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  2. 18-Crown-6 - Wikipedia

    en.wikipedia.org/wiki/18-Crown-6

    Thus, reaction of 18-crown-6 with strong acids gives the cation [H 3 O·18-crown-6] +. For example, interaction of 18-crown-6 with HCl gas in toluene with a little moisture gives an ionic liquid layer with the composition [H 3 O·18-crown-6] + [HCl 2 ] − ·3.8C 6 H 5 Me, from which the solid [H 3 O·18-crown-6] + [HCl 2 ] − can be isolated ...

  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. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    The case for S N 2 reactions is quite different, as the lack of solvation on the nucleophile increases the rate of an S N 2 reaction. In either case (S N 1 or S N 2), the ability to either stabilize the transition state (S N 1) or destabilize the reactant starting material (S N 2) acts to decrease the ΔG ‡ activation and thereby increase the ...

  5. Beverage opener - Wikipedia

    en.wikipedia.org/wiki/Beverage_opener

    A beverage opener (also known as a multi-opener) is a device used to open beverage cans, plastic bottles or glass bottles, which are the three most common beverage containers. [ 1 ] Types

  6. Bottle opener - Wikipedia

    en.wikipedia.org/wiki/Bottle_opener

    Under most use, a bottle opener functions as a second-class lever: the fulcrum is the far end of the bottle opener, placed on the top of the crown, with the output at the near end of the bottle opener, on the crown edge, between the fulcrum and the hand: in these cases, one pushes up on the lever.

  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. Electrolysis of water - Wikipedia

    en.wikipedia.org/wiki/Electrolysis_of_water

    An AA battery in a glass of tap water with salt showing hydrogen produced at the negative terminal. Electrolysis of water is using electricity to split water into oxygen (O 2) and hydrogen (H 2) gas by electrolysis. Hydrogen gas released in this way can be used as hydrogen fuel, but must be kept apart from the oxygen as the mixture would be ...

  9. Heterogeneous water oxidation - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_Water_Oxidation

    Heterogeneous OER is sensitive to the surface which the reaction takes place and is also affected by the pH of the solution. The general mechanism for acidic and alkaline solutions is shown below. Under acidic conditions water binds to the surface with the irreversible removal of one electron and one proton to form a platinum hydroxide. [4]