Yes an aliphatic hydrocarbon chain with an OH group on is called an alcohol - if it is an aromatic hydrocarbon it can often be called a phenol
alcohol homologous series OH is the functional group of ethanol
There are two functional groups: 1. Carboxyl group 2. Ester group
Phenol is an aromatic alcohol, i.e. it has the alcohol functional group (-OH) attached to a benzene ring. It is also known as carbolic acid, and was the first antiseptic. Alcohol can be any of a large number of compounds that contain the -OH group bonded to a carbon atom. The most common, and often just referred to as "alcohol" is ethyl alcohol, which is CH3CH2OH.
because, phenol it self neucleophilic group.
the functional group of thymol is phenol because it got an OH group connected to aromatic ring (AR-OH)
Yes an aliphatic hydrocarbon chain with an OH group on is called an alcohol - if it is an aromatic hydrocarbon it can often be called a phenol
A benzenol is another term for a phenol - any of a class of aromatic organic compounds having at least one hydroxyl group attached directly to the benzene ring.
alcohol homologous series OH is the functional group of ethanol
There are two functional groups: 1. Carboxyl group 2. Ester group
Phenol is an aromatic alcohol, i.e. it has the alcohol functional group (-OH) attached to a benzene ring. It is also known as carbolic acid, and was the first antiseptic. Alcohol can be any of a large number of compounds that contain the -OH group bonded to a carbon atom. The most common, and often just referred to as "alcohol" is ethyl alcohol, which is CH3CH2OH.
because, phenol it self neucleophilic group.
Yes,phenol is an alcohol.It contains a benzene ring and a hydoxile group.
phenol is more acidic because of the benzene ring present in the molecule,when you lose the H form the OH group it is possible to delocalise the charge around the aromatic system due to the pi electron cloud,straight chain alcohols cannot do this so it is less favourable to deprotonate them hance it is easier to deprotonate a phenol,hence we say it is more acidic
The nitration of phenol is more rapid than that of toluene.
Because the -OH group present in phenol is more ring activating than -OCH3 group in anisole.
Phenol does not undergo nucleophilic substitution for several reasons: phenol is a relatively stable compound, OH on its own is not one of the best leaving groups, and the aromatic ring does provides an extremely high energy barrier which prevents the initiation of either the SN1 or SN2 substitution mechanisms under normal conditions. When looking at the keto-enol tautomerization resonance forms, the enolate is the major contributor due to the aromatic stabilization. In order to substitute in place of the phenol, the hydroxy group needs to be converted to a better leaving group such as a Toluenesulfonate ester. It is possible to acylate phenols to form other compounds such as aspirin (o-Acetylsalicylic acid). It is alos possible to form aryl ethers with phenols. Benzediols (quinones) can be readily oxidized, allowing even more chemistry to be done to the aromatic system.