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A nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in a reaction. All molecules or ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they are by definition Lewis bases.
Nucleophilic describes the affinity of a nucleophile to the nuclei. Nucleophilicity, sometimes referred to as nucleophile strength, refers to a substance''s nucleophilic character and is often used to compare the affinity of atoms.
Neutral nucleophilic reactions with solvents such as alcohols and water are named solvolysis. Nucleophiles may take part in nucleophilic substitution, whereby a nucleophile becomes attracted to a full or partial positive charge.
Electrocatalysis is a branch of electrochemistry dealing with anodically and cathodically induced radical reaction mechanisms utilizing the electrochemical reactivity of an organom
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Group which gives out electron pair to an electrophile.
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