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  2. Wallace Carothers - Wikipedia

    en.wikipedia.org/wiki/Wallace_Carothers

    Wallace Hume Carothers (/ k ə ˈ r ʌ ð ər z /; April 27, 1896 – April 29, 1937) was an American chemist, inventor, and the leader of organic chemistry at DuPont, who was credited with the invention of nylon.

  3. Trifluoroperacetic acid - Wikipedia

    en.wikipedia.org/wiki/Trifluoroperacetic_acid

    At standard ambient temperature and pressure, trifluoroperacetic acid is a colourless liquid with a boiling point of 162 °C. [8] It is soluble in acetonitrile, dichloromethane, diethyl ether, and sulfolane, and readily reacts with water. [5]

  4. Marvin H. Caruthers - Wikipedia

    en.wikipedia.org/wiki/Marvin_H._Caruthers

    Marvin H. Caruthers (born February 11, 1940) is an American biochemist who is a distinguished professor at the University of Colorado Boulder.. Caruthers earned a B.S in chemistry at the Iowa State University in 1962 and a Ph.D. in biochemistry 1968 at Northwestern University with Robert Letsinger.

  5. Carothers equation - Wikipedia

    en.wikipedia.org/wiki/Carothers_equation

    The simplest case refers to the formation of a strictly linear polymer by the reaction (usually by condensation) of two monomers in equimolar quantities. An example is the synthesis of nylon-6,6 whose formula is [−NH−(CH 2) 6 −NH−CO−(CH 2) 4 −CO−] n from one mole of hexamethylenediamine, H 2 N(CH 2) 6 NH 2, and one mole of adipic acid, HOOC−(CH 2) 4 −COOH.

  6. File:Organic Chemistry.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Organic_Chemistry.pdf

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Donate

  7. Physical organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Physical_organic_chemistry

    Physical organic chemistry is the study of the relationship between structure and reactivity of organic molecules.More specifically, physical organic chemistry applies the experimental tools of physical chemistry to the study of the structure of organic molecules and provides a theoretical framework that interprets how structure influences both mechanisms and rates of organic reactions.

  8. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Cadiot–Chodkiewicz coupling; Cadogan-Sundberg indole synthesis; Camps quinoline synthesis; Cannizzaro reaction; Carbohydrate acetalisation; Carbonyl reduction

  9. 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 ...