When.com Web Search

Search results

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

    en.wikipedia.org/wiki/Triphenylcarbethoxym...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  3. Wittig reagents - Wikipedia

    en.wikipedia.org/wiki/Wittig_reagents

    Wittig reagents are usually described as a combination of two resonance structures: Ph 3 P + CR 2 − ↔ Ph 3 P=CR 2. The former is called the ylide form and the latter is called the phosphorane form, which is the more familiar representation. Crystallographic characterization of methylenetriphenylphosphorane shows that the phosphorus atom is ...

  4. Carbomethoxymethylenetriphenylphosphorane - Wikipedia

    en.wikipedia.org/wiki/Carbomethoxymethylenetri...

    This article about an organic compound is a stub. You can help Wikipedia by expanding it.

  5. Wittig reaction - Wikipedia

    en.wikipedia.org/wiki/Wittig_reaction

    The Wittig reaction or Wittig olefination is a chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide called a Wittig reagent.Wittig reactions are most commonly used to convert aldehydes and ketones to alkenes.

  6. Clar's rule - Wikipedia

    en.wikipedia.org/wiki/Clar's_rule

    Clar's rule states that for a benzenoid polycyclic aromatic hydrocarbon (i.e. one with only hexagonal rings), the resonance structure with the largest number of disjoint aromatic π-sextets is the most important to characterize its chemical and physical properties. Such a resonance structure is called a Clar structure. In other words, a ...

  7. Methylenetriphenylphosphorane - Wikipedia

    en.wikipedia.org/wiki/Methylenetriphenylphosphorane

    Methylenetriphenylphosphorane is prepared from methyltriphenylphosphonium bromide by its deprotonation using a strong base like butyllithium: [1]. Ph 3 PCH 3 Br + BuLi → Ph 3 PCH 2 + LiBr + BuH

  8. Resonance (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Resonance_(chemistry)

    Contributing structures of the carbonate ion. In chemistry, resonance, also called mesomerism, is a way of describing bonding in certain molecules or polyatomic ions by the combination of several contributing structures (or forms, [1] also variously known as resonance structures or canonical structures) into a resonance hybrid (or hybrid structure) in valence bond theory.

  9. Triphenyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Triphenyl_phosphate

    Triphenyl phosphate has been detected in the environment. [9] Other triaryl phosphates have been known to enter aquatic environments through volatilization and leaching from plastics, through hydraulic fluid leakages, and, to a lesser degree, through manufacturing processes. [5]

  1. Related searches carbethoxymethylene triphenylphosphorane resonance structures pictures of 10

    melting point of triphenylcarbeth methylenephosphoranetriphenylcarbethoxymethylmethylene