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  2. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Indicative of its high reactivity (relative to alkyl chlorides), benzyl chloride slowly reacts with water in a hydrolysis reaction to form benzyl alcohol and hydrochloric acid. In contact with mucous membranes, hydrolysis produces hydrochloric acid. Thus, benzyl chloride is a lachrymator and has been used in chemical warfare. It is also very ...

  3. 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. [6]

  4. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    In IUPAC nomenclature, the prefix benzyl refers to a C 6 H 5 CH 2 substituent, for example benzyl chloride or benzyl benzoate. Benzyl is not to be confused with phenyl with the formula C 6 H 5. The term benzylic is used to describe the position of the first carbon bonded to a benzene or other aromatic ring.

  5. Acid salt - Wikipedia

    en.wikipedia.org/wiki/Acid_salt

    The solution is expected to be neutral only when K a = K b. [12] Other possible factors that could vary pH level of a solution are the relevant equilibrium constants and the additional amounts of any base or acid. For example, in ammonium chloride solution, NH + 4 is the main influence for acidic solution.

  6. Benzoyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_chloride

    Benzoyl chloride, also known as benzenecarbonyl chloride, is an organochlorine compound with the formula C 7 H 5 ClO. It is a colourless, fuming liquid with an irritating odour, and consists of a benzene ring ( C 6 H 6 ) with an acyl chloride ( −C(=O)Cl ) substituent .

  7. Phenylsodium - Wikipedia

    en.wikipedia.org/wiki/Phenylsodium

    In the original synthesis, diphenylmercury and sodium was shown to yield a suspension of phenylsodium: (C 6 H 5) 2 Hg + 3 Na → 2 C 6 H 5 Na + NaHg. The Shorigen reaction is also used in the generation of phenylsodium, where an alkyl sodium compound is treated with benzene: [3]

  8. Benzyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloroformate

    Benzyl chloroformate, also known as benzyl chlorocarbonate or Z-chloride, is the benzyl ester of chloroformic acid. It can be also described as the chloride of the benzyloxycarbonyl (Cbz or Z) group. In its pure form it is a water-sensitive oily colorless liquid, although impure samples usually appear yellow.

  9. Alkali salt - Wikipedia

    en.wikipedia.org/wiki/Alkali_salt

    The chloride from the hydrochloric acid in sodium chloride does not hydrolyze, though, so sodium chloride is not basic. The difference between a basic salt and an alkali is that an alkali is the soluble hydroxide compound of an alkali metal or an alkaline earth metal. A basic salt is any salt that hydrolyzes to form a basic solution.