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  2. Category:Bases (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Category:Bases_(chemistry)

    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.

  3. Base (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Base_(chemistry)

    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 ...

  4. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    a strong base used in organic synthesis Sodium hydroxide: strong base with many industrial uses; in the laboratory, used with acids to produce the corresponding salt, also used as an electrolyte: Sodium hypochlorite: frequently used as a disinfectant or a bleaching agent Sodium nitrite: used to convert amines into diazo compounds Sulfuric acid

  5. List of chemical databases - Wikipedia

    en.wikipedia.org/wiki/List_of_chemical_databases

    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

  6. Non-nucleophilic base - Wikipedia

    en.wikipedia.org/wiki/Non-nucleophilic_base

    2,6-Di-tert-butylpyridine, a weak non-nucleophilic base [2] pK a = 3.58; Phosphazene bases, such as t-Bu-P 4 [3] Non-nucleophilic bases of high strength are usually anions. For these species, the pK a s of the conjugate acids are around 35–40. Lithium diisopropylamide (LDA), pK a = 36

  7. Category:Chemical compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Chemical_compounds

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikimedia Commons; ... Bases (chemistry) (8 C, 20 P) Binary compounds (3 C, 9 P) C.

  8. Organic base - Wikipedia

    en.wikipedia.org/wiki/Organic_base

    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 ...

  9. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    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 −