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In addition, bromine water is commonly used to test for the presence of an alkene which contains a double covalent bond, reacting with the bromine water, changing its color from an intense yellow to a colorless solution. Bromine water is also commonly used to check for the presence of an aldehyde group in compounds. In this reaction, the color ...
Bromothymol blue is synthesized by addition of elemental bromine to thymol blue in a solution in glacial acetic acid. [ 6 ] To prepare a solution for use as pH indicator, dissolve 0.10 g in 8.0 cm 3 N/50 (a.k.a. 0.02 Normal ) NaOH and dilute with water to 250 cm 3 .
Bromine was discovered independently by two chemists, Carl Jacob Löwig [13] and Antoine Balard, [14] [15] in 1825 and 1826, respectively. [16] Löwig isolated bromine from a mineral water spring from his hometown Bad Kreuznach in 1825. Löwig used a solution of the mineral salt saturated with chlorine and extracted the bromine with diethyl ...
Bromine readily reacts with water, i.e. it undergoes hydrolysis: Br 2 + H 2 O → HOBr + HBr. This forms hypobromous acid (HOBr), and hydrobromic acid (HBr in water). The solution is called "bromine water". The hydrolysis of bromine is more favorable in the presence of base, for example sodium hydroxide: Br 2 + NaOH → NaOBr + NaBr
The hypobromite ion, also called alkaline bromine water, is BrO −. Bromine is in the +1 oxidation state. The Br–O bond length is 1.82 Å. [1] Hypobromite is the bromine compound analogous to hypochlorites found in common bleaches, and in immune cells. In many ways, hypobromite functions in the same manner as hypochlorite, and is also used ...
Bromophenol is also used as a colour marker to monitor the process of agarose gel electrophoresis and polyacrylamide gel electrophoresis.Since bromophenol blue carries a slight negative charge at moderate pH, it will migrate in the same direction as DNA or protein in a gel; the rate at which it migrates varies according to gel density and buffer composition, but in a typical 1% agarose gel in ...