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Methyllithium is the simplest organolithium reagent, with the empirical formula LiCH3. This s-block organometallic compound adopts an oligomeric structure both in solution and in the solid state. This highly reactive compound, invariably used in solution with an ether as the solvent, is a reagent in organic synthesis as well as organometallic chemistry.…
Reactivity, Structure & Synthesis
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lithium carbon methyl meli compound ether compounds prepared reactive solution reagent used well formula state highly water structure synthesis organometallic
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Methyllithium | is a | simplest organolithium reagent | 0.90 | text |
| benzene favour formation of the hexamer | instance of | Hydrocarbon solvents | 0.80 | text |
| whereas ethereal solvents favour the tetramer.BondingThese clusters are considered | instance of | Hydrocarbon solvents | 0.80 | text |
| Methyllithium | related to Reactivity | In | 0.60 | section |
| Methyllithium | related to Reactivity | BuLi | 0.60 | section |
| Methyllithium | related to Reactivity | MeLi | 0.60 | section |
| Methyllithium | related to Reactivity | THF | 0.60 | section |
| Methyllithium | related to Reactivity | Water | 0.60 | section |
| Methyllithium | related to Reactivity | Most | 0.60 | section |
| Methyllithium | related to Reactivity | Although MeLi | 0.60 | section |
| Methyllithium | related to Reactivity | For | 0.60 | section |
| Methyllithium | related to Synthesis | In | 0.60 | section |
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