Cause's cancer as the shape is just right to fit in the major grove of DNA. Journal of Hazardous Materials
Volume 155, Issues 1-2, 30 June 2008, Pages 83-89
First line in absract - "Phenol is a carcinogen" the article discusses a new technique for its removal from waste water. American Conference of Governmental Industrial Hygienists Standards (ACGIH) Manual, 2005, and United States Environmental Protection Agency, EPA, 816-F-01-007, 2006. EPA state phenol is a carcinogen....
Answer:
Phenol can:
* corrode skin and tissue (cause chemical burns) * is poisonous when ingested or injectd or through dermal exposure * EPA at one time had classified phenol as a Group D, "not classifiable as a human carcinogen "based on a lack of data concerning carcinogenic effects in humans * (in controlled amounts) be used for its antibiotic properties in throat lozenges
When an Elodea leaf is added to a phenol red solution, the leaf will release oxygen through photosynthesis. The oxygen will cause the phenol red solution to change color, indicating the presence of oxygen production.
Phenol should always be stored in a closed container. If it overheats it could build pressure causing it to explode. It could also produce toxic or irritating fumes.
After recovering from a phenol drink, it is advisable to stick to a bland and easily digestible diet. This can include items like plain rice, toast, boiled potatoes, cooked vegetables, yogurt, and fruits. Avoid spicy, acidic, or hard-to-digest foods to allow your stomach to fully recover.
The derivative of Phenol is Carbolic acid.
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
tribromophenol is formed.
tribromophenol is formed.
In the reaction between phenol and sodium metal, sodium donates an electron to the oxygen atom in the phenol molecule, forming a sodium phenoxide salt and hydrogen gas. This process is a type of redox reaction where the sodium is oxidized and the phenol is reduced.
When an Elodea leaf is added to a phenol red solution, the leaf will release oxygen through photosynthesis. The oxygen will cause the phenol red solution to change color, indicating the presence of oxygen production.
Phenol should always be stored in a closed container. If it overheats it could build pressure causing it to explode. It could also produce toxic or irritating fumes.
When phenol is treated with sodium borohydride, a reduction reaction occurs and the oxygen atom in the hydroxyl group of phenol gets reduced to a hydroxide ion. This reaction usually leads to the formation of cyclohexanol as the main product.
phenol
When sodium phenoxide is reacted with CO2 and HCl, the phenoxide anion is protonated by HCl to form phenol. The phenol then reacts with CO2 to form salicylic acid.
Chemically, the major difference between phenol and alcohol is that phenol is a hydroxyl unit attached to a benzene ring and alcohol has a hydroxyl unit attached to a carbon chain. More generally the major difference is that swallowing a small amount of phenol can kill you. Swallowing a small amount of alcohol (ethanol) may give you a buzz, but you would have to drink a great deal for it to kill you quickly.
After recovering from a phenol drink, it is advisable to stick to a bland and easily digestible diet. This can include items like plain rice, toast, boiled potatoes, cooked vegetables, yogurt, and fruits. Avoid spicy, acidic, or hard-to-digest foods to allow your stomach to fully recover.
In the reaction between phenol and sodium hydroxide, the phenol is deprotonated by the base, forming the phenolate ion. This reaction is an acid-base reaction where phenol acts as an acid and donates a proton to form water. The products of the reaction are the phenolate ion and water.
The derivative of Phenol is Carbolic acid.