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  2. Linear molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Linear_molecular_geometry

    The linear molecular geometry describes the geometry around a central atom bonded to two other atoms (or ligands) placed at a bond angle of 180°. Linear organic molecules, such as acetylene (HC≡CH), are often described by invoking sp orbital hybridization for their carbon centers. Two sp orbitals

  3. Tetrafluoroberyllate - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroberyllate

    The Be–F bond length is between 145 and 153 pm.The beryllium is sp 3 hybridized, leading to a longer bond than in BeF 2, where beryllium is sp hybridized. [11] In trifluoroberyllates, there are actually BeF 4 tetrahedra arranged in a triangle, so that three fluorine atoms are shared on two tetrahedra each, resulting in a formula of Be 3 F 9.

  4. Beryllium fluoride - Wikipedia

    en.wikipedia.org/wiki/Beryllium_fluoride

    Molecular BeF 2 in the gaseous state is isoelectronic to carbon dioxide. As a liquid, beryllium fluoride has a tetrahedral structure. The density of liquid BeF 2 decreases near its freezing point, as Be 2+ and F − ions begin to coordinate more strongly with one another, leading to the expansion of voids between formula units. [11]

  5. Carbon–fluorine bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–fluorine_bond

    The carbon–fluorine bond is a polar covalent bond between carbon and fluorine that is a component of all organofluorine compounds. It is one of the strongest single bonds in chemistry (after the B–F single bond, Si–F single bond, and H–F single bond), and relatively short, due to its partial ionic character.

  6. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    The fluorine–fluorine bond of the difluorine molecule is relatively weak when compared to the bonds of heavier dihalogen molecules. The bond energy is significantly weaker than those of Cl 2 or Br 2 molecules and similar to the easily cleaved oxygen–oxygen bonds of peroxides or nitrogen–nitrogen bonds of hydrazines. [8]

  7. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carboncarbon_bond

    Carbon is one of the few elements that can form long chains of its own atoms, a property called catenation.This coupled with the strength of the carboncarbon bond gives rise to an enormous number of molecular forms, many of which are important structural elements of life, so carbon compounds have their own field of study: organic chemistry.

  8. Covalent bond - Wikipedia

    en.wikipedia.org/wiki/Covalent_bond

    A covalent bond forming H 2 (right) where two hydrogen atoms share the two electrons. A covalent bond is a chemical bond that involves the sharing of electrons to form electron pairs between atoms. These electron pairs are known as shared pairs or bonding pairs.

  9. Carbon - Wikipedia

    en.wikipedia.org/wiki/Carbon

    Atomic carbon is a very short-lived species and, therefore, carbon is stabilized in various multi-atomic structures with diverse molecular configurations called allotropes. The three relatively well-known allotropes of carbon are amorphous carbon, graphite, and diamond.