enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/Electrophilic_halogenation

    Halogenation of phenols is faster in polar solvents in a basic environment due to the dissociation of phenol, with phenoxide ions being more susceptible to electrophilic attack as they are more electron-rich. Chlorination of toluene with chlorine without catalyst requires a polar solvent as well such as acetic acid.

  3. Hydrogen bromide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_bromide

    Hydrogen bromide is the inorganic compound with the formula HBr.It is a hydrogen halide consisting of hydrogen and bromine. A colorless gas, it dissolves in water, forming hydrobromic acid, which is saturated at 68.85% HBr by weight at room temperature.

  4. Polar aprotic solvent - Wikipedia

    en.wikipedia.org/wiki/Polar_aprotic_solvent

    A polar aprotic solvent is a solvent that lacks an acidic proton and is polar. Such solvents lack hydroxyl and amine groups. In contrast to protic solvents, these solvents do not serve as proton donors in hydrogen bonding, although they can be proton acceptors. Many solvents, including chlorocarbons and hydrocarbons, are classifiable as aprotic ...

  5. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula C 6 H 5 OH. [5] It is a white crystalline ...

  6. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    The simplest is phenol, C 6 H 5 OH. Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule. Phenol – the simplest of the phenols Chemical structure of salicylic acid, the active metabolite of aspirin. Phenols are both synthesized industrially and produced by plants and ...

  7. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    Phenol ethers, similarly to regular ethers, are less hydrophilic than its precursors, phenols and alcohols, both of which can donate and accept hydrogen bonds. Phenol ethers, however, are still able to accept hydrogen bonds through the ethereal oxygen, allowing for its slight solubility in polar solvents.

  8. Hydrobromic acid - Wikipedia

    en.wikipedia.org/wiki/Hydrobromic_acid

    Hydrobromic acid is an aqueous solution of hydrogen bromide.It is a strong acid formed by dissolving the diatomic molecule hydrogen bromide (HBr) in water. "Constant boiling" hydrobromic acid is an aqueous solution that distills at 124.3 °C (255.7 °F) and contains 47.6% HBr by mass, which is 8.77 mol/L. Hydrobromic acid is one of the strongest mineral acids known.

  9. Diphenyl ether - Wikipedia

    en.wikipedia.org/wiki/Diphenyl_ether

    PhOH + PhBr → PhOPh + HBr. Involving similar reactions, diphenyl ether is a significant side product in the high-pressure hydrolysis of chlorobenzene in the production of phenol. [7] Related compounds are prepared by Ullmann reactions. [8]