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  2. 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 ...

  3. 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".

  4. Anomer - Wikipedia

    en.wikipedia.org/wiki/Anomer

    Download as PDF; Printable version; ... 1 = Fischer projection with C-1 at the top of the anomeric centre. C-5 is the anomeric reference atom. 2, 3 = Haworth projections.

  5. Monosaccharide - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide

    The Fischer projection is a systematic way of drawing the skeletal formula of an acyclic monosaccharide so that the handedness of each chiral carbon is well specified. Each stereoisomer of a simple open-chain monosaccharide can be identified by the positions (right or left) in the Fischer diagram of the chiral hydroxyls (the hydroxyls attached ...

  6. Glucose - Wikipedia

    en.wikipedia.org/wiki/Glucose

    From left to right: Haworth projections and ball-and-stick structures of the α- and β- anomers of D-glucopyranose (top row) and D-glucofuranose (bottom row) In solutions, the open-chain form of glucose (either " D -" or " L -") exists in equilibrium with several cyclic isomers , each containing a ring of carbons closed by one oxygen atom.

  7. Pyranose - Wikipedia

    en.wikipedia.org/wiki/Pyranose

    Haworth Projection of β-D-glucopyranose. Hermann Emil Fischer won the Nobel Prize in Chemistry (1902) for his work in determining the structure of the D-aldohexoses. [1] However, the linear, free-aldehyde structures that Fischer proposed represent a very minor percentage of the forms that hexose sugars adopt in solution.

  8. File:Alpha-D-Fructofuranose.svg - Wikipedia

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

    English: Structure of alpha-D-fructofuranose (Haworth projection). Esperanto: Fruktozo, monosakarido, kiel Haworth projekcio. Español: Estructura química de alfa-D-fructofuranosa.

  9. File:Alpha-D-Ribofuranose.svg - Wikipedia

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

    Deutsch: Struktur von alpha-D-Ribofuranose (Haworth-Schreibweise). English: Structure of alpha-D- ribofuranose ( Haworth projection ). Español: Molécula de β-D- Ribofuranosa ( Proyección de Haworth ).