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  2. Non-covalent interaction - Wikipedia

    en.wikipedia.org/wiki/Non-covalent_interaction

    A dipole-induced dipole interaction (Debye force) is due to the approach of a molecule with a permanent dipole to another non-polar molecule with no permanent dipole. This approach causes the electrons of the non-polar molecule to be polarized toward or away from the dipole (or "induce" a dipole) of the approaching molecule. [13]

  3. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    Because electrons have a negative charge, the unequal sharing of electrons within a bond leads to the formation of an electric dipole: a separation of positive and negative electric charge. Because the amount of charge separated in such dipoles is usually smaller than a fundamental charge , they are called partial charges , denoted as δ ...

  4. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Unlike many compounds with the acet-prefix which have a 2-carbon chain, acetone has a 3-carbon chain. That has caused confusion because there cannot be a ketone with 2 carbons. The prefix refers to acetone's relation to vinegar ( acetum in Latin , also the source of the words "acid" and "acetic"), rather than its chemical structure.

  5. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    Note the decreased ΔG ‡ activation for the non-polar-solvent reaction conditions. Polar solvents stabilize the reactants to a greater extent than the non-polar-solvent conditions by solvating the negative charge on the nucleophile, making it less available to react with the electrophile. Solvent effects on SN1 and SN2 reactions

  6. 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]

  7. 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]

  8. Ionic bonding - Wikipedia

    en.wikipedia.org/wiki/Ionic_bonding

    Atoms that lose electrons make positively charged ions (called cations). This transfer of electrons is known as electrovalence in contrast to covalence . In the simplest case, the cation is a metal atom and the anion is a nonmetal atom, but these ions can be more complex, e.g. polyatomic ions like NH +

  9. Electronegativity - Wikipedia

    en.wikipedia.org/wiki/Electronegativity

    Electrostatic potential map of a water molecule, where the oxygen atom has a more negative charge (red) than the positive (blue) hydrogen atoms. Electronegativity, symbolized as χ, is the tendency for an atom of a given chemical element to attract shared electrons (or electron density) when forming a chemical bond. [1]