Nucleophile

In chemistry, a nucleophile (literally nucleus lover) is a reagent which is attracted to centres of positive charge. A nucleophile participates in a chemical reaction by donating electrons to a species known as an electrophile in order to form a chemical bond. Because nucleophiles donate electrons, they are by definition Lewis bases (see acid-base reaction theories). All molecules or ions with a free pair of electrons can act as nucleophiles, although negative ions (anions) are more potent than neutral reagents. Neutral nucleophilic reactions such as with alcohols, ROH, and water, HOH, are named solvolysis.

Related Topics:
Chemistry - Reagent - Chemical reaction - Electron - Electrophile - Chemical bond - Lewis base - Acid-base reaction theories - Molecule - Ion - Anions - Solvolysis

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Nucleophiles may take part in nucleophilic substitution, whereby a nucleophile becomes attracted to a full or partial positive charge on an element and displaces the group it is bonded to.

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Nucleophilic is an adjective that describes the affinity of a nucleophile to the nuclei, while nucleophilicity or nucleophile strength refers to the nucleophilic character. Nucleophilicity is often used to compare an atom's relative affinity to another's.

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The more basic the ions (high pKa) the more reactive they are as a nucleophile. Polarizability is also important in the determination of the nucleophilicity. Larger atoms contain more electrons; therefore distortion is easier so they are more nucleophilic. eg. I- is more nucleophilic than F-

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An ambident nucleophile is one that can attack from two or more places, resulting in two or more products. For example, thiocyanate ion (SCN−) may attack from either the {{sulfur}} or the {{nitrogen}}. For this reason, the SN2 reaction of an alkyl halide with SCN− often leads to a mixture of RSCN (an alkyl thiocyanate) and RNCS (an alkyl isothiocyanate).

Related Topics:
Thiocyanate - Isothiocyanate

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