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  2. Optical rotation - Wikipedia

    en.wikipedia.org/wiki/Optical_rotation

    The lowercase "d-" and "l-" prefixes are distinct from the SMALL CAPS "D-" and "L-" prefixes. The "D-" and "L-" prefixes are used to specify the enantiomer of chiral organic compounds in biochemistry and are based on the compound's absolute configuration relative to (+)-glyceraldehyde, which is the D-form by definition.

  3. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    There are three common naming conventions for specifying one of the two enantiomers (the absolute configuration) of a given chiral molecule: the R/S system is based on the geometry of the molecule; the (+)- and (−)- system (also written using the obsolete equivalents d- and l-) is based on its optical rotation properties; and the D/L system is based on the molecule's relationship to ...

  4. Chirality (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Chirality_(chemistry)

    Chirality can also arise from isotopic differences between atoms, such as in the deuterated benzyl alcohol PhCHDOH; which is chiral and optically active ([α] D = 0.715°), even though the non-deuterated compound PhCH 2 OH is not. [7]

  5. Deuterium - Wikipedia

    en.wikipedia.org/wiki/Deuterium

    In chemistry, biochemistry and environmental sciences, deuterium is used as a non-radioactive, stable isotopic tracer, for example, in the doubly labeled water test. In chemical reactions and metabolic pathways , deuterium behaves somewhat similarly to ordinary hydrogen (with a few chemical differences, as noted).

  6. Specific rotation - Wikipedia

    en.wikipedia.org/wiki/Specific_rotation

    In chemistry, specific rotation ([α]) is a property of a chiral chemical compound. [ 1 ] : 244 It is defined as the change in orientation of monochromatic plane-polarized light , per unit distance–concentration product, as the light passes through a sample of a compound in solution.

  7. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    The D- and L- labeling of the isomers above is not the same as the d- and l- labeling more commonly seen, explaining why these may appear reversed to those familiar with only the latter naming convention. A Fischer projection can be used to differentiate between L- and D- molecules Chirality (chemistry). For instance, by definition, in a ...

  8. Here Are All the Big Differences Between the ‘Lessons in ...

    www.aol.com/big-differences-between-lessons...

    Here are all the notable differences between the Love in Chemistry book and TV show. 1. In the book: Elizabeth Zott is a chemist at the Hastings Research Institute, with her own lab technicians ...

  9. Partition coefficient - Wikipedia

    en.wikipedia.org/wiki/Partition_coefficient

    In the physical sciences, a partition coefficient (P) or distribution coefficient (D) is the ratio of concentrations of a compound in a mixture of two immiscible solvents at equilibrium. This ratio is therefore a comparison of the solubilities of the solute in these two liquids.