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  2. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    According to some authors, organyl derivatives of acidic hydrogen of other acids are esters as well (e.g. amides), but not according to the IUPAC. [1] An example of an ester formation is the substitution reaction between a carboxylic acid (R−C(=O)−OH) and an alcohol (R'OH), forming an ester (R−C(=O)−O−R'), where R and R′ are organyl ...

  3. 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]

  4. -oate - Wikipedia

    en.wikipedia.org/wiki/-oate

    The suffix-oate is the IUPAC nomenclature used in organic chemistry to form names of compounds formed with ester. They are of two types: They are of two types: Formed by replacing the hydrogen atom in the –COOH by some other radical , usually an alkyl or aryl radical forming an ester .

  5. Bis(2-Hydroxyethyl) terephthalate - Wikipedia

    en.wikipedia.org/wiki/Bis(2-hydroxyethyl)_tere...

    Preferred IUPAC name. Bis(2-hydroxyethyl) benzene-1,4-dicarboxylate [1] ... (BHET) is an organic compound; it is the ester of ethylene glycol and terephthalic acid.

  6. Octyl acetate - Wikipedia

    en.wikipedia.org/wiki/Octyl_acetate

    It is classified as an ester that is formed from 1-octanol (octyl alcohol) and acetic acid. It is found in oranges, grapefruits, and other citrus products. [10] Octyl acetate can be synthesized by the Fischer esterification of 1-octanol and acetic acid: CH 3 (CH 2) 7 OH + CH 3 CO 2 H → CH 3 (CH 2) 7 O 2 CCH 3 + H 2 O

  7. Phenyl acetate - Wikipedia

    en.wikipedia.org/wiki/Phenyl_acetate

    Phenyl acetate is the ester of phenol and acetic acid.It can be produced by reacting phenol with acetic anhydride or acetyl chloride.. Phenyl acetate can be separated into phenol and an acetate salt, via saponification: heating the phenyl acetate with a strong base, such as sodium hydroxide, will produce phenol and an acetate salt (sodium acetate, if sodium hydroxide were used).

  8. Formate - Wikipedia

    en.wikipedia.org/wiki/Formate

    Formate (IUPAC name: methanoate) is the conjugate base of formic acid. Formate is an anion ( HCO − 2 ) or its derivatives such as ester of formic acid . The salts and esters are generally colorless.

  9. Triethyl citrate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_citrate

    Triethyl citrate is an ester of citric acid. It is a colorless, odorless liquid used as a food additive, emulsifier and solvent (E number E1505) [4] to stabilize foams, especially as whipping aid for egg white. [5] It is also used in pharmaceutical coatings and plastics. [6]