enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    Chlorobenzene (abbreviated PhCl) is an aryl chloride and the simplest of the chlorobenzenes, consisting of a benzene ring substituted with one chlorine atom. Its chemical formula is C 6 H 5 Cl. This colorless, flammable liquid is a common solvent and a widely used intermediate in the manufacture of other chemicals.

  3. Acetyl hypochlorite - Wikipedia

    en.wikipedia.org/wiki/Acetyl_hypochlorite

    Acetyl hypochlorite is reported to be produced by the reaction of acetic anhydride and dichlorine monoxide at very low temperatures: [2]. Cl 2 O + (CH3CO) 2 O → 2CH 3 COOCl. The liquid can be distilled at reduced pressure, however it cannot be heated, as it violently decomposes at 100 °C to acetic anhydride, oxygen, and chlorine gas, and reacts with water and alcohols.

  4. Sodium acetate - Wikipedia

    en.wikipedia.org/wiki/Sodium_acetate

    Any of these reactions produce sodium acetate and water. When a sodium and carbonate ion-containing compound is used as the reactant, the carbonate anion from sodium bicarbonate or carbonate, reacts with the hydrogen from the carboxyl group (-COOH) in acetic acid, forming carbonic acid. Carbonic acid readily decomposes under normal conditions ...

  5. Iodobenzene - Wikipedia

    en.wikipedia.org/wiki/Iodobenzene

    Iodobenzene is commercially available, or it can be prepared in the laboratory from aniline via the diazotization reaction. In the first step, the amine functional group is diazotized with hydrochloric acid and sodium nitrite. Potassium iodide is added to the resultant phenyldiazonium chloride, causing nitrogen gas to evolve. The product is ...

  6. Dow process (phenol) - Wikipedia

    en.wikipedia.org/wiki/Dow_process_(phenol)

    Benzene can be readily converted to chlorobenzene by nucleophilic aromatic substitution via a benzyne intermediate. [1] Chlorobenzene is treated with aqueous sodium hydroxide at 350 °C and 300 bar or molten sodium hydroxide at 350 °C to convert it to sodium phenoxide, which yields phenol upon acidification. [2]

  7. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    The reaction mechanism for chlorination of benzene is the same as bromination of benzene. Iron(III) bromide and iron(III) chloride become inactivated if they react with water, including moisture in the air. Therefore, they are generated by adding iron filings to bromine or chlorine. Here is the mechanism of this reaction:

  8. Cooling bath - Wikipedia

    en.wikipedia.org/wiki/Cooling_bath

    However, adding a salt such as sodium chloride will lower the temperature through the property of freezing-point depression. Although the exact temperature can be hard to control, the weight ratio of salt to ice influences the temperature: −10 °C can be achieved with a 1:2.5 mass ratio of calcium chloride hemihydrate to ice.

  9. Common-ion effect - Wikipedia

    en.wikipedia.org/wiki/Common-ion_effect

    Sodium acetate is a strong electrolyte, so it dissociates completely in solution. Acetic acid is a weak acid , so it only ionizes slightly. According to Le Chatelier's principle , the addition of acetate ions from sodium acetate will suppress the ionization of acetic acid and shift its equilibrium to the left.