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  2. Carbon tetrafluoride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrafluoride

    Tetrafluoromethane, also known as carbon tetrafluoride or R-14, is the simplest perfluorocarbon (C F 4).As its IUPAC name indicates, tetrafluoromethane is the perfluorinated counterpart to the hydrocarbon methane.

  3. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    Through the use of Lewis structures, the placement of electrons, whether it is in a bond or in lone pairs, will allow for the identification of the formal charges of the atoms in the molecule to understand the stability and determine the most likely molecule (based on molecular geometry difference) that would be formed in a reaction.

  4. List of compounds with carbon number 4 - Wikipedia

    en.wikipedia.org/wiki/List_of_compounds_with...

    Chemical formula Synonyms CAS number; C 4 Br 2: dibromobutadiyne: 36333-41-2 C 4 Ce: cerium tetracarbide: 12151-79-0 C 4 ClF 7 O: heptafluorobutyryl chloride: 375-16-6 C 4 Cl 2 F 4 O 2: tetrafluorosuccinyl chloride: 356-15-0 C 4 Cl 2 F 4 O 3: chlorodifluoroacetic anhydride: 2834-23-3 C 4 Cl 2 O 4 Rh 2: dirhodium tetracarbonyl dichloride: 14523 ...

  5. Fluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Fluorocarbon

    Perfluoroalkanes are very stable because of the strength of the carbon–fluorine bond, one of the strongest in organic chemistry. [4] Its strength is a result of the electronegativity of fluorine imparting partial ionic character through partial charges on the carbon and fluorine atoms, which shorten and strengthen the bond (compared to carbon-hydrogen bonds) through favorable covalent ...

  6. Carbon–fluorine bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–fluorine_bond

    The wide range is due to the sensitivity of the stretching frequency to other substituents in the molecule. Monofluorinated compounds have a strong band between 1000 and 1110 cm −1 ; with more than one fluorine atoms, the band splits into two bands, one for the symmetric mode and one for the asymmetric. [ 13 ]

  7. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    In the latter case, it significantly increases the acidity of a molecule: the anion formed after giving the proton off becomes stable as a result. Consider acetic acid and its mono- , di-, and trifluoroacetic derivatives and their pK a values (4.74, 2.66, 1.24, and 0.23 [ note 2 ] ); [ 28 ] in other words, the trifluoro derative is 33,800 times ...

  8. Tetrahedral molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_molecular_geometry

    In a tetrahedral molecular geometry, a central atom is located at the center with four substituents that are located at the corners of a tetrahedron. The bond angles are arccos (− ⁠ 1 / 3 ⁠ ) = 109.4712206...° ≈ 109.5° when all four substituents are the same, as in methane ( CH 4 ) [ 1 ] [ 2 ] as well as its heavier analogues .

  9. Square planar molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Square_planar_molecular...

    Structure of cisplatin, an example of a molecule with the square planar coordination geometry. In chemistry, the square planar molecular geometry describes the stereochemistry (spatial arrangement of atoms) that is adopted by certain chemical compounds. As the name suggests, molecules of this geometry have their atoms positioned at the corners.