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  2. Anti-periplanar - Wikipedia

    en.wikipedia.org/wiki/Anti-periplanar

    Figure 5 shows 2-chloro-2,3-dimethylbutane in a sawhorse projection with chlorine and a hydrogen anti-periplanar to each other. Syn-periplanar or synperiplanar is similar to anti-periplanar. In the syn-periplanar conformer, the A and D are on the same side of the plane of the bond, with the dihedral angle of A−B and C−D between +30° and ...

  3. 2-Chlorobutane - Wikipedia

    en.wikipedia.org/wiki/2-Chlorobutane

    This is because 2-chlorobutane possesses two different sets of β-hydrogens at the first and third carbons respectively, resulting in 1-butene or 2-butene. It is important to note that as a secondary alkyl halide, both E2 and Sn2 reactions are equally likely when reacting with a substance that can act as both a base and a nucleophile.

  4. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  5. Rotamers - Wikipedia

    en.wikipedia.org/wiki/Rotamers

    Relative conformation energy diagram of butane as a function of dihedral angle. [8] A: antiperiplanar, anti or trans. B: synclinal or gauche. C: anticlinal or eclipsed. D: synperiplanar or cis. [1] Rotating their carbon–carbon bonds, the molecules ethane and propane have three local energy minima.

  6. Cieplak effect - Wikipedia

    en.wikipedia.org/wiki/Cieplak_Effect

    The Cieplak effect relies on the stabilizing interaction of mixing full and empty orbitals to delocalize electrons, known as hyperconjugation. [2] When the highest occupied molecular orbital of one system and the lowest unoccupied molecular orbital of another system have comparable energies and spatial overlap, the electrons can delocalize and sink into a lower energy level.

  7. Pentane interference - Wikipedia

    en.wikipedia.org/wiki/Pentane_interference

    Pentane interference or syn-pentane interaction is the steric hindrance that the two terminal methyl groups experience in one of the chemical conformations of n-pentane.The possible conformations are combinations of anti conformations and gauche conformations and are anti-anti, anti-gauche +, gauche + - gauche + and gauche + - gauche − of which the last one is especially energetically ...

  8. C4-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C4-Benzenes

    The saturated compounds have formula C 10 H 14 and molecular weight 134.22 g/mol. C 4-benzenes are found in petroleum. [1] Petrol (gasoline) can contain 5-8% C 4 -benzenes. [ 2 ]

  9. Category:Chloroalkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Chloroalkanes

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