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  2. Ethyl cyanoacrylate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacrylate

    Ethyl cyanoacrylate is prepared by the condensation of formaldehyde with ethyl cyanoacetate: NCCH 2 CO 2 C 2 H 5 + CH 2 O → H 2 C=C(CN)CO 2 C 2 H 5 + H 2 O. This exothermic reaction affords the polymer, which is subsequently sintered, thermally "cracked" to give the monomer. Alternatively, it can be prepared by the ethoxycarbonylation of ...

  3. Cyanoacrylate - Wikipedia

    en.wikipedia.org/wiki/Cyanoacrylate

    Structure of the backbone of a cyanoacrylate polymer. Cyanoacrylates are a family of strong fast-acting adhesives with industrial, medical, and household uses. They are derived from ethyl cyanoacrylate and related esters. The cyanoacrylate group in the monomer rapidly polymerizes in the presence of water to form long, strong chains. [1]

  4. Rate equation - Wikipedia

    en.wikipedia.org/wiki/Rate_equation

    In chemistry, the rate equation (also known as the rate law or empirical differential rate equation) is an empirical differential mathematical expression for the reaction rate of a given reaction in terms of concentrations of chemical species and constant parameters (normally rate coefficients and partial orders of reaction) only. [1]

  5. Acrylate - Wikipedia

    en.wikipedia.org/wiki/Acrylate

    Acrylates are industrially prepared by treating acrylic acid with the corresponding alcohol in presence of a catalyst. The reaction with lower alcohols (methanol, ethanol) takes place at 100–120 °C with acidic heterogeneous catalysts (cation exchanger).

  6. Ethyl cyanoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacetate

    Ethyl cyanoacrylate, used as superglue, via reaction with formaldehyde; Ethyl cyanoacetate is also used to prepare 3,3-diphenylpropan-1-amine, which is the precursor used in the synthesis of Prenylamine & Droprenilamine.

  7. Pharmacology of ethanol - Wikipedia

    en.wikipedia.org/wiki/Pharmacology_of_ethanol

    The reaction from ethanol to carbon dioxide and water proceeds in at least 11 steps in humans. C 2 H 6 O (ethanol) is converted to C 2 H 4 O (acetaldehyde), then to C 2 H 4 O 2 (acetic acid), then to acetyl-CoA. Once acetyl-CoA is formed, it is free to enter directly into the citric acid cycle (TCA) and is converted to 2 CO 2 molecules in 8 ...

  8. Cyanoacetic acid - Wikipedia

    en.wikipedia.org/wiki/Cyanoacetic_acid

    In its largest scale application, cyanoacetic acid is first esterified to give ethyl cyanoacetate. Condensation of that ester with formaldehyde gives ethyl cyanoacrylate , which used as superglue. As of 2007, more than 10,000 tons of cyanoacetic acid were produced annually.

  9. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    rate = k[RCHO] 2 [OH −] + k'[RCHO] 2 [OH −] 2. The k' pathway implicates a reaction between the doubly charged anion (RCHO 2 2−) and the aldehyde. The direct transfer of hydride ion is evident from the observation that the recovered alcohol does not contain any deuterium attached to the α-carbon when the reaction is performed in the ...