Search results
Results from the WOW.Com Content Network
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]
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 ...
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). For example, lithium dissolves in liquid ammonia to give a blue solution (solvated electron) of lithium amide: 2 Li + 2 NH 3 → 2 LiNH 2 + H 2
Bases of carbon, nitrogen and oxygen without resonance stabilization are usually very strong, or superbases, which cannot exist in a water solution due to the acidity of water. Resonance stabilization, however, enables weaker bases such as carboxylates; for example, sodium acetate is a weak base.
A Lewis base is an atomic or molecular species where the highest occupied molecular orbital (HOMO) is highly localized. Typical Lewis bases are conventional amines such as ammonia and alkyl amines. Other common Lewis bases include pyridine and its derivatives. Some of the main classes of Lewis bases are
Similarly, when ammonia is the solvent, the strongest acid is ammonium (NH 4 +), thus HCl and a super acid exert the same acidifying effect. The same argument applies to bases. In water, OH − is the strongest base. Thus, even though sodium amide (NaNH 2) is an exceptional base (pK a of NH 3 ~ 33), in water it
Most organic bases are considered to be weak.Many factors can affect the strength of the compounds. One such factor is the inductive effect.A simple explanation of the term would state that electropositive atoms (such as carbon groups) attached in close proximity to the potential proton acceptor have an "electron-releasing" effect, such that the positive charge acquired by the proton acceptor ...
As the salt of a weak acid and a weak base, ammonium acetate is often used with acetic acid to create a buffer solution.Ammonium acetate is volatile at low pressures. Because of this, it has been used to replace cell buffers that contain non-volatile salts in preparing samples for mass spectrometry. [8]