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  2. Triiodide - Wikipedia

    en.wikipedia.org/wiki/Triiodide

    The following exergonic equilibrium gives rise to the triiodide ion: . I 2 + I − ⇌ I − 3. In this reaction, iodide is viewed as a Lewis base, and the iodine is a Lewis acid.The process is analogous to the reaction of S 8 with sodium sulfide (which forms polysulfides) except that the higher polyiodides have branched structures.

  3. Isovalent hybridization - Wikipedia

    en.wikipedia.org/wiki/Isovalent_hybridization

    In chemistry, isovalent or second order hybridization is an extension of orbital hybridization, the mixing of atomic orbitals into hybrid orbitals which can form chemical bonds, to include fractional numbers of atomic orbitals of each type (s, p, d). It allows for a quantitative depiction of bond formation when the molecular geometry deviates ...

  4. Polyiodide - Wikipedia

    en.wikipedia.org/wiki/Polyiodide

    The polyiodides are a class of polyhalogen anions composed entirely of iodine atoms. [1] [2] The most common member is the triiodide ion, I −3.Other known larger polyiodides include [I 4] 2−, [I 5] −, [I 6] 2−, [I 7] −, [I 8] 2−, [I 9] −, [I 10] 2−, [I 10] 4−, [I 11] 3−, [I 12] 2−, [I 13] 3−, [I 14] 4-, [I 16] 2−, [I 22] 4−, [I 26] 3−, [I 26] 4−, [I 28] 4− and ...

  5. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    Bent's rule can be extended to rationalize the hybridization of nonbonding orbitals as well. On the one hand, a lone pair (an occupied nonbonding orbital) can be thought of as the limiting case of an electropositive substituent, with electron density completely polarized towards the central atom.

  6. Iodine clock reaction - Wikipedia

    en.wikipedia.org/wiki/Iodine_clock_reaction

    An alternative protocol uses a solution of iodate ion (for instance potassium iodate) to which an acidified solution (again with sulfuric acid) of sodium bisulfite is added. [3] In this protocol, iodide ion is generated by the following slow reaction between the iodate and bisulfite: IO − 3 + 3 HSO − 3 → I − + 3 HSO − 4

  7. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    Chemist Linus Pauling first developed the hybridisation theory in 1931 to explain the structure of simple molecules such as methane (CH 4) using atomic orbitals. [2] Pauling pointed out that a carbon atom forms four bonds by using one s and three p orbitals, so that "it might be inferred" that a carbon atom would form three bonds at right angles (using p orbitals) and a fourth weaker bond ...

  8. Thallium triiodide - Wikipedia

    en.wikipedia.org/wiki/Thallium_triiodide

    Unlike the other thallium trihalides, which contain thallium(III), TlI 3 is a thallium(I) salt and contains the triiodide ion, I − 3. An appreciation as to why Tl + is not oxidised to Tl 3+ in the reaction: Tl 3+ + 2 I − → Tl + + I 2. can be gained by considering the standard reduction potentials of the half cells which are: Tl 3+ + 2 e −

  9. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    Monochloroacetic acid (pK a =2.82), though, is stronger than formic acid, due to the electron-withdrawing effect of chlorine promoting ionization. In benzoic acid, the carbon atoms which are present in the ring are sp 2 hybridised. As a result, benzoic acid (pK a =4.20) is a stronger acid than cyclohexanecarboxylic acid (pK a =4.87).