What is the chemical formula of Tribromophenol?
What is the chemical formula of Tribromophenol?
C6H3Br3O2,4,6-Tribromophenol / Formula
How do you make Tribromophenol?
Take 1 gm acetanilide in a beaker and dissolve it in 3.5 mL glacial acetic acid. Keep the beaker in an ice bath for 10 minutes. Now dropwise add 2.5 mL solution of bromine in acetic acid taken in test tube and stirr well. The color of mixture turns orange due to bromination reaction.
What is the common name for 2,4,6-tribromophenol?
2,4,6-Tribromophenol, also known as 2,4,6-TBP or bromol, belongs to the class of organic compounds known as p-bromophenols. These are bromophenols carrying a iodine at the C4 position of the benzene ring.
Which solvent is used in the preparation of 246 Tribromophenol?
A method of producing 2,4,6-tribromophenol by phenol bromination using a metal bromide salt, characterized in that the process is carried out under the action of hydrogen peroxide on a metal bromide salt in a sulfuric acid solution, where bromine is generated and regenerated from the resulting hydrobromic acid.
How do you convert phenol to Tribromophenol?
React Phenol with bromine ( Br ) in the presence of water ( H O ) or aqueous condition, 2,4,6-tribromophenol is formed . In aqueous conditions , more B is formed and more addition is taking place . 2,4,6-Tribromophenol (TBP) is used as a wood preservative and also as a fungicide.
What is the density of 2,4,6-tribromophenol?
2,4,6-Tribromophenol
| Common Name | 2,4,6-Tribromophenol | |
|---|---|---|
| Density | 2.4±0.1 g/cm3 | 286.8±0.0 °C at 760 mmHg |
| Molecular Formula | C6H3Br3O | 90-94 °C(lit.) |
| MSDS | Chinese USA | 109.7±25.9 °C |
| Symbol | GHS07, GHS09 | Warning |
What is the melting point of 2 4 6 Tribromophenol?
203.9°F (95.5°C)2,4,6-Tribromophenol / Melting point
Why does phenol give Tribromophenol on bromination with bromine water?
Phenol reacts with bromine water to give 2,4,6-tribromophenol. And Bromine ions are highly stabilized in ionic solvents.So the formation of strong o/p directing group and stabilization of Br+ enhances the formation of tribromophenol.
How is phenol converted to 2,4,6-tribromophenol explain with equation?
When concentrated nitric acid is added to phenol in the presence of sulphuric acid it gives 2, 4, 6-trinitrophenol.
What is the structure of 2,4,6-tribromophenol?
2,4,6-tribromophenol is a bromophenol that is phenol in which the hydrogens at positions 2, 4 and 6 have been replaced by bromines. It is commonly used as a fungicide and in the preparation of flame retardants. It has a role as an environmental contaminant, a fungicide and a marine metabolite.
Which of the following on reaction with bromine water will give 2,4,6-tribromophenol?
phenol
Therefore, the answer is – option (d) – When phenol is treated with excess bromine water, it gives 2,4,6-tribromophenol.
Why is phenol acidic than ethanol?
Phenoxide ion is aromatic and can undergo resonance but ethoxide ion can’t. Phenol is more acidic than that of ethanol because phenoxide ion is stabilized through delocalisation. An acid loses H+ ions in water. When phenol loses an H+ ion, the ion formed is known as phenoxide ion.
What is 2 4 6 tribromophenol used for?
2,4,6-tribromophenol is a bromophenol that is phenol in which the hydrogens at positions 2, 4 and 6 have been replaced by bromines. It is commonly used as a fungicide and in the preparation of flame retardants.
What does tribromophenol look like?
IDENTIFICATION: 2,4,6-Tribromophenol is a white to almost white crystalline powder with an acrid odor like phenol. 2,4,6-Tribromophenol is an intermediate in the synthesis of fire retardants.
What is a bromophenol used for?
A bromophenol that is phenol substituted by bromo groups at positions 2, 4 and 6. It is commonly used as a fungicide and in the preparation of flame retardants. ChEBI CHEBI:47696
What is a bromine based phenol?
A bromophenol that is phenol in which the hydrogens at positions 2, 4 and 6 have been replaced by bromines. It is commonly used as a fungicide and in the preparation of flame retardants. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:47696
