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  2. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    A Lewis base is often a Brønsted–Lowry base as it can donate a pair of electrons to H +; [11] the proton is a Lewis acid as it can accept a pair of electrons. The conjugate base of a Brønsted–Lowry acid is also a Lewis base as loss of H + from the acid leaves those electrons which were used for the A—H bond as a lone pair on the ...

  3. Nucleophile - Wikipedia

    en.wikipedia.org/wiki/Nucleophile

    A hydroxide ion acting as a nucleophile in an S N 2 reaction, converting a haloalkane into an alcohol. In chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they ...

  4. Periodic trends - Wikipedia

    en.wikipedia.org/wiki/Periodic_trends

    Similarly, nucleophilicity is defined as the affinity of an electron-rich species, known as a nucleophile, to donate electrons to another species. [29] Trends in the periodic table are useful for predicting an element's nucleophilicity and electrophilicity.

  5. HSAB theory - Wikipedia

    en.wikipedia.org/wiki/HSAB_theory

    An application of HSAB theory is the so-called Kornblum's rule (after Nathan Kornblum) which states that in reactions with ambident nucleophiles (nucleophiles that can attack from two or more places), the more electronegative atom reacts when the reaction mechanism is S N 1 and the less electronegative one in a S N 2 reaction.

  6. Azide - Wikipedia

    en.wikipedia.org/wiki/Azide

    In chemistry, azide (/ ˈ eɪ z aɪ d /, AY-zyd) is a linear, polyatomic anion with the formula N − 3 and structure − N=N + =N −.It is the conjugate base of hydrazoic acid HN 3. Organic azides are organic compounds with the formula RN 3, containing the azide functional group. [1]

  7. Electron pair - Wikipedia

    en.wikipedia.org/wiki/Electron_pair

    This also limits the number of electrons in the same orbital to two. The pairing of spins is often energetically favorable, and electron pairs therefore play a large role in chemistry. They can form a chemical bond between two atoms, or they can occur as a lone pair of valence electrons. They also fill the core levels of an atom.

  8. Carbones - Wikipedia

    en.wikipedia.org/wiki/Carbones

    Carbones possess high-energy orbitals with both σ- and π-symmetry, making them strong Lewis bases and strong π-backdonor substituents. [2] Carbones possess high proton affinities [3] [4] and are strong nucleophiles which allows them to function as ligands in a variety of main group and transition metal complexes. [5]

  9. Charge number - Wikipedia

    en.wikipedia.org/wiki/Charge_number

    In that case, the charge of an ion could be written as =. The charge number in chemistry normally relates to an electric charge. This is a property of specific subatomic atoms. These elements define the electromagnetic contact between the two elements. A chemical charge can be found by using the periodic table.