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For example, sulfuric acid (H 2 SO 4) is a diprotic acid. Since only 0.5 mol of H 2 SO 4 are needed to neutralize 1 mol of OH −, the equivalence factor is: f eq (H 2 SO 4) = 0.5. If the concentration of a sulfuric acid solution is c(H 2 SO 4) = 1 mol/L, then its normality is 2 N. It can also be called a "2 normal" solution.
For example, dissolution of iron ores in hydrochloric acid gives a mixture of ferrous and ferric chlorides: [4] Fe 3 O 4 + 8 HCl → FeCl 2 + 2 FeCl 3 + 4 H 2 O. The iron(II) chloride is converted to the iron(III) derivative by treatment with oxygen and hydrochloric acid: 4 FeCl 2 + O 2 + 4 HCl → 4 FeCl 3 + 2 H 2 O
At room temperature, it is a colorless gas, which forms white fumes of hydrochloric acid upon contact with atmospheric water vapor. Hydrogen chloride gas and hydrochloric acid are important in technology and industry. Hydrochloric acid, the aqueous solution of hydrogen chloride, is also commonly given the formula HCl.
When a strong acid is dissolved in water, it reacts with it to form hydronium ion (H 3 O +). [2] An example of this would be the following reaction, where "HA" is the strong acid: HA + H 2 O → A − + H 3 O + Any acid that is stronger than H 3 O + reacts with H 2 O to form H 3 O +. Therefore, no acid stronger than H 3 O + exists in H 2 O.
In a paper published in 1894, it was formally proposed to add chlorine to water to render it "germ-free". Two other authorities endorsed this proposal and published it in many other papers in 1895. [4] Early attempts at implementing water chlorination at a water treatment plant were made in 1893 in Hamburg, Germany.
Heavy water, D 2 O, self-ionizes less than normal water, H 2 O; D 2 O + D 2 O ⇌ D 3 O + + OD −. This is due to the equilibrium isotope effect, a quantum mechanical effect attributed to oxygen forming a slightly stronger bond to deuterium because the larger mass of deuterium results in a lower zero-point energy.
2 NaCl + 2 H 2 O → 2 NaOH + H 2 + Cl 2. Without a membrane, the OH − ions produced at the cathode are free to diffuse throughout the electrolyte. As the electrolyte becomes more basic due to the production of OH −, less Cl 2 emerges from the solution as it begins to disproportionate to form chloride and hypochlorite ions at the anode:
Sodium chlorate can be used with hydrochloric acid (or also sulfuric acid and sodium chloride, the reaction of which generates HCl) to chlorinate aromatic compounds without the use of organic solvents. In this case its function is to oxidize the HCl to obtain either HOCl or Cl 2 (depending upon the pH) in-situ which are the active chlorinating ...