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  2. Tollens' reagent - Wikipedia

    en.wikipedia.org/wiki/Tollens'_reagent

    Tollens' reagent (chemical formula ()) is a chemical reagent used to distinguish between aldehydes and ketones along with some alpha-hydroxy ketones which can tautomerize into aldehydes. The reagent consists of a solution of silver nitrate , ammonium hydroxide and some sodium hydroxide (to maintain a basic pH of the reagent solution).

  3. Fehling's solution - Wikipedia

    en.wikipedia.org/wiki/Fehling's_solution

    In organic chemistry, Fehling's solution is a chemical reagent used to differentiate between water-soluble carbohydrate and ketone (>C=O) functional groups, and as a test for reducing sugars and non-reducing sugars, supplementary to the Tollens' reagent test. The test was developed by German chemist Hermann von Fehling in 1849. [1]

  4. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    Reagents are "substances or compounds that are added to a system in order to bring about a chemical reaction or are added to see if a reaction occurs." [1] Some reagents are just a single element. However, most processes require reagents made of chemical compounds. Some of the most common ones used widely for specific reactive functions are ...

  5. Phloroglucinol - Wikipedia

    en.wikipedia.org/wiki/Phloroglucinol

    Phloroglucinol is a reagent of the Tollens' test for pentoses. This test relies on reaction of the furfural with phloroglucinol to produce a colored compound with high molar absorptivity. [26] A solution of hydrochloric acid and phloroglucinol is also used for the detection of lignin (Wiesner test).

  6. Ammonia solution - Wikipedia

    en.wikipedia.org/wiki/Ammonia_solution

    Like many amines, it gives a deep blue coloration with copper(II) solutions. Ammonia solution can dissolve silver oxide residues, such as those formed from Tollens' reagent. It is often found in solutions used to clean gold, silver, and platinum jewelry, but may have adverse effects on porous gem stones like opals and pearls. [22]

  7. Conversion (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Conversion_(chemistry)

    Conversion and its related terms yield and selectivity are important terms in chemical reaction engineering.They are described as ratios of how much of a reactant has reacted (X — conversion, normally between zero and one), how much of a desired product was formed (Y — yield, normally also between zero and one) and how much desired product was formed in ratio to the undesired product(s) (S ...

  8. 2,4-Dinitrophenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrophenylhydrazine

    Brady's reagent or Borche's reagent, is prepared by dissolving DNPH in a solution containing methanol and some concentrated sulfuric acid. This solution is used to detect ketones and aldehydes . A positive test is signalled by the formation of a yellow, orange or red precipitate of the dinitrophenylhydrazone.

  9. N-Phenylhydroxylamine - Wikipedia

    en.wikipedia.org/wiki/N-Phenylhydroxylamine

    N-Phenylhydroxylamine is the organic compound with the formula C 6 H 5 NHOH. It is an intermediate in the redox-related pair C 6 H 5 NH 2 and C 6 H 5 NO . N -Phenylhydroxylamine should not be confused with its isomer α-phenylhydroxylamine or O -phenylhydroxylamine.