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  2. Carbon tetrafluoride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrafluoride

    Tetrafluoromethane is the product when any carbon compound, including carbon itself, is burned in an atmosphere of fluorine. With hydrocarbons, hydrogen fluoride is a coproduct. It was first reported in 1926. [7] It can also be prepared by the fluorination of carbon dioxide, carbon monoxide or phosgene with sulfur tetrafluoride.

  3. Tetrafluoride - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoride

    Toggle the table of contents. ... A tetrafluoride is a chemical compound with four fluorines in its formula. ... Carbon tetrafluoride (tetrafluoromethane)

  4. List of chemical elements - Wikipedia

    en.wikipedia.org/wiki/List_of_chemical_elements

    A chemical element, often simply called an element, is a type of atom which has a specific number of protons in its atomic nucleus (i.e., a specific atomic number, or Z). [ 1 ] The definitive visualisation of all 118 elements is the periodic table of the elements , whose history along the principles of the periodic law was one of the founding ...

  5. Periodic table - Wikipedia

    en.wikipedia.org/wiki/Periodic_table

    Each chemical element has a unique atomic number (Z— for "Zahl", German for "number") representing the number of protons in its nucleus. [4] Each distinct atomic number therefore corresponds to a class of atom: these classes are called the chemical elements. [5] The chemical elements are what the periodic table classifies and organizes.

  6. Tetrafluoroethylene - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroethylene

    A convenient, safe method for generating TFE is the pyrolysis of the sodium salt of pentafluoropropionic acid: [6]. C 2 F 5 CO 2 Na → C 2 F 4 + CO 2 + NaF. The depolymerization reaction – vacuum pyrolysis of PTFE at 650–700 °C (1,200–1,290 °F) in a quartz vessel – is a traditional laboratory synthesis of TFE.

  7. Carbon–fluorine bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–fluorine_bond

    Carbon–fluorine bonds can have a bond dissociation energy (BDE) of up to 130 kcal/mol. [2] The BDE (strength of the bond) of C–F is higher than other carbon–halogen and carbon–hydrogen bonds. For example, the BDEs of the C–X bond within a CH 3 –X molecule is 115, 104.9, 83.7, 72.1, and 57.6 kcal/mol for X = fluorine, hydrogen ...

  8. List of inorganic compounds - Wikipedia

    en.wikipedia.org/wiki/List_of_inorganic_compounds

    Diphosphorus tetrafluoride – P 2 F 4; Diphosphorus tetraiodide – P 2 I 4; Hexachlorophosphazene – (NPCl 2) 3; Phosphine – PH 3; Phosphomolybdic acid – H 3 PMo 12 O 40; Phosphoric acid – H 3 PO 4; Phosphorous acid (Phosphoric(III) acid) – H 3 PO 3; Phosphoroyl nitride – NPO; Phosphorus pentabromide – PBr 5; Phosphorus ...

  9. Tetrahalomethane - Wikipedia

    en.wikipedia.org/wiki/Tetrahalomethane

    Tetrahalomethanes are fully halogenated methane derivatives of general formula CF k Cl l Br m I n At p, where: + + + + = Tetrahalomethanes are on the border of inorganic and organic chemistry, thus they can be assigned both inorganic and organic names by IUPAC: tetrafluoromethane - carbon tetrafluoride, tetraiodomethane - carbon tetraiodide, dichlorodifluoromethane - carbon dichloride difluoride.