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  2. Zinc sulfate - Wikipedia

    en.wikipedia.org/wiki/Zinc_sulfate

    Zn + H 2 SO 4 + 7 H 2 O → ZnSO 4 ·7H 2 O + H 2. Pharmaceutical-grade zinc sulfate is produced by treating high-purity zinc oxide with sulfuric acid: ZnO + H 2 SO 4 + 6 H 2 O → ZnSO 4 ·7H 2 O. In aqueous solution, all forms of zinc sulfate behave identically. These aqueous solutions consist of the metal aquo complex [Zn(H 2 O) 6] 2+ and SO ...

  3. Single displacement reaction - Wikipedia

    en.wikipedia.org/wiki/Single_displacement_reaction

    A single-displacement reaction, also known as single replacement reaction or exchange reaction, is an archaic concept in chemistry. It describes the stoichiometry of some chemical reactions in which one element or ligand is replaced by atom or group. [ 1 ][ 2 ][ 3 ] It can be represented generically as: where either.

  4. Zinc compounds - Wikipedia

    en.wikipedia.org/wiki/Zinc_compounds

    The composition of this layer can be complex, but one constituent is probably basic zinc carbonate, Zn 5 (OH) 6 CO 3. [8] The reaction of zinc with water is slowed by this passive layer. When this layer is corroded by acids such as hydrochloric acid and sulfuric acid, the reaction proceeds with the evolution of hydrogen gas. [1] [9] Zn + 2 H ...

  5. Standard electrode potential (data page) - Wikipedia

    en.wikipedia.org/wiki/Standard_electrode...

    Standard electrode potential (data page) The data below tabulates standard electrode potentials (E °), in volts relative to the standard hydrogen electrode (SHE), at: Temperature 298.15 K (25.00 °C; 77.00 °F); Effective concentration (activity) 1 mol/L for each aqueous or amalgamated (mercury-alloyed) species; Unit activity for each solvent ...

  6. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    RXNO:0000369. The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring. [1] Friedel–Crafts reactions are of two main types: alkylation reactions and acylation reactions. Both proceed by electrophilic aromatic substitution. [2][3][4][5]

  7. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    RXNO:0000170. In organic chemistry, the Schmidt reaction is an organic reaction in which an azide reacts with a carbonyl derivative, usually an aldehyde, ketone, or carboxylic acid, under acidic conditions to give an amine or amide, with expulsion of nitrogen. [1][2][3] It is named after Karl Friedrich Schmidt (1887–1971), who first reported ...

  8. Hydrolysis - Wikipedia

    en.wikipedia.org/wiki/Hydrolysis

    Hydrolysis (/ haɪˈdrɒlɪsɪs /; from Ancient Greek hydro- 'water' and lysis 'to unbind') is any chemical reaction in which a molecule of water breaks one or more chemical bonds. The term is used broadly for substitution, elimination, and solvation reactions in which water is the nucleophile. [ 1 ]

  9. Zinc - Wikipedia

    en.wikipedia.org/wiki/Zinc

    In aqueous solution an octahedral complex, [Zn(H 2 O) 6] 2+ is the predominant species. [51] The volatilization of zinc in combination with zinc chloride at temperatures above 285 °C indicates the formation of Zn 2 Cl 2, a zinc compound with a +1 oxidation state. [48] No compounds of zinc in positive oxidation states other than +1 or +2 are ...