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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. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Tollens reagent; Transfer hydrogenation; Trapp mixture; Transesterification; Traube purine synthesis; Truce–Smiles rearrangement; Tscherniac–Einhorn reaction; Tschitschibabin reaction; Tschugajeff reaction; Tsuji–Trost reaction; Tsuji–Wilkinson decarbonylation reaction; Twitchell process; Tyrer sulfonation process

  6. 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.

  7. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    The simplest class have the formula (CH 2) n CO, where n varies from 2 for cyclopropanone ((CH 2) 2 CO) to the tens. Larger derivatives exist. Larger derivatives exist. Cyclohexanone ( (CH 2 ) 5 CO ), a symmetrical cyclic ketone, is an important intermediate in the production of nylon .

  8. Reagent - Wikipedia

    en.wikipedia.org/wiki/Reagent

    In chemistry, a reagent (/ r i ˈ eɪ dʒ ən t / ree-AY-jənt) or analytical reagent is a substance or compound added to a system to cause a chemical reaction, or test if one occurs. [1] The terms reactant and reagent are often used interchangeably, but reactant specifies a substance consumed in the course of a chemical reaction. [ 1 ]

  9. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.