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  2. Dibromomethane - Wikipedia

    en.wikipedia.org/wiki/Dibromomethane

    Dibromomethane or methylene bromide, or methylene dibromide is a halomethane with the formula CH 2 Br 2. It is slightly soluble in water but very soluble in organic solvents . It is a colorless liquid.

  3. 1,1-Dibromoethane - Wikipedia

    en.wikipedia.org/wiki/1,1-Dibromoethane

    1,1-Dibromoethane is a clear, slightly brown, flammable chemical compound. [3] It is classified as the organobromine compound, and has the chemical formula C 2 H 4 Br 2 [4] and it is a position isomer of 1,2-dibromoethane.

  4. File:Dibromomethane Structural Formula V1.svg - Wikipedia

    en.wikipedia.org/wiki/File:Dibromomethane...

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  5. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.

  6. Bromoform - Wikipedia

    en.wikipedia.org/wiki/Bromoform

    Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.

  7. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    The bond order of diatomic nitrogen is three, and it is a diamagnetic molecule. [12] The bond order for dinitrogen (1σ g 2 1σ u 2 2σ g 2 2σ u 2 1π u 4 3σ g 2) is three because two electrons are now also added in the 3σ MO. The MO diagram correlates with the experimental photoelectron spectrum for nitrogen. [19]

  8. Three-center four-electron bond - Wikipedia

    en.wikipedia.org/.../Three-center_four-electron_bond

    As a result of unusual bonding situation, the donor lone pair ends up with significant electron density on the central atom, while the acceptor is the "out-of-phase" combination of the p orbitals on the peripheral atoms. This bonding scheme is depicted in Figure 3 for the theoretical noble gas dihalide NeF 2.

  9. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    The overall geometry is further refined by distinguishing between bonding and nonbonding electron pairs. The bonding electron pair shared in a sigma bond with an adjacent atom lies further from the central atom than a nonbonding (lone) pair of that atom, which is held close to its positively charged nucleus. VSEPR theory therefore views ...