conjugate base of an alcohol and therefore consists of an organic group bonded to a negatively charged oxygen atom. They can be written as RO−, where R is the organic substituent. Alkoxides are strong bases and, when R is not bulky, good nucleophiles and good ligands. Alkoxides, although generally not stable in protic solvents such as water, occur widely as intermediates in various reactions, including the Williamson ether synthesis.".
- Alkoxide label "Alcoolate".
- Alkoxide label "Alcossido".
- Alkoxide label "Alcóxido".
- Alkoxide label "Alcóxido".
- Alkoxide label "Alkoholany".
- Alkoxide label "Alkoholate".
- Alkoxide label "Alkoxide".
- Alkoxide label "Alkoxide".
- Alkoxide label "Алкоголяты".
- Alkoxide label "アルコキシド".
- Alkoxide label "醇盐".
- Alkoxide sameAs Alkoxid.
- Alkoxide sameAs Alkoholate.
- Alkoxide sameAs Alcóxido.
- Alkoxide sameAs Alcoolate.
- Alkoxide sameAs Alcossido.
- Alkoxide sameAs アルコキシド.
- Alkoxide sameAs Alkoxide.
- Alkoxide sameAs Alkoholany.
- Alkoxide sameAs Alcóxido.
- Alkoxide sameAs m.02g781.
- Alkoxide sameAs Q278540.
- Alkoxide sameAs Q278540.
- Alkoxide sameAs Alkoxide.
- Alkoxide wasDerivedFrom Alkoxide?oldid=597741121.
- Alkoxide depiction Alkoxide_General_Formulae_V.1.png.
- Alkoxide isPrimaryTopicOf Alkoxide.