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  2. Glucose - Wikipedia

    en.wikipedia.org/wiki/Glucose

    The fact that d-glucose is dextrorotatory is a combined effect of its four chiral centres, not just of C-5; some of the other d-aldohexoses are levorotatory. The conversion between the two anomers can be observed in a polarimeter since pure α-d-glucose has a specific rotation angle of +112.2° mL/(dm·g), pure β-d-glucose of +17.5° mL/(dm·g ...

  3. Haworth projection - Wikipedia

    en.wikipedia.org/wiki/Haworth_projection

    In chemistry, a Haworth projection is a common way of writing a structural formula to represent the cyclic structure of monosaccharides with a simple three-dimensional perspective. Haworth projection approximate the shapes of the actual molecules better for furanoses —which are in reality nearly planar—than for pyranoses that exist in ...

  4. File:Alpha-D-Glucopyranose.svg - Wikipedia

    en.wikipedia.org/wiki/File:Alpha-D-Glucopyranose.svg

    This image of a simple structural formula is ineligible for copyright and therefore in the public domain, because it consists entirely of information that is common property and contains no original authorship.

  5. Norman Haworth - Wikipedia

    en.wikipedia.org/wiki/Norman_Haworth

    Sir Walter Norman Haworth FRS [1] (19 March 1883 [2] – 19 March 1950) was a British chemist best known for his groundbreaking work on ascorbic acid while working at the University of Birmingham. He received the 1937 Nobel Prize in Chemistry "for his investigations on carbohydrates and vitamin C".

  6. α-Glucosidase - Wikipedia

    en.wikipedia.org/wiki/Α-Glucosidase

    It is defined as "catalysis of the hydrolysis of terminal, non-reducing alpha-linked alpha-D-glucose residue with release of alpha-D-glucose." In this sense, "alpha-glucosidase" can encompass a wide range of enzyme activitiess, differing by the linkage of their terminal (1→3, 1→4, or 1→6), the specific identity of their substrate (sucrose ...

  7. File:Beta-D-glucose Haworth formula.svg - Wikipedia

    en.wikipedia.org/wiki/File:Beta-D-glucose...

    This structural formula is saved in human-editable plain text format. Any editing of the image or creation of any derivative work should be performed using a text editor . Please do not upload edits saved or exported with Inkscape or similar vector graphics editors , as well as with automated tools such as SVG Translate .

  8. Amylose - Wikipedia

    en.wikipedia.org/wiki/Amylose

    Amylose A is a parallel double-helix of linear chains of glucose. Amylose is made up of α(1→4) bound glucose molecules. The carbon atoms on glucose are numbered, starting at the aldehyde (C=O) carbon, so, in amylose, the 1-carbon on one glucose molecule is linked to the 4-carbon on the next glucose molecule (α(1→4) bonds). [3]

  9. File:Alpha-D-glucose Haworth.svg - Wikipedia

    en.wikipedia.org/wiki/File:Alpha-D-glucose...

    This image of a simple structural formula is ineligible for copyright and therefore in the public domain, because it consists entirely of information that is common property and contains no original authorship.