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A strong base is a basic chemical compound that can remove a proton (H +) from (or deprotonate) a molecule of even a very weak acid (such as water) in an acid–base reaction. Common examples of strong bases include hydroxides of alkali metals and alkaline earth metals, like NaOH and Ca(OH) 2, respectively. Due to their low solubility, some ...
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 is only as good as sodium hydroxide. On the other hand, NaNH 2 is a far more basic reagent in ammonia than is NaOH. The pH range allowed by a particular solvent is called the acid-base discrimination window. [1]
The Schlosser base (or Lochmann-Schlosser base), the combination of n-butyllithium and potassium tert-butoxide, is commonly cited as a superbase. n -Butyllithium and potassium tert -butoxide form a mixed aggregate of greater reactivity than either component reagent.
Water is amphoteric: it has the ability to act as either an acid or a base in chemical reactions. [87] According to the Brønsted-Lowry definition, an acid is a proton (H +) donor and a base is a proton acceptor. [88] When reacting with a stronger acid, water acts as a base; when reacting with a stronger base, it acts as an acid. [88]
It is a highly stable +1 cation in aqueous solution due to the efficient resonance stabilization of the charge and efficient solvation by water molecules. As a result, its pK aH is 13.6 [2] (pK b of 0.4) meaning that guanidine is a very strong base in water; in neutral water, it exists almost exclusively as guanidinium. Due to this, most ...
In water, measurable pK a values range from about −2 for a strong acid to about 12 for a very weak acid (or strong base). A buffer solution of a desired pH can be prepared as a mixture of a weak acid and its conjugate base. In practice, the mixture can be created by dissolving the acid in water, and adding the requisite amount of strong acid ...
For example, carbon monoxide is a very weak Brønsted–Lowry base but it forms a strong adduct with BF 3. In another comparison of Lewis and Brønsted–Lowry acidity by Brown and Kanner, [ 19 ] 2,6-di- t -butylpyridine reacts to form the hydrochloride salt with HCl but does not react with BF 3 .
In chemistry, the Verkade base (or Verkade superbase) is a powerful superbase with the formula P(MeNCH 2 CH 2) 3 N. A colorless oil, it is an aminophosphine although its inventor John Verkade called it proazaphosphatrane. The trimethyl derivative or 2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane is the simplest. [1]