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  2. Hypervalent organoiodine compounds - Wikipedia

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

    These iodine compounds are hypervalent because the iodine atom formally contains in its valence shell more than the 8 electrons required for the octet rule. Hypervalent iodine oxyanions are known for oxidation states +1, +3, +5, and +7; organic analogues of these moieties are known for each oxidation state except +7.

  3. (Diacetoxyiodo)benzene - Wikipedia

    en.wikipedia.org/wiki/(Diacetoxyiodo)benzene

    The PIDA molecule is termed hypervalent as its iodine atom (technically a hypervalent iodine) is in its +III oxidation state and has more than typical number of covalent bonds. [9] It adopts a T-shaped molecular geometry , with the phenyl group occupying one of the three equatorial positions of a trigonal bipyramid ( lone pairs occupy the other ...

  4. (Bis(trifluoroacetoxy)iodo)benzene - Wikipedia

    en.wikipedia.org/wiki/(Bis(trifluoroacetoxy)iodo...

    The reaction can also be carried out under mildly acidic conditions by way of the same intermediate using a hypervalent iodine compound in aqueous solution. [1] An example published in Organic Syntheses is the conversion of cyclobutanecarboxamide , easily synthesized from cyclobutylcarboxylic acid , to cyclobutylamine . [ 2 ]

  5. Melzer's reagent - Wikipedia

    en.wikipedia.org/wiki/Melzer's_reagent

    Melzer's reagent is an aqueous solution of chloral hydrate, potassium iodide, and iodine.Depending on the formulation, it consists of approximately 2.50-3.75% potassium iodide and 0.75–1.25% iodine, with the remainder of the solution being 50% water and 50% chloral hydrate.

  6. Bis (pyridine)iodonium (I) tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Bis(pyridine)iodonium(I...

    Bis(pyridine)iodonium(I) tetrafluoroborate or Barluenga's reagent, named after José Barluenga, [1] is a mild iodinating reagent. Commercially available, it may be prepared by reacting iodine with pyridine in the presence of silver tetrafluoroborate supported on silica gel .

  7. Iodine compounds - Wikipedia

    en.wikipedia.org/wiki/Iodine_compounds

    Iodine trichloride, which exists in the solid state as the planar dimer I 2 Cl 6, is a bright yellow solid, synthesised by reacting iodine with liquid chlorine at −80 °C; caution is necessary during purification because it easily dissociates to iodine monochloride and chlorine and hence can act as a strong chlorinating agent.

  8. Experimental: Create your own iodine clock reaction in 12 ...

    www.aol.com/news/experimental-create-own-iodine...

    Try this experiment at home with the kids to introduce them to the basic tenet of physics, kinetics! ... Transform iodine with a few simple ingredients: 3 plastic cups. 1000 MG Vitamin C.

  9. Iodosobenzene - Wikipedia

    en.wikipedia.org/wiki/Iodosobenzene

    The related diacetate, C 6 H 5 I(O 2 CCH 3) 2, illustrates the ability of iodine(III) to adopt a T-shaped geometry without multiple bonds. [8] Theoretical studies show that the bonding between the iodine and oxygen atoms in iodosobenzene represents a single dative I-O sigma bond, confirming the absence of the double I=O bond.