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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 halide salt is prepared by the reaction of triethylamine and an ethyl halide: + + This method works well for the preparation of tetraethylammonium iodide (where X = I). [1] Most tetraethylammonium salts are prepared by salt metathesis reactions.
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]
Sodium trimethylsiloxide is useful for generating metal complexes by salt metathesis reactions. A very bulky siloxide is tert-butyl 3 SiO −, sometimes called silox. Siloxides are weaker net donors than alkoxides because p π-d donation has to compete with backbonding from the oxygen atom into the low-lying Si-C σ * orbitals. [1]
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
Metal thiolate complexes are commonly prepared by reactions of metal complexes with thiols (RSH), thiolates (RS −), and disulfides (R 2 S 2). The salt metathesis reaction route is common. In this method, an alkali metal thiolate is treated with a transition metal halide to produce an alkali metal halide and the metal thiolate complex:
Although this reaction is suitable for the common halides, tetramethylammonium salts with more complex anions may be prepared by salt metathesis reactions, e.g. tetramethylammonium borohydride has been made from tetramethylammonium hydroxide as shown: [8] Me 4 N + [OH] − + Na + [BH 4] − → Me 4 N + [BH 4] − + Na + + HO −
Redox reactions (see list of oxidants and reductants) Reduction; Reductive elimination; Reppe synthesis; Riley oxidation; Salt metathesis; Sarett oxidation; Sharpless epoxidation; Shell higher olefin process; Silylation; Simmons–Smith reaction; Sonogashira coupling; Staudinger reaction; Stille reaction; Sulfidation; Suzuki reaction ...