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IB Chemistry · Structure 2 Models of bonding and structure

S2.4 From models to materials

Summary to follow. 6 syllabus statements (1 HL) · 17 questions · about twenty minutes.

Compiled from the IB Chemistry guide (first assessment 2025) and our question bank · Specialist review in progress · How these pages are made

In this topic — 6 syllabus statements, 1 HL
  1. S2.4.1 Bonding continuum
  2. S2.4.2 Electronegativity (χ)
  3. S2.4.3 Alloy
  4. S2.4.4 Polymer (macromolecule)
  5. S2.4.5 Addition polymerization
  6. S2.4.6 Condensation polymerization HL

Assessed in Paper 1A (multiple choice), Paper 1B (data-based) and Paper 2 (short and extended response). IB Chemistry guide (first assessment 2025).

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In preparation: 0 of 6 sections compiled and reviewed. The rest show key terms and common misconceptions from our question bank until they are.

S2.4.1 Bonding continuum

Bonding continuum
The idea that ionic, covalent and metallic bonding are idealized models at the ends of a continuous range, not three separate boxes. The bonding in most real substances has some character of more than one model, in proportions that vary smoothly from one substance to another. Sodium chloride is described well by the ionic model, silicon tetrachloride by the covalent model, and aluminium chloride lies between them.
Bonding triangle
A triangular diagram that places a substance according to two electronegativity-based coordinates. The x-axis is the average electronegativity of the two elements, (χA + χB)/2; the y-axis is the electronegativity difference, Δχ = |χA − χB|. The metallic vertex is at the bottom left (low average, Δχ = 0), the covalent vertex at the bottom right (high average, Δχ = 0) and the ionic vertex at the top (largest Δχ). In a standard construction the metallic vertex is caesium (χ = 0.8), the covalent vertex is fluorine (χ = 4.0) and the ionic vertex is caesium fluoride (average 2.4, Δχ = 3.2). Points inside the triangle represent bonding with mixed character.
Using bonding models to explain properties
Each model predicts a characteristic set of properties. Ionic: a lattice of ions, high melting point, brittle, conducts electricity when molten or in aqueous solution but not as a solid, because the ions are fixed in the solid. Covalent (molecular): discrete molecules held by weak intermolecular forces, low melting and boiling points, does not conduct. Covalent (giant network): very high melting point, generally does not conduct (graphite is an exception). Metallic: a lattice of cations and delocalized electrons, conducts electricity as a solid, malleable and ductile.

Students often think A compound with intermediate bonding contains a mixture of bonds of the pure types: some are fully ionic and the rest are fully covalent (or fully metallic), in proportions given by its percentage character. In fact No. Each bond has intermediate character; all the equivalent bonds in the compound are alike.

Students often think An ionic compound is made of molecules, such as MgO or NaCl molecules, each formed by one electron transfer; the molecules split into ions when the compound melts or dissolves. In fact No. It is a giant lattice of Mg²⁺ and O²⁻ ions; each ion is attracted to all the neighbouring ions of opposite charge, and there are no discrete MgO molecules.

S2.4.2 Electronegativity (χ)

Electronegativity (χ)
The relative ability of an atom to attract a shared pair of electrons in a covalent bond. Pauling electronegativity has no units. Rounded Pauling values include Na 0.9, Mg 1.3, Al 1.6, Si 1.9, P 2.2, S 2.6, Cl 3.2, O 3.4 and F 4.0.
Average electronegativity
The mean of the electronegativities of the two elements in a binary compound, (χA + χB)/2, whatever the formula. It is the x-coordinate in the bonding triangle. For AlCl₃ with χ(Al) = 1.6 and χ(Cl) = 3.2 it is (1.6 + 3.2)/2 = 2.4; the three chlorine atoms in the formula are not counted separately. A low average places a compound towards the metallic side, a high average towards the covalent side.
Electronegativity difference (Δχ)
The difference between the electronegativities of the two elements, Δχ = |χA − χB|. It is the y-coordinate in the bonding triangle: the larger Δχ, the higher the compound lies and the greater its ionic character. For AlCl₃, Δχ = 3.2 − 1.6 = 1.6; for NaCl, Δχ = 3.2 − 0.9 = 2.3.
Percentage bonding character
A description of how much each bonding model contributes to the bonding in a compound, judged from its position in the bonding triangle: the nearer a compound lies to a vertex, the greater that model's contribution. It describes every bond in the compound, not a fraction of the bonds. For example, NaCl (Δχ = 2.3) has mainly ionic character, AlCl₃ (Δχ = 1.6) has substantial ionic and covalent character, and PCl₃ (Δχ = 1.0) is mainly covalent. Percentage ionic character is not calculated at this level.
Predicting properties from position
A compound near the ionic vertex is predicted to have ionic properties (high melting point, conducts when molten); one low in the triangle towards the covalent vertex is predicted to be covalent, often molecular with low melting and boiling points; one near the metallic vertex is predicted to conduct electricity as a solid. Tin(IV) chloride, SnCl₄ (Δχ = 1.2), lies low in the triangle and is a molecular liquid that boils at 114 °C, although it contains a metal.

