When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  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

    Alternately, it can be named as a "carboxy" or "carboxylic acid" substituent on another parent structure, such as 2-carboxyfuran. The carboxylate anion (R−COO − or R−CO − 2) of a carboxylic acid is usually named with the suffix -ate, in keeping with the general pattern of -ic acid and -ate for a conjugate acid and its conjugate base ...

  4. Category:Carboxylate anions - Wikipedia

    en.wikipedia.org/wiki/Category:Carboxylate_anions

    Category: Carboxylate anions. 18 languages. Беларуская (тарашкевіца) ... Download as PDF; Printable version; In other projects Wikimedia Commons;

  5. Salt bridge (protein and supramolecular) - Wikipedia

    en.wikipedia.org/wiki/Salt_bridge_(protein_and...

    Hydrogen bonds contribute to the stability of ion pairs with e.g. protonated ammonium ions, and with anions is formed by deprotonation as in the case of carboxylate, phosphate etc; then the association constants depend on the pH. Entropic driving forces for ion pairing (in absence of significant H-bonding contributions) are also found in ...

  6. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    Acyl anions are almost always unstable—usually too unstable to be exploited synthetically. They readily react with the neutral aldehyde to form an acyloin dimer. Hence, synthetic chemists have developed various acyl anion synthetic equivalents, such as dithianes, as surrogates.

  7. 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 ...

  8. Vinylogy - Wikipedia

    en.wikipedia.org/wiki/Vinylogy

    For example, a carboxylic acid is defined as a carbonyl group (C=O) directly attached to a hydroxyl group (OH): O=C–OH. A vinylogous carboxylic acid has a vinyl unit (−HC=CH−, vinylene) between the two groups that define the acid: O=C–C=C–OH. The usual resonance of a

  9. Acetate - Wikipedia

    en.wikipedia.org/wiki/Acetate

    acetate anion. The acetate anion, [CH 3 COO] −,(or [C 2 H 3 O 2] −) is one of the carboxylate family. It is the conjugate base of acetic acid. Above a pH of 5.5, acetic acid converts to acetate: [1] CH 3 COOH ⇌ CH 3 COO − + H + Many acetate salts are ionic, indicated by their tendency to dissolve well in water.