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  2. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    [1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [ 4 ] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.

  3. Molecular solid - Wikipedia

    en.wikipedia.org/wiki/Molecular_solid

    The halogen bonding between the bromine and 1,4-dioxane molecules partially guides the organization of the crystal lattice structure. [27] (a) A lewis dot structure and ball and stick model of bromine and 1,4-dioxane. The halogen bond is between the bromine and 1,4-dioxane.

  4. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    BF 3 + OMe 2 → BF 3 OMe 2. Both BF 4 − and BF 3 OMe 2 are Lewis base adducts of boron trifluoride. Many adducts violate the octet rule, such as the triiodide anion: I 2 + I − → I − 3. The variability of the colors of iodine solutions reflects the variable abilities of the solvent to form adducts with the Lewis acid I 2.

  5. Carbon tetrabromide - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrabromide

    Br· + CH 4 → ·CH 3 + HBr. ·CH 3 + Br 2 → CH 3 Br + Br ... Due to its symmetrically substituted tetrahedral structure, its dipole moment is 0 Debye. Critical ...

  6. Tetrabromoethane - Wikipedia

    en.wikipedia.org/wiki/Tetrabromoethane

    1,1,2,2-Tetrabromoethane, or simply tetrabromoethane (TBE), is a halogenated hydrocarbon, chemical formula C 2 H 2 Br 4.Although three bromine atoms may bind to one of the carbon atoms creating 1,1,1,2-tetrabromoethane this is not thermodynamically favorable, so in practice tetrabromoethane is equal to 1,1,2,2-tetrabromoethane, where each carbon atom binds two bromine atoms.

  7. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Silver bromide (AgBr). Nearly all elements in the periodic table form binary bromides. The exceptions are decidedly in the minority and stem in each case from one of three causes: extreme inertness and reluctance to participate in chemical reactions (the noble gases, with the exception of xenon in the very unstable XeBr 2; extreme nuclear instability hampering chemical investigation before ...

  8. Dibromomethane - Wikipedia

    en.wikipedia.org/wiki/Dibromomethane

    6 CH 2 BrCl + 3 Br 2 + 2 Al → 6 CH 2 Br 2 + 2 AlCl 3 CH 2 BrCl + HBr → CH 2 Br 2 + HCl. In the laboratory, it is prepared from bromoform using sodium arsenite and sodium hydroxide: [4] CHBr 3 + Na 3 AsO 3 + NaOH → CH 2 Br 2 + Na 3 AsO 4 + NaBr. Another way is to prepare it from diiodomethane and bromine.

  9. Halomethane - Wikipedia

    en.wikipedia.org/wiki/Halomethane

    Using CH 4 in large excess generates primarily CH 3 Cl and using Cl 2 in large excess generates primarily CCl 4, but mixtures of other products will still be present. Halogenation of methanol. This method is used for the production of the mono-chloride, -bromide, and -iodide. CH 3 OH + HCl → CH 3 Cl + H 2 O 4 CH 3 OH + 3 Br 2 + S → 4 CH 3 ...