Students often think The type of element decides the bond: a metal with a non-metal gives an ionic compound and two non-metals give a covalent compound, so the bond type switches sharply where the metals end. In fact No. The bonding depends on the electronegativities of the two elements. Many metal compounds have substantial covalent character (AlCl₃, SnCl₄), and bonding character changes gradually rather than switching at the metal/non-metal boundary.

Students often think Bond type is set by the electronegativity difference alone, on a single line from ionic (large Δχ) to covalent (Δχ close to zero), so any substance with Δχ close to zero is covalent. In fact No. Δχ decides how far the substance lies from the bottom edge of the triangle, but a substance with small Δχ can be metallic or covalent; the average electronegativity decides which.

S2.4.3 Alloy

Alloy
A mixture of a metal with one or more other metals or non-metals. Its composition can vary, so it has no fixed formula. Alloys usually have enhanced properties compared with the pure metal, such as greater hardness and strength, or better resistance to corrosion. Illustrative examples: bronze (copper with tin), brass (copper with zinc), stainless steel (iron with chromium, nickel and a little carbon); specific alloys do not have to be learned.
Non-directional bonding in alloys
Metallic bonding is the attraction between a lattice of cations and delocalized electrons, and it acts in all directions. Because it does not depend on particular atoms being bonded to particular neighbours, atoms of a different element and size can be included in the lattice while it stays metallically bonded, so an alloy still conducts electricity and can be shaped. The different-sized atoms disrupt the regular layers of the pure metal, so the layers slide over each other less easily and the alloy is harder than the pure metal.

Students often think Metallic bonding exists only in a pure metal element; once another element is present, as in an alloy or a compound, the bonding must be covalent or ionic. In fact No. Metallic bonding is found wherever a lattice of cations is held by delocalized electrons: in pure metals, in alloys and in compounds of metals with low electronegativity.

Students often think An alloy is a compound: the metals react with each other and bond in a fixed ratio, with a single fixed formula, and this new compound is what makes the alloy harder. In fact No. An alloy is a mixture; its composition can vary (brasses contain from about 5% to 45% zinc) and it has no fixed formula.

S2.4.4 Polymer (macromolecule)

Polymer (macromolecule)
A very large molecule made of many repeating subunits called monomers, joined by covalent bonds into long chains. A sample of a polymer is a collection of chain molecules of similar structure but differing lengths.
Monomer
A small molecule that can join repeatedly to other monomer molecules to form a polymer. Examples: ethene for poly(ethene), glucose for starch and cellulose, amino acids for proteins.
Natural and synthetic polymers
Natural polymers are made by living organisms, for example cellulose and starch (from glucose), proteins (from amino acids), DNA (from nucleotides) and natural rubber. Synthetic polymers are made industrially, for example poly(ethene), poly(chloroethene) (PVC), nylon and polyesters. Fats (triglycerides) and simple sugars such as glucose are not polymers.
Properties of plastics
Plastics are synthetic polymers that can be moulded. Their common properties follow from their structure of long chains of covalently bonded atoms. They are electrical insulators because all their valence electrons are held in localized covalent bonds and they contain no ions. Many soften on heating because only the weak intermolecular forces between chains are overcome; the covalent bonds within the chains stay intact. They are unreactive and persist in the environment because their chains are held together by strong covalent bonds (in poly(ethene), non-polar C–C and C–H bonds) that few reagents or microorganisms break down. They have low density.

