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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.
It is the potassium salt of tetraiodoplatinate, a square planar complex of platinum(II). The compound crystallizes from water as the dihydrate, [ 1 ] whereas the related chloride and bromide K 2 PtCl 4 and K 2 PtBr 4 are obtained only as the anhydrous salts.
The Petasis reagent is prepared by the salt metathesis reaction of methylmagnesium chloride or methyllithium [2] with titanocene dichloride: [3] Cp 2 TiCl 2 + 2 CH 3 MgCl → Cp 2 Ti(CH 3) 2 + 2 MgCl 2. This compound is used for the transformation of carbonyl groups to terminal alkenes. It exhibits similar reactivity to the Tebbe reagent and ...
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]
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.
I wouldnt add it, although your observations are insightful. My reasoning: (1) salt metathesis is really intended for salt-like reagents, (2) Wikipedia guidelines urge us not to make it into a textbook. The encylopedia is intended to give and explain facts, but not to go much farther.
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 ...
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]