Comparison

Hydrogen Bonds vs Covalent Bonds: Strength, Length and Role

Bonding & Molecular StructureIntermediate8 min read
On this page
  1. The short version
  2. Side-by-side comparison
  3. Why they are so different
  4. What actually breaks when water boils
  5. When each one matters
  6. The grey zone
  7. Common mistakes
  8. Key takeaways

Ask a class what happens to water molecules when a kettle boils and a surprising number of students will say the molecules “break apart into hydrogen and oxygen”. It’s an understandable slip. Both the forces involved are called bonds, both involve hydrogen, and textbook diagrams often draw them sitting side by side. But the two are separated by more than a factor of twenty in strength, and they do completely different jobs.

This post puts hydrogen bonds and covalent bonds next to each other, number by number, and then looks at the situations where one or the other is the thing you should be thinking about.

The short version

A covalent bond is a shared pair of electrons holding two atoms together inside a molecule. It decides what the molecule is.

A hydrogen bond is an electrostatic attraction between a hydrogen atom that is already covalently bonded to nitrogen, oxygen or fluorine and a lone pair on a nearby N, O or F atom. It usually acts between molecules (sometimes between two parts of one large molecule) and decides how molecules behave together: whether they stick, how high they boil, how they fold.

In water you can see both at once. Written as O–H···O, the solid dash is the covalent O–H bond and the dotted line is the hydrogen bond to the next molecule.

Side-by-side comparison

Feature Covalent bond (O–H in water) Hydrogen bond (O–H···O between water molecules)
What it is A shared electron pair between two nuclei An attraction between a δ+ hydrogen and a lone pair on N, O or F
Where it acts Within a molecule (intramolecular) Mostly between molecules (intermolecular)
Typical energy About 463 kJ/mol for O–H Around 20 kJ/mol in water; roughly 5–40 kJ/mol for most hydrogen bonds
Typical length About 96 pm (O to H) About 280 pm from one oxygen to the next, so roughly 180–190 pm from H to the accepting O
Directionality Strongly directional, fixed by orbitals Directional; strongest when O–H···O is close to a straight line
Lifetime in liquid water Effectively permanent at room temperature Constantly breaking and re-forming, on a picosecond timescale
Broken by Chemical reactions, high-energy processes Warming, melting, boiling, dissolving
Changes the substance? Yes: breaking it makes new substances No: water is still water after its hydrogen bonds break
Controls Identity, formula, shape, reactivity Boiling point, viscosity, surface tension, solubility, folding of proteins and DNA

The energy row is the one to remember. With the O–H bond at about 463 kJ/mol and a typical water hydrogen bond near 20 kJ/mol, the covalent bond is over twenty times stronger. The length row tells the same story from another angle: the hydrogen bond is almost twice as long, and longer bonds are weaker bonds.

Why they are so different

Sharing versus attracting

In a covalent bond, the electron pair sits in the region between two nuclei and is attracted to both of them. The atoms’ orbitals genuinely overlap. That overlap is what makes covalent bonds strong and gives them fixed lengths and angles.

A hydrogen bond has only a small amount of that character. Oxygen is much more electronegative than hydrogen, so in each O–H bond the shared pair is pulled towards oxygen. The hydrogen is left with a partial positive charge (δ+), and because hydrogen has no inner electrons, its nucleus is unusually exposed. A lone pair on a neighbouring oxygen, which carries a partial negative charge (δ−), is drawn towards it. Most of the attraction is electrostatic, with a modest contribution from orbital overlap and from dispersion. That is enough to matter enormously in bulk, but not enough to rival a shared pair.

A useful analogy

Think of a covalent bond as two people holding hands with fingers laced together. Pulling them apart takes real effort. A hydrogen bond is more like two people standing close at a crowded party, drawn together by conversation. They drift apart and find new partners all the time, yet at any moment most people in the room are talking to someone. Water is that crowded party: individual hydrogen bonds last only for moments, but the network as a whole is always there.

What actually breaks when water boils

When water boils, the energy you supply goes into pulling molecules away from their neighbours. That means breaking hydrogen bonds (and weaker dispersion forces), not the O–H covalent bonds. The steam that leaves the kettle is still H₂O. You can check this with the numbers: the enthalpy of vaporisation of water is about 41 kJ/mol at 100 °C, which fits with overcoming a couple of hydrogen bonds’ worth of attraction per molecule. Breaking two O–H bonds per molecule would need more than 900 kJ/mol.