Students often think When a covalent substance melts, boils or softens, its covalent bonds break, so a substance with strong covalent bonds must have a high boiling point and a plastic softens because its chains break up. In fact No, not in a molecular substance or a plastic. Melting, boiling and softening overcome the intermolecular forces between molecules or chains; the covalent bonds within them stay intact.

Students often think Polymers are synthetic plastics; substances made by living things, such as cellulose or proteins, are not polymers. In fact No. Many polymers are natural, including cellulose, starch, proteins, DNA and natural rubber.

S2.4.5 Addition polymerization

Addition polymerization
The joining of many unsaturated monomer molecules into one long chain. In each monomer one of the two bonds of the C=C double bond breaks, and the carbon atoms form new single bonds to neighbouring monomers. No other product forms, so the polymer contains every atom of the monomers. Example: n CH₂=CHCH₃ → [–CH₂–CH(CH₃)–]ₙ.
Repeating unit of an addition polymer
The part of the chain formed from one monomer, written with open bonds at each end. It has the same atoms as the monomer, but its two former C=C carbons are joined by a single bond and are the only atoms in the main chain; other groups become side groups. From chloroethene, CH₂=CHCl, the repeating unit is –CH₂–CH(Cl)–. The polymer is written [–CH₂–CH(Cl)–]ₙ, where n is the number of repeating units in one chain. The monomer is deduced from a chain by taking a two-carbon unit of the main chain and restoring the C=C.

Students often think The C=C double bond of the monomer is still present in the repeating unit: the monomers simply link end to end without their own bonds changing. In fact No. One of the two bonds of each C=C breaks and the carbon atoms form single bonds to neighbouring units, so the repeating unit has only single bonds in the main chain.

Students often think Every carbon atom of the monomer is part of the main chain of the polymer, so side groups are drawn into the chain. In fact No. Only the two carbon atoms of the C=C form the main chain; the CH₃ group becomes a side group.

S2.4.6 Condensation polymerization HL

Condensation polymerization
The formation of a polymer by reaction between functional groups on different monomers, with the release of a small molecule, such as H₂O or HCl, at each link. Each monomer must have two reacting functional groups so that the chain can grow at both ends. Two monomers of different kinds (for example a diamine and a dicarboxylic acid) give a repeating unit that contains one residue of each.
Polyamide
A condensation polymer whose monomer units are joined by amide links, –CONH–. From hexane-1,6-diamine, H₂N(CH₂)₆NH₂, and hexanedioic acid, HOOC(CH₂)₄COOH (H₂O released), or hexanedioyl dichloride, ClOC(CH₂)₄COCl (HCl released), the repeating unit of nylon-6,6 is –NH(CH₂)₆NHCO(CH₂)₄CO–. Proteins are natural polyamides formed from amino acids.
Polyester
A condensation polymer whose monomer units are joined by ester links, –COO–. From ethane-1,2-diol, HOCH₂CH₂OH, and hexanedioic acid, HOOC(CH₂)₄COOH, the repeating unit is –OCH₂CH₂OOC(CH₂)₄CO– and water is released at each ester link.
Hydrolysis of biological macromolecules
The breaking of a bond by reaction with water, the reverse of condensation. All biological macromolecules form by condensation reactions and are broken down by hydrolysis: proteins to amino acids (amide, or peptide, links), polysaccharides such as starch to glucose, nucleic acids to nucleotides. One water molecule is used for each link broken.

Students often think The small molecule released in a condensation reaction is always water, whatever the functional groups. In fact No. It depends on the functional groups: a carboxylic acid group reacting with an amine or alcohol releases H₂O, but an acyl chloride group (–COCl) releases HCl.

Students often think All polymers form like addition polymers, with monomers simply adding together, so no atoms are lost and the repeating unit contains every atom of its monomers. In fact No. Each link in a condensation polymer forms with the release of a small molecule, such as H₂O or HCl, so the polymer contains fewer atoms than the monomers used.

Diagnostic a bearings check, not a test

10 questions, one per part of the topic where we can. Answer them, then see which statements you own and which to read.

1 Magnesium oxide (χ: Mg 1.3, O 3.4; Δχ = 2.1) lies high in the bonding triangle, towards the ionic vertex. Solid magnesium oxide does not conduct electricity, but molten magnesium oxide does. Which explanation is correct?

