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Grignard Reagent

Grignard reagent ( grin′yär rē′ājənt ) ( organic chemistry ) RMgX The organometallic halide formed in the Grignard reaction; an example is C 2 H 5.

Grignard Reagent is described in multiple online sources, as addition to our editors' articles, see section below for printable documents, Grignard Reagent books and related discussion.

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REPRINTED FROM HANDBOOK OF GRIGNARD REAGENTS by G. Silverman Grignard reaction for the formation of the silicon-carbon bond [1].
Nucleophilic Addition to Carbonyl: Grignard Reaction with an
Grignard reagent across the carbonyl of an aldehyde. Characterize the INFORMATION.
14.6 Synthesis of Alcohols Using Grignard Reagents Grignard
14.6. Synthesis of Alcohols Using.
are called “Grignardreagents after their inventor.
Experiment #8: Grignard Reaction
Nov. 5. Experiment #8: Grignard Reaction.

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U.S. Patents Awarded to Inventors in Louisiana (April 27)
In methods according to this invention, at least one halogenated transition metal, an amine compound and a solvent are combined, followed by the addition of an alkylated metal or a Grignard reagent to produce the transition metal amide and/or imido.

Suggested Web Resources

Grignard reaction - Wikipedia, the free encyclopedia
grignard reagents
An introduction to the formation of Grignard reagents from halogenoalkanes, and to some of their reactions.
Grignard Reaction
Grignard Reagents
Grignard Reagents. So far, we have built a small repertoire of reactions that can be used to convert one functional group to another.
Grignard Synthesis
A compound with a carbon-magnesium bond is called a Grignard reagent.

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