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Basic copper carbonate is a chemical compound, more properly called copper(II) carbonate hydroxide.It can be classified as a coordination polymer or a salt.It consists of copper(II) bonded to carbonate and hydroxide with formula Cu 2 (CO 3)(OH) 2.
2 mixture by knowing the partial pressure of each species and the value of K eq. For instance, in a high temperature reducing environment, such as that created for the reduction of iron oxide in a blast furnace or the preparation of carburizing atmospheres, [ 5 ] carbon monoxide is the stable oxide of carbon.
2 fe(co) 5 + c 10 h 12 → (η 5-c 5 h 5) 2 fe 2 (co) 4 + 6 co + h 2 In this preparation, dicyclopentadiene cracks to give cyclopentadiene, which reacts with Fe(CO) 5 with loss of CO . Thereafter, the pathways for the photochemical and thermal routes differ subtly but both entail formation of a hydride intermediate. [ 5 ]
Structure of [Co 2 (OH 2) 10] 4+ color code: red = O, white = H, blue = Co. In the binuclear ion [Co 2 (OH 2 ) 10 ] 4+ each bridging water molecule donates one pair of electrons to one cobalt ion and another pair to the other cobalt ion.
Paul Sabatier (1854-1941) winner of the Nobel Prize in Chemistry in 1912 and discoverer of the reaction in 1897. The Sabatier reaction or Sabatier process produces methane and water from a reaction of hydrogen with carbon dioxide at elevated temperatures (optimally 300–400 °C) and pressures (perhaps 3 MPa [1]) in the presence of a nickel catalyst.
The mineral of the formula Cu(OH) 2 is called spertiniite. Copper(II) hydroxide is rarely found as an uncombined mineral because it slowly reacts with carbon dioxide from the atmosphere to form a basic copper(II) carbonate. Thus copper(II) hydroxide slowly acquires a dull green coating in moist air by the reaction: 2 Cu(OH) 2 + CO 2 → Cu 2 CO ...
Cobalt(II) hydroxide precipitates as a solid when an alkali metal hydroxide is added to an aqueous solution of Co 2+ salt. [4] For example, Co 2+ + 2 NaOH → Co(OH) 2 + 2 Na + The compound can be prepared by reacting cobalt(II) nitrate in water with a solution of triethylamine N(C 2 H 5) 3 as both the base and a complexing agent. [3]
The compound can be prepared by treating nickel or nickel(II) carbonate with acetic acid: . NiCO 3 + 2 CH 3 CO 2 H + 3 H 2 O → Ni(CH 3 CO 2) 2 ·4 H 2 O + CO 2. The mint-green tetrahydrate has been shown by X-ray crystallography to adopt an octahedral structure, the central nickel centre being coordinated by four water molecules and two acetate ligands. [5]