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  2. 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.

  3. 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 ...

  4. Rotamers - Wikipedia

    en.wikipedia.org/wiki/Linear_alkane_conformation

    The ring-flip proceeds at a rates of approximately 10 5 ring-flips/sec, with an overall energy barrier of 10 kcal/mol (42 kJ/mol). This barrier precludes separation at ambient temperatures. [ 20 ] However, at low temperatures below the coalescence point one can directly monitor the equilibrium by NMR spectroscopy and by dynamic, temperature ...

  5. 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]

  6. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    A secondary deuterium isotope effect of slightly larger than 1 (commonly 1 - 1.5) is observed. There is no antiperiplanar requirement. An example is the pyrolysis of a certain sulfonate ester of menthol: E1 elimination Nash 2008, antiperiplanar relationship in blue Only reaction product A results from antiperiplanar

  7. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    A: antiperiplanar, anti or trans. B: synclinal or gauche. C: anticlinal or eclipsed. D: synperiplanar or cis. [2] Rotating their carbon–carbon bonds, the molecules ethane and propane have three local energy minima. They are structurally and energetically equivalent, and are called the staggered conformers.

  8. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    20 C20. 21 C21. 22 C22. 23 C23. 24 C24. 25 C25. 26 C26. Toggle the table of contents. List of carboxylic acids. ... (CH 2) 10 COOH benzene-1,2,3,4,5,6-hexacarboxylic ...

  9. Category:Chloroalkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Chloroalkanes

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