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  2. Iodine Clock Reaction [Video] - AOL

    www.aol.com/news/iodine-clock-reaction-155728609...

    This experiment is about much more than just watching Iodine solution turn royal blue from reddish brown. Try this experiment at home with the kids to introduce them to the basic tenet of physics ...

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

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

    This experiment is about much more than just watching Iodine solution turn royal blue from reddish brown. Try this experiment at home with the kids to introduce them to the basic tenet of physics ...

  4. Iodine clock reaction - Wikipedia

    en.wikipedia.org/wiki/Iodine_clock_reaction

    The iodine clock reaction is a classical chemical clock demonstration experiment to display chemical kinetics in action; it was discovered by Hans Heinrich Landolt in 1886. [1] The iodine clock reaction exists in several variations, which each involve iodine species ( iodide ion, free iodine, or iodate ion) and redox reagents in the presence of ...

  5. Thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Thiocyanate

    [7] [8] [9] Thus the complete absence of thiocyanate or reduced thiocyanate [10] in the human body, (e.g., cystic fibrosis) is damaging to the human host defense system. [11] [12] Thiocyanate is a potent competitive inhibitor of the thyroid sodium-iodide symporter. [13] Iodine is an essential component of thyroxine. Since thiocyanates will ...

  6. Chemical oscillator - Wikipedia

    en.wikipedia.org/wiki/Chemical_oscillator

    The Bray–Liebhafsky reaction is a chemical clock first described by W. C. Bray in 1921 with the oxidation of iodine to iodate: 5 H 2 O 2 + I 2 → 2 IO − 3 + 2 H + + 4 H 2 O. and the reduction of iodate back to iodine: 5 H 2 O 2 + 2 IO − 3 + 2 H + → I 2 + 5 O 2 + 6 H 2 O [4]

  7. Organic thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Organic_thiocyanates

    In methyl thiocyanate, N≡C and C−S distances are 116 and 176 pm. By contrast, N=C and C=S distances are 117 and 158 pm in isothiocyanates. [7] Typical bond angles for C−S−C are 100°. [3] By contrast C−N=C in aryl isothiocyanates is 165°. Again, the thiocyanate isomers are quite different with C−S−C angle near 100°.

  8. Organoiodine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoiodine_chemistry

    Organoiodine chemistry is the study of the synthesis and properties of organoiodine compounds, or organoiodides, organic compounds that contain one or more carbon–iodine bonds. They occur widely in organic chemistry, but are relatively rare in nature.

  9. Briggs–Rauscher reaction - Wikipedia

    en.wikipedia.org/wiki/Briggs–Rauscher_reaction

    Oscillogram made in July 1972 by Briggs and Rauscher. The Briggs–Rauscher oscillating reaction is one of a small number of known oscillating chemical reactions.It is especially well suited for demonstration purposes because of its visually striking colour changes: the freshly prepared colourless solution slowly turns an amber colour, then suddenly changes to a very dark blue.