IB Chemistry HL Topic 2 — Models of Bonding & Structure Paper 1 & 2 Core skill ~9 min read

Physical Properties of Covalent Substances

This page is where the whole topic pays off. Once you know the shape of a molecule, whether it is polar, and which intermolecular forces it has, you can predict how it behaves without ever having seen it — whether it is a gas, what it dissolves in, and whether it conducts.

📘 What you need to know

Melting point, boiling point and volatility

To boil a molecular substance you have to pull the molecules apart from each other. You do not have to break anything inside them. So the question is always the same: how strongly do these molecules grip one another?

A substance with a low boiling point is described as volatile — it evaporates readily. Petrol is volatile; motor oil is not, because its far longer molecules have much greater contact area.

🧩 How to compare two boiling points

  1. Compare the number of electrons. Similar? Then dispersion forces are similar and the answer lies elsewhere.
  2. Check polarity. Is either molecule polar? That adds dipole–dipole attractions.
  3. Check for hydrogen bonding. Is there an O–H, N–H or F–H bond? That trumps everything else.
  4. Check shape. For isomers, the straighter molecule has more contact area and boils higher.
  5. Name the strongest force in each and say which needs more energy to overcome.
Three molecules of almost the same mass
Same size, very different boiling points Mₕ of 58, 58 and 60, so dispersion forces are almost identical in all three −20 0 50 100 boiling point / °C −0.5°C 56°C 97°C butane propanone propan-1-ol nonpolar polar C=O has an O—H group dispersion only plus dipole—dipole plus hydrogen bonds Each new force stacks on the ones below it and lifts the boiling point again.
This is the comparison examiners keep returning to, because it isolates one variable at a time. Mass is controlled, so any difference must come from the type of intermolecular force.
Learn this trio as a set: butane, propanone, propan-1-ol. If you can explain their order fluently you can handle almost any boiling point comparison the IB sets.

Solubility: like dissolves like

For something to dissolve, the solvent has to form attractions with the solute that are comparable to the ones it is breaking. Polar solvents can do that for polar solutes; nonpolar solvents can do it for nonpolar solutes. Mix the two kinds and neither can offer the other a good enough deal.

Why ethanol mixes with water and hexane does not
Can the solute offer water anything in return? Water will only make room for a molecule it can bond to ETHANOL: DISSOLVES HEXANE: DOES NOT C C O H O hydrogen bond to water O nothing to bond with Ethanol brings an O—H group. Hexane brings only carbon and hydrogen. Water would have to break its own hydrogen bonds and get nothing back.
Solubility in water falls as an alcohol chain grows. Ethanol mixes with water in any proportion; hexan-1-ol barely dissolves, because the long nonpolar tail now outweighs the one polar group.

Conductivity

To conduct electricity you need charged particles that can move. Molecular covalent substances have neither free electrons nor free ions — every electron is tied into a bond and every molecule is neutral. So as a rule they do not conduct in any state.

There are two exceptions worth knowing:

PropertyNonpolar molecularPolar molecularGiant covalent
Melting and boiling pointlowlow to moderatevery high
Volatilityhighmoderatevery low
Solubility in waterinsolubleoften solubleinsoluble
Solubility in hexanesolubleoften insolubleinsoluble
Conducts as a solidnonoonly graphite and graphene
Conducts in solutionnoonly if it ionisesdoes not dissolve

Worked examples

WE 1

Place in order of increasing boiling point: CH3CH2CH2CH3, CH3COCH3, CH3CH2CH2OH

Step 1: compare relative molecular masses 58, 58 and 60 — near enough identical, so dispersion forces are similar. Step 2: identify the strongest force in each Butane: nonpolar → dispersion only Propanone: polar C=O → dispersion + dipole–dipole Propan-1-ol: has O–H → dispersion + hydrogen bonding Step 3: rank by force strength butane < propanone < propan-1-ol state the Mₕ values first — it shows you ruled out the size explanation
WE 2

Explain why ethanol dissolves in water but hexane does not [3]

Mark 1: describe the solvent Water is polar and forms hydrogen bonds with itself. Mark 2: what ethanol offers Ethanol has an O–H group, so it can form hydrogen bonds with water and replace the ones broken. Mark 3: what hexane cannot offer Hexane is nonpolar with only C–H and C–C bonds. It can form only weak dispersion forces with water, not enough to replace the hydrogen bonds lost. Like dissolves like: ethanol matches water, hexane does not the phrase “replace the forces broken” is what turns a description into an explanation
WE 3

Substance Y melts at −114°C, does not conduct as a pure liquid, but its aqueous solution does. Suggest what Y is.

Step 1: read the melting point Very low, so simple molecular, not giant or ionic. Step 2: it does not conduct when pure Confirms neutral molecules with no free electrons or ions. Step 3: but it does in water So it must ionise when it dissolves. A polar covalent molecule that ionises in water, such as HCl the “only in solution” clue is the giveaway for a covalent acid every time

💡 Exam tips

⚠ Common mix-ups

Up next: Chromatography — a separation technique built entirely on the intermolecular forces you have just learned, and one that gives you a number to calculate.

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