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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 .
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 ...
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.
Two important hexoses, in the Fischer projection. In chemistry , a hexose is a monosaccharide (simple sugar) with six carbon atoms. [ 1 ] [ 2 ] The chemical formula for all hexoses is C 6 H 12 O 6 , and their molecular weight is 180.156 g/mol. [ 3 ]
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.
Fischer projections depicting the two enantiomers of erythrose Erythrose was first isolated in 1849 from rhubarb by the French pharmacist Louis Feux Joseph Garot (1798-1869), [ 4 ] and was named as such because of its red hue in the presence of alkali metals (ἐρυθρός, "red").
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L-Ribose Fischer Projection. Ribose is a simple sugar and carbohydrate with molecular formula C 5 H 10 O 5 and the linear-form composition H−(C=O)−(CHOH) 4 −H. The naturally occurring form, d-ribose, is a component of the ribonucleotides from which RNA is built, and so this compound is necessary for coding, decoding, regulation and expression of genes.