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  2. Sodium hydride - Wikipedia

    en.wikipedia.org/wiki/Sodium_hydride

    Sodium hydride is the chemical compound with the empirical formula Na H.This alkali metal hydride is primarily used as a strong yet combustible base in organic synthesis.NaH is a saline (salt-like) hydride, composed of Na + and H − ions, in contrast to molecular hydrides such as borane, silane, germane, ammonia, and methane.

  3. Water-reactive substances - Wikipedia

    en.wikipedia.org/wiki/Water-reactive_substances

    Group 1: Alkali metals Reaction of sodium (Na) and water Reaction of potassium (K) in water. The alkali metals (Li, Na, K, Rb, Cs, and Fr) are the most reactive metals in the periodic table - they all react vigorously or even explosively with cold water, resulting in the displacement of hydrogen.

  4. Hydride - Wikipedia

    en.wikipedia.org/wiki/Hydride

    The hydride adds to an electrophilic center, typically unsaturated carbon. Hydrides such as sodium hydride and potassium hydride are used as strong bases in organic synthesis. The hydride reacts with the weak Bronsted acid releasing H 2. Hydrides such as calcium hydride are used as desiccants, i.e. drying agents, to remove trace water from ...

  5. How to Make Iced Tea - AOL

    www.aol.com/food/how-make-iced-tea

    Let your tea cool down to room temperature, transfer the concentrate into a 2-quart pitcher, and dilute with cold water according to taste. Serve with ice, and garnish with a lemon wedge if you'd ...

  6. Non-nucleophilic base - Wikipedia

    en.wikipedia.org/wiki/Non-nucleophilic_base

    Other strong non-nucleophilic bases are sodium hydride and potassium hydride. These compounds are dense, salt-like materials that are insoluble and operate by surface reactions. These compounds are dense, salt-like materials that are insoluble and operate by surface reactions.

  7. Trimethylsulfoxonium - Wikipedia

    en.wikipedia.org/wiki/Trimethylsulfoxonium

    Treated with sodium hydride, trimethylsulfoxonium forms dimethylsulfoxonium methylide. [1] Trimethylsulfoxonium can polymerise to yield polyethylene. [2] [3] Copper, zinc and palladium ions in water react with trimethylsulfoxonium and sodium hydroxide to form sulfur ylide complexes. [4]

  8. 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).

  9. How to Depuff Your Face for a Refreshed and Rested Look - AOL

    www.aol.com/lifestyle/depuff-face-refreshed...

    Dip Your Face in Ice Cold Water. Fill a bowl with cold water and ice cubes. “You can submerge your face for ten seconds at a time or massage your skin with an ice cube, applying slight pressure ...