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  2. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    A molecule is composed of one or more chemical bonds between molecular orbitals of different atoms. A molecule may be polar either as a result of polar bonds due to differences in electronegativity as described above, or as a result of an asymmetric arrangement of nonpolar covalent bonds and non-bonding pairs of electrons known as a full ...

  3. Polarizability - Wikipedia

    en.wikipedia.org/wiki/Polarizability

    In atoms, this occurs because larger atoms have more loosely held electrons in contrast to smaller atoms with tightly bound electrons. [9] [10] On rows of the periodic table, polarizability therefore decreases from left to right. [9] Polarizability increases down on columns of the periodic table. [9]

  4. Carbon–oxygen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–oxygen_bond

    A carbon–oxygen bond is a polar covalent bond between atoms of carbon and oxygen. [1] [2] [3]: 16–22 Carbon–oxygen bonds are found in many inorganic compounds such as carbon oxides and oxohalides, carbonates and metal carbonyls, [4] and in organic compounds such as alcohols, ethers, and carbonyl compounds.

  5. Molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Molecular_geometry

    For four atoms bonded together in a chain, the torsional angle is the angle between the plane formed by the first three atoms and the plane formed by the last three atoms. There exists a mathematical relationship among the bond angles for one central atom and four peripheral atoms (labeled 1 through 4) expressed by the following determinant.

  6. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    In benzoic acid, the carbon atoms which are present in the ring are sp 2 hybridised. As a result, benzoic acid ( pK a =4.20 ) is a stronger acid than cyclohexanecarboxylic acid ( pK a =4.87 ). Also, in aromatic carboxylic acids, electron-withdrawing groups substituted at the ortho and para positions can enhance the acid strength.

  7. Carbonyl group - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_group

    The polarity of C=O bond also enhances the acidity of any adjacent C-H bonds. Due to the positive charge on carbon and the negative charge on oxygen, carbonyl groups are subject to additions and/or nucleophilic attacks. A variety of nucleophiles attack, breaking the carbon-oxygen double bond, and leading to addition-elimination reactions.

  8. Tetrahedral molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_molecular_geometry

    Geometrical constraints in a molecule can cause a severe distortion of idealized tetrahedral geometry. In compounds featuring "inverted" tetrahedral geometry at a carbon atom, all four groups attached to this carbon are on one side of a plane. [6] The carbon atom lies at or near the apex of a square pyramid with the other four groups at the ...

  9. 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]

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