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  2. Carboxylate - Wikipedia

    en.wikipedia.org/wiki/Carboxylate

    Carboxylate ion Acrylate ion. In organic chemistry, a carboxylate is the conjugate base of a carboxylic acid, RCOO − (or RCO − 2). It is an anion, an ion with negative charge. Carboxylate salts are salts that have the general formula M(RCOO) n, where M is a metal and n is 1, 2,....

  3. Carboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Carboxylic_acid

    Structure of a carboxylic acid Carboxylate anion 3D structure of a carboxylic acid. In organic chemistry, a carboxylic acid is an organic acid that contains a carboxyl group (−C(=O)−OH) [1] attached to an R-group.

  4. Category:Carboxylate anions - Wikipedia

    en.wikipedia.org/wiki/Category:Carboxylate_anions

    Pages in category "Carboxylate anions" The following 21 pages are in this category, out of 21 total. This list may not reflect recent changes. ...

  5. Oxocarbon anion - Wikipedia

    en.wikipedia.org/wiki/Oxocarbon_anion

    An oxocarbon anion C x O n− y can be seen as the result of removing all protons from a corresponding acid C x H n O y. Carbonate CO 2− 3, for example, can be seen as the anion of carbonic acid H 2 CO 3. Sometimes the "acid" is actually an alcohol or other species; this is the case, for example, of acetylenediolate C 2 O 2− 2 that would ...

  6. Skeletal formula - Wikipedia

    en.wikipedia.org/wiki/Skeletal_formula

    Thus, in cases where two or more canonical forms contribute with equal weight (e.g., in benzene, or a carboxylate anion) and one of the canonical forms is selected arbitrarily, the skeletal formula is understood to depict the true structure, containing equivalent bonds of fractional order, even though the delocalized bonds are depicted as ...

  7. HBTU - Wikipedia

    en.wikipedia.org/wiki/HBTU

    This scheme depicts the general mechanistic steps of HBTU creating an activated ester out of the carboxylate anion of the acid substrate. The deprotination of the carboxylic acid and the aminolysis of the activated ester are not shown. HBTU activates carboxylic acids by forming a stabilized HOBt (Hydroxybenzotriazole) leaving group.

  8. Transition metal carboxylate complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal...

    Structure of hydrated nickel acetate. Transition metal carboxylate complexes are coordination complexes with carboxylate (RCO 2 −) ligands. Reflecting the diversity of carboxylic acids, the inventory of metal carboxylates is large. Many are useful commercially, and many have attracted intense scholarly scrutiny.

  9. Arachidonic acid - Wikipedia

    en.wikipedia.org/wiki/Arachidonic_acid

    In chemical structure, arachidonic acid is a carboxylic acid with a 20-carbon chain and four cis-double bonds; the first double bond is located at the sixth carbon from the omega end. Some chemistry sources define 'arachidonic acid' to designate any of the eicosatetraenoic acids .