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  2. Non-nucleophilic base - Wikipedia

    en.wikipedia.org/wiki/Non-nucleophilic_base

    Normal bases are also nucleophiles, but often chemists seek the proton-removing ability of a base without any other functions. Typical non-nucleophilic bases are bulky, such that protons can attach to the basic center but alkylation and complexation is inhibited.

  3. Nucleophile - Wikipedia

    en.wikipedia.org/wiki/Nucleophile

    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 are Lewis bases. Nucleophilic describes the affinity of a nucleophile to bond with positively charged ...

  4. Superbase - Wikipedia

    en.wikipedia.org/wiki/Superbase

    Organometallic compounds of electropositive metals are superbases, but they are generally strong nucleophiles. Examples include organolithium and organomagnesium ( Grignard reagent ) compounds. Another type of organometallic superbase has a reactive metal exchanged for a hydrogen on a heteroatom , such as oxygen (unstabilized alkoxides ) or ...

  5. Organolithium reagent - Wikipedia

    en.wikipedia.org/wiki/Organolithium_reagent

    Thus, organolithium reagents are strongly basic and nucleophilic. Some of the most common applications of organolithium reagents in synthesis include their use as nucleophiles, strong bases for deprotonation, initiator for polymerization, and starting material for the preparation of other organometallic compounds.

  6. 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.

  7. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    tert-Butoxide, on the other hand, is a strong base, but a poor nucleophile, because of its three methyl groups hindering its approach to the carbon. Nucleophile strength is also affected by charge and electronegativity : nucleophilicity increases with increasing negative charge and decreasing electronegativity.

  8. Base (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Base_(chemistry)

    A strong base is a basic chemical compound that can remove a proton (H +) from (or deprotonate) a molecule of even a very weak acid (such as water) in an acid–base reaction. Common examples of strong bases include hydroxides of alkali metals and alkaline earth metals, like NaOH and Ca(OH) 2, respectively. Due to their low solubility, some ...

  9. Electron-rich - Wikipedia

    en.wikipedia.org/wiki/Electron-rich

    with regards to acid-base reactions, electron-rich species have high pKa's and react with weak Lewis acids. [ 4 ] with regards to nucleophilic substitution reactions , electron-rich species are relatively strong nucleophiles, as judged by rates of attack by electrophiles.