Intermolecular Hydrogen Bond
Intermolecular Hydrogen Bond
Intermolecular Hydrogen Bond
The H-bond formed between two different molecules (of same or different compounds) is
referred to as intermolecular H-bond. In this case, hydrogen of one molecule makes H-bond with
electronegative atom of another molecule. These molecules may belong to same compound or
different compounds.
E.g.
Note: In above diagrams, directional nature of H-bonding is not taken into account.
Consequences of intermolecular hydrogen bonding
1) The boiling point, melting point, sublimation point as well as enthalpy of vaporization of
compounds increase due to intermolecular H-bonding.
E.g. The boiling point of H
2
O is high (373 K) due to intermolecular hydrogen bonding and
hence it exist as liquid at room temperature, whereas H-bonds are absent in H
2
S and hence it has
low boiling point and exists as a gas at room temperature.
Note: Though sulfur is an electronegative element, it cannot form hydrogen bonds due to
larger size. There is no ample charge density on either sulfur or hydrogen to make a H-bond.
2) The solubility of compounds, showing intermolecular H-bonding, in water increases due to
formation of intermolecular H-bonds with water.
E.g. Ethyl alcohol, methyl alcohol, ammonia, HF, acetic acid etc., are fairly soluble in water
due to their ability to form intermolecular hydrogen bonds with water molecules.
Intermolecular H-bonding between water and ammonia molecules is shown below.
3) Due to intermolecular H-bonding, para isomers have higher boiling points and are fairly
soluble in water. Therefore they cannot be separated by steam distillation.
E.g. Para hydroxy benzaldehyde has high boiling point and is more soluble in water, than its
ortho isomer, due to intermolecular H-bonding and hence cannot be separated by steam
distillation.
4) Some molecules exist as dimers or trimers or polymers in non-aqueous medium or in vapor
state due to strong intermolecular H-bonding.
E.g. Acetic acid exists as dimer in benzene.