The ionisation constant of phenol is higher than that of ethanol because
- phenoxide ion is a stronger base than that of ethoxide ion
- phenoxide ion is stabilized through delocalization
- phenoxide ion is less stable than ethoxide ion
- phenoxide ion is bulkier than ethoxide ion.Phenol
The Correct Option is B
Solution and Explanation
Note: Ionization constant (Ka) of phenol is more than that of ethanol indicates phenol is more acidic than alcohol. Phenol on ionization gives phenoxide ion it is stabilized by resonance.
Top Questions on Phenols
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- Phenolic group can be identified by a positive
- The product (X) obtained in the following reaction is:
Questions Asked in COMEDK UGET exam
A solid cylinder of mass 2 kg and radius 0.2 m is rotating about its own axis without friction with angular velocity 5 rad/s. A particle of mass 1 kg moving with a velocity of 5 m/s strikes the cylinder and sticks to it as shown in figure.
The angular velocity of the system after the particle sticks to it will be:- COMEDK UGET - 2024
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Concepts Used:
Phenols
Phenol is a different class of organic compounds that are usually found in wide usage in an extensive range of industries and also for domestic purposes. Phenol is formed when a hydrogen atom in a benzene molecule is replaced by the chemical -OH group.
Phenol is also called as Carbolic acid. It is an aromatic organic compound having the molecular formula C6H5OH. It is a volatile white crystalline solid. The molecule consists of a phenyl group (−C6H5) bonded to a hydroxy group (−OH). Phenol is mildly acidic, it requires careful handling because it can cause chemical burns.
Classification of Phenol
On the basis of the different number of hydroxyl groups attached, the phenols can be classified further into three types.
- Monohydric phenols: These contain one -OH group.
- Dihydric phenols: These contain two -OH groups. These may be ortho-, meta- or para- derivative.
- Trihydric phenols: These contain three -OH groups.
Properties of Phenol
- Phenol is an organic compound that is appreciably soluble in water, with about 84.2 g dissolving in 1000 mL (0.895 M).
- It is a weak acid.
- is highly reactive toward electrophilic aromatic substitution.