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  2. Chemical chameleon - Wikipedia

    en.wikipedia.org/wiki/Chemical_chameleon

    The chemical chameleon reaction shows the process in reverse, by reducing violet potassium permanganate first to green potassium manganate and eventually to brown manganese dioxide: [1] [2] [5] KMnO 4 (violet) → K 2 MnO 4 (green) → MnO 2 (brown/yellow suspension) Blue potassium hypomanganate may also form as an intermediate. [6]

  3. Potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_permanganate

    The reagent is an alkaline solution of potassium permanganate. Reaction with double or triple bonds (R 2 C=CR 2 or R−C≡C−R) causes the color to fade from purplish-pink to brown. Aldehydes and formic acid (and formates) also give a positive test. [43] The test is antiquated. Baeyer's reagent reaction

  4. Alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene

    Gattermann-Koch reaction: named after German chemists Ludwig Gattermann and Julius Arnold Koch, the Gattermann-Koch reaction is a catalyzed formylation of alkylbenzenes with carbon monoxide and hydrochloric acid. [5] Alkylbenzene sulfonation reaction: electrophilic addition of a sulfonic acid group onto the aromatic ring. [4]

  5. 4-Nitrotoluene - Wikipedia

    en.wikipedia.org/wiki/4-Nitrotoluene

    Together with other isomers, 4-nitrotoluene is prepared by nitration of toluene, [4] commonly using titanium(IV) nitrate. [5] It undergoes the reactions typical for nitrobenzene derivatives, e.g. hydrogenation gives p-toluidine. Oxidation of the methyl substituent of 4-nitrotoluene has been extensively investigated.

  6. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  7. On-water reaction - Wikipedia

    en.wikipedia.org/wiki/On-water_reaction

    The reaction of quadricyclane with DEAD is a 2σ + 2σ + 2π cycloaddition that on water takes place within 10 minutes at room temperature with 82% yield. The same reaction in toluene takes 24 hours at 80 °C with 70% yield. An emulsion reaction in fluorinated cyclohexane takes 36 hours and the neat reaction takes even longer (48 hours).

  8. Beverage opener - Wikipedia

    en.wikipedia.org/wiki/Beverage_opener

    Beverage openers are useful for opening every day beverage containers for those who have limited hand strength as it eliminates the need for strong twisting or pulling motions. Plastic bottles may become stuck due to a high volume of carbonation released during shipping or overtightening.

  9. Bottle opener - Wikipedia

    en.wikipedia.org/wiki/Bottle_opener

    Wall-mounted bottle opener with magnet to catch lids. Works the same as the lever variation, except that it is attached to the wall, to allow for simpler bottle-opening, which can be done with one hand. The bottle cap can fall into a bottle cap catcher mounted below the opener, or it can be retrieved after removal from the bottle.