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Ammonium iodide is the inorganic compound with the formula NH 4 I. A white solid. It is an ionic compound, although impure samples appear yellow. This salt consists of ammonium cation and an iodide anion. [1] It can be prepared by the action of hydroiodic acid on ammonia. It is easily soluble in water, from which it crystallizes in cubes.
Using its low solubility in water, it can also be precipitated from an iodate solution with an ammonium salt. 2 KIO 3 + (NH 4) 2 SO 4 → 2 NH 4 IO 3 + K 2 SO 4. Unlike other iodates, ammonium iodate can't be prepared by dissolving iodine in an ammonium hydroxide solution, instead the highly explosive nitrogen triiodide is formed. 3 I 2 + 5 NH ...
The iodide is regenerated, meaning the reaction runs with the iodide/hypoiodite as a catalyst in the presence of excess of the original strong oxidizing agent. Ammonium hypoiodites are capable of oxidizing benzylic methyl groups, [ 2 ] initiating oxidative dearomatization , [ 3 ] and oxidative decarboxylation of β-keto lactones . [ 4 ]
The enthalpy of formation Δ f H 0 of tetra-n-butylammonium iodide is −499 kJ/mol, which is lower than that for the bromide or chloride (−540, −564 kJ/mol). [2] At lower temperatures with water tetra-n-butylammonium iodide forms a clathrate hydrate. [2] The tetra-n-butylammonium cation is large and hydrophobic.
Tetraethylammonium iodide is a quaternary ammonium compound with the chemical formula C 8 H 20 N + I −. It has been used as the source of tetraethylammonium ions in pharmacological and physiological studies, but is also used in organic chemical synthesis.
This clock reaction uses sodium, potassium or ammonium persulfate to oxidize iodide ions to iodine. Sodium thiosulfate is used to reduce iodine back to iodide before the iodine can complex with the starch to form the characteristic blue-black color. Iodine is generated: 2 I − + S 2 O 2− 8 → I 2 + 2 SO 2− 4. And is then removed:
It is the iodide salt of the dimethylaminomethylene cation [(CH 3) 2 NCH 2] +. The dimethylaminomethylene cation is a strong dimethylaminomethylating agent, used to prepare derivatives of the type RCH 2 N(CH 3) 2. [1] [2] Enolates, silyl enol ethers, and even more acidic ketones undergo efficient dimethylaminomethylation.
The low solubility of silver iodide and lead iodide reflects the covalent character of these metal iodides. A test for the presence of iodide ions is the formation of yellow precipitates of these compounds upon treatment of a solution of silver nitrate or lead(II) nitrate. [2] Aqueous solutions of iodide salts dissolve iodine better than pure ...