Answer and reasoning
  1. Melting splits its MgO molecules into separate ions, which then carry the current. — A student who pictures ionic compounds as made of molecules picks this. Solid MgO contains no molecules; it is already a lattice of Mg²⁺ and O²⁻ ions. Melting does not create ions, it lets the existing ions move.
  2. Its ions become liquid when it melts, and liquid ions can carry charge but solid ones cannot. — A student who gives single particles the properties of the bulk material picks this. An ion is not solid or liquid; 'liquid' describes how the particles are arranged. In the melt the same ions are no longer held in fixed positions, so they can move.
  3. Its ions cannot move in the solid, but in the melt they move and carry the current. — High in the triangle, the ionic model applies: MgO is a lattice of Mg²⁺ and O²⁻ ions. In the solid the ions cannot move, so no current flows; when it melts the ions become mobile and carry the current.
  4. Melting sets electrons free, which then move through the liquid and carry the current. — A student who thinks current is always carried by electrons picks this. MgO has no delocalized electrons, solid or molten; in the melt the current is carried by Mg²⁺ and O²⁻ ions moving to the electrodes.

Syllabus statement S2.4.1 · Read this in Learn

2 The position of a binary compound in the bonding triangle is found from the electronegativities of its two elements. In the triangle the metallic vertex is at the bottom left, the covalent vertex at the bottom right and the ionic vertex at the top; the two bottom vertices are elements, for which Δχ = 0. For aluminium chloride, AlCl₃, χ(Al) = 1.6 and χ(Cl) = 3.2. What is the x-coordinate of AlCl₃ in the bonding triangle?

Answer and reasoning
  1. 2.8 — A student who averages over every atom in the formula gets (1.6 + 3 × 3.2)/4 = 2.8. The x-coordinate is the mean of the two elements' electronegativities, (1.6 + 3.2)/2 = 2.4; the number of chlorine atoms does not enter.
  2. 4.8 — A student who adds the electronegativities without dividing by 2 gets 4.8. The x-coordinate is an average, (1.6 + 3.2)/2 = 2.4; 4.8 is off the scale, since no element has χ above 4.0.
  3. 1.6 — A student who interchanges the axes gives Δχ = 3.2 − 1.6 = 1.6 as the x-coordinate. The bottom vertices have Δχ = 0, so Δχ (1.6) is the y-coordinate, which measures ionic character; the x-axis is the average electronegativity (2.4).
  4. 2.4 — Both bottom vertices have Δχ = 0 and the ionic vertex at the top has the largest Δχ, so Δχ is the y-coordinate and x is the average electronegativity of the two elements: (1.6 + 3.2)/2 = 2.4. Each element is counted once, whatever the formula.

Working The bottom edge (both bottom vertices) has Δχ = 0 and the ionic vertex at the top has the largest Δχ, so Δχ is the vertical (y) coordinate and the horizontal (x) coordinate is the average electronegativity. x = (χ(Al) + χ(Cl))/2 = (1.6 + 3.2)/2 = 2.4 (no units). The y-coordinate, Δχ = 3.2 − 1.6 = 1.6, is not asked.

Syllabus statement S2.4.2 · Read this in Learn

3 Which description of an alloy is correct?

Answer and reasoning
  1. A compound of a metal with other elements, bonded in a fixed ratio by formula — A student who thinks the metals react to form a compound picks this. An alloy is a mixture with variable composition and no fixed formula; the atoms of the added element sit in the metallic lattice.
  2. A mixture of a metal with other metals or non-metals, in variable amounts — An alloy is a mixture, so its composition can vary, and the added element can be a metal (zinc in brass) or a non-metal (carbon in steel). Alloys usually have enhanced properties, such as greater hardness.
  3. A mixture of two or more metals, with no atoms of a non-metal present in it — A student who learned the definition 'a mixture of metals' picks this. Alloys can contain non-metals: steel is iron with a small percentage of carbon.
  4. A mixture of a metal with another element, made so that it is softer — A student who thinks mixing weakens a metal picks this. Alloys are usually harder and stronger than the pure metal, because the added atoms disrupt the layers so they slide less easily.

