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Salt metathesis is a common technique for exchanging counterions. The choice of reactants is guided by a solubility chart or lattice energy. HSAB theory can also be used to predict the products of a metathesis reaction. Salt metathesis is often employed to obtain salts that are soluble in organic solvents.
The [BAr F 4] − anion with four fluorinated aryl groups distributed tetrahedrally about a central boron atom. Tetrakis[3,5-bis(trifluoromethyl)phenyl]borate is an anion with chemical formula [{3,5-(CF 3) 2 C 6 H 3} 4 B] −, which is commonly abbreviated as [BAr F 4] −, indicating the presence of fluorinated aryl (Ar F) groups.
Metathesis (linguistics), alteration of the order of phonemes within a word Quantitative metathesis , exchange of long and short roles, without changing order of vowel sounds Chemical change in which a pair of molecules exchange electronic patterns of bonding
Tetrabutylammonium bromide (TBAB) is a quaternary ammonium salt with a bromide commonly used as a phase transfer catalyst. [4] It is used to prepare many other tetrabutylammonium salts by salt metathesis reactions. The anhydrous form is a white solid. [2]
In some reactions between highly reactive metals (usually from Group 1 or Group 2) and highly electronegative halogen gases, or water, the atoms can be ionized by electron transfer, [16] a process thermodynamically understood using the Born–Haber cycle. [17] Salts are formed by salt-forming reactions. A base and an acid, e.g., NH 3 + HCl → ...
The reaction is driven by the low solubility of potassium chlorate in water. The equilibrium of the reaction is shifted to the right hand side by the continuous precipitation of the product (Le Chatelier's Principle). The precursor sodium chlorate is produced industrially in very large quantities by electrolysis of sodium chloride, common table ...
Most of this article is about the homogeneous (one-phase) reaction of preformed organolithium compounds: R−Li + R′−X → R−X + R′−Li. Butyllithium is commonly used. Gilman and Wittig independently discovered this method in the late 1930s. [1] It is not a salt metathesis reaction, as no salt is produced.
It is prepared from tetraethylammonium bromide by salt metathesis, using a hydroxide-loaded ion exchange column or by the action of silver oxide. [3] Attempted isolation of Et 4 NOH induces Hofmann elimination, leading to triethylamine and ethylene. Treatment of Et 4 NOH with a wide range of acids gives water and the other tetraethylammonium salts: