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nucleophile - translation to russian
![alcohol]]](https://commons.wikimedia.org/wiki/Special:FilePath/Hydrox subst.png?width=200 "alcohol]]")
['nju:kliəfail]
химия
нуклеофильный реагент
электронно-донорное вещество
существительное
химия
нуклеофильный реагент
электронно-донорное вещество
общая лексика
нуклеофильный
![Chiral oxy[<sup>2</sup>''H''<sub>1</sub>]methyllithiums. Bu stands for butyl, ''i''-Pr stands for isopropyl.](https://commons.wikimedia.org/wiki/Special:FilePath/PhosphatePhosphonateRearrangement.png?width=200 "Chiral oxy[<sup>2</sup>''H''<sub>1</sub>]methyllithiums. Bu stands for butyl, ''i''-Pr stands for isopropyl.")
Definition
Wikipedia
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 atomic 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, and nucleophilic addition. Nucleophilicity is closely related to basicity.
