When.com Web Search

  1. Ads

    related to: chemistry of acid anhydrides pdf book class

Search results

  1. Results From The WOW.Com Content Network
  2. Acid anhydride - Wikipedia

    en.wikipedia.org/wiki/Acid_anhydride

    An acid anhydride is a type of chemical compound derived by the removal of water molecules from an acid. In organic chemistry, organic acid anhydrides contain the functional group −C(=O)−O−C(=O)−. Organic acid anhydrides often form when one equivalent of water is removed from two equivalents of an organic acid in a dehydration reaction.

  3. Organic acid anhydride - Wikipedia

    en.wikipedia.org/wiki/Organic_acid_anhydride

    A common type of organic acid anhydride is a carboxylic anhydride, where the parent acid is a carboxylic acid, the formula of the anhydride being (RC(O)) 2 O. Symmetrical acid anhydrides of this type are named by replacing the word acid in the name of the parent carboxylic acid by the word anhydride. [2] Thus, (CH 3 CO) 2 O is called acetic ...

  4. Acetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_anhydride

    Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH 3 CO) 2 O. Commonly abbreviated Ac 2 O, it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis. It is a colorless liquid that smells strongly of acetic acid, which is formed by its reaction with ...

  5. Amino acid N-carboxyanhydride - Wikipedia

    en.wikipedia.org/wiki/Amino_acid_N-carboxyanhydride

    Amino acid N-carboxyanhydrides, also called Leuchs' anhydrides, are a family of heterocyclic organic compounds derived from amino acids. They are white, moisture-reactive solids. They have been evaluated for applications the field of biomaterials. [1] [2] [3]

  6. Acyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acyl_chloride

    In organic chemistry, an acyl chloride (or acid chloride) is an organic compound with the functional group −C(=O)Cl. Their formula is usually written R−COCl , where R is a side chain . They are reactive derivatives of carboxylic acids ( R−C(=O)OH ).

  7. Perkin reaction - Wikipedia

    en.wikipedia.org/wiki/Perkin_reaction

    The Perkin reaction is an organic reaction developed by English chemist William Henry Perkin in 1868 that is used to make cinnamic acids.It gives an α,β-unsaturated aromatic acid or α-substituted β-aryl acrylic acid by the aldol condensation of an aromatic aldehyde and an acid anhydride, in the presence of an alkali salt of the acid.

  8. Shiina esterification - Wikipedia

    en.wikipedia.org/wiki/Shiina_Esterification

    Therefore, the aromatic carboxylic acid anhydride and the mixed anhydride (MA) coexist in the system. Furthermore, aliphatic carboxylic acid anhydride produced via disproportionation of the MA is simultaneously present in the system; thus, it is directly used as a mixture without being separated.

  9. Imide - Wikipedia

    en.wikipedia.org/wiki/Imide

    A general linear imide functional group. In organic chemistry, an imide is a functional group consisting of two acyl groups bound to nitrogen. [1] The compounds are structurally related to acid anhydrides, although imides are more resistant to hydrolysis.

  1. Ad

    related to: chemistry of acid anhydrides pdf book class