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  2. Neighbouring group participation - Wikipedia

    en.wikipedia.org/wiki/Neighbouring_group...

    In organic chemistry, neighbouring group participation (NGP, also known as anchimeric assistance) has been defined by the International Union of Pure and Applied Chemistry (IUPAC) as the interaction of a reaction centre with a lone pair of electrons in an atom or the electrons present in a sigma or pi bond contained within the parent molecule but not conjugated with the reaction centre.

  3. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    In Organic chemistry, the inductive effect in a molecule is a local change in the electron density due to electron-withdrawing or electron-donating groups elsewhere in the molecule, resulting in a permanent dipole in a bond. [1] It is present in a σ (sigma) bond, unlike the electromeric effect which is present in a π (pi) bond.

  4. Imidogen - Wikipedia

    en.wikipedia.org/wiki/Imidogen

    Interstellar NH was identified in the diffuse clouds toward ζ Persei and HD 27778 from high-resolution high-signal-to-noise spectra of the NH A 3 Π→X 3 Σ (0,0) absorption band near 3358 Å. [7] A temperature of about 30 K (−243 °C) favored an efficient production of CN from NH within the diffuse cloud.

  5. Mesomeric effect - Wikipedia

    en.wikipedia.org/wiki/Mesomeric_effect

    In chemistry, the mesomeric effect (or resonance effect) is a property of substituents or functional groups in a chemical compound.It is defined as the polarity produced in the molecule by the interaction of two pi bonds or between a pi bond and lone pair of electrons present on an adjacent atom. [1]

  6. Pi-interaction - Wikipedia

    en.wikipedia.org/wiki/Pi-interaction

    In chemistry, π-effects or π-interactions are a type of non-covalent interaction that involves π systems.Just like in an electrostatic interaction where a region of negative charge interacts with a positive charge, the electron-rich π system can interact with a metal (cationic or neutral), an anion, another molecule and even another π system. [1]

  7. Nitrenium ion - Wikipedia

    en.wikipedia.org/wiki/Nitrenium_ion

    A nitrenium ion (also called: aminylium ion or imidonium ion (obsolete)) in organic chemistry is a reactive intermediate based on nitrogen with both an electron lone pair and a positive charge and with two substituents (R 2 N +). [1] [2] Nitrenium ions are isoelectronic with carbenes, and can exist in either a singlet or a triplet state.

  8. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    Bent's rule can be extended to rationalize the hybridization of nonbonding orbitals as well. On the one hand, a lone pair (an occupied nonbonding orbital) can be thought of as the limiting case of an electropositive substituent, with electron density completely polarized towards the central atom.

  9. Amino radical - Wikipedia

    en.wikipedia.org/wiki/Amino_radical

    The rate constant (k 1) for this reaction was determined to be 1.0 × 10 8 M −1 s −1, while the parallel reaction of OH with NH + 4 was found to be much slower. This rate was redetermined by using two-pulse radiolysis competition methods with benzoate and thiocyanate ions at pH 11.4. A value of k 1 = (9 + 1) × 10 7 M −1 s −1 was