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  2. Monosaccharide - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide

    The number of open chain stereoisomers for an aldose monosaccharide is larger by one than that of a ketose monosaccharide of the same length. Every ketose will have 2 (n−3) stereoisomers where n > 2 is the number of carbons. Every aldose will have 2 (n−2) stereoisomers where n > 2 is the number of carbons. These are also referred to as ...

  3. Monosaccharide nomenclature - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide_nomenclature

    The carbohydrate part of the molecule is called glycone, the -O- bridge is the glycosisdic oxygen, and the attached group is the aglycone. Glycosides are named by giving the aglyconic alcohol HOR, followed by the saccharide name with the '-e' ending replaced by '-ide'; as in [[phenol D -glucopyranoside]].

  4. Carbohydrate - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate

    A carbohydrate is a biomolecule consisting of carbon (C), hydrogen (H) and oxygen (O) atoms, usually with a hydrogen–oxygen atom ratio of 2:1 (as in water) and thus with the empirical formula C m (H 2 O) n (where m may or may not be different from n), which does not mean the H has covalent bonds with O (for example with CH 2 O, H has a covalent bond with C but not with O).

  5. Hexose - Wikipedia

    en.wikipedia.org/wiki/Hexose

    The 2-ketohexoses psicose, fructose and tagatose occur naturally as the D-isomers, whereas sorbose occurs naturally as the L-isomer. D-Sorbose is commonly used in the commercial synthesis of ascorbic acid. [10] D-Tagatose is a rare natural ketohexose that is found in small quantities in food. [11]

  6. Glucose - Wikipedia

    en.wikipedia.org/wiki/Glucose

    The clinical importance of the glycemic index is controversial, [123] [124] as foods with high fat contents slow the resorption of carbohydrates and lower the glycemic index, e.g. ice cream. [124] An alternative indicator is the insulin index , [ 125 ] measured as the impact of carbohydrate consumption on the blood insulin levels.

  7. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    The two isomeric complexes, cisplatin and transplatin, are examples of square planar MX 2 Y 2 molecules with M = Pt. Cis and trans isomers also occur in inorganic coordination compounds , such as square planar MX 2 Y 2 {\displaystyle {\ce {MX2Y2}}} complexes and octahedral MX 4 Y 2 {\displaystyle {\ce {MX4Y2}}} complexes.

  8. Oligosaccharide nomenclature - Wikipedia

    en.wikipedia.org/wiki/Oligosaccharide_nomenclature

    Two common examples are cellulose, a main component of the cell wall in plants, and starch, a name derived from the Anglo-Saxon stercan, meaning to stiffen. [ 2 ] To name a polysaccharide composed of a single type of monosaccharide, that is a homopolysaccharide, the ending “-ose” of the monosaccharide is replaced with “-an”. [ 3 ]

  9. Erythrose - Wikipedia

    en.wikipedia.org/wiki/Erythrose

    Erythrose is a tetrose saccharide with the chemical formula C 4 H 8 O 4. It has one aldehyde group, and is thus part of the aldose family. The natural isomer is D-erythrose; it is a diastereomer of D-threose. [3] Fischer projections depicting the two enantiomers of erythrose