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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. Sodium bromide - Wikipedia

    en.wikipedia.org/wiki/Sodium_bromide

    Sodium bromide is an inorganic compound with the formula Na Br. It is a high-melting white, crystalline solid that resembles sodium chloride . It is a widely used source of the bromide ion and has many applications.

  4. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Structure of N-bromosuccinimide, a common brominating reagent in organic chemistry. Like the other carbon–halogen bonds, the C–Br bond is a common functional group that forms part of core organic chemistry. Formally, compounds with this functional group may be considered organic derivatives of the bromide anion.

  5. Gallium(III) bromide - Wikipedia

    en.wikipedia.org/wiki/Gallium(III)_bromide

    The somewhat high oxidation state of Ga in Ga(III)Br 3, low electronegativity, and high polarizability allow GaBr 3 to behave as a "soft acid" in terms of the Hard-Soft-Acid-Base (HSAB) theory. The Lewis acidity of all the gallium trihalides, GaBr 3 included, has been extensively studied thermodynamically, and the basicity of GaBr 3 has been ...

  6. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    A Lewis base is also a Brønsted–Lowry base, but a Lewis acid does not need to be a Brønsted–Lowry acid. The classification into hard and soft acids and bases ( HSAB theory ) followed in 1963. The strength of Lewis acid-base interactions, as measured by the standard enthalpy of formation of an adduct can be predicted by the Drago–Wayland ...

  7. Cyanogen bromide - Wikipedia

    en.wikipedia.org/wiki/Cyanogen_bromide

    Cyanogen bromide is a common reagent in organic synthesis. In most reactions, it acts as a source of electrophilic cyanogen and nucleophilic bromide; carbocations preferentially attack the nitrogen atom. [4] In the presence of a Lewis acid, it cyanidates arenes. [9] BrCN converts alcohols to cyanates; amines to cyanamides or dicyanamides. [4]

  8. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    Structure of N-bromosuccinimide, a common brominating reagent in organic chemistry. Like the other carbon–halogen bonds, the C–Br bond is a common functional group that forms part of core organic chemistry. Formally, compounds with this functional group may be considered organic derivatives of the bromide anion.

  9. Sodium hypobromite - Wikipedia

    en.wikipedia.org/wiki/Sodium_hypobromite

    Sodium hypobromite is an inorganic compound with the chemical formula Na O Br. It is a sodium salt of hypobromous acid. It consists of sodium cations Na + and hypobromite anions − OBr. It is usually obtained as the pentahydrate, so the compound that is usually called sodium hypobromite actually has the formula NaBrO·5H 2 O. It is a yellow ...