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  2. Sodium amide - Wikipedia

    en.wikipedia.org/wiki/Sodium_amide

    Sodium amide is a standard base for dehydrohalogenations. [9] It induces the loss of two equivalents of hydrogen bromide from a vicinal dibromoalkane to give a carbon–carbon triple bond , as in a preparation of phenylacetylene . [ 10 ]

  3. Leveling effect - Wikipedia

    en.wikipedia.org/wiki/Leveling_effect

    Similarly the strength of a strong base is leveled by the acidity of the solvent. When a strong acid is dissolved in water, it reacts with it to form hydronium ion (H 3 O +). [2] An example of this would be the following reaction, where "HA" is the strong acid: HA + H 2 O → A − + H 3 O + Any acid that is stronger than H 3 O + reacts with H ...

  4. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  5. 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 ...

  6. Sodium compounds - Wikipedia

    en.wikipedia.org/wiki/Sodium_compounds

    Sodium tends to form water-soluble compounds, such as halides, sulfates, nitrates, carboxylates and carbonates. The main aqueous species are the aquo complexes [Na(H 2 O) n ] + , where n = 4–8; with n = 6 indicated from X-ray diffraction data and computer simulations.

  7. Amide - Wikipedia

    en.wikipedia.org/wiki/Amide

    Compared to amines, amides are very weak bases. While the conjugate acid of an amine has a pK a of about 9.5, the conjugate acid of an amide has a pK a around −0.5. Therefore, compared to amines, amides do not have acid–base properties that are as noticeable in water. This relative lack of basicity is explained by the withdrawing of ...

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  9. Weak base - Wikipedia

    en.wikipedia.org/wiki/Weak_base

    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] When there is a hydrogen ion gradient between two sides of the biological membrane, the concentration of some weak bases are focused on only one side of the membrane. [6]