Search results
Results From The WOW.Com Content Network
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]
The ammonium ion is generated when ammonia, a weak base, reacts with Brønsted acids (proton donors): H + + NH 3 → [NH 4] + The ammonium ion is mildly acidic, reacting with Brønsted bases to return to the uncharged ammonia molecule: [NH 4] + + B − → HB + NH 3. Thus, the treatment of concentrated solutions of ammonium salts with a strong ...
The salts produced by the action of ammonia on acids are known as the ammonium salts and all contain the ammonium ion ([NH 4] +). [38] Although ammonia is well known as a weak base, it can also act as an extremely weak acid. It is a protic substance and is capable of formation of amides (which contain the NH − 2 ion).
Ammonium bromide is a weak acid with a pK a of approximately 9 in water. It is an acid salt because the ammonium ion hydrolyzes slightly in water. Ammonium bromide is a strong electrolyte when put in water: NH 4 Br(s) → NH + 4 (aq) + Br − (aq) Ammonium bromide decomposes to ammonia and hydrogen bromide when heated at elevated temperatures ...
The following exergonic equilibrium gives rise to the triiodide ion: . I 2 + I − ⇌ I − 3. In this reaction, iodide is viewed as a Lewis base, and the iodine is a Lewis acid.The process is analogous to the reaction of S 8 with sodium sulfide (which forms polysulfides) except that the higher polyiodides have branched structures.
In chemistry, an acid–base reaction is a chemical reaction that occurs between an acid and a base.It can be used to determine pH via titration.Several theoretical frameworks provide alternative conceptions of the reaction mechanisms and their application in solving related problems; these are called the acid–base theories, for example, Brønsted–Lowry acid–base theory.
General structure of an imine. Schiff bases are imines in which R 3 is an alkyl or aryl group (not a hydrogen). R 1 and R 2 may be hydrogens General structure of an azomethine compound. In organic chemistry, a Schiff base (named after Hugo Schiff) is a compound with the general structure R 1 R 2 C=NR 3 (R 3 = alkyl or aryl, but not hydrogen).
A general linear imide functional group. In organic chemistry, an imide is a functional group consisting of two acyl groups bound to nitrogen. [1] The compounds are structurally related to acid anhydrides, although imides are more resistant to hydrolysis.