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  2. Diphenylphosphoryl azide - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphoryl_azide

    It is now suggested that this reaction proceeds through the intermediate mixed anhydride, resulting from attack by the nucleophilic carboxylate anion on the phosphorus atom, with expulsion of the azide ion. The latter then attacks the carbonyl carbon atom, to give the acyl azide and loss of the diphenylphosphate anion, known to be a good ...

  3. Diphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphine

    For example, in the presence of concentrated hydrochloric acid at 100 °C, diphenylphosphine adds to the carbon atom in benzaldehyde to give (phenyl-(phenylmethyl)phosphoryl)benzene. Ph 2 PH + PhCHO → Ph 2 P(O)CH 2 Ph. Compared to tertiary phosphines, diphenylphosphine is weakly basic. The pKa of the protonated derivative is 0.03: [4]

  4. Organic azide - Wikipedia

    en.wikipedia.org/wiki/Organic_azide

    The azide functional group can be shown by two resonance structures. An organic azide is an organic compound that contains an azide (– N 3) functional group. [1] Because of the hazards associated with their use, few azides are used commercially although they exhibit interesting reactivity for researchers.

  5. Phenyl azide - Wikipedia

    en.wikipedia.org/wiki/Phenyl_azide

    Phenyl azide is an organic compound with the formula C 6 H 5 N 3. It is one of the prototypical organic azides. It is a pale yellow oily liquid with a pungent odor. The structure consists of a linear azide substituent bound to a phenyl group. The C−N=N angle is approximately 116°.

  6. Diphenylphosphite - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphite

    Diphenyl phosphite is a diorganophosphite with the formula (C 6 H 5 O) 2 P(O)H. The molecule is tetrahedral. It is a colorless viscous liquid. The compounds can be prepared by treating phosphorus trichloride with phenol. Many analogues can be prepared similarly.

  7. Diphenylphosphine oxide - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphine_oxide

    Diphenylphosphine oxide exists in equilibrium with its minor tautomer diphenylphosphinous acid, ((C 6 H 5) 2 POH: (C 6 H 5) 2 P(O)H ⇌ (C 6 H 5) 2 POH. Diphenylphosphine oxide is used in Buchwald-Hartwig coupling reactions to introduce diphenylphosphino substituents.

  8. Puppy lovin' dog days: Westminster's Best in Show is ... - AOL

    www.aol.com/puppy-lovin-dog-days-westminsters...

    No more parading around in a tennis facility. After a four-year absence, the Westminster Dog Show is back at its longtime home, Madison Square Garden in Midtown Manhattan, for its 149 th edition.

  9. List of gases - Wikipedia

    en.wikipedia.org/wiki/List_of_gases

    This list is sorted by boiling point of gases in ascending order, but can be sorted on different values. "sub" and "triple" refer to the sublimation point and the triple point, which are given in the case of a substance that sublimes at 1 atm; "dec" refers to decomposition. "~" means approximately. Blue type items have an article available by ...