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  2. 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 ...

  3. Reducing sugar - Wikipedia

    en.wikipedia.org/wiki/Reducing_sugar

    Reducing form of glucose(the aldehyde groupis on the far right) A reducing sugaris any sugarthat is capable of acting as a reducing agent.[1] In an alkalinesolution, a reducing sugar forms some aldehydeor 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 ...

  4. 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.

  5. Disaccharide - Wikipedia

    en.wikipedia.org/wiki/Disaccharide

    A disaccharide (also called a double sugar or biose) [ 1 ] is the sugar formed when two monosaccharides are joined by glycosidic linkage. [ 2 ] Like monosaccharides, disaccharides are simple sugars soluble in water. Three common examples are sucrose, lactose, and maltose. Disaccharides are one of the four chemical groupings of carbohydrates ...

  6. Aldonic acid - Wikipedia

    en.wikipedia.org/wiki/Aldonic_acid

    Aldonic acids are the products of the oxidation of aldoses by Benedict's or Fehling's reagents. [ 6 ] Copper ions react with an aldose to form a red precipitate, Cu 2 O. The reaction scheme of an aldose being oxidized by the copper ions in a Benedict's reagent solution. The R group provided is an example of a sugar backbone.

  7. Stanley Rossiter Benedict - Wikipedia

    en.wikipedia.org/wiki/Stanley_Rossiter_Benedict

    Stanley Benedict was part of many Chemistry societies. He was a member of the National Academy of Sciences, [1] American Association for the Advancement of Science, [1] American Society of Biological Chemists (President 1919-1920), American Physiological Society, [4] Phi Beta Kappa, [1] Corresponding Member of the Societe Biologie de Paris, [1] Sigma Xi, [4] Alpha Omega Alpha, [1] The Harvey ...

  8. Ketose - Wikipedia

    en.wikipedia.org/wiki/Ketose

    In organic chemistry, a ketose is a monosaccharide containing one ketone (>C=O) group per molecule. [1][2] The simplest ketose is dihydroxyacetone ((CH2OH)2C=O), which has only three carbon atoms. It is the only ketose with no optical activity. All monosaccharide ketoses are reducing sugars, because they can tautomerize into aldoses via an ...

  9. Glycosuria - Wikipedia

    en.wikipedia.org/wiki/Glycosuria

    Glycosuria is the excretion of glucose into the urine. Ordinarily, urine contains no glucose because the kidneys are able to reabsorb all of the filtered glucose from the tubular fluid back into the bloodstream. Glycosuria is nearly always caused by an elevated blood sugar level, most commonly due to untreated diabetes.

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