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  2. Reformatsky reaction - Wikipedia

    en.wikipedia.org/wiki/Reformatsky_reaction

    The Reformatsky reaction (sometimes transliterated as Reformatskii reaction) is an organic reaction which condenses aldehydes or ketones with α-halo esters using metallic zinc to form β-hydroxy-esters: [1] [2] The Reformatsky reaction. The organozinc reagent, also called a 'Reformatsky enolate', is prepared by treating an alpha-halo ester ...

  3. Ester pyrolysis - Wikipedia

    en.wikipedia.org/wiki/Ester_pyrolysis

    Ester pyrolysis in organic chemistry is a vacuum pyrolysis reaction converting esters containing a β-hydrogen atom into the corresponding carboxylic acid and the alkene.The reaction is an E i elimination and operates in a syn fashion.

  4. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).

  5. Zeisel determination - Wikipedia

    en.wikipedia.org/wiki/Zeisel_determination

    The ensuing reaction results in the cleavage of the ether or the ester into an alkyl iodide and respectively an alcohol or a carboxylic acid. Zeisel determination By heating this mixture, the gases are allowed to come into contact with a piece of paper higher up the test tube saturated with silver nitrate .

  6. Saponification - Wikipedia

    en.wikipedia.org/wiki/Saponification

    Saponification is a process of cleaving esters into carboxylate salts and alcohols by the action of aqueous alkali. Typically aqueous sodium hydroxide solutions are used. [1] [2] It is an important type of alkaline hydrolysis. When the carboxylate is long chain, its salt is called a soap.

  7. Malonic ester synthesis - Wikipedia

    en.wikipedia.org/wiki/Malonic_ester_synthesis

    On heating, the di-ester undergoes thermal decarboxylation, yielding an acetic acid substituted by the appropriate R group. [1] Thus, the malonic ester can be thought of being equivalent to the − CH 2 COOH synthon. The esters chosen are usually the same as the base used, i.e. ethyl esters with sodium ethoxide.

  8. Hagemann's ester - Wikipedia

    en.wikipedia.org/wiki/Hagemann's_ester

    Hagemann's ester, ethyl 2-methyl-4-oxo-2-cyclohexenecarboxylate, is an organic compound that was first prepared and described in 1893 by German chemist Carl Hagemann. The compound is used in organic chemistry as a reagent in the synthesis of many natural products including sterols , trisporic acids , and terpenoids .

  9. Ester hydrolysis - Wikipedia

    en.wikipedia.org/wiki/Ester_hydrolysis

    Ester hydrolysis is an organic reaction which hydrolyzes an ester to a carboxylic acid or carboxylate, and an alcohol. It can be performed with acid as catalyst, or ...