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  2. 2,3,4-Trimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3,4-Trimethylpentane

    2,3,4-Trimethylpentane Skeletal formula of 2,3,4-trimethylpentane with some implicit hydrogens added: Names Preferred IUPAC name. 2,3,4-Trimethylpentane [1] Identifiers

  3. Chiral inversion - Wikipedia

    en.wikipedia.org/wiki/Chiral_inversion

    Chiral inversion is the process of conversion of one enantiomer of a chiral molecule to its mirror-image version with no other change in the molecule. [1] [2] [3] [4]Chiral inversion happens depending on various factors (viz. biological-, solvent-, light-, temperature- induced, etc.) and the energy barrier energy barrier associated with the stereogenic element present in the chiral molecule. 2 ...

  4. Trimethylpentane - Wikipedia

    en.wikipedia.org/wiki/Trimethylpentane

    2,3,4-Trimethylpentane This page was last edited on 10 January 2019, at 23:34 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4. ...

  5. Gas exchange - Wikipedia

    en.wikipedia.org/wiki/Gas_exchange

    Gas exchange is the physical process by which gases move passively by diffusion across a surface. For example, this surface might be the air/water interface of a water body, the surface of a gas bubble in a liquid, a gas-permeable membrane, or a biological membrane that forms the boundary between an organism and its extracellular environment.

  6. Triptane - Wikipedia

    en.wikipedia.org/wiki/Triptane

    Triptane, or 2,2,3-trimethylbutane, is an organic chemical compound with the molecular formula C 7 H 16 or (H 3 C-) 3 C-C(-CH 3) 2 H. It is therefore an alkane , specifically the most compact and heavily branched of the heptane isomers, the only one with a butane (C 4 ) backbone.

  7. 2,2,4-Trimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,2,4-Trimethylpentane

    2,2,4-Trimethylpentane, also known as isooctane or iso-octane, is an organic compound with the formula (CH 3) 3 CCH 2 CH(CH 3) 2. It is one of several isomers of octane (C 8 H 18 ). This particular isomer is the standard 100 point on the octane rating scale (the zero point is n -heptane ).

  8. Chiral analysis - Wikipedia

    en.wikipedia.org/wiki/Chiral_analysis

    Moreover, the moment a racemic therapeutic is placed in a biological system, a chiral environment, it is no more 50:50 due enantioselective absorption, distribution, metabolism, and elimination (ADME) process. Hence to track the individual enantiomeric profile there is a need for chiral analysis tool.

  9. Chiral thin-layer chromatography - Wikipedia

    en.wikipedia.org/wiki/Chiral_thin-layer...

    The chiral stationary phase can be prepared by mixing chirally pure reagents such as L-amino acid, or brucine, or a chiral ligand exchange reagent with silica gel slurry, [2] [3] or by impregnation of the TLC plate in the solution of a chiral reagent. [4] The principle can also be applied to chemically modify the stationary phase before making ...