Syllabus statement S2.4.3 · Read this in Learn

4 Which statement about polymers is correct?

Answer and reasoning
  1. Polymers are synthetic plastics; substances made by living things are not. — A student who equates 'polymer' with 'plastic' picks this. Many polymers are natural: cellulose, starch, proteins, DNA and natural rubber are all macromolecules made of repeating monomer units.
  2. Fats are natural polymers made of many glycerol and fatty acid units. — A student who assumes every large biological molecule is a polymer picks this. A fat (triglyceride) contains one glycerol and three fatty acid units; it has no long chain of repeating units, so it is not a polymer.
  3. Glucose is a natural polymer, as it is the building block of starch and cellulose. — A student who confuses monomer with polymer picks this. Glucose is the monomer; starch and cellulose are the polymers made from many glucose units.
  4. Cellulose (natural) and nylon (synthetic) are both polymers built from monomers. — Cellulose is a natural polymer of glucose, made by plants; nylon is a synthetic polyamide made industrially. Both are macromolecules built from many repeating monomer units, so being a polymer does not depend on being natural or synthetic.

Syllabus statement S2.4.4 · Read this in Learn

5 Propene, CH₂=CHCH₃, forms the addition polymer poly(propene), written as [repeating unit]ₙ. Which option gives the repeating unit and describes it correctly?

Answer and reasoning
  1. –CH₂=CH(CH₃)–, keeping each monomer's C=C — A student who thinks the monomer's double bond survives picks this. Polymerization happens because one bond of each C=C breaks; if the C=C remained, each carbon here would have five bonds.
  2. –CH₂–CH(CH₃)–, one unit of a single long chain — One bond of each C=C breaks and the two former C=C carbons form the main chain, with CH₃ as a side group. The formula [–CH₂–CH(CH₃)–]ₙ represents one chain molecule containing n of these units.
  3. –CH₂–CH₂–CH₂–, all three carbons in the main chain — A student who puts every carbon of the monomer into the chain picks this. Only the two C=C carbons form the main chain; the CH₃ group becomes a side group, so the chain has CH₃ branches on alternate carbons.
  4. CH₃CH₂CH₃, one of n separate small molecules — A student who reads n as a number of separate molecules writes the unit as a complete molecule, CH₃CH₂CH₃ (propane). The repeating unit has open bonds at both ends because each unit is covalently bonded to the next in one long chain, [–CH₂–CH(CH₃)–]ₙ; propane has no C=C and cannot polymerize.

Syllabus statement S2.4.5 · Read this in Learn

6 Which statement about biological macromolecules is correct? HL

Answer and reasoning
  1. Starch forms from glucose by hydrolysis, with a water molecule released at each link. — A student who interchanges the two terms picks this. Starch forms from glucose by condensation, which releases water; hydrolysis is the reverse, which uses water to break the links.
  2. Proteins are hydrolyzed to amino acids, with water used to break each amide link. — All biological macromolecules form by condensation and are broken down by hydrolysis. In the hydrolysis of a protein, one water molecule reacts with each amide (peptide) link, giving the amino acids.
  3. DNA is hydrolyzed simply as it dissolves in water, without any covalent bonds breaking. — A student who equates hydrolysis with dissolving picks this. Hydrolysis is a chemical reaction that breaks covalent links by reaction with water; dissolving breaks no covalent bonds.
  4. Cellulose forms from glucose by addition, with no atoms at all lost from the monomers. — A student who thinks every polymer forms like an addition polymer picks this. Glucose has no C=C to open; cellulose forms by condensation, with one water molecule released for each glycosidic link.

Syllabus statement S2.4.6 · Read this in Learn

7 Using the electronegativities Na 0.9, Mg 1.3, Al 1.6, Si 1.9, P 2.2 and Cl 3.2, the electronegativity differences for NaCl, MgCl₂, AlCl₃, SiCl₄ and PCl₃ are 2.3, 1.9, 1.6, 1.3 and 1.0. Which statement about the bonding in this series is correct?

