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  2. 1,1-Diiodoethane - Wikipedia

    en.wikipedia.org/wiki/1,1-Diiodoethane

    In the presence of aluminium trichloride, 1,1-dichloroethane will converted to 1,1-diiodoethane. [3] The preparation of 1,1-diiodoethane from gem-dihaloalkanes [3] To be specific, mix 0.4 mol (~39.6 g) of 1,1-dichloroethane with 1.2 mol (~187 g) of ethyl iodide, and ~2.0 g of aluminium chloride. Heat for three hours using steam bath.

  3. Ethyl iodide - Wikipedia

    en.wikipedia.org/wiki/Ethyl_iodide

    Ethyl iodide (also iodoethane) is a colorless flammable chemical compound. It has the chemical formula C 2 H 5 I and is prepared by heating ethanol with iodine and phosphorus . [ 2 ] On contact with air, especially on the effect of light, it decomposes and turns yellow or reddish from dissolved iodine.

  4. 1,2-Diiodoethane - Wikipedia

    en.wikipedia.org/wiki/1,2-Diiodoethane

    1,2-Diiodoethane can be prepared by the reaction of ethylene with iodine (I 2): [2] C 2 H 4 + I 2 ⇌ C 2 H 4 I 2. 1,2-Diiodoethane is most commonly used in organic synthesis in the preparation of samarium(II) iodide or ytterbium(II) iodide in an inert solvent such as THF. [3] Sm + ICH 2 CH 2 I → SmI 2 + H 2 C=CH 2

  5. Sodium iodide - Wikipedia

    en.wikipedia.org/wiki/Sodium_iodide

    Sodium iodide (chemical formula NaI) is an ionic compound formed from the chemical reaction of sodium metal and iodine. Under standard conditions, it is a white, water-soluble solid comprising a 1:1 mix of sodium cations (Na +) and iodide anions (I −) in a crystal lattice. It is used mainly as a nutritional supplement and in organic chemistry.

  6. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    Ether synthesis by reaction of salicylaldehyde with chloroacetic acid and sodium hydroxide [1] The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol . This reaction was developed by Alexander Williamson in 1850. [2]

  7. Leveling effect - Wikipedia

    en.wikipedia.org/wiki/Leveling_effect

    When a strong acid is dissolved in water, it reacts with it to form hydronium ion (H 3 O +). [2] An example of this would be the following reaction, where "HA" is the strong acid: HA + H 2 O → A − + H 3 O + Any acid that is stronger than H 3 O + reacts with H 2 O to form H 3 O +. Therefore, no acid stronger than H 3 O + exists in H 2 O.

  8. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  9. Iron oxide adsorption - Wikipedia

    en.wikipedia.org/wiki/Iron_oxide_adsorption

    The addition of ferric chloride, FeCl 3, to well water immediately after the well at the influent to the treatment plant creates ferric hydroxide, Fe(OH) 3, and hydrochloric acid, HCl. 3H 2 O + FeCl 3 → Fe(OH) 3 + 3HCl. Fe(OH) 3 in water is a strong adsorbent of arsenate, As(V), provided that the pH is low.