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Iodomethane, also called methyl iodide, and commonly abbreviated "MeI", is the chemical compound with the formula CH 3 I. It is a dense, colorless, volatile liquid. In terms of chemical structure, it is related to methane by replacement of one hydrogen atom by an atom of iodine. It is naturally emitted in small amounts by rice plantations. [5]
The potential for methyl iodide to replace the ubiquitous dependence on methyl bromide as a soil fumigant has been considered, however limited information is available on environmental behavior of the former. [5] Ioxynil (3,5-diiodo-4-hydroxybenzonitrile), which inhibits photosynthesis at photosystem II, is among the very few organoiodine ...
deactivating any unreacted reagents by quenching a reaction. cooling the reaction mixture or adding an antisolvent to induce precipitation, and collecting or removing the solids by filtration, decantation, or centrifugation. changing the protonation state of the products or impurities by adding an acid or base.
In materials science, quenching is the rapid cooling of a workpiece in water, gas, oil, polymer, air, or other fluids to obtain certain material properties. A type of heat treating , quenching prevents undesired low-temperature processes, such as phase transformations, from occurring.
Diiodomethane or methylene iodide, commonly abbreviated "MI", is an organoiodine compound. Diiodomethane is a very dense colorless liquid; however, it decomposes upon exposure to light liberating iodine, which colours samples brownish. It is slightly soluble in water, but soluble in organic solvents.
This reaction can be optimized by carefully controlling the amount of organolithium reagent addition, or using trimethylsilyl chloride to quench excess lithium reagent. [40] A more common way to synthesize ketones is through the addition of organolithium reagents to Weinreb amides (N-methoxy-N-methyl amides).
The alkylphosphonium salt is deprotonated with a strong base such as n-butyllithium: [Ph 3 P + CH 2 R]X − + C 4 H 9 Li → Ph 3 P=CHR + LiX + C 4 H 10. Besides n-butyllithium (n BuLi), other strong bases like sodium and potassium t-butoxide (t BuONa, t BuOK), lithium, sodium and potassium hexamethyldisilazide (LiHMDS, NaHMDS, KHDMS, where HDMS = N(SiMe 3) 2), or sodium hydride (NaH) are also ...
Methyl acetate is used in place of methanol as a source of methyl iodide. [5] CH 3 CO 2 CH 3 + CO → (CH 3 CO) 2 O. In this process lithium iodide converts methyl acetate to lithium acetate and methyl iodide, which in turn affords, through carbonylation, acetyl iodide. Acetyl iodide reacts with acetate salts or acetic acid to give the anhydride.