| Nucleophilic Attack |
Article Index for Nucleophilic |
Information AboutNucleophilic Attack |
| CATEGORIES ABOUT NUCLEOPHILE | |
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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. 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. 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, ''e.g.,'' the Iodide ion (I−) is more nucleophilic than the Fluoride ion (F−). An ambident nucleophile is one that can attack from two or more places, resulting in two or more products. For example, the Thiocyanate ion (SCN−) may attack from either the or the . 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 ). COMMON EXAMPLES In the example below, the Oxygen of the hydroxide ion donates an electron to bond with the Carbon at the end of the bromopropane molecule. The bond between the carbon and the Bromine then undergoes Heterolytic Fission , with the bromine atom taking the pair of electrons and becoming the Bromide ion (Br−): Carbon nucleophiles
Oxygen nucleophiles Sulfur nucleophiles
Nitrogen nucleophiles SEE ALSO |
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