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in the presence of con.h2so4 anisole will convert into phenol and hi

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Is phenol a hydrocarbon?

No, phenol is not a hydrocarbon. It is an aromatic compound that contains a hydroxyl group (-OH) attached to a benzene ring, making it an alcohol. While it has a hydrocarbon structure due to its benzene component, the presence of the hydroxyl group classifies it as a phenolic compound rather than a simple hydrocarbon.


Why acylation occur at phenol rather than carboxylic acid in salicylic acid?

Acylation occurs at the phenol group in salicylic acid due to the higher reactivity of the phenol hydroxyl group compared to the carboxylic acid group. The phenol group is more nucleophilic and readily reacts with acetyl chloride to form acetylsalicylic acid (aspirin). Additionally, the carboxylic acid group can interfere with the reaction due to its ability to form hydrogen bonds, making it less reactive towards acylation.


How do you separate fluorenone and anisole?

Since they have different boiling points ( that differ by more than 50 degrees C) you can use fractional distillation ( or simple distillation) where you boil one compound out ( leting the vapors condense into a certain container and then collect the condensed vapors of the second compound (fluornene in this case) ... note: that the first vapors are [mostly] comming from the compound with a lower boiling point.


What are the ingredients of photosenthesis?

Photosynthesis is the process where plants convert sunlight into energy (in very simple terms). There are not ingredients.


What simple experiment can be used to determine if a liquid compound contains polar molecules?

Thin Layer Chromatography (TLC) procedure can be used

Related Questions

How will you synthesis of phenol in small scale'?

There are many known syntheses of phenol. However, a few simple ones are: 1) hydrolysis of chlorobenzene: - chlorobenzene + water --> phenol + hydrochloric acid 2) oxidation of toluene: - toluene + oxygen --> phenol + carbon dioxide + water 3) oxidation of benzene with nitrous oxide: - benzene + nitrous oxide --> phenol + nitrogen


How Differentiate phenol and chloroform layer?

To differentiate between phenol and chloroform layers, you can carry out a simple test by adding a few drops of water to the layers. Phenol is water-soluble and will mix with the water, turning the solution into a cloudy emulsion. Chloroform, on the other hand, is insoluble in water and will remain as a distinct layer separate from the water-phenol emulsion.


What is simple procedure?

unraavel


How many atoms of each element are present in one molecule of phenol?

Simple phenol is mono hydroxy benzene and has the formula, C6H5OH So there are six carbon, six oxygen and one oxygen present in a molecule of phenol.


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What are the differences between phenyl and phenol, and how do they affect the properties and reactivity of organic compounds?

Phenyl is a hydrocarbon group with a benzene ring, while phenol is a hydroxyl group attached to a benzene ring. Phenol is more reactive due to the presence of the hydroxyl group, which can participate in hydrogen bonding and other reactions. Phenyl, being a simple hydrocarbon group, is less reactive in comparison. The presence of the hydroxyl group in phenol can also affect the solubility and acidity of organic compounds.


Does a simple vaginal tightning procedure can cause bleeding on wedding night?

A simple vaginal tightening procedure causes the diameter of the vagina to be smaller. Depending on the size of the man, this can cause a tear.


What is chemical content of material for Backalite?

Bakelite is based on the thermosetting phenol formaldehyde resin polyoxybenzylmethylenglycolanhydride, developed in 1907–1909 by Belgian Dr. Leo Baekeland, formed by the reaction under heat and pressure of phenol (a toxic, colourless crystalline solid) and formaldehyde (a simple organic compound).


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