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  2. Phosphite ester - Wikipedia

    en.wikipedia.org/wiki/Phosphite_ester

    The general structure of a phosphite ester showing the lone pairs on the P. In organic chemistry, a phosphite ester or organophosphite usually refers to an organophosphorous compound with the formula P(OR) 3. They can be considered as esters of an unobserved tautomer phosphorous acid, H 3 PO 3, with the simplest example being trimethylphosphite ...

  3. Gas constant - Wikipedia

    en.wikipedia.org/wiki/Gas_constant

    The gas constant occurs in the ideal gas law: = = where P is the absolute pressure, V is the volume of gas, n is the amount of substance, m is the mass, and T is the thermodynamic temperature. R specific is the mass-specific gas constant. The gas constant is expressed in the same unit as molar heat.

  4. Organophosphate - Wikipedia

    en.wikipedia.org/wiki/Organophosphate

    [14] [15] Current models rely on either negative hyperconjugation, [16] or a more complex arraignment with a dative-type bond from P to O, combined with back-donation from an oxygen 2p orbital. [ 15 ] [ 17 ] These models agree with the experimental observations of the phosphoryl as being shorter than P-OR bonds [ 18 ] and much more polarised.

  5. Phosphate - Wikipedia

    en.wikipedia.org/wiki/Phosphate

    The phosphate ion has a molar mass of 94.97 g/mol, and consists of a central phosphorus atom surrounded by four oxygen atoms in a tetrahedral arrangement. It is the conjugate base of the hydrogen phosphate ion H(PO 4) 2−, which in turn is the conjugate base of the dihydrogen phosphate ion H 2 (PO 4) −

  6. Oxyanion - Wikipedia

    en.wikipedia.org/wiki/Oxyanion

    The phosphite ion, PO 3− 3, is a strong base, and so always carries at least one proton. In this case the proton is attached directly to the phosphorus atom with the structure HPO 2− 3 . In forming this ion, the phosphite ion is behaving as a Lewis base and donating a pair of electrons to the Lewis acid, H + .

  7. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    In organic chemistry, a ketone / ˈ k iː t oʊ n / is an organic compound with the structure R−C(=O)−R', where R and R' can be a variety of carbon-containing substituents. Ketones contain a carbonyl group −C(=O)− (a carbon-oxygen double bond C=O). The simplest ketone is acetone (where R and R' are methyl), with the formula (CH 3) 2 CO ...

  8. Phosphonate - Wikipedia

    en.wikipedia.org/wiki/Phosphonate

    General ester of phosphonic acid; in fact, the phosphorus has a formal charge of +1, the oxygen above it has a formal charge of −1, and the bond between them is single. In organic chemistry, phosphonates or phosphonic acids are organophosphorus compounds containing C−PO(OR) 2 groups, where R is an organic group (alkyl, aryl).

  9. Phosphite (ion) - Wikipedia

    en.wikipedia.org/wiki/Phosphite_(ion)

    From the commercial perspective, the most important phosphite salt is basic lead phosphite. Many salts containing the phosphite ion have been investigated structurally, these include sodium phosphite pentahydrate (Na 2 HPO 3 ·5H 2 O). (NH 4) 2 HPO 3 ·H 2 O, CuHPO 3 ·H 2 O, SnHPO 3 and Al 2 (HPO 3) 3 ·4H 2 O. [4] The structure of HPO 2− 3 ...