nucleophilic - definizione. Che cos'è nucleophilic
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Cosa (chi) è nucleophilic - definizione

CHEMICAL SPECIES THAT DONATES AN ELECTRON PAIR TO FORM A CHEMICAL BOND IN RELATION TO A REACTION
Nucleophilicity; Nucleophiles; Nucleophilic; Nucleophilic attack; Ambident nucleophile; Nucleophyl
  • benzhydrylium ions used in the determination of Mayr–Patz equation
  • alcohol]]
  • Mayr equation also includes SN2 reactions
  • Nucleophiles used in the determination of Mayr–Patz equation, X = tetrafluoroborate anion
  • Ritchie equation diazonium ion reactions

nucleophilic         
[?nju:kl??(?)'f?l?k]
¦ adjective Chemistry having a tendency to donate electrons or react with protons. Often contrasted with electrophilic.
Derivatives
nucleophile noun
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.
Nucleophilic substitution         
  • 1-phenylethylchloride methanolysis
  • SN1 reaction mechanism
  • mechanism
  • A graph showing the relative reactivities of the different alkyl halides towards S<sub>N</sub>1 and S<sub>N</sub>2 reactions (also see Table 1).
CLASS OF CHEMICAL REACTIONS IN WHICH A LEAVING GROUP(ELECTROPHILE) IS REPLACED BY AN ELECTRON RICH COMPOUND(NUCLEOPHILE).
Nucleophilic substitution reaction; Nucleophilic Substitution; Nucleophilic aliphatic Substitution; Sn reactions; SN Reactions; Nucleophilic aliphatic substitution; SN reaction; Nucleophilic displacement; Intramolecular nucleophilic substitution
In chemistry, a nucleophilic substitution is a class of chemical reactions in which an electron-rich chemical species (known as a nucleophile) replaces a functional group within another electron-deficient molecule (known as the electrophile). The molecule that contains the electrophile and the leaving functional group is called the substrate.

Wikipedia

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 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.