

Bromine Water 1 liter
KSh1,750.00 Original price was: KSh1,750.00.KSh1,600.00Current price is: KSh1,600.00.
Bromine water is a solution of bromine (Brā) in water. It is a reactive and strong oxidizing agent used primarily in chemical analysis and organic chemistry. Here are some key points about bromine water:
Properties
- Appearance: It has a reddish-brown color due to the presence of bromine.
- Odor: It has a strong, unpleasant smell similar to chlorine.
- Solubility: Bromine is only slightly soluble in water but dissolves better in organic solvents.
Uses of Bromine Water
1. Testing for Unsaturation in Organic Compounds
Bromine water is widely used to test for the presence of unsaturated compounds (alkenes and alkynes). When added to an unsaturated compound, the bromine adds across the double or triple bonds, leading to the decolorization of the bromine water.
- Example Reaction: C2H4(ethene)+Br2āC2H4Br2(1,2-dibromoethane)text{C}_2text{H}_4 (text{ethene}) + text{Br}_2 rightarrow text{C}_2text{H}_4text{Br}_2 (text{1,2-dibromoethane})C2āH4ā(ethene)+Br2āāC2āH4āBr2ā(1,2-dibromoethane)
2. Detection of Phenols
Phenols react with bromine water to form a white precipitate of 2,4,6-tribromophenol, indicating the presence of a phenolic group.
- Example Reaction: C6H5OH(phenol)+3Br2āC6H2Br3OH(2,4,6-tribromophenol)+3HBrtext{C}_6text{H}_5text{OH} (text{phenol}) + 3text{Br}_2 rightarrow text{C}_6text{H}_2text{Br}_3text{OH} (text{2,4,6-tribromophenol}) + 3text{HBr}C6āH5āOH(phenol)+3Br2āāC6āH2āBr3āOH(2,4,6-tribromophenol)+3HBr
3. Oxidation Reactions
Bromine water can oxidize certain functional groups in organic compounds, such as converting aldehydes to carboxylic acids.
- Example Reaction: RCHO(aldehyde)+Br2+H2OāRCOOH(carboxylic acid)+2HBrtext{RCHO} (text{aldehyde}) + text{Br}_2 + text{H}_2text{O} rightarrow text{RCOOH} (text{carboxylic acid}) + 2text{HBr}RCHO(aldehyde)+Br2ā+H2āOāRCOOH(carboxylic acid)+2HBr
4. Identification of Aliphatic Amines
Primary and secondary aliphatic amines can be distinguished from tertiary amines using bromine water. Primary and secondary amines react with bromine to form N-bromoamines, while tertiary amines do not react.
5. Detection of Aniline and Its Derivatives
Aniline and its derivatives react with bromine water to form a precipitate of 2,4,6-tribromoaniline, which is a useful test for identifying these compounds.
- Example Reaction: C6H5NH2(aniline)+3Br2āC6H2Br3NH2(2,4,6-tribromoaniline)+3HBrtext{C}_6text{H}_5text{NH}_2 (text{aniline}) + 3text{Br}_2 rightarrow text{C}_6text{H}_2text{Br}_3text{NH}_2 (text{2,4,6-tribromoaniline}) + 3text{HBr}C6āH5āNH2ā(aniline)+3Br2āāC6āH2āBr3āNH2ā(2,4,6-tribromoaniline)+3HBr
6. Bleaching and Disinfection
Due to its strong oxidizing properties, bromine water can be used for bleaching certain substances and as a disinfectant in laboratory settings.
7. Analytical Chemistry
Bromine water is used in various qualitative and quantitative analyses to identify and measure specific organic and inorganic substances.
Related products
2 Propanol 2.5 litres (IPA)
Acetaldehyde
- Chemical Structure: Acetaldehyde consists of two carbon atoms, one oxygen atom, and four hydrogen atoms. Its structure is CH3CHO, where the carbon atom in the middle is doubly bonded to an oxygen atom and singly bonded to a hydrogen atom and a methyl group (CH3).
- Occurrence: Acetaldehyde can be found naturally in various ripe fruits, coffee, and heated milk. It is also produced by the oxidation of ethanol (alcohol) by enzymes in the liver and other tissues in humans, making it an intermediate product in alcohol metabolism.
Aluminum Fine Powder
Aluminum Oxide 500 grams
Ammonia Acetate
Properties
- Chemical Formula: NH4C2H3O2
- Molecular Weight: 77.08 g/mol
- Appearance: White, crystalline solid
- Solubility: Highly soluble in water
- Melting Point: Decomposes upon heating
Reviews
There are no reviews yet.