When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Phosphonium - Wikipedia

    en.wikipedia.org/wiki/Phosphonium

    They are derived from phosphonium salts. A strong base such as butyllithium or sodium amide is required for the deprotonation: [Ph 3 P + CH 2 R]X − + C 4 H 9 Li → Ph 3 P=CHR + LiX + C 4 H 10. One of the simplest ylides is methylenetriphenylphosphorane (Ph 3 P=CH 2). [6] The compounds Ph 3 PX 2 (X = Cl, Br) are used in the Kirsanov reaction ...

  3. Adopt Me! - Wikipedia

    en.wikipedia.org/wiki/Adopt_Me!

    Adopt Me! (stylized in all caps ) is a massively multiplayer online video game developed by Uplift Games (formerly known as DreamCraft) on the gaming and game development platform Roblox . [ 2 ]

  4. Phosphenium - Wikipedia

    en.wikipedia.org/wiki/Phosphenium

    P(NMe 2) 3 + 2 HOTf → [P(NMe 2) 2]OTf + [HNMe 2]OTf. Weakly coordinating anions are desirable. Triflic acid is often used. [3] N-heterocyclic phosphenium (NHP) have also been reported. [5] Reaction of PI 3 with the α-diimine yields the NHP cation by reduction of the diimine and oxidation of iodine. Redox synthesis of N-heterocyclic ...

  5. Phosphonium iodide - Wikipedia

    en.wikipedia.org/wiki/Phosphonium_iodide

    Phosphonium iodide is a powerful substitution reagent in organic chemistry; for example, it can convert a pyrilium into a phosphinine via substitution. [3] In 1951, Glenn Halstead Brown found that PH 4 I reacts with acetyl chloride to produce an unknown phosphine derivative, possibly CH 3 C(=PH)PH 2 ·HI .

  6. Talk:Adopt Me! - Wikipedia

    en.wikipedia.org/wiki/Talk:Adopt_Me!

    Literally nothing about the section on Adopt Me has any reference to roleplaying or adoption mentioning players, the two most obvious aspects of the gameplay, and is instead focused on pets. I understand the importance of pets, but the game does not revolve around just pets. 01052021a 00:29, 10 May 2021 (UTC)

  7. Diphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphine

    In the laboratory, diphenylphosphine is a common intermediate. It can be deprotonated to give diphenylphosphide derivatives: [2] Ph 2 PH + n BuLi → Ph 2 PLi + n BuH. The preparation of phosphine ligands, Wittig-Horner reagents, and phosphonium salts are commonly accomplished by alkylating diphenylphosphine.

  8. Phosphine oxides - Wikipedia

    en.wikipedia.org/wiki/Phosphine_oxides

    PMePh 2 + H 2 O 2 → OPMePh 2 + H 2 O. Phosphine oxides are generated as a by-product of the Wittig reaction: R 3 PCR' 2 + R" 2 CO → R 3 PO + R' 2 C=CR" 2. Another albeit unconventional route to phosphine oxides is the thermolysis of phosphonium hydroxides: [PPh 4]Cl + NaOH → Ph 3 PO + NaCl + PhH. The hydrolysis of phosphorus(V) dihalides ...

  9. Phosphonite - Wikipedia

    en.wikipedia.org/wiki/Phosphonite

    Although they are derivatives of phosphonous acid (RP(OH) 2), [2] they are not prepared from such precursors. Phosphonites are prepared by alcoholysis of organophosphinous chlorides. For example, treatment of dichlorophenylphosphine with methanol and base gives dimethyl phenylphosphonite: