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  2. Fischer projection - Wikipedia

    en.wikipedia.org/wiki/Fischer_projection

    In chemistry, the Fischer projection, devised by Emil Fischer in 1891, is a two-dimensional representation of a three-dimensional organic molecule by projection. Fischer projections were originally proposed for the depiction of carbohydrates and used by chemists, particularly in organic chemistry and biochemistry .

  3. L-Glucose - Wikipedia

    en.wikipedia.org/wiki/L-Glucose

    l-Glucose is an organic compound with formula C 6 H 12 O 6 or O=CH[CH(OH)] 5 H, specifically one of the aldohexose monosaccharides.As the l-isomer of glucose, it is the enantiomer of the more common d-glucose.

  4. Anomer - Wikipedia

    en.wikipedia.org/wiki/Anomer

    Different projections of α-D-glucopyranose. 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. Emil Fischer - Wikipedia

    en.wikipedia.org/wiki/Emil_Fischer

    Hermann Emil Louis Fischer FRS FRSE FCS (German pronunciation: [ˈeːmiːl ˈfɪʃɐ] ⓘ; 9 October 1852 – 15 July 1919) was a German chemist and 1902 recipient of the Nobel Prize in Chemistry. He discovered the Fischer esterification. He also developed the Fischer projection, a symbolic way of drawing asymmetric carbon atoms. He also ...

  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. NYT ‘Connections’ Hints and Answers Today, Tuesday, December 10

    www.aol.com/nyt-connections-hints-answers-today...

    Get ready for all of today's NYT 'Connections’ hints and answers for #548 on Tuesday, December 10, 2024. Today's NYT Connections puzzle for Tuesday, December 10, 2024The New York Times.

  9. 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 ...