it is used for cleansing dental denture. that's all what i know
Cyclohexene and cyclohexane are both insoluble in water and bases. Cyclohexene is insoluble in weak acids and soluble in strong acids and is thus considered a neutral compound. Cyclohexane is insoluble in everything, and is considered an inert compound.
Phenol is soluble in sodium bicarbonate because it reacts with the bicarbonate ions present in the solution to form a water-soluble salt, sodium phenoxide, which is highly soluble in water. This reaction converts the non-polar phenol molecule into a highly soluble ionic compound.
Sodium phenoxide ion is more soluble in water than phenol. This is because sodium phenoxide ion is an ionic compound, which dissociates into ions in water and forms interactions with water molecules, increasing its solubility compared to the non-ionic phenol molecule.
When bromine reacts with phenol, it undergoes electrophilic aromatic substitution to brominate the aromatic ring. The reaction takes place under mild conditions without a catalyst, and the product formed is a bromophenol compound.
Phenol + 3Br2 = 2,4,6-tribromophenol + 3HBr Everything you need to know :) http://www.chemguide.co.uk/organicprops/phenol/ring.html
Trifluoperazine is a synthetic compound.
Phenol and carbolic acid are actually the same compound. "Carbolic acid" is an older, colloquial term for phenol.
The type of bond that the compound phenol salicylate has is a covalent bond. It is created by heating phenol and salicylic acid together.
Cresol is a derivative of phenol. It is an organic compound with a similar structure to phenol, but with a methyl group attached to the benzene ring.
Phenol is an aromatic compound found in creosote and coal tar. It is used in the production of various chemicals, including plastics, pharmaceuticals, and disinfectants. Phenol is also known for its antiseptic properties.
Phenol is an organic compound. It is composed of a benzene ring with a hydroxyl group attached, making it an organic compound due to its carbon-containing structure.
The empirical formula for phenol is C6H5OH, which represents the simplest whole-number ratio of atoms present in the compound.
The phenol coefficient is a measure used to evaluate the disinfecting power of a chemical compared to phenol. It is determined by comparing the dilution of a test compound that achieves a specific level of microbial kill to that of phenol under identical conditions. A phenol coefficient greater than 1 indicates that the test compound is more effective than phenol, while a coefficient less than 1 indicates lower effectiveness. This metric helps in assessing the potency of disinfectants in microbiological applications.
Phenolphthalein is made up of, H20, C14, O4,
Phenol is not miscible in silicone oil. Phenol is a polar compound, while silicone oil is nonpolar. This difference in polarity makes them immiscible in each other.
The compound formed by the combination of benzene and alcohol is named as phenol.
The conjugate base of phenol is phenolate. Phenol is a weak acid, but when it loses a proton to become phenolate, it forms a stable negative charge, making it more stable and less likely to accept a proton back. This stability increases the acidity of phenol.