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  2. Nucleophile - Wikipedia

    en.wikipedia.org/wiki/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 ...

  3. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    In chemistry, a nucleophilic substitution (S N) 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.

  4. Template:Periodic table (electron configuration) - Wikipedia

    en.wikipedia.org/wiki/Template:Periodic_table...

    4 9 F 2 5 10 Ne 2 6 [Ne] 3s: 3p: 11 Na 1 - 12 Mg 2 - 13 Al 2 1 14 Si 2 2 15 P 2 3 16 S 2 4 17 Cl 2 5 18 Ar 2 6 [Ar] 4s: 3d: 4p: 19 K 1-- 20 Ca 2-- 21 Sc 2 1 - 22 Ti 2 2 - 23 V 2 3 - 24 Cr 1 5 - 25 Mn 2 5 - 26 Fe 2 6 - 27 Co 2 7 - 28 Ni 2 8 - 29 Cu 1 10 - 30 Zn 2 10 - 31 Ga 2 10 1 32 Ge 2 10 2 33 As 2 10 3 34 Se 2 10 4 35 Br 2 10 5 36 Kr 2 10 6 ...

  5. Aluminium(I) nucleophiles - Wikipedia

    en.wikipedia.org/wiki/Aluminium(I)_nucleophiles

    The first isolation of a nucleophilic aluminium center was achieved in 2018 by Aldridge, Goicoechea and coworkers when they were able to synthesize the first aluminyl anion, [5] following the discoveries of gallium [6] [7] [8] and indium [9] analogues, heavier group 13 analogues which are more stable than aluminium in the lower +1 oxidation ...

  6. Electron-withdrawing group - Wikipedia

    en.wikipedia.org/wiki/Electron-withdrawing_group

    When it comes to nucleophilic substitution reactions, electron-withdrawing groups are more prone to nucleophilic substitution. For example, chlorodinitrobenzene is far more susceptible to reactions displacing chloride compared to chlorobenzene. [4]

  7. Electron configurations of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Electron_configurations_of...

    However there are numerous exceptions; for example the lightest exception is chromium, which would be predicted to have the configuration 1s 2 2s 2 2p 6 3s 2 3p 6 3d 4 4s 2, written as [Ar] 3d 4 4s 2, but whose actual configuration given in the table below is [Ar] 3d 5 4s 1. Note that these electron configurations are given for neutral atoms in ...

  8. Polyhedral skeletal electron pair theory - Wikipedia

    en.wikipedia.org/wiki/Polyhedral_skeletal...

    5 H 45, hydrogen atoms omitted. Example: [11] B 5 H 45. Electron count: 5 × B + 5 × H + 4 (for the negative charge) = 5 × 3 + 5 × 1 + 4 = 24 Since n = 5, 4n + 4 = 24, so the cluster is nido. Starting from an octahedron, one of the vertices is removed. The rules are useful in also predicting the structure of carboranes. Example: C 2 ...

  9. Electron pair - Wikipedia

    en.wikipedia.org/wiki/Electron_pair

    In chemistry, an electron pair or Lewis pair consists of two electrons that occupy the same molecular orbital but have opposite spins. Gilbert N. Lewis introduced the concepts of both the electron pair and the covalent bond in a landmark paper he published in 1916. [1] [2]