BIOCHEM2027 Specialised Subject · 2.1
2027 · High School Specialised Subject · Biochemistry

2.1 Weak Interactions in Aqueous Solutions

Hydrogen bonds, the hydrophobic effect, colligative properties

Hydrogen bonding and electrostatics, entropy of dissolution, the hydrophobic effect, van der Waals contacts, and how weak interactions together stabilise macromolecules and set colligative properties.

10 SECTIONS19 FIGURESEnglish edition
01

Hydrogen bonding gives water its unusual properties

  • Two O–H bonds at about 104.5° give a bent, strongly dipolar molecule
  • Each water can donate two hydrogen bonds and accept two, forming a dynamic network
  • Consequences: high boiling point, high surface tension, high heat capacity, open ice lattice
02

Water hydrogen-bonds with polar solutes

  • Hydration shells surround hydroxyl, amino and carbonyl groups
  • Sugars, amino acids and short peptides dissolve because hydration compensates for lost crystal contacts
  • Directionality of hydrogen bonds makes recognition specific rather than merely tight
03

Water interacts electrostatically with charged solutes

  • Ion–dipole orientation: cations attract oxygen lone pairs, anions attract hydrogens
  • Solvation shells screen charge–charge attraction
  • Dielectric constant of water near 78 at 25 °C weakens salt bridges compared with vacuum
04

Dissolution of crystalline solids increases entropy

  • A crystal has few accessible arrangements; a solution has many
  • The entropy gain of dispersal offsets part of the lattice enthalpy
  • ΔG = ΔH − TΔS decides whether dissolution is favourable
05

Nonpolar gases are poorly soluble in water

  • Cavity formation costs energy that a nonpolar solute cannot repay
  • Water around a nonpolar surface becomes more ordered: an entropic cost
  • Gas solubility falls with rising temperature, so warm water holds less oxygen
06

Nonpolar compounds disturb the structure of water

  • Nonpolar groups cluster to minimise the ordered water surface around them
  • Driving force is the entropy gained by released water, not attraction between nonpolar groups
  • Underlies bilayer formation, protein cores, micelles and ligand binding
07

Van der Waals interactions are weak attractions between atoms

  • Fluctuating dipoles induce dipoles in neighbouring atoms
  • Attractive as 1/r⁶ with strong short-range repulsion; optimum at contact distance
  • 0.4–4 kJ/mol per contact, but hundreds act together across a complementary surface
08

Weak interactions appear together in many combinations

  • An interface typically combines hydrogen bonds, ion pairs, hydrophobic contacts and packing
  • Individually weak energies sum to tens of kJ/mol for a well-matched surface
  • Geometry requirements create specificity; weak bonds allow reversible assembly
09

Weak interactions are central to macromolecular structure and function

  • Protein folding: hydrophobic core, backbone hydrogen bonds, side-chain packing
  • Nucleic acids: base pairing plus base stacking
  • Membranes, enzyme recognition, hormone–receptor binding and allostery all use this toolkit
10

Solutes affect the colligative properties of aqueous solutions

  • Osmotic pressure, boiling-point elevation, freezing-point depression depend on particle number
  • π = iMRT for dilute ideal solutions
  • Cells regulate osmolarity to control water movement
  • ΔTf = i·Kf·m underlies biological antifreeze strategies
참조 자료
본문의 참조 표시를 누르면 이 창에서 원문 그림·표를 크게 볼 수 있습니다.