To split water into hydrogen and oxygen you need a chemical process such as electrolysis, which is a completely different scale of energy. The bond enthalpy calculator lets you see how covalent bond energies add up in reactions where bonds really are broken and made.

When each one matters

Covalent bonds decide identity and reactivity

If the question is about what a substance is or what it turns into, you are dealing with covalent bonds (or ionic bonds). Examples:

  • Why methane burns: C–H and O=O bonds break and C=O and O–H bonds form.
  • Why ethanol and dimethyl ether are different compounds even though both are C₂H₆O: their atoms are covalently connected in different orders.
  • Why a water molecule is bent: the shape comes from the covalent bonds and lone pairs around oxygen.

For a refresher on how shared pairs form, see covalent bonding explained.

Hydrogen bonds decide physical behaviour

If the question is about melting, boiling, dissolving, sticking or folding, hydrogen bonds are often the main character:

  • Boiling points. Water boils at 100 °C while hydrogen sulfide, a heavier molecule, boils far below zero. Ethanol boils well above dimethyl ether for the same reason: ethanol has an O–H group that can hydrogen bond; the ether does not.
  • Solubility. Sugar and ethanol dissolve readily in water because they can hydrogen bond with it. Oils cannot, so they separate.
  • Ice floating. The hydrogen-bond network holds ice in an open framework, so ice is less dense than liquid water.
  • Biology. The two strands of DNA are held together by hydrogen bonds between base pairs, which is why they can be “unzipped” for copying while each strand’s covalent backbone stays intact.

The general idea of forces inside versus between molecules is covered in intramolecular vs intermolecular forces.

The grey zone

Real chemistry does not always sort neatly into two boxes.

  • Unusually strong hydrogen bonds. In a few species, such as the hydrogen difluoride ion [F–H–F]⁻, the hydrogen sits almost midway between two fluorines and the interaction is strong enough that it is treated as having substantial covalent character. These are exceptions, not the norm.
  • Weak covalent bonds. Some covalent bonds, like the O–O single bond in peroxides, are relatively weak. Even so, they are still several times stronger than a normal hydrogen bond.
  • Intramolecular hydrogen bonds. A hydrogen bond can form between two groups in the same large molecule, as in the folding of a protein chain. It is still a hydrogen bond, not a covalent one, even though no second molecule is involved.

So the dividing line is really about the physics: is there a shared electron pair holding the atoms together, or a mainly electrostatic attraction between separate bonded groups?

Common mistakes

  1. “Boiling water breaks the bonds in H₂O.” Boiling breaks hydrogen bonds between molecules. The covalent O–H bonds survive.
  2. “A hydrogen bond is a bond to a hydrogen atom.” Every O–H covalent bond involves hydrogen, but that doesn’t make it a hydrogen bond. The hydrogen bond is the second, weaker contact that the hydrogen makes to another atom’s lone pair.
  3. “Any hydrogen can hydrogen bond.” The hydrogen needs to be attached to N, O or F. The C–H hydrogens in methane are not polarised enough to form ordinary hydrogen bonds.
  4. “Hydrogen bonds are weak, so they don’t matter.” Individually they are weak, but there are huge numbers of them. Collectively they give water its high boiling point and hold DNA’s strands together.
  5. Drawing the hydrogen bond at the wrong atom. The dotted line goes from the hydrogen of one molecule to the lone pair of the N, O or F on the other, not from hydrogen to hydrogen or oxygen to oxygen.

Key takeaways

  • A covalent bond is a shared electron pair inside a molecule; a hydrogen bond is a mostly electrostatic attraction between a δ+ hydrogen (on N, O or F) and a lone pair on another N, O or F.
  • In water, the covalent O–H bond is about 463 kJ/mol and 96 pm long; a hydrogen bond is about 20 kJ/mol, with oxygen atoms about 280 pm apart.
  • Covalent bonds decide a substance’s identity and reactions. Hydrogen bonds decide physical properties such as boiling point, solubility and density.
  • Boiling, melting and dissolving break hydrogen bonds, not covalent bonds.
  • For more on the weaker partner, read the full guide to hydrogen bonding.

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