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  2. 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.

  3. Iodomethane - Wikipedia

    en.wikipedia.org/wiki/Iodomethane

    MeI can also be used to prepare dimethylmercury, by reacting 2 moles of MeI with a 2/1-molar sodium amalgam (2 moles of sodium, 1 mol of mercury). Iodomethane and other organic iodine compounds do form under the conditions of a serious nuclear accident, [ 11 ] after both Chernobyl and Fukushima , Iodine-131 was detected in organic iodine ...

  4. 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]

  5. Sodium iodide - Wikipedia

    en.wikipedia.org/wiki/Sodium_iodide

    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. It is produced industrially as the salt formed when acidic iodides react with sodium hydroxide. [11] It is a ...

  6. Hydrolysis - Wikipedia

    en.wikipedia.org/wiki/Hydrolysis

    For example, sodium acetate dissociates in water into sodium and acetate ions. Sodium ions react very little with the hydroxide ions whereas the acetate ions combine with hydronium ions to produce acetic acid. In this case the net result is a relative excess of hydroxide ions, yielding a basic solution. Strong acids also undergo hydrolysis.

  7. 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.

  8. Sodium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_hydroxide

    Sodium hydroxide, also known as lye and caustic soda, [1] [2] is an inorganic compound with the formula NaOH. It is a white solid ionic compound consisting of sodium cations Na + and hydroxide anions OH −. Sodium hydroxide is a highly corrosive base and alkali that decomposes lipids and proteins at ambient temperatures and may cause severe ...

  9. Basic oxide - Wikipedia

    en.wikipedia.org/wiki/Basic_oxide

    All oxides of group 1 & 2 elements are basic (except BeO), they react with water to form a base: [2] Lithium oxide reacts with water to produce lithium hydroxide: Li 2 O + H 2 O → 2 LiOH; Sodium oxide reacts with water to produce sodium hydroxide: Na 2 O + H 2 O → 2 NaOH; Potassium oxide reacts with water to produce potassium hydroxide: K 2 ...