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  2. Grignard reagent - Wikipedia

    en.wikipedia.org/wiki/Grignard_reagent

    The oxide layer can also be broken up using ultrasound, using a stirring rod to scratch the oxidized layer off, [6] or by adding a few drops of iodine or 1,2-Diiodoethane. Another option is to use sublimed magnesium or magnesium anthracene. [7] "Rieke magnesium" is prepared by a reduction of an anhydrous magnesium chloride with an potassium:

  3. Methylaluminoxane - Wikipedia

    en.wikipedia.org/wiki/Methylaluminoxane

    MAO serves multiple functions in the activation process. First it alkylates the metal-chloride pre-catalyst species giving Ti/Zr-methyl intermediates. Second, it abstracts a ligand from the methylated precatalysts, forming an electrophilic, coordinatively unsaturated catalysts that can undergo ethylene insertion.

  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. Group 2 organometallic chemistry - Wikipedia

    en.wikipedia.org/wiki/Group_2_organometallic...

    Mixed alkyl/aryl-halide compounds, which contain a single C-M bond and a C-X bond, are typically prepared by oxidative addition. Magnesium-containing compounds of this configuration are known as the Grignard reagents, though some calcium Grignard's are known and more reactive and sensitive to decomposition. Calcium grignard's must be pre ...

  6. Alkoxide - Wikipedia

    en.wikipedia.org/wiki/Alkoxide

    Structure of the methoxide anion. Although alkali metal alkoxides are not salts and adopt complex structures, they behave chemically as sources of RO −. The structure of the methoxide ion. In chemistry, an alkoxide is the conjugate base of an alcohol and therefore consists of an organic group bonded to a negatively charged oxygen atom.

  7. Allyl group - Wikipedia

    en.wikipedia.org/wiki/Allyl_group

    Structure of the allyl group. In organic chemistry, an allyl group is a substituent with the structural formula −CH 2 −HC=CH 2. It consists of a methylene bridge (−CH 2 −) attached to a vinyl group (−CH=CH 2). [1] [2] The name is derived from the scientific name for garlic, Allium sativum.

  8. Amine oxide - Wikipedia

    en.wikipedia.org/wiki/Amine_oxide

    Alkyl dimethyl amine oxide (chain lengths C10–C16) is the most commercially used amine oxide. [3] They are considered a high production volume class of compounds in more than one member country of the Organisation for Economic Co-operation and Development ( OECD ); with annual production over 26,000, 16,000 and 6,800 tonnes (28,700, 17,600 ...

  9. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    The term alkyl is intentionally unspecific to include many possible substitutions. An acyclic alkyl has the general formula of −C n H 2n+1. A cycloalkyl group is derived from a cycloalkane by removal of a hydrogen atom from a ring and has the general formula −C n H 2n−1. [2] Typically an alkyl is a part of a larger molecule.