Answer and reasoning
  1. The bonds are ionic up to AlCl₃ and covalent from SiCl₄ on, where the metals end. — A student who decides bond type by metal/non-metal class picks this. The Δχ values show no break at aluminium: the step from AlCl₃ (1.6) to SiCl₄ (1.3) is no larger than the others. AlCl₃ already has substantial covalent character (it sublimes at about 180 °C as Al₂Cl₆ molecules), and SiCl₄ still has polar bonds.
  2. Ionic character decreases and covalent character increases gradually along the series. — Δχ falls in small steps (2.3, 1.9, 1.6, 1.3, 1.0), so each compound lies a little lower in the bonding triangle than the one before and a little further towards the covalent side. The bonding changes by degrees: NaCl is mainly ionic, PCl₃ mainly covalent, and AlCl₃ lies between them.
  3. Ionic character increases along the series, as the average electronegativity rises. — A student who treats average electronegativity as the measure of ionic character picks this. The average does rise (2.05, 2.25, 2.4, 2.55, 2.7), but that moves compounds towards the covalent side. Ionic character is measured by Δχ, which falls along the series.
  4. In SiCl₄ some of the Si–Cl bonds are ionic and the others are fully covalent. — A student who reads intermediate character as a mixture of bond types picks this. The four Si–Cl bonds in SiCl₄ are equivalent: each is a polar covalent bond with the same partial ionic character (Δχ = 1.3).

Syllabus statement S2.4.1 · Read this in Learn

8 With χ(Sn) = 2.0 and χ(Cl) = 3.2, tin(IV) chloride, SnCl₄, has an electronegativity difference of 1.2 and an average electronegativity of 2.6. Sodium chloride has an electronegativity difference of 2.3. Which prediction about SnCl₄ is correct?

Answer and reasoning
  1. It has a low boiling point, as its molecules are held by weak intermolecular forces. — With Δχ = 1.2 and a high average, SnCl₄ lies low in the triangle towards the covalent vertex, far below NaCl. It is predicted to be molecular; indeed it is a liquid that boils at 114 °C, because only weak London forces hold its tetrahedral SnCl₄ molecules together.
  2. It has a high melting point, as a metal chloride is a lattice of metal and chloride ions. — A student who classifies every metal–non-metal compound as ionic picks this. The electronegativities, not the element classes, decide the position: Δχ = 1.2 is small, so SnCl₄ has mainly covalent character and is a molecular liquid at room temperature.
  3. Its vapour consists of separate Sn and Cl atoms, as boiling must break its Sn–Cl bonds. — A student who thinks boiling breaks covalent bonds picks this. Boiling a molecular substance separates whole SnCl₄ molecules by overcoming the intermolecular forces between them; the Sn–Cl bonds stay intact, so the vapour consists of SnCl₄ molecules and the boiling point is low (114 °C).
  4. It conducts electricity when solid, as it contains atoms of the metal tin. — A student who expects a compound to behave like the metal it contains picks this. SnCl₄ has no delocalized electrons and no ions; its electrons are in Sn–Cl bonds within molecules, so it does not conduct in any state.

Syllabus statement S2.4.2 · Read this in Learn

9 A bronze used for springs and bearings is an alloy of copper containing about 5% tin. Tin atoms are larger than copper atoms, and pure tin is a soft metal. Which statement comparing this bronze with pure copper is correct?

Answer and reasoning
  1. Bronze is harder, as the larger tin atoms disrupt the layers of copper atoms. — In pure copper the layers of identical cations slide over each other easily. The larger tin atoms distort the regular layers, so the layers cannot slide as easily and bronze is harder. The non-directional metallic bonding holds the tin atoms in the lattice, so bronze remains a metal.
  2. Bronze is softer, as a mixture of metals is weaker than a pure metal. — A student who thinks a mixture must be weaker than a pure substance picks this. Alloying normally makes a metal harder: bronze is harder than copper, which is why it was used for tools and weapons.
  3. Bronze is softer, as its tin atoms are themselves soft and pass this on to the alloy. — A student who gives atoms the properties of the bulk metal picks this. A tin atom is not soft or hard; softness is a property of pure tin as a material. In bronze, the tin atoms make the copper harder by disrupting its layers.
  4. Bronze is harder, as copper and tin form a compound with a fixed formula. — A student who thinks an alloy is a compound picks this. Bronze is a mixture whose tin content can vary; its hardness comes from different-sized atoms disrupting the layers, not from a new compound.

Syllabus statement S2.4.3 · Read this in Learn

10 Poly(ethene) is a plastic that softens when heated and can then be moulded into a new shape. What happens in the plastic as it softens?

