Edexcel International A Level (IAL) Chemistry (YCH11) - Unit 2 - 7.6 Solvent choice and intermolecular forces-Study Notes - New Syllabus

Edexcel International A Level (IAL) Chemistry (YCH11) -Unit 2 – 7.6 Solvent choice and intermolecular forces- Study Notes- New syllabus

Edexcel International A Level (IAL) Chemistry (YCH11) -Unit 2 – 7.6 Solvent choice and intermolecular forces- Study Notes -International A Level (IAL) Chemistry (YCH11) – per latest Syllabus.

Key Concepts:

7.6 understand factors that influence the choice of solvents, including:
i water, to dissolve some ionic compounds, in terms of the hydration of the ions
ii water, to dissolve simple alcohols, in terms of hydrogen bonding
iii water, as a poor solvent for compounds (to include polar molecules such as halogenoalkane), in terms of inability to form hydrogen bonds
iv non-aqueous solvents, for compounds that have similar intermolecular forces to those in the solvent

Edexcel International A Level (IAL) Chemistry (YCH11) -Concise Summary Notes- All Topics

7.6 Factors Influencing Choice of Solvents 

(i) Water as a Solvent for Ionic Compounds

Key Idea: Hydration of Ions

Water dissolves ionic compounds because ions become surrounded by water molecules (hydration).

Explanation 

  • Water is a polar molecule:
    • Oxygen has \( \delta^- \) charge
    • Hydrogen has \( \delta^+ \) charge
  • When an ionic compound dissolves:
    • Positive ions attract the \( \delta^- \) oxygen end
    • Negative ions attract the \( \delta^+ \) hydrogen end
  • This forms ion–dipole interactions.
  • Ions become hydrated and separated from the lattice.

Example

\( \mathrm{NaCl(s) \rightarrow Na^+(aq) + Cl^-(aq)} \)

Key Conclusion

Water dissolves ionic compounds due to strong ion–dipole attractions (hydration).

(ii) Water as a Solvent for Simple Alcohols

Key Idea: Hydrogen Bonding

Simple alcohols dissolve in water because they can form hydrogen bonds with water molecules.

Explanation 

  • Alcohols contain –OH group.
  • This group is polar.
  • Hydrogen bonding occurs between:
    • \( \mathrm{H^{\delta+}} \) of –OH
    • Lone pair on oxygen of water
  • These strong interactions allow alcohol molecules to mix with water.

Effect of Chain Length

  • Small alcohols (e.g. methanol, ethanol) → fully miscible.
  • Larger alcohols → less soluble.
  • Due to increasing non-polar hydrocarbon chain.

Example

\( \mathrm{C_2H_5OH(l) + H_2O(l)} \) → hydrogen bonding between molecules

Key Conclusion

Alcohols dissolve in water due to hydrogen bonding between –OH groups and water molecules.

Summary 

  • Ionic compounds dissolve due to hydration (ion–dipole forces).
  • Alcohols dissolve due to hydrogen bonding.

Therefore, solubility in water depends on the ability to form strong interactions with water molecules.

Example 1:

Explain why sodium chloride dissolves readily in water but not in hexane.

▶️ Answer/Explanation

Water is polar and forms ion–dipole interactions with ions.

Hexane is non-polar and cannot stabilise ions.

Therefore, NaCl dissolves in water but not in hexane.

Example 2 :

Explain why ethanol is soluble in water but hexanol is only slightly soluble.

▶️ Answer/Explanation

Both form hydrogen bonds via –OH group.

Hexanol has a longer non-polar hydrocarbon chain.

Non-polar part reduces overall polarity.

Therefore, solubility decreases with chain length.

(iii) Water as a Poor Solvent for Some Compounds

Key Idea: Inability to Form Hydrogen Bonds

Water is a poor solvent for many organic compounds because they cannot form hydrogen bonds with water.

Explanation 

  • Water is polar and forms strong hydrogen bonds.
  • Some compounds (e.g. halogenoalkanes):
    • May be slightly polar
    • But do not form hydrogen bonds with water
  • Therefore:
    • Weak interactions with water
    • Cannot replace strong water–water hydrogen bonds
  • Result: substance is insoluble or only slightly soluble.

Example

Halogenoalkanes (e.g. \( \mathrm{CH_3Cl} \)) are not soluble in water.

Conclusion

If a substance cannot form hydrogen bonds with water, it is unlikely to dissolve.

(iv) Non-aqueous Solvents and “Like Dissolves Like”

A substance dissolves best in a solvent that has similar intermolecular forces.

Explanation 

  • Non-aqueous solvents (e.g. hexane) are non-polar.
  • They interact via London dispersion forces.
  • Non-polar solutes:
    • Also have London forces
    • Therefore dissolve easily
  • Polar solutes:
    • Do not dissolve well in non-polar solvents

Examples

  • Iodine dissolves in hexane (both non-polar).
  • Oil dissolves in organic solvents, not in water.

Summary 

  • Water cannot dissolve substances that cannot hydrogen bond.
  • Solubility depends on similarity of intermolecular forces.
  • “Like dissolves like” explains solvent choice.

Therefore, solvent selection depends on intermolecular interactions between solute and solvent.

Example 1 :

Explain why chloromethane is only slightly soluble in water.

▶️ Answer/Explanation

Chloromethane is polar but cannot form hydrogen bonds with water.

Water–water hydrogen bonds are strong.

Weak interactions cannot replace them.

Therefore, low solubility.

Example 2 :

Explain why iodine dissolves in hexane but not in water.

▶️ Answer/Explanation

Iodine is non-polar.

Hexane is non-polar → similar London forces.

Therefore, iodine dissolves in hexane.

Water is polar and cannot interact effectively.

Therefore, iodine is insoluble in water.

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