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  2. Acetate - Wikipedia

    en.wikipedia.org/wiki/Acetate

    An acetate is a salt formed by the combination of acetic acid with a base (e.g. alkaline, earthy, metallic, nonmetallic or radical base). "Acetate" also describes the conjugate base or ion (specifically, the negatively charged ion called an anion) typically found in aqueous solution and written with the chemical formula C 2 H 3 O − 2.

  3. 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).

  4. Acetylation - Wikipedia

    en.wikipedia.org/wiki/Acetylation

    Acetate esters [5] and acetamides [6] are generally prepared by acetylations. Acetylations are often used in making C-acetyl bonds in Friedel-Crafts reactions . [ 7 ] [ 8 ] Carbanions and their equivalents are susceptible to acetylations.

  5. Ester - Wikipedia

    en.wikipedia.org/wiki/Ester

    An ester of a carboxylic acid.R stands for any group (typically hydrogen or organyl) and R ′ stands for any 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 ′). [1]

  6. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    The major esters of acetic acid are commonly used as solvents for inks, paints and coatings. The esters include ethyl acetate, n-butyl acetate, isobutyl acetate, and propyl acetate. They are typically produced by catalyzed reaction from acetic acid and the corresponding alcohol: CH 3 COO−H + HO−R → CH 3 COO−R + H 2 O, R = general alkyl ...

  7. Acetoacetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetoacetic_acid

    Acetoacetic esters are used for the acetoacetylation reaction, which is widely used in the production of arylide yellows and diarylide dyes. [3] Although the esters can be used in this reaction, diketene also reacts with alcohols and amines to the corresponding acetoacetic acid derivatives in a process called acetoacetylation .

  8. Acetoacetic ester synthesis - Wikipedia

    en.wikipedia.org/wiki/Acetoacetic_Ester_Synthesis

    Acetoacetic ester synthesis is a chemical reaction where ethyl acetoacetate is alkylated at the α-carbon to both carbonyl groups and then converted into a ketone, or more specifically an α-substituted acetone. This is very similar to malonic ester synthesis. Acetoacetic ester synthesis equation

  9. Hexyl acetate - Wikipedia

    en.wikipedia.org/wiki/Hexyl_acetate

    Hexyl acetate is an ester with the molecular formula C 8 H 16 O 2. It is mainly used as a solvent for resins , polymers , fats and oils . It is also used as a paint additive to improve its dispersion on a surface.