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  2. Phosphorus trichloride - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride

    Phosphorus trichloride is commonly used to convert primary and secondary alcohols to the corresponding chlorides. [14] As discussed above, the reaction of alcohols with phosphorus trichloride is sensitive to conditions. The mechanism for the ROH →RCl conversion involves the reaction of HCl with phosphite esters: P(OR) 3 + HCl ⇌ HP(OR) + 3 ...

  3. Phosphorus-31 nuclear magnetic resonance - Wikipedia

    en.wikipedia.org/wiki/Phosphorus-31_nuclear...

    Phosphorus-31 NMR spectroscopy is an analytical chemistry technique that uses nuclear magnetic resonance (NMR) to study chemical compounds that contain phosphorus. Phosphorus is commonly found in organic compounds and coordination complexes (as phosphines), making it useful to measure 31 - NMR spectra routinely.

  4. Thiophosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Thiophosphoryl_chloride

    Thiophosphoryl chloride has tetrahedral molecular geometry and C 3v molecular symmetry, with the structure S=PCl 3.According to gas electron diffraction, the phosphorus–sulfur bond length is 189 pm and the phosphorus–chlorine bond length is 201 pm, while the Cl−P−Cl bond angle is 102°.

  5. Triethyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Triethyl_phosphite

    The molecule features a pyramidal phosphorus(III) center bound to three ethoxide groups. Its 31 P NMR spectrum features a signal at around +139 ppm vs phosphoric acid standard. Triethylphosphite is prepared by treating phosphorus trichloride with ethanol in the presence of a base, typically a tertiary amine: [1]

  6. Phosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_chloride

    Phosphoryl chloride (commonly called phosphorus oxychloride) is a colourless liquid with the formula P O Cl 3. It hydrolyses in moist air releasing phosphoric acid and fumes of hydrogen chloride . It is manufactured industrially on a large scale from phosphorus trichloride and oxygen or phosphorus pentoxide . [ 4 ]

  7. Chlorodiphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Chlorodiphenylphosphine

    Chlorodiphenylphosphine is produced on a commercial scale from benzene and phosphorus trichloride (PCl 3). Benzene reacts with phosphorus trichloride at extreme temperatures around 600 °C to give dichlorophenylphosphine (PhPCl 2) and HCl. Redistribution of PhPCl 2 in the gas phase at high temperatures results in chlorodiphenylphosphine. [2] [3]

  8. Phosphorus trichloride (data page) - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride...

    The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet for this chemical from a reliable source such as SIRI, and follow its directions.

  9. Phosphorus halide - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_halide

    Phosphorus trichloride is a major industrial chemical and widely used starting material for phosphorus chemistry. Phosphorus tribromide is used in organic chemistry to convert alcohols to alkyl bromides and carboxylic acids to acyl bromides (e.g. in the Hell-Volhard-Zelinsky reaction).