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  2. Chloral hydrate - Wikipedia

    en.wikipedia.org/wiki/Chloral_hydrate

    Chloral hydrate is a geminal diol with the formula Cl 3 C−CH(OH) 2. It was first used as a sedative and hypnotic in Germany in the 1870s. Over time it was replaced by safer and more effective alternatives but it remained in usage in the United States until at least the 1970s. [ 4 ]

  3. Chloral - Wikipedia

    en.wikipedia.org/wiki/Chloral

    Chloral tends to form adducts with water (to give chloral hydrate) and alcohols. Aside from its tendency to hydrate, chloral is notable as a building block in the synthesis of DDT. For this purpose, chloral is treated with chlorobenzene in the presence of a catalytic amount of sulfuric acid: Cl 3 CCHO + 2 C 6 H 5 Cl → Cl 3 CCH(C 6 H 4 Cl) 2 ...

  4. Haloform reaction - Wikipedia

    en.wikipedia.org/wiki/Haloform_reaction

    In chemistry, the haloform reaction (also referred to as the Lieben haloform reaction) is a chemical reaction in which a haloform (CHX 3, where X is a halogen) is produced by the exhaustive halogenation of an acetyl group (R−C(=O)CH 3, where R can be either a hydrogen atom, an alkyl or an aryl group), in the presence of a base.

  5. Trichloroethylene - Wikipedia

    en.wikipedia.org/wiki/Trichloroethylene

    The earliest record of trichloroethylene synthesis dates back to 1836. It was obtained from the action of potassium hydroxide on 1,1,2,2-tetrachloroethane and 1,1,1,2-tetrachloroethane by Auguste Laurent and notated as C 4 HCl 3 (then the atomic weight of carbon was thought to be the half of it really was).

  6. Chloroform - Wikipedia

    en.wikipedia.org/wiki/Chloroform

    The haloform reaction can also occur inadvertently in domestic settings. Sodium hypochlorite solution (chlorine bleach) mixed with common household liquids such as acetone, methyl ethyl ketone, ethanol, or isopropyl alcohol can produce some chloroform, in addition to other compounds, such as chloroacetone or dichloroacetone. [citation needed]

  7. Geminal diol - Wikipedia

    en.wikipedia.org/wiki/Geminal_diol

    Similarly, the conversion of chloral (Cl 3 C)HC =O to chloral hydrate is strongly favored by influence of the trichloromethyl group . In some cases, such as decahydroxycyclopentane and dodecahydroxycyclohexane , the geminal diol is stable while the corresponding ketone is not.

  8. Chlorobutanol - Wikipedia

    en.wikipedia.org/wiki/Chlorobutanol

    Chlorobutanol (trichloro-2-methyl-2-propanol) is an organic compound with the formula CCl 3 C(OH)(CH 3) 2.The compound is a chlorohydrin.The compound is a preservative, sedative, hypnotic and weak local anesthetic similar in nature to chloral hydrate.

  9. Melzer's reagent - Wikipedia

    en.wikipedia.org/wiki/Melzer's_reagent

    Melzer's reagent is an aqueous solution of chloral hydrate, potassium iodide, and iodine.Depending on the formulation, it consists of approximately 2.50-3.75% potassium iodide and 0.75–1.25% iodine, with the remainder of the solution being 50% water and 50% chloral hydrate.