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[23] 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.
Bases are defined by the Brønsted–Lowry theory as chemical substances that can accept a proton, i.e., a hydrogen ion. In water this is equivalent to a hydronium ion). The Lewis theory instead defines a Base as an electron-pair donor. The Lewis definition is broader — all Brønsted–Lowry bases are also Lewis bases.
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 ...
The most common Lewis bases are anions. The strength of Lewis basicity correlates with the pK a of the parent acid: acids with high pK a 's give good Lewis bases. As usual, a weaker acid has a stronger conjugate base. Examples of Lewis bases based on the general definition of electron pair donor include: simple anions, such as H − and F −
In chemistry, an alkali (/ ˈ æ l k ə l aɪ /; from the Arabic word al-qāly, القلوي) is a basic, ionic salt of an alkali metal or an alkaline earth metal. An alkali can also be defined as a base that dissolves in water. A solution of a soluble base has a pH greater than 7.0.
List of Lists safety data sheets, regulation "LOLI". Mcule supplied chemicals InChI, SMILES, SDF, physichochemical properties "Mcule". 45,000,000 MediaDB Institute for Systems Biology: growth media "MediaDB". 288 Merck Index: Royal Society of Chemistry: drugs "Merck-Index". 11,500 MeSH Medical Subject Headings: US National Library of Medicine
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 ...
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