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  2. Grignard reagent - Wikipedia

    en.wikipedia.org/wiki/Grignard_reagent

    Many methods have been developed to weaken this passivating layer, thereby exposing highly reactive magnesium to the organic halide. Mechanical methods include crushing of the Mg pieces in situ, rapid stirring, and sonication. [4] Iodine, methyl iodide, and 1,2-dibromoethane are common activating agents.

  3. 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 ...

  4. Organic acid anhydride - Wikipedia

    en.wikipedia.org/wiki/Organic_acid_anhydride

    Acetic anhydride is mainly produced by the carbonylation of methyl acetate. [6] Maleic anhydride is produced by the oxidation of benzene or butane. Laboratory routes emphasize the dehydration of the corresponding acids. The conditions vary from acid to acid, but phosphorus pentoxide is a common dehydrating agent:

  5. 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.

  6. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    An organic group's migration propensity depends on its ability to stabilize negative charge: alkynyl > aryl ≈ alkenyl > primary alkyl > secondary alkyl > tertiary alkyl. [32] Bis(norbornyl)borane and 9-BBN are often hydroboration reagents for this reason — only the hydroborated olefin is likely to migrate upon nucleophilic activation.

  7. 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 ...

  8. Why Experts Say This Underrated Supplement Is Key To Building ...

    www.aol.com/why-experts-underrated-supplement...

    "Hearst Magazines and Yahoo may earn commission or revenue on some items through these links." There are about as many performance supplements on the market as there are protein-packed foods in a ...

  9. Magnesium carbonate - Wikipedia

    en.wikipedia.org/wiki/Magnesium_carbonate

    Magnesium carbonate is ordinarily obtained by mining the mineral magnesite. Seventy percent of the world's supply is mined and prepared in China. [9] Magnesium carbonate can be prepared in laboratory by reaction between any soluble magnesium salt and sodium bicarbonate: MgCl 2 (aq) + 2 NaHCO 3 (aq) → MgCO 3 (s) + 2 NaCl(aq) + H 2 O(l) + CO 2 (g)

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