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  2. Gilman test - Wikipedia

    en.wikipedia.org/wiki/Gilman_test

    The Gilman test is a chemical test for the detection of Grignard reagents and organolithium reagents. [1] [2] A 0.5 mL sample is added to a 1% solution of Mischler's ketone in benzene or toluene. To this solution is added 1 mL of water for hydrolysis to take place and then several drops of 0.2% iodine in glacial acetic acid.

  3. Grignard reagent - Wikipedia

    en.wikipedia.org/wiki/Grignard_reagent

    Grignard reagents or Grignard compounds are chemical compounds with the general formula R−Mg−X, where X is a halogen and R is an organic group, normally an alkyl or aryl. Two typical examples are methylmagnesium chloride Cl−Mg−CH 3 and phenylmagnesium bromide (C 6 H 5)−Mg−Br. They are a subclass of the organomagnesium compounds.

  4. Grignard reaction - Wikipedia

    en.wikipedia.org/wiki/Grignard_reaction

    A solution of a carbonyl compound is added to a Grignard reagent. (See gallery) An example of a Grignard reaction (R 2 or R 3 could be hydrogen). The Grignard reaction (French:) is an organometallic chemical reaction in which, according to the classical definition, carbon alkyl, allyl, vinyl, or aryl magnesium halides (Grignard reagent) are added to the carbonyl groups of either an aldehyde or ...

  5. Trimethyl borate - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_borate

    It is a useful reagent in organic synthesis, as a precursor to boronic acids, which are used in Suzuki couplings. These boronic acids are prepared via reaction of the trimethyl borate with Grignard reagents followed by hydrolysis:. [3] [4] ArMgBr + B(OCH 3) 3 → MgBrOCH 3 + ArB(OCH 3) 2 ArB(OCH 3) 2 + 2 H 2 O → ArB(OH) 2 + 2 HOCH 3

  6. Bouveault aldehyde synthesis - Wikipedia

    en.wikipedia.org/wiki/Bouveault_aldehyde_synthesis

    The first step of the Bouveault aldehyde synthesis is the formation of the Grignard reagent. Upon addition of a N , N -disubstituted formamide (such as dimethylformamide ) a hemiaminal is formed, which can easily be hydrolyzed into the desired aldehyde.

  7. Organotin chemistry - Wikipedia

    en.wikipedia.org/wiki/Organotin_chemistry

    Organotin compounds are those with tin linked to hydrocarbons. The compound on the picture is trimethyltin chloride, an example of organotin compounds.. Organotin chemistry is the scientific study of the synthesis and properties of organotin compounds or stannanes, which are organometallic compounds containing tin–carbon bonds.

  8. Zerewitinoff determination - Wikipedia

    en.wikipedia.org/wiki/Zerewitinoff_determination

    A sample is treated with the Grignard reagent, methylmagnesium iodide, which reacts with any acidic hydrogen atom to form methane. This gas can be determined quantitatively by measuring its volume. This gas can be determined quantitatively by measuring its volume.

  9. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Geminal halide hydrolysis; Gewald reaction; Gibbs phthalic anhydride process; Gilman reagent; Glaser coupling; Glycol cleavage; Goldberg reaction; Gomberg–Bachmann reaction; Gomberg–Bachmann–Hey reaction; Gomberg radical reaction; Gould–Jacobs reaction; Graebe–Ullmann synthesis; Grignard degradation; Griesbaum coozonolysis; Grignard ...