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  2. Organoiodine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoiodine_chemistry

    For example, in the molecules represented by CH 3 X, where X is a halide, the carbon-X bonds have strengths, or bond dissociation energies, of 115, 83.7, 72.1, and 57.6 kcal/mol for X = fluoride, chloride, bromide, and iodide, respectively. [2] Of the halides, iodide usually is the best leaving group.

  3. Iodide - Wikipedia

    en.wikipedia.org/wiki/Iodide

    The low solubility of silver iodide and lead iodide reflects the covalent character of these metal iodides. A test for the presence of iodide ions is the formation of yellow precipitates of these compounds upon treatment of a solution of silver nitrate or lead(II) nitrate. [2] Aqueous solutions of iodide salts dissolve iodine better than pure ...

  4. Hypervalent organoiodine compounds - Wikipedia

    en.wikipedia.org/wiki/Hypervalent_organoiodine...

    Alternatively, the Meyer-Hartmann reaction applies: a silver alkoxide reacts with elemental iodine to give the hypoiodite and silver iodide. They are unstable to visible light, cleaving into alkoxyl and iodine radicals. [12] The synthesis of organyl periodyl derivatives (λ 7-iodanes) has been attempted since the early 20th century. [13]

  5. Iodine compounds - Wikipedia

    en.wikipedia.org/wiki/Iodine_compounds

    (Nonetheless, nitrogen triiodide is named as an iodide as it is analogous to the other nitrogen trihalides.) [7] Given the large size of the iodide anion and iodine's weak oxidising power, high oxidation states are difficult to achieve in binary iodides, the maximum known being in the pentaiodides of niobium, tantalum, and protactinium. Iodides ...

  6. Iodine - Wikipedia

    en.wikipedia.org/wiki/Iodine

    This is an accepted version of this page This is the latest accepted revision, reviewed on 9 January 2025. This article is about the chemical element. For other uses, see Iodine (disambiguation). Chemical element with atomic number 53 (I) Iodine, 53 I Iodine Pronunciation / ˈ aɪ ə d aɪ n, - d ɪ n, - d iː n / (EYE -ə-dyne, -⁠din, -⁠deen) Appearance lustrous metallic gray solid, black ...

  7. Ammonium - Wikipedia

    en.wikipedia.org/wiki/Ammonium

    Ammonia or ammonium ion when added to Nessler's reagent gives a brown color precipitate known as the iodide of Million's base in basic medium. Ammonium ion when added to chloroplatinic acid gives a yellow precipitate of ammonium hexachloroplatinate(IV). H 2 [PtCl 6](aq) + [NH 4] + (aq) → [NH 4] 2 [PtCl 6](s) + 2 H +

  8. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    A Lewis base is often a Brønsted–Lowry base as it can donate a pair of electrons to H +; [11] the proton is a Lewis acid as it can accept a pair of electrons. The conjugate base of a Brønsted–Lowry acid is also a Lewis base as loss of H + from the acid leaves those electrons which were used for the A—H bond as a lone pair on the ...

  9. Base pair - Wikipedia

    en.wikipedia.org/wiki/Base_pair

    An unnatural base pair (UBP) is a designed subunit (or nucleobase) of DNA which is created in a laboratory and does not occur in nature. DNA sequences have been described which use newly created nucleobases to form a third base pair, in addition to the two base pairs found in nature, A-T (adenine – thymine) and G-C (guanine – cytosine).