Solubility of Ionic & Molecular Compounds (College Board AP® Chemistry): Revision Note

Martín

Written by: Martín

Reviewed by: Stewart Hird

Updated on

Solubility of Ionic & Molecular Compounds

  • The solubility of two substances depends on their intermolecular interactions

  • Ions and molecules can exhibit can exhibit the following interactions:

Relative strength comparison between the intermolecular interactions

Interaction

Relative strength

Ion-dipole

Strongest

Hydrogen bonding

 

Dipole-dipole

 

London dispersion forces

Weakest

  • A solution is made from two components a solvent and a solute

  • In a solution system, intermolecular interactions exist in three possible scenarios:

    • Solvent–solute, i.e. solvent particles with solute particles

    • Solvent–solvent, i.e. solvent particles with themselves

    • Solute–solute, i.e. solute particles with themselves

When does a solution form?

  • Substances with similar intermolecular interactions tend to be miscible or soluble in one another, because the solute–solvent attractions can replace the solute–solute and solvent–solvent attractions

    • Two liquids that mix completely in all proportions are miscible; a solid that dissolves in a liquid is soluble

    • E.g. ethanol and water molecules hydrogen bond to each other, so ethanol and water are miscible

  • When the solvent-solvent interaction and the solute-solute interaction are not equal, the strength of the solvent-solute interaction must be considered

The three interactions between the particles of solute and solvent

Beaker of mixed solvent (blue) and solute (pink) particles beside two solvent and two solute particles joined by dashed lines labeled solvent–solvent, solute–solute and solvent–solute.

Solvent-solvent, solvent-solute and solute-solute interactions must be considered for solubility

  • A solution is formed when the solvent-solute interactions are stronger than the solvent-solvent interactions

    • E.g. Salt and water present ion-dipole interactions. Water molecules present hydrogen bonding between themselves

ion-dipole > hydrogen bonding

  • Therefore, they are miscible in one another

  • A solution is unlikely to form when the solute–solvent attractions are much weaker than the solvent–solvent attractions they would have to replace

    • E.g. the weak attractions between hexane and water molecules cannot replace the hydrogen bonds between water molecules

  • Therefore, they are not miscible in one another

  • The rules of solution formation are summarized in the table below

Rules of Solution Formation by comparing the intermolecular interactions strengths

Comparison of the strength between intermolecular interactions

Solution formed?

Solvent-solute = Solvent-solvent

Yes

Solvent-solute > Solvent-solvent

Yes

Solvent-solute < Solvent-solvent

May or may not form

Examiner Tips and Tricks

  • Explain solubility using the attractions between solute and solvent particles. Describing only the forces in the pure solute or the pure solvent does not earn credit

  • When a molecular solute such as ethanol dissolves, its molecules separate: no covalent bonds break and no ions form

Worked Example

Predict if a solution will be formed when chloroform is mixed with an acetone solvent.

Displayed formulas of acetone, CH3COCH3, with a C=O double bond, and chloroform, CHCl3, drawn with wedge and dash bonds.

Answer:

Step 1 (Optional): Draw the molecular structure of the solvent molecules and the solute molecules. This step is not applicable to ions since they exist as lattice structures

Step 2: Identify the solvent-solvent intermolecular interactions

  • Acetone is the solvent. Since oxygen is more electronegative than carbon, a dipole moment will be formed

Two acetone molecules with delta minus on oxygen and delta plus on the carbonyl carbon, joined by a dashed line labeled dipole–dipole.
  • Therefore, acetone molecules attract each other through dipole–dipole forces in addition to London dispersion forces

Step 3: Identify the solute-solute intermolecular interactions

  • Chloroform is the solute. Since it is a non-symmetrical molecule and chlorine is more electronegative than carbon, dipole moments will be formed

Two chloroform molecules with delta plus on carbon and delta minus on each chlorine, joined by dashed lines labeled dipole–dipole.
  • Therefore, chloroform molecules attract each other through dipole–dipole forces in addition to London dispersion forces

Step 4: Identify the solute–solvent attractions and compare them with the solute–solute and solvent–solvent attractions they must replace

  • Acetone and chloroform molecules attract each other through dipole–dipole and London dispersion forces that are similar in strength to the attractions in each pure liquid, so acetone and chloroform are miscible

Worked Example

Predict if a solution will be formed when hexane is mixed with water as solvent.

Displayed formulas of hexane, C6H14, a six-carbon chain, and water, H2O.

Answer:

Step 1 (Optional): Draw the molecular structure of the solvent molecules and the solute molecules. This step is not applicable to ions since they exist as lattice structures

Step 2: Identify the solvent-solvent intermolecular interactions

  • Water is the solvent. Since hydrogen is bonded to a highly electronegative atom such as oxygen, a strong dipole moment will be formed

  • Therefore, water molecules attract each other through hydrogen bonding (and London dispersion forces)

Two water molecules with delta minus oxygens and delta plus hydrogens; a dashed line labeled hydrogen bonding joins the oxygen of one to a hydrogen of the other.

Step 3: Identify the solute-solute intermolecular interactions

  • Hexane is the solute. Since hexane is a symmetrical molecule, all its dipole moments are canceled out

Two hexane molecules with dashed lines between hydrogen atoms of neighboring molecules, labeled London dispersion forces.
  • Therefore, the only attractions between hexane molecules are London dispersion forces

Step 4: Identify the solute–solvent attractions and compare them with the solute–solute and solvent–solvent attractions they must replace

  • The solvent-solvent interaction is not the same as solute-solute interaction

  • The solvent-solute interaction must be considered

water-and-hexane-showing-london-dispersion-forceswater-and-hexane-showing-london-dispersion-forces
  • As shown in the image above, water and hexane attract each other through dipole–induced dipole forces (the water dipole induces a temporary dipole in hexane) and London dispersion forces

  • The attractions between hexane and water molecules are much weaker than the hydrogen bonds between water molecules that they would have to replace

  • So water molecules stay hydrogen-bonded to each other, hexane and water are not miscible, and they form two layers

Unlock more, it's free!

Join the 100,000+ Students that ❤️ Save My Exams

the (exam) results speak for themselves:

Build on this topic

Martín

Author: Martín

Expertise: Chemistry Content Creator

Martín, a dedicated chemistry teacher and tutor, excels in guiding students through IB, AP, and IGCSE Chemistry. As an IB Chemistry student, he came from hands-on preparation, focusing on practical exam techniques and rigorous practice. While at Universidad San Francisco de Quito, his academic journey sparked a passion for computational and physical chemistry. Martín specializes in chemistry, and he knows that SaveMyExams is the right place if he wants to have a positive impact all around the world.

Stewart Hird

Reviewer: Stewart Hird

Expertise: Chemistry Content Creator

Stewart has been an enthusiastic GCSE, IGCSE, A Level and IB teacher for more than 30 years in the UK as well as overseas, and has also been an examiner for IB and A Level. As a long-standing Head of Science, Stewart brings a wealth of experience to creating Topic Questions and revision materials for Save My Exams. Stewart specialises in Chemistry, but has also taught Physics and Environmental Systems and Societies.