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  2. Diethyl ether (data page) - Wikipedia

    en.wikipedia.org/wiki/Diethyl_ether_(data_page)

    Material Safety Data Sheet The handling of this chemical may incur notable safety precautions. ... Vapor-liquid Equilibrium for Diethyl Ether/Methanol [4] P = 700 ...

  3. Diethyl ether - Wikipedia

    en.wikipedia.org/wiki/Diethyl_ether

    Diethyl ether, or simply ether, is an organic compound with the chemical formula (CH 3 CH 2) 2 O, sometimes abbreviated as Et 2 O. [ a ] It is a colourless, highly volatile , sweet-smelling ("ethereal odour"), extremely flammable liquid .

  4. Fluoroboric acid - Wikipedia

    en.wikipedia.org/wiki/Fluoroboric_acid

    Fluoroboric acid is corrosive and attacks the skin. It is available commercially as a solution in water and other solvents such as diethyl ether. It is a strong acid with a weakly coordinating, non-oxidizing conjugate base. [2] It is structurally similar to perchloric acid, but lacks the hazards associated with oxidants.

  5. Benzenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Benzenesulfonic_acid

    Benzenesulfonic acid (conjugate base benzenesulfonate) is an organosulfur compound with the formula C 6 H 6 O 3 S.It is the simplest aromatic sulfonic acid.It forms white deliquescent sheet crystals or a white waxy solid that is soluble in water and ethanol, slightly soluble in benzene and insoluble in nonpolar solvents like diethyl ether.

  6. Phenylmagnesium bromide - Wikipedia

    en.wikipedia.org/wiki/Phenylmagnesium_bromide

    Phenylmagnesium bromide is commercially available as solutions of diethyl ether or THF. Laboratory preparation involves treating bromobenzene with magnesium metal, usually in the form of turnings. A small amount of iodine may be used to activate the magnesium to initiate the reaction.

  7. Benzophenone - Wikipedia

    en.wikipedia.org/wiki/Benzophenone

    1 g/6 mL in diethyl ether. [2] ... Safety data sheet (SDS) ... less well-known reaction to produce benzophenone is the pyrolysis of anhydrous calcium benzoate.

  8. Iron(III) chloride - Wikipedia

    en.wikipedia.org/wiki/Iron(III)_chloride

    Aside from lability, which applies to anhydrous and hydrated forms, the reactivity of anhydrous ferric chloride reveals two trends: It is a Lewis acid and an oxidizing agent. [20] Reactions of anhydrous iron(III) chloride reflect its description as both oxophilic and a hard Lewis acid. Myriad manifestations of the oxophiliicty of iron(III ...

  9. 1,4-Dioxane - Wikipedia

    en.wikipedia.org/wiki/1,4-Dioxane

    1,4-Dioxane (/ d aɪ ˈ ɒ k s eɪ n /) is a heterocyclic organic compound, classified as an ether. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether. The compound is often called simply dioxane because the other dioxane isomers (1,2-and 1,3-) are rarely encountered.

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