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  2. Keller's reagent (organic) - Wikipedia

    en.wikipedia.org/wiki/Keller's_reagent_(organic)

    In organic chemistry, Keller's reagent is a mixture of anhydrous (glacial) acetic acid, concentrated sulfuric acid, and small amounts of ferric chloride, used to detect alkaloids. Keller's reagent can also be used to detect other kinds of alkaloids via reactions in which it produces products with a wide range of colors.

  3. Reducing sugar - Wikipedia

    en.wikipedia.org/wiki/Reducing_sugar

    Reducing form of glucose (the aldehyde group is on the far right). 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.

  4. Fructose - Wikipedia

    en.wikipedia.org/wiki/Fructose

    Fructose is also 73% sweeter than sucrose at room temperature, allowing diabetics to use less of it per serving. Fructose consumed before a meal may reduce the glycemic response of the meal. [65] Fructose-sweetened food and beverage products cause less of a rise in blood glucose levels than do those manufactured with either sucrose or glucose. [12]

  5. Combining These Two Types of Sugars Will Fuel Your ... - AOL

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  6. Keller's reagent - Wikipedia

    en.wikipedia.org/wiki/Keller's_reagent

    Keller's reagent can refer to two different reagents: Keller's reagent (metallurgy), used to etch aluminum alloys; Keller's reagent (organic), used to detect alkaloids

  7. Keller's reagent (metallurgy) - Wikipedia

    en.wikipedia.org/wiki/Keller's_reagent_(metallurgy)

    In metallurgy, Keller's reagent is a mixture of nitric acid, hydrochloric acid, and hydrofluoric acid, used to etch aluminum alloys to reveal their grain boundaries and orientations. [1] It is also sometimes called Dix–Keller reagent , after E. H. Dix, Jr., and Fred Keller of the Aluminum Corporation of America , who pioneered the use of this ...

  8. Hydrolysis - Wikipedia

    en.wikipedia.org/wiki/Hydrolysis

    When a carbohydrate is broken into its component sugar molecules by hydrolysis (e.g., sucrose being broken down into glucose and fructose), this is recognized as saccharification. [2] Hydrolysis reactions can be the reverse of a condensation reaction in which two molecules join into a larger one and eject a water molecule. Thus hydrolysis adds ...

  9. Invertase - Wikipedia

    en.wikipedia.org/wiki/Invertase

    β-Fructofuranosidase is an enzyme that catalyzes the hydrolysis (breakdown) of the table sugar sucrose into fructose and glucose. [1] [2] Alternative names for β-fructofuranosidase EC 3.2.1.26 include invertase, saccharase, glucosucrase, β-fructosidase, invertin, fructosylinvertase, alkaline invertase, and acid invertase.