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  2. Cyanoacetic acid - Wikipedia

    en.wikipedia.org/wiki/Cyanoacetic_acid

    Cyanoacetic acid is prepared by treatment of chloroacetate salts with sodium cyanide followed by acidification. [1] [2] Electrosynthesis by cathodic reduction of carbon dioxide and anodic oxidation of acetonitrile also affords cyanoacetic acid. [3] Cyanoacetic acid is used to do cyanoacetylation, first convenient method described by J. Slätt. [4]

  3. Ethyl cyanoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacetate

    Ethyl cyanoacetate is an organic compound that contains a carboxylate ester and a nitrile. It is a colourless [ 1 ] liquid with a pleasant odor. This material is useful as a starting material for synthesis due to its variety of functional groups and chemical reactivity.

  4. Sodium chloroacetate - Wikipedia

    en.wikipedia.org/wiki/Sodium_chloroacetate

    Reaction with cyanide salts gives cyanoacetate NCCH 2 CO 2 Na. [3] Cyanoacetate is a precursor to malonic acid. Sodium chloroacetate is a common laboratory reagent in organic chemistry as illustrated by many entries in the book series Organic Syntheses. With bifunctional nucleophiles, sodium chloroacetate is a precursor to heterocycles. [4] [5 ...

  5. Cyanoacrylate - Wikipedia

    en.wikipedia.org/wiki/Cyanoacrylate

    This reaction also occurs with fiberglass and carbon fiber. The heat released may cause serious burns [ 34 ] or release irritating white smoke. Material safety data sheets for cyanoacrylate instruct users not to wear cotton (jeans) or wool clothing, especially cotton gloves, when applying or handling cyanoacrylates.

  6. Cyanate - Wikipedia

    en.wikipedia.org/wiki/Cyanate

    Sodium cyanate is isostructural with sodium fulminate, confirming the linear structure of the cyanate ion. [3] It is made industrially by heating a mixture of sodium carbonate and urea. [4] Na 2 CO 3 + 2 OC(NH 2) 2 → 2 NaNCO + CO 2 + 2 NH 3 + H 2 O. A similar reaction is used to make potassium cyanate. Cyanates are produced when cyanides are ...

  7. Finkelstein reaction - Wikipedia

    en.wikipedia.org/wiki/Finkelstein_reaction

    The classic Finkelstein reaction entails the conversion of an alkyl chloride or an alkyl bromide to an alkyl iodide by treatment with a solution of sodium iodide in acetone. Sodium iodide is soluble in acetone while sodium chloride and sodium bromide are not; [ 3 ] therefore, the reaction is driven toward products by mass action due to the ...

  8. 21 High-Fiber Breakfasts for Better Blood Sugar - AOL

    www.aol.com/21-high-fiber-breakfasts-better...

    Spin leftovers from taco night into this easy salsa-topped avocado toast for an easy breakfast. Add an egg on top for extra protein. Chia seeds, a good source of healthy omega-3 fatty acids, are ...

  9. Sodium acetate - Wikipedia

    en.wikipedia.org/wiki/Sodium_acetate

    Any of these reactions produce sodium acetate and water. When a sodium and carbonate ion-containing compound is used as the reactant, the carbonate anion from sodium bicarbonate or carbonate, reacts with the hydrogen from the carboxyl group (-COOH) in acetic acid, forming carbonic acid. Carbonic acid readily decomposes under normal conditions ...