An unshielded hydrogen nucleus covalently bound to an electron-withdrawing oxygen or nitrogen atom can interact with an unshared electron pair on another oxygen or nitrogen atom to form a hydrogen bond. Since water molecules contain both of these features, hydrogen bonding favors the self-association of water molecules into ordered arrays. Hydrogen bonding profoundly influences the physical properties of
water and accounts for its exceptionally high viscosity, surface tension, and boiling point. On average, each molecule in liquid water associates through hydrogen bonds with 3.5 others. These bonds are both relatively weak and transient, with a half-life of about one microsecond. Rupture of a hydrogen bond in liquid water requires only about 4.5 kcal/mol, less than 5% of the energy required to rupture a covalent O-H bond.
Hydrogen bonding enables water to dissolve many organic biomolecules that contain functional groups
which can participate in hydrogen bonding. The oxygen atoms of aldehydes, ketones, and amides provide
pairs of electrons that can serve as hydrogen acceptors. Alcohols and amines can serve both as hydrogen acceptors and as donors of unshielded hydrogen atoms for formation of hydrogen bonds.
water and accounts for its exceptionally high viscosity, surface tension, and boiling point. On average, each molecule in liquid water associates through hydrogen bonds with 3.5 others. These bonds are both relatively weak and transient, with a half-life of about one microsecond. Rupture of a hydrogen bond in liquid water requires only about 4.5 kcal/mol, less than 5% of the energy required to rupture a covalent O-H bond.
Hydrogen bonding enables water to dissolve many organic biomolecules that contain functional groups
which can participate in hydrogen bonding. The oxygen atoms of aldehydes, ketones, and amides provide
pairs of electrons that can serve as hydrogen acceptors. Alcohols and amines can serve both as hydrogen acceptors and as donors of unshielded hydrogen atoms for formation of hydrogen bonds.
