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  2. Potassium methoxide - Wikipedia

    en.wikipedia.org/wiki/Potassium_methoxide

    The carbonylation of methanol with carbon monoxide to methyl formate (methyl methanoate) is catalyzed by strong bases, such as potassium methoxide. [7] [8] The main application of potassium methoxide is use as basic transesterification catalyst in biodiesel synthesis (as a 25-32% methanolic solution).

  3. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    A Lewis base is often a Brønsted–Lowry base as it can donate a pair of electrons to H +; [11] the proton is a Lewis acid as it can accept a pair of electrons. The conjugate base of a Brønsted–Lowry acid is also a Lewis base as loss of H + from the acid leaves those electrons which were used for the A—H bond as a lone pair on the ...

  4. 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 ...

  5. Amphoterism - Wikipedia

    en.wikipedia.org/wiki/Amphoterism

    Metal oxides which react with both acids as well as bases to produce salts and water are known as amphoteric oxides. Many metals (such as zinc, tin, lead, aluminium, and beryllium) form amphoteric oxides or hydroxides. Aluminium oxide (Al 2 O 3) is an example of an amphoteric oxide. Amphoterism depends on the oxidation states of the oxide.

  6. Sodium methoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_methoxide

    Sodium methoxide is prepared by treating methanol with sodium: 2 Na + 2 CH 3 OH → 2 CH 3 ONa + H 2. The reaction is so exothermic that ignition is possible. The resulting solution, which is colorless, is often used as a source of sodium methoxide, but the pure material can be isolated by evaporation followed by heating to remove residual methanol.

  7. Lewis acid catalysis - Wikipedia

    en.wikipedia.org/wiki/Lewis_Acid_Catalysis

    Common Lewis acid catalysts are based on main group metals such as aluminum, boron, silicon, and tin, as well as many early (titanium, zirconium) and late (iron, copper, zinc) d-block metals. The metal atom forms an adduct with a lone-pair bearing electronegative atom in the substrate, such as oxygen (both sp 2 or sp 3), nitrogen, sulfur, and ...

  8. Methyl formate - Wikipedia

    en.wikipedia.org/wiki/Methyl_formate

    In the laboratory, methyl formate can be produced by the condensation reaction of methanol and formic acid, as follows: . HCOOH + CH 3 OH → HCOOCH 3 + H 2 O. Industrial methyl formate, however, is usually produced by the combination of methanol and carbon monoxide (carbonylation) in the presence of a strong base, such as sodium methoxide: [4]

  9. Formate - Wikipedia

    en.wikipedia.org/wiki/Formate

    Methanol and carbon monoxide react in the presence of a strong base, such as sodium methoxide: [1] CH 3 OH + CO → HCOOCH 3. Hydrolysis of methyl formate gives formic acid and regenerates methanol: HCOOCH 3 → HCOOH + CH 3 OH. Formic acid is used for many applications in industry. Formate esters often are fragrant or have distinctive odors.