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  2. Alkoxy group - Wikipedia

    en.wikipedia.org/wiki/Alkoxy_group

    The term alkoxide refers to the anionic conjugate bases of alcohols (RO −) or to ionic compounds containing such an anion. Alkoxide compounds are derivatives of alcohols where the hydrogen of the –OH group is replaced by a metal ; [ 2 ] for example, the sodium salt of ethanol ( CH 3 CH 2 OH ) is sodium ethoxide , containing ethoxide anions ...

  3. Alkoxide - Wikipedia

    en.wikipedia.org/wiki/Alkoxide

    Structure of the methoxide anion. Although alkali metal alkoxides are not salts and adopt complex structures, they behave chemically as sources of RO −. The structure of the methoxide ion. In chemistry, an alkoxide is the conjugate base of an alcohol and therefore consists of an organic group bonded to a negatively charged oxygen atom.

  4. Transition metal alkoxide complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_alkoxide...

    Structure of the methoxide anion. Although alkali metal alkoxides are not salts and adopt complex structures, they behave chemically as sources of RO −.. A transition metal alkoxide complex is a kind of coordination complex containing one or more alkoxide ligands, written as RO −, where R is the organic substituent.

  5. Sodium methoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_methoxide

    Sodium methoxide is prepared by treating methanol with sodium: 2 Na + 2 CH 3 OH → 2 CH 3 ONa + H 2. The reaction is so exothermic that ignition is possible. The resulting solution, which is colorless, is often used as a source of sodium methoxide, but the pure material can be isolated by evaporation followed by heating to remove residual methanol.

  6. Sodium ethoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_ethoxide

    It is easily prepared in the laboratory by treating sodium metal with absolute ethanol: [3] 2 CH 3 CH 2 OH + 2 Na → 2 CH 3 CH 2 ONa + H 2. The reaction of sodium hydroxide with anhydrous ethanol suffers from incomplete conversion to the ethoxide, but can still produce dry NaOEt by precipitation using acetone, [4] or by drying using additional ...

  7. Acetoxy group - Wikipedia

    en.wikipedia.org/wiki/Acetoxy_group

    Anhydrous base such as sodium methoxide in methanol. Very useful when a methyl ester of a carboxylic acid is also present in the molecule, as it will not hydrolyze it like an aqueous base would. (Same also holds with an ethoxide in ethanol with ethyl esters) [ 8 ]

  8. Methoxy group - Wikipedia

    en.wikipedia.org/wiki/Methoxy_group

    The structure of a typical methoxy group. In organic chemistry, a methoxy group is the functional group consisting of a methyl group bound to oxygen.This alkoxy group has the formula R−O−CH 3.

  9. Hydroxide - Wikipedia

    en.wikipedia.org/wiki/Hydroxide

    The hydroxide ion by itself is not a strong enough base, but it can be converted in one by adding sodium hydroxide to ethanol. OH − + EtOH ⇌ EtO − + H 2 O. to produce the ethoxide ion. The pK a for self-dissociation of ethanol is about 16, so the alkoxide ion is a strong enough base. [49]