When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Haloform reaction - Wikipedia

    en.wikipedia.org/wiki/Haloform_reaction

    Substrates are broadly limited to methyl ketones and secondary alcohols oxidizable to methyl ketones, such as isopropanol.The only primary alcohol and aldehyde to undergo this reaction are ethanol and acetaldehyde, respectively. 1,3-Diketones such as acetylacetone also undergo this reaction. β-ketoacids such as acetoacetic acid will also give the test upon heating.

  3. 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]

  4. Sodium formate - Wikipedia

    en.wikipedia.org/wiki/Sodium_formate

    In the laboratory, sodium formate can be prepared by neutralizing formic acid with sodium carbonate. It can also be obtained by reacting chloroform with an alcoholic solution of sodium hydroxide. CHCl 3 + 4 NaOH → HCOONa + 3 NaCl + 2 H 2 O. or by reacting sodium hydroxide with chloral hydrate. C 2 HCl 3 (OH) 2 + NaOH → CHCl 3 + HCOONa + H 2 O

  5. Bargellini reaction - Wikipedia

    en.wikipedia.org/wiki/Bargellini_reaction

    The original reaction was a mixture of the reagents phenol, chloroform, and acetone in the presence of a sodium hydroxide solution. [2] Prior to Bargellini's research, the product attributed to this multi-component reaction (MCR) had been described as a phenol derivative in chemistry texts at the time.

  6. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Benzyl ethers are often derived from benzyl chloride. Benzyl chloride reacts with aqueous sodium hydroxide to give dibenzyl ether. In organic synthesis, benzyl chloride is used to introduce the benzyl protecting group in reaction with alcohols, yielding the corresponding benzyl ether, carboxylic acids, and benzyl ester.

  7. Ethyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_chloroformate

    Preparation. Ethyl chloroformate can be prepared using ethanol and phosgene: Safety. Ethyl chloroformate is a highly toxic, flammable, corrosive substance. It causes ...

  8. Ethanol - Wikipedia

    en.wikipedia.org/wiki/Ethanol

    Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula CH 3 CH 2 OH. It is an alcohol, with its formula also written as C 2 H 5 OH, C 2 H 6 O or EtOH, where Et stands for ethyl. Ethanol is a volatile, flammable, colorless liquid with a characteristic wine-like ...

  9. Dichlorocarbene - Wikipedia

    en.wikipedia.org/wiki/Dichlorocarbene

    Dichlorocarbene as a reactive intermediate was first proposed by Anton Geuther in 1862 who viewed chloroform as CCl 2. HCl [9] Its generation was reinvestigated by Hine in 1950. [10] The preparation of dichlorocarbene from chloroform and its utility in synthesis was reported by William von Eggers Doering in 1954. [11]