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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. Benedict's reagent - Wikipedia

    en.wikipedia.org/wiki/Benedict's_reagent

    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. [2]

  5. 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

  6. 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 ...

  7. Invertase - Wikipedia

    en.wikipedia.org/wiki/Invertase

    This specific invertase (β-fructofuranosidase) cleaves the molecule from its fructose end resulting in the two monosaccharides. It does this by adding a hydrogen ion to the glycosidic atom by an imidazolium cation. From there, an unstable intermediate carbonium ion will be left behind by the leaving of an alcohol group.

  8. Dog Trainer Reveals Big Mistake People Make When Teaching ...

    www.aol.com/dog-trainer-reveals-big-mistake...

    Reward good behavior and reacting correctly to commands with treats, toys, or verbal praise to encourage your dog. Negative reinforcements, like yelling or striking your dog, does more harm than good.

  9. Sugars in wine - Wikipedia

    en.wikipedia.org/wiki/Sugars_in_wine

    At time of harvest, there is usually an equal amount of glucose and fructose molecules in the grape; however, as the grape overripens the level of fructose will become higher. In wine, fructose can taste nearly twice as sweet as glucose and is a key component in the creation of sweet dessert wines. During fermentation, glucose is consumed first ...