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  2. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    Usually, both occur without preference. The result is racemization. The stability of a carbocation (C +) depends on how many other carbon atoms are bonded to it. This results in S N 1 reactions usually occurring on atoms with at least two carbons bonded to them. [2] A more detailed explanation of this can be found in the main SN1 reaction page.

  3. Crystallographic defect - Wikipedia

    en.wikipedia.org/wiki/Crystallographic_defect

    Electron microscopy of antisites (a, Mo substitutes for S) and vacancies (b, missing S atoms) in a monolayer of molybdenum disulfide.Scale bar: 1 nm. [1]A crystallographic defect is an interruption of the regular patterns of arrangement of atoms or molecules in crystalline solids.

  4. Hume-Rothery rules - Wikipedia

    en.wikipedia.org/wiki/Hume-Rothery_rules

    For alloys containing transition metal elements there is a difficulty in interpretation of the Hume-Rothery electron concentration rule, as the values of e/a values (number of itinerant electrons per atom) for transition metals have been quite controversial for a long time, and no satisfactory solutions have yet emerged. [9] [10]

  5. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    The two main mechanisms were the S N 1 reaction and the S N 2 reaction, where S stands for substitution, N stands for nucleophilic, and the number represents the kinetic order of the reaction. [ 4 ] In the S N 2 reaction, the addition of the nucleophile and the elimination of leaving group take place simultaneously (i.e. a concerted reaction ).

  6. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    The unimolecular nucleophilic substitution (S N 1) reaction is a substitution reaction in organic chemistry. The Hughes-Ingold symbol of the mechanism expresses two properties—"S N " stands for " nucleophilic substitution ", and the "1" says that the rate-determining step is unimolecular .

  7. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    Once a substitution is made on a parent molecule, its structural symmetry is usually reduced, meaning that atoms that were formerly equivalent may no longer be so. Thus substitution of two or more equivalent atoms by the same element may generate more than one positional isomer. The classical example is the derivatives of benzene. Its six ...

  8. Coupled substitution - Wikipedia

    en.wikipedia.org/wiki/Coupled_substitution

    Coupled substitution is the geological process by which two elements simultaneous substitute into a crystal in order to maintain overall electrical neutrality and keep the charge constant. [1] In forming a solid solution series, ionic size is more important than ionic charge , as this can be compensated for elsewhere in the structure.

  9. Markovnikov's rule - Wikipedia

    en.wikipedia.org/wiki/Markovnikov's_rule

    The same is true when an alkene reacts with water in an additional reaction to form an alcohol that involves carbocation formation. The hydroxyl group (OH) bonds to the carbon that has the greater number of carbon-carbon bonds, while the hydrogen bonds to the carbon on the other end of the double bond, that has more carbon–hydrogen bonds.