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Boron tribromide is commercially available and is a strong Lewis acid.. It is an excellent demethylating or dealkylating agent for the cleavage of ethers, also with subsequent cyclization, often in the production of pharmaceuticals.
The trihalides adopt a planar trigonal structure. These compounds are Lewis acids in that they readily form adducts with electron-pair donors, which are called Lewis bases. For example, fluoride (F −) and boron trifluoride (BF 3) combined to give the tetrafluoroborate anion, BF 4 −. Boron trifluoride is used in the petrochemical industry as ...
In a Lewis adduct, the Lewis acid and base share an electron pair furnished by the Lewis base, forming a dative bond. [1] In the context of a specific chemical reaction between NH 3 and Me 3 B, a lone pair from NH 3 will form a dative bond with the empty orbital of Me 3 B to form an adduct NH 3 •BMe 3.
Expressing resonance when drawing Lewis structures may be done either by drawing each of the possible resonance forms and placing double-headed arrows between them or by using dashed lines to represent the partial bonds (although the latter is a good representation of the resonance hybrid which is not, formally speaking, a Lewis structure).
Boron trifluoride is a versatile Lewis acid that forms adducts with such Lewis bases as fluoride and ethers: CsF + BF 3 → Cs[BF 4] O(CH 2 CH 3) 2 + BF 3 → BF 3 ·O(CH 2 CH 3) 2. Tetrafluoroborate salts are commonly employed as non-coordinating anions.
In its pure state, boron triiodide forms colorless, otherwise reddish, shiny, air and hydrolysis-sensitive [3] crystals, which have a hexagonal crystal structure (a = 699.09 ± 0.02 pm, c = 736.42 ± 0.03 pm, space group P6 3 /m (space group no. 176)). [4] Boron triiodide is a strong Lewis acid and soluble in carbon disulfide. [2]
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Phosphorus tribromide, like PCl 3 and PF 3, has both properties of a Lewis base and a Lewis acid. For example, with a Lewis acid such as boron tribromide it forms stable 1 :1 adducts such as Br 3 B · PBr 3. At the same time PBr 3 can react as an electrophile or Lewis acid in many of its reactions, for example with amines.