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Chromium(III) hydroxide is a gelatinous green inorganic compound with the chemical formula Cr(OH) 3. It is a polymer with an undefined structure and low solubility. It is amphoteric, dissolving in both strong alkalis and strong acids. [2] In alkali: Cr(OH) 3 + OH − → CrO − 2 + 2 H 2 O In acid: Cr(OH) 3 (OH 2) 3 + 3 H + → Cr(OH 2) 6 3+
The Pourbaix diagram for chromium in pure water, perchloric acid, or sodium hydroxide [1] [2] Chromium compounds are compounds containing the element chromium (Cr). Chromium is a member of group 6 of the transition metals. The +3 and +6 states occur most commonly within chromium compounds, followed by +2; charges of +1, +4 and +5 for chromium ...
A large number of chromium(III) compounds are known, such as chromium(III) nitrate, chromium(III) acetate, and chromium(III) oxide. [33] Chromium(III) can be obtained by dissolving elemental chromium in acids like hydrochloric acid or sulfuric acid, but it can also be formed through the reduction of chromium(VI) by cytochrome c7. [34] The Cr 3+
An amphiprotic molecule (or ion) can either donate or accept a proton, thus acting either as an acid or a base. Water , amino acids , hydrogencarbonate ion (or bicarbonate ion) HCO − 3 , dihydrogen phosphate ion H 2 PO − 4 , and hydrogensulfate ion (or bisulfate ion) HSO − 4 are common examples of amphiprotic species.
In acid solution the aquated Cr 3+ ion is produced. Cr 2 O 2− 7 + 14 H + + 6 e − → 2 Cr 3+ + 7 H 2 O ε 0 = 1.33 V. In alkaline solution chromium(III) hydroxide is produced. The redox potential shows that chromates are weaker oxidizing agent in alkaline solution than in acid solution. [6] CrO 2− 4 + 4 H 2 O + 3 e − → Cr(OH) 3 + 5 OH −
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.
A variety of other chromium(III) sulfates are known, but also contain hydroxide or oxide ligands. Most important commercially is basic chromium sulfate, which is thought to be [Cr 2 (H 2 O) 6 (OH) 4]SO 4 (CAS#39380-78-4). [2] It results from the partial neutralization of the hexahydrates. Other chromium(III) hydroxides have been reported. [3]
Solutions of metal aquo complexes are acidic owing to the ionization of protons from the water ligands. In dilute solution chromium(III) aquo complex has a pK a of about 4.3, affording a metal hydroxo complex: [Cr(H 2 O) 6] 3+ ⇌ [Cr(H 2 O) 5 (OH)] 2+ + H + Thus, the aquo ion is a weak acid, of comparable strength to acetic acid (pK a of about ...