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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. HSAB theory - Wikipedia

    en.wikipedia.org/wiki/HSAB_theory

    An application of HSAB theory is the so-called Kornblum's rule (after Nathan Kornblum) which states that in reactions with ambident nucleophiles (nucleophiles that can attack from two or more places), the more electronegative atom reacts when the reaction mechanism is S N 1 and the less electronegative one in a S N 2 reaction.

  4. Nucleotide base - Wikipedia

    en.wikipedia.org/wiki/Nucleotide_base

    Similarly, the simple-ring structure of cytosine, uracil, and thymine is derived of pyrimidine, so those three bases are called the pyrimidine bases. [ 6 ] Each of the base pairs in a typical double- helix DNA comprises a purine and a pyrimidine: either an A paired with a T or a C paired with a G.

  5. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    In the context of a specific chemical reaction between NH 3 and Me 3 B, a lone pair from NH 3 will form a dative bond with the empty orbital of Me 3 B to form an adduct NH 3 •BMe 3. The terminology refers to the contributions of Gilbert N. Lewis. [2] The terms nucleophile and electrophile are sometimes interchangeable with Lewis base and ...

  6. Base (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Base_(chemistry)

    G. N. Lewis realized that water, ammonia, and other bases can form a bond with a proton due to the unshared pair of electrons that the bases possess. [3] In the Lewis theory, a base is an electron pair donor which can share a pair of electrons with an electron acceptor which is described as a Lewis acid. [4]

  7. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    The nucleophile may be electrically neutral or negatively charged, whereas the substrate is typically neutral or positively charged. An example of nucleophilic substitution is the hydrolysis of an alkyl bromide, R-Br under basic conditions, where the attacking nucleophile is hydroxyl (OH −) and the leaving group is bromide (Br −).

  8. Electron pair - Wikipedia

    en.wikipedia.org/wiki/Electron_pair

    This also limits the number of electrons in the same orbital to two. The pairing of spins is often energetically favorable, and electron pairs therefore play a large role in chemistry. They can form a chemical bond between two atoms, or they can occur as a lone pair of valence electrons. They also fill the core levels of an atom.

  9. Chemical reaction - Wikipedia

    en.wikipedia.org/wiki/Chemical_reaction

    In the first type, a nucleophile, an atom or molecule with an excess of electrons and thus a negative charge or partial charge, replaces another atom or part of the "substrate" molecule. The electron pair from the nucleophile attacks the substrate forming a new bond, while the leaving group departs with an electron pair. The nucleophile may be ...