IB Chemistry SL Topic 2 — Covalent Bonding Paper 1 & 2 Structure & properties ~11 min read

Properties of Covalent Substances

Now everything pays off. Melting point, volatility, solubility, conductivity — all of it comes from two questions: is this a molecule or a network? and what forces sit between the molecules?

📚 What you need to know

Melting and boiling point

The single most important sentence in this topic: when a simple molecular substance melts or boils, the covalent bonds stay exactly where they are. Only the weak forces holding one molecule to the next are overcome.

Those forces are weak, which is why so many covalent substances are gases or liquids at room temperature. Compare that with a giant covalent structure, where melting really does mean breaking covalent bonds — hence the enormous difference in melting points.

LIQUIDGASmolecules held close byintermolecular forcesheat inforces brokenmolecules free and far apartbut each one is still intactthe covalent bonds INSIDE each molecule are never broken by boiling
Heating separates the molecules but leaves each one whole. The green dashes are what your energy is actually paying for.

What decides how strong the forces are

Three things, and you should check them in this order:

🧩 Comparing two molecular substances

  1. Type of force first. Hydrogen bonding beats dipole–dipole, which beats London forces. If one substance can hydrogen bond and the other cannot, that usually settles it.
  2. Then the number of electrons. If both have the same type of force, the one with more electrons has stronger London forces.
  3. Then the shape. For isomers with identical electron counts, the longer, straighter molecule packs better and boils higher.

Here is all three ideas in one comparison. These molecules have almost the same number of electrons, so London forces are similar — the difference is entirely in what else they can do:

SIMILAR SIZE, VERY DIFFERENT BOILING POINTSbutane, C₄H₁₀0 °CLondon onlypropanone, CH₃COCH₃56 °CLondon + dipole–dipolepropan-1-ol, C₃H₇OH97 °CLondon + dipole–dipole + H bonding0255075100boiling point / °Call three have 32–34 electrons
Almost identical electron counts, so the difference in boiling point comes entirely from the extra types of force available.
WORKED EXAMPLE

Place CH3CH2CH2OH, CH3COCH3 and CH3CH2CH2CH3 in order of increasing boiling point and explain.

Step 1 — check the electron counts 32–34 electrons each, so London forces are about the same. Not the deciding factor. Step 2 — identify the strongest force in each Butane: nonpolar → London only. Propanone: polar C=O → London + dipole–dipole. Propan-1-ol: has an O–H → London + dipole–dipole + hydrogen bonding. butane < propanone < propan-1-ol

Volatility

Volatile just means “evaporates easily”. It is the flip side of boiling point — weak intermolecular forces mean a low boiling point and high volatility. That is why petrol and nail varnish remover evaporate in seconds while water takes hours.

Solubility

The rule is “like dissolves like”, and the reason is energy. Dissolving something means pulling the solvent particles apart to make room, then slotting the solute in. That only works if the new solute–solvent attractions are strong enough to pay for the ones you had to break.

ETHANOL IN WATER — DISSOLVESHEXANE IN WATER — DOES NOTOHC₂H₅δ+OHHhydrogen bondpolar –OH group can hydrogen bond to waterenergy released pays for separating the waterhexane layerwater layernonpolar — only London forces to offernot enough to break water’s hydrogen bonds
Ethanol can join water’s hydrogen bonding network; hexane cannot, so it is pushed out into its own layer.
Size matters too. Small alcohols like ethanol (C2H5OH) dissolve completely in water because the –OH group dominates. As the carbon chain grows, the nonpolar hydrocarbon part takes over and solubility drops sharply — hexan-1-ol (C6H13OH) is only slightly soluble. Same functional group, very different behaviour.

Giant covalent substances are insoluble in everything. No solvent can supply the energy needed to break a continuous network of covalent bonds.

Electrical conductivity

To conduct, a substance needs charged particles that can move. Most covalent substances have neither free electrons nor ions, so the answer is usually no:

Summary table

Nonpolar molecularPolar molecularGiant covalent
Forces to overcomeLondon onlyLondon + dipole–dipole (± H bonding)Covalent bonds
Melting / boiling pointLowLow to moderateVery high
VolatilityHighModerateVery low
Soluble in water?NoOften yesNo
Soluble in nonpolar solvents?YesSometimesNo
Conducts?NoNo, unless it ionises in waterNo, except graphite & graphene
ExampleBr2, CH4H2O, HClDiamond, SiO2
WORKED EXAMPLE

A substance X melts at 1450 °C and conducts electricity poorly both as a solid and when molten. Deduce its structure.

Very high melting point → must be a giant structure That leaves ionic, metallic or giant covalent. Does not conduct when molten → rules out ionic Molten ionic compounds have free-moving ions. Does not conduct as a solid → rules out metallic giant covalent, like diamond or SiO₂

💡 Exam tip

⚠️ Common mix-up

Up next: Chromatography — a practical technique built entirely on the ideas from these last few pages, since separation depends on which intermolecular forces each component can form.

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