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  2. Acetate - Wikipedia

    en.wikipedia.org/wiki/Acetate

    Acetate esters have the general formula CH 3 CO 2 R, where R is an organyl group. The esters are the dominant forms of acetate in the marketplace. Unlike the acetate salts, acetate esters are often liquids, lipophilic, and sometimes volatile.

  3. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    In IUPAC nomenclature, an acetyl group is called an ethanoyl group. An acetyl group contains a methyl group ( −CH 3 ) that is single-bonded to a carbonyl ( C=O ), making it an acyl group . The carbonyl center of an acyl radical has one non-bonded electron with which it forms a chemical bond to the remainder (denoted with the letter R ) of the ...

  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. Cellulose acetate - Wikipedia

    en.wikipedia.org/wiki/Cellulose_acetate

    The most common form of cellulose acetate fiber has an acetate group on approximately two of every three hydroxyls. This cellulose diacetate is known as secondary acetate, or simply as "acetate". After it is formed, cellulose acetate is dissolved in acetone, forming a viscous solution for extrusion through spinnerets (which resemble a shower ...

  6. Acetylation - Wikipedia

    en.wikipedia.org/wiki/Acetylation

    It introduces an acetyl group into a chemical compound. Such compounds are termed acetate esters or simply acetates. Deacetylation is the opposite reaction, the removal of an acetyl group from a chemical compound.

  7. Category:Acetates - Wikipedia

    en.wikipedia.org/wiki/Category:Acetates

    This page was last edited on 1 November 2023, at 00:46 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  8. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    The most important esters with common protecting-group use are the acetate, benzoate, and pivalate esters, for these exhibit differential removal. Sterically hindered esters are less susceptible to nucleophilic attack: Chloroacetyl > acetyl > benzoyl > pivaloyl

  9. Moiety (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Moiety_(chemistry)

    It also contains an ester functional group (in red), and an acetyl functional group (encircled with dark green). Other divisions can be made. Other divisions can be made. In organic chemistry , a moiety ( / ˈ m ɔɪ ə t i / MOY -ə-tee ) is a part of a molecule [ 1 ] [ 2 ] that is given a name because it is identified as a part of other ...