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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. 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. ...

  4. 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 ).

  5. 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 ...

  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. Chiral analysis - Wikipedia

    en.wikipedia.org/wiki/Chiral_analysis

    This term has become very popular and commonly used in practice. But the appropriate expression is "enantioselective chromatography". [34] Chiral chromatography has advanced to turn into the most preferred technique for the determination of enantiomeric purity as well as separation of pure enantiomers both on analytical and preparative scale.

  8. 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 ...

  9. 2,4-Dimethylpentane - Wikipedia

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

    2,4-Dimethylpentane is an alkane with the chemical formula [(H 3 C) 2 CH] 2 CH 2. This colorless hydrocarbon is produced in large quantities in oil refineries. It results from the alkylation of isobutane by propylene. [1] Often referred to as "alkylate", it is blended with other gasoline components to give a high octane fuel.