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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

    Monosaccharides. 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.

  4. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    Ketones give positive results in Brady's test, the reaction with 2,4-dinitrophenylhydrazine to give the corresponding hydrazone. Ketones may be distinguished from aldehydes by giving a negative result with Tollens' reagent or with Fehling's solution. Methyl ketones give positive results for the iodoform test. [7] Ketones also give positive ...

  5. Benedict's reagent - Wikipedia

    en.wikipedia.org/wiki/Benedict's_reagent

    Reducing sugars. Benedict's reagent (often called Benedict's qualitative solution or Benedict's solution) is a chemical reagent and complex mixture of sodium carbonate, sodium citrate, and copper (II) sulfate pentahydrate. [1] It is often used in place of Fehling's solution to detect the presence of reducing sugars and other reducing substances ...

  6. Acyloin - Wikipedia

    en.wikipedia.org/wiki/Acyloin

    α-hydroxy ketones give positive Tollens' and Fehling's test. Some acyloins rearrange with positions swapped under the influence of base in the Lobry–de Bruyn–van Ekenstein transformation A similar reaction is the so-called Voigt amination [ 6 ] where an acyloin reacts with a primary amine and phosphorus pentoxide to an α-keto amine: [ 7 ]

  7. Reducing sugar - Wikipedia

    en.wikipedia.org/wiki/Reducing_sugar

    A reducing sugar is any sugar that is capable of acting as a reducing agent. [1] In an alkaline solution, a reducing sugar forms some aldehyde or ketone, which allows it to act as a reducing agent, for example in Benedict's reagent. In such a reaction, the sugar becomes a carboxylic acid. All monosaccharides are reducing sugars, along with some ...

  8. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    In this test, an aldehyde is treated with Tollens' reagent, which is prepared by adding a drop of sodium hydroxide solution into silver nitrate solution to give a precipitate of silver(I) oxide, and then adding just enough dilute ammonia solution to redissolve the precipitate in aqueous ammonia to produce [Ag(NH 3) 2] + complex. This reagent ...

  9. Hydroxy ketone - Wikipedia

    en.wikipedia.org/wiki/Hydroxy_ketone

    In organic chemistry, a hydroxy ketone (often referred to simply as a ketol) is a functional group consisting of a ketone (>C=O) flanked by a hydroxyl group (−OH). Chemicals in this group can be classified by the position of the hydroxyl relative to the ketone. The two main classes have the hydroxyl on the alpha or beta carbon, that is, on ...