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Those with five organic substituents are rare, although P(C 6 H 5) 5 is known, being derived from P(C 6 H 5) 4 + by reaction with phenyllithium. Phosphorus ylides are unsaturated phosphoranes, known as Wittig reagents, e.g. CH 2 P(C 6 H 5) 3. These compounds feature tetrahedral phosphorus(V) and are considered relatives of phosphine oxides.
The latter is a common feature of the chemistry of phosphorus. As a result, the lone pair of trimethylphosphine has predominantly s-character as is the case for phosphine, PH 3. [10] Tertiary phosphines are pyramidal. When the organic substituents all differ, the phosphine is chiral and
Organophosphate flame retardants are part of a wider family of phosphorus-based agents which include organic phosphonate and phosphinate esters, in addition to inorganic salts. [ 58 ] [ 59 ] When some prominent brominated flame retardant were banned in the early 2000s phosphorus-based agents were promoted as safer replacements.
Methylphosphonyl dichloride is produced by oxidation of methyldichlorophosphine, with sulfuryl chloride: [3]. CH 3 PCl 2 + SO 2 Cl 2 → CH 3 P(O)Cl 2 + SOCl 2. It can also be produced from a range of methylphosphonates (e.g. dimethyl methylphosphonate) via chlorination with thionyl chloride.
Phosphate rich organic manure is a type of fertilizer used as an alternative to diammonium phosphate and single super phosphate.. Phosphorus is required by all plants but is limited in soil, creating a problem in agriculture In many areas phosphorus must be added to soil for the extensive plant growth that is desired for crop production.
Phosphogypsum is a by-product from the production of phosphoric acid by treating phosphate ore with sulfuric acid according to the following reaction: . Ca 5 (PO 4) 3 X + 5 H 2 SO 4 + 10 H 2 O → 3 H 3 PO 4 + 5 (CaSO 4 · 2 H 2 O) + HX
Wellness influencers say yes, but their claims are slippery at best. Experts explain what seed oils are, their benefits, and why they get so much hate.
Dimethyl methylphosphonate can be prepared from trimethyl phosphite and a halomethane (e.g. iodomethane) via the Michaelis–Arbuzov reaction. [2]Dimethyl methylphosphonate is a schedule 2 chemical as it may be used in the production of chemical weapons.