--%>

Explain alcohols and phenols in organic chemistry.

Alcohols and phenols are the compounds containing one or more hydroxyl groups (- OH). The alcohols contain the -OH group attached to alkyl group whereas in phenols, the -OH group is attached to aromatic ring. These are classified as mono-, di- and trihydric alcohols or phenols according to the number of -OH groups contained in their molecules. Some examples of mono-, di- and trihydric alcohols and phenols are as follows:

    Alcohols

2399_alcohol and phenol.png 

It may be noted that the aromatic compounds in which -OH group is not directly attached to benzene ring are not phenols but are called aromatic alcohols. These may also be called as aryl derivatives of aliphatic alcohols. When four or more hydroxyl groups are present, they are called polyhydric alcohols or polyhydric phenols.

Monohydric alcohols may be further classified according to the hybrid state of the carbon atom to which the -OH group is attached.
    
Compounds containing Csp3 ) -OH bond

In this type of alcohols, the -OH group is attached to a sp3 hybridised carbon atom. They are further classify as follows:

Primary (1°), secondary (2°) and tertiary (3°) alcohols

Monohydric alcohols are classified as primary, secondary or tertiary alcohols depending upon whether the hydroxyl group is attached to a primary, secondary or tertiary carbon atom. For instance,

1240_alcohol and phenol1.png 

Allylic alcohols: in allylic alcohols, the -OH group is attached to a sp3-hybridised carbon next to the carbon-carbon double bond, that is to an allylic carbon. For instance,

2066_alcohol and phenol2.png 

Benzylic alcohols: in benzlylic alcohols, the -OH group is attached to a sp3 -hybridised carbon atom next to an aromatic ring. Allylic and benzylic alcohols can be secondary, primary or tertiary.
    
Compounds containing Csp3 )-OH bond:

These alcohols include -OH group bonded to a carbon-carbon double bond i.e. to a vinylic carbon or to an aryl carbon. For example, vinylic alcohols and phenols belong to this class of compounds.

   Related Questions in Chemistry

  • Q : Net charge of a non-ionized atom

    Describe the net charge of a non-ionized atom?

  • Q : Molar concentration of hydrogen 20 g of

    20 g of hydrogen is present in 5 litre of vessel. Determine he molar concentration of hydrogen: (a) 4  (b) 1 (c) 3 (d) 2 Choose the right answer from above.

  • Q : Moles of HCl present in .70 L of a .33

    Detail the moles of HCl which are present in .70 L of a .33 M HCl solution?

  • Q : Problem on decomposition reaction

    Nitrogen tetroxide (melting point: -11.2°C, normal boiling point 21.15°C) decomposes into nitrogen dioxide according to the following reaction: N2O4(g) ↔ 2 NO2(g)<

  • Q : Molarity based question Help me to

    Help me to solve this problem. 4.0 gm of NaOH are contained in one decilitre of solution. Its molarity would be: (a) 4 M (b)2 M (c)1 M (d)1.5 M

  • Q : Reducible Representations The number of

    The number of times each irreducible representation occurs in a reducible representation can be calculated.Consider the C2v point group as described or Appendix C. you can see that (1) sum of

  • Q : Molecular Diameters The excluded volume

    The excluded volume b, introduced by vander Wall's as an empirical correction term, can be related to the size gas molecules. To do so, we assume the excluded volume is the result of the pairwise coming together of molecules. This assumption is justified when b values

  • Q : Mole fraction of hydrogen Give me

    Give me answer of this question. In a mixture of 1 gm H2 and 8 gm O2 , the mole fraction of hydrogen is: (a) 0.667 (b) 0.5 (c) 0.33 (d) None of these

  • Q : Solutions The relative lowering of

    The relative lowering of vapour pressure of 0.2 molal solution in which solvent is benzene

  • Q : Relationship between free energy and

    The free energy of a gas depends on the pressure that confines the gas. The standard free energies of formation, like those allow predictions to be made of the possibility of a reaction at 25°C for each reagent at