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  2. Carbon tetrafluoride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrafluoride

    Commercially it is manufactured by the reaction of hydrogen fluoride with dichlorodifluoromethane or chlorotrifluoromethane; it is also produced during the electrolysis of metal fluorides MF, MF 2 using a carbon electrode. Although it can be made from a myriad of precursors and fluorine, elemental fluorine is expensive and difficult to handle.

  3. Hypervalent molecule - Wikipedia

    en.wikipedia.org/wiki/Hypervalent_molecule

    On the other hand, some compounds that are normally written with ionic bonds in order to conform to the octet rule, such as ozone O 3, nitrous oxide NNO, and trimethylamine N-oxide (CH 3) 3 NO, are found to be genuinely hypervalent. Examples of γ calculations for phosphate PO 3− 4 (γ(P) = 2.6, non-hypervalent) and orthonitrate NO 3−

  4. Carbon–nitrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–nitrogen_bond

    A carbon–nitrogen bond is a covalent bond between carbon and nitrogen and is one of the most abundant bonds in organic chemistry and biochemistry. [ 1 ] Nitrogen has five valence electrons and in simple amines it is trivalent , with the two remaining electrons forming a lone pair .

  5. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Count valence electrons. Nitrogen has 5 valence electrons; each oxygen has 6, for a total of (6 × 2) + 5 = 17. The ion has a charge of −1, which indicates an extra electron, so the total number of electrons is 18. Connect the atoms by single bonds. Each oxygen must be bonded to the nitrogen, which uses four electrons—two in each bond.

  6. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    The covalent radius of fluorine of about 71 picometers found in F 2 molecules is significantly larger than that in other compounds because of this weak bonding between the two fluorine atoms. [9] This is a result of the relatively large electron and internuclear repulsions, combined with a relatively small overlap of bonding orbitals arising ...

  7. Carbon tetrachloride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrachloride

    Kolbe made carbon tetrachloride in 1845 by passing chlorine over carbon disulfide through a porcelain tube. [16] Prior to the 1950s, carbon tetrachloride was manufactured by the chlorination of carbon disulfide at 105 to 130 °C: [17] CS 2 + 3 Cl 2 → CCl 4 + S 2 Cl 2. But now it is mainly produced from methane: CH 4 + 4 Cl 2 → CCl 4 + 4 HCl

  8. Quadruple bond - Wikipedia

    en.wikipedia.org/wiki/Quadruple_bond

    The octachlorodirhenate(III) anion, [Re 2 Cl 8] 2−, which features a quadruple Re–Re bond Formation of a delta bond by the overlap of two d orbitals. The [Re 2 Cl 8] 2ion adopts an eclipsed conformation as shown at left. The delta bonding orbital is then formed by overlap of the d orbitals on each rhenium atom, which are perpendicular ...

  9. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_bond

    These effects become more pronounced for the heavier elements. The distannene (Me 3 Si) 2 CHSn=SnCH(SiMe 3) 2 has a tin-tin bond length just a little shorter than a single bond, a trans bent structure with pyramidal coordination at each tin atom, and readily dissociates in solution to form (Me 3 Si) 2 CHSn: (stannanediyl, a carbene analog). The ...

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