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  2. Le Bel–Van 't Hoff rule - Wikipedia

    en.wikipedia.org/wiki/Le_Bel–Van_'t_Hoff_rule

    [3] As an example, four of the carbon atoms of the aldohexose class of molecules are asymmetric, therefore the Le Bel–Van 't Hoff rule gives a calculation of 2 4 = 16 stereoisomers. This is indeed the case: these chemicals are two enantiomers each of eight different diastereomers : allose , altrose , glucose , mannose , gulose , idose ...

  3. Bromobutane - Wikipedia

    en.wikipedia.org/wiki/Bromobutane

    Bromobutane (molecular formula: C 4 H 9 Br, molar mass: 137.02 g/mol) may refer to either of two chemical compounds: 1-Bromobutane (n-butyl bromide)

  4. 2-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/2-Bromobutane

    2-Bromobutane is an isomer of 1-bromobutane. Both compounds share the molecular formula C 4 H 9 Br. 2-Bromobutane is also known as sec-butyl bromide or methylethylbromomethane. Because it contains bromine, a halogen, it is part of a larger class of compounds known as alkyl halides. It is a colorless liquid with a pleasant odor.

  5. C4H9Br - Wikipedia

    en.wikipedia.org/wiki/C4H9Br

    The molecular formula C 4 H 9 Br, (molar mass: 137.02 g/mol, exact mass: 135.9888 u) may refer to: 1-Bromobutane; 2-Bromobutane; tert-Butyl bromide;

  6. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    2 Li + C 4 H 9 X → C 4 H 9 Li + LiX where X = Cl, Br. The lithium for this reaction contains 1-3% sodium. When bromobutane is the precursor, the product is a homogeneous solution, consisting of a mixed cluster containing both LiBr and LiBu. 1-Fluorobutane can be obtained by reacting 1-bromobutane with potassium fluoride in ethylene glycol. [5]

  7. Monosaccharide - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide

    For example, there are 16 distinct aldohexose stereoisomers, but the name "glucose" means a specific pair of mirror-image aldohexoses. In the Fischer projection, one of the two glucose isomers has the hydroxyl at left on C3, and at right on C4 and C5; while the other isomer has the reversed pattern.

  8. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    [2] [3] [4] The ring-flip of substituted cyclohexanes constitutes a common form of conformers. [5] The study of the energetics of bond rotation is referred to as conformational analysis. [6] In some cases, conformational analysis can be used to predict and explain product selectivity, mechanisms, and rates of reactions. [7]

  9. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    The most common one in nature (myo-inositol) has the hydroxyls on carbons 1, 2, 3 and 5 on the same side of that plane, and can therefore be called cis-1,2,3,5-trans-4,6-cyclohexanehexol. And each of these cis - trans isomers can possibly have stable "chair" or "boat" conformations (although the barriers between these are significantly lower ...