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Ammonia solution, also known as ammonia water, ammonium hydroxide, ammoniacal liquor, ammonia liquor, aqua ammonia, aqueous ammonia, or (inaccurately) ammonia, is a solution of ammonia in water. It can be denoted by the symbols NH 3 (aq). Although the name ammonium hydroxide suggests a salt with the composition [NH + 4][OH −
Household ammonia or ammonium hydroxide is a solution of ammonia in ... 4 NH 3 + 3 O 2 → 2 N 2 + 6 H 2 O(g), ... to remove hair from hides in preparation for ...
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 ...
Illustrative is the preparation of tetramethylammonium fluoride: [6] NMe 4 + OH − + HF → NMe 4 + F − + H 2 O. Solutions of TMAH may be used to make other tetramethylammonium salts in metathesis reactions with ammonium (NH 4 +) salts. For example, tetramethylammonium thiocyanate may be prepared from ammonium thiocyanate as follows: [7]
An example of a weak base is ammonia. It does not contain hydroxide ions, but it reacts with water to produce ammonium ions and hydroxide ions. [4] The position of equilibrium varies from base to base when a weak base reacts with water. The further to the left it is, the weaker the base. [5]
Tetrapropylammonium (TPA) is a quaternary ammonium cation with the formula [N(C 3 H 7) 4] +, also denoted [NPr 4] + (where Pr = propyl group). It is a precursor to several significant industrial and laboratory catalysts .
The Solvay process or ammonia–soda process is the major industrial process for the production of sodium carbonate (soda ash, Na 2 CO 3).The ammonia–soda process was developed into its modern form by the Belgian chemist Ernest Solvay during the 1860s. [1]
In organic chemistry, the Mannich reaction is a three-component organic reaction that involves the amino alkylation of an acidic proton next to a carbonyl (C=O) functional group by formaldehyde (H−CHO) and a primary or secondary amine (−NH 2) or ammonia (NH 3). [1]