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  2. Fructose - Wikipedia

    en.wikipedia.org/wiki/Fructose

    In solution, fructose exists as an equilibrium mixture of the tautomers β-d-fructopyranose, β-d-fructofuranose, α-d-fructofuranose, α-d-fructopyranose and keto-d-fructose (the non-cyclic form). [16] The distribution of d-fructose tautomers in solution is related to several variables, such as solvent and temperature.

  3. Glucose - Wikipedia

    en.wikipedia.org/wiki/Glucose

    A open-chain form of glucose makes up less than 0.02% of the glucose molecules in an aqueous solution at equilibrium. [57] The rest is one of two cyclic hemiacetal forms. In its open-chain form, the glucose molecule has an open (as opposed to cyclic ) unbranched backbone of six carbon atoms, where C-1 is part of an aldehyde group H(C=O)− .

  4. Mutarotation - Wikipedia

    en.wikipedia.org/wiki/Mutarotation

    Mutarotation. In stereochemistry, mutarotation is the change in optical rotation of a chiral material in a solution due to a change in proportion of the two constituent anomers (i.e. the interconversion of their respective stereocenters) until equilibrium is reached. Cyclic sugars show mutarotation as α and β anomeric forms interconvert. [1]

  5. Blue bottle experiment - Wikipedia

    en.wikipedia.org/wiki/Blue_bottle_experiment

    Blue bottle reaction video. The blue bottle experiment is a color-changing redox chemical reaction. An aqueous solution containing glucose, sodium hydroxide, methylene blue is prepared in a closed bottle containing some air. Upon standing, it spontaneously turns from blue to colorless due to reduction of methylene blue by the alkaline glucose ...

  6. Sugar - Wikipedia

    en.wikipedia.org/wiki/Sugar

    Sugar is the generic name for sweet-tasting, soluble carbohydrates, many of which are used in food. Simple sugars, also called monosaccharides, include glucose, fructose, and galactose. Compound sugars, also called disaccharides or double sugars, are molecules made of two bonded monosaccharides; common examples are sucrose (glucose + fructose ...

  7. Fructose 1,6-bisphosphate - Wikipedia

    en.wikipedia.org/wiki/Fructose_1,6-bisphosphate

    Fructose 1,6-bisphosphate, known in older publications as Harden-Young ester, is fructose sugar phosphorylated on carbons 1 and 6 (i.e., is a fructosephosphate). The β- D -form of this compound is common in cells. [1] Upon entering the cell, most glucose and fructose is converted to fructose 1,6-bisphosphate. [2][3]

  8. Hexose - Wikipedia

    en.wikipedia.org/wiki/Hexose

    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] Hexoses exist in two forms, open-chain or cyclic, that easily convert into each other in aqueous solutions. [4] The open-chain form of a hexose, which ...

  9. Glucose oxidase - Wikipedia

    en.wikipedia.org/wiki/Glucose_oxidase

    Infobox references. The glucose oxidase enzyme (GOx or GOD) also known as notatin (EC number 1.1.3.4) is an oxidoreductase that catalyses the oxidation of glucose to hydrogen peroxide and D-glucono-δ-lactone. This enzyme is produced by certain species of fungi and insects and displays antibacterial activity when oxygen and glucose are present.