Answer and reasoning
  1. The chains gain enough energy to overcome the forces between them and slide past each other. — Poly(ethene) consists of long chains held together only by intermolecular (London) forces. Heating gives the chains enough energy to overcome these forces partly, so they slide past each other and the plastic can be reshaped. The covalent bonds in the chains are not broken.
  2. Heat flows into the gaps between the chains as a substance and pushes the chains apart. — A student who pictures heat as a substance picks this. Heat is energy transferred to the plastic, not a material that fills the gaps; the chains gain kinetic energy, partly overcome the intermolecular forces between them and slide past each other.
  3. The covalent bonds between neighbouring chains break, so the chains separate. — A student who pictures the chains as covalently bonded to each other picks this. In poly(ethene) there are no covalent bonds between chains; the chains are held together by intermolecular forces.
  4. Each chain molecule itself becomes soft, so the plastic as a whole softens. — A student who gives molecules the properties of the bulk material picks this. Softness is a property of the material; it softens because the chains can move past each other more easily, not because each molecule becomes soft.

Syllabus statement S2.4.4 · Read this in Learn

Verify confirm before you go

7 more questions. Every wrong answer here is a real misconception, and you see why it is wrong straight away.

1 In the bonding triangle, the x-axis is the average electronegativity of the two elements and the y-axis is their electronegativity difference, Δχ. The metallic vertex is at the bottom left (low average, Δχ = 0), the covalent vertex at the bottom right (high average, Δχ = 0) and the ionic vertex at the top. Compound P is formed from two metals with χ = 1.0 and 1.3 (average 1.15, Δχ = 0.3). Carbon disulfide, CS₂, with χ(C) = 2.6 and χ(S) = 2.6, has average 2.6 and Δχ = 0. Which prediction about P does the bonding triangle support?

Answer and reasoning
  1. It is a molecular substance like CS₂, as its small Δχ means shared electron pairs. — A student who uses Δχ alone picks this. A small Δχ places a substance near the bottom edge, but the average electronegativity decides where: CS₂ (average 2.6) is at the covalent side, P (average 1.15) at the metallic side.
  2. It conducts when molten but not as a solid, as its unequal χ values mean it has ions. — A student who thinks any electronegativity difference creates ions picks this. A Δχ of 0.3 is far too small for electron transfer; P lies near the bottom of the triangle, close to the metallic vertex, not near the ionic vertex at the top.
  3. Some of its bonds are ionic and the rest are metallic, as its Δχ is small but not zero. — A student who reads intermediate character as a mixture of bond types picks this. The bonding in P has a single character throughout: with Δχ = 0.3 and a low average electronegativity, P lies just above the bottom edge near the metallic vertex, so it is metallic bonding with slight polarity, not a mixture of separate ionic and metallic bonds.
  4. It conducts electricity as a solid, as its valence electrons are delocalized. — P and CS₂ both lie on or near the bottom edge, but P has a low average electronegativity and so lies near the metallic vertex. Atoms with low electronegativity hold their valence electrons weakly, so these electrons are delocalized, and P is predicted to conduct as a solid, like a metal.

Syllabus statement S2.4.2 · Read this in Learn

2 Brass is an alloy of copper and zinc. Like copper, brass conducts electricity and can be hammered into shape. Which statement about the bonding in brass is correct?

Answer and reasoning
  1. Copper and zinc atoms bond in a fixed ratio, as they would in a compound of the two. — A student who thinks an alloy is a compound picks this. Brasses contain from about 5% to 45% zinc; there is no fixed ratio, because the bonding is non-directional metallic bonding, not bonding between particular pairs of atoms.
  2. Covalent bonds join the atoms, as metallic bonding needs atoms of a single element. — A student who confines metallic bonding to pure elements picks this. Directional covalent bonds would give no mobile electrons, so brass could not conduct. Brass keeps the metallic bonding of copper.
  3. Delocalized electrons hold all the cations, as the bonding is non-directional. — Brass is held by metallic bonding, which is non-directional: the delocalized electrons attract every cation, whatever its element. So zinc atoms fit into the lattice, the delocalized electrons carry current, and layers can be moved without breaking the bonding.
  4. Zinc atoms give electrons to copper atoms, so that ionic bonds form between them. — A student who thinks any difference in electronegativity leads to electron transfer picks this. Copper (χ 1.9) and zinc (χ 1.7) differ very little, so no ions of opposite charge form; an ionic solid would also be brittle and would not conduct when solid.

Syllabus statement S2.4.3 · Read this in Learn

3 Which property of poly(ethene) is correctly explained in terms of its structure?

Answer and reasoning
  1. It is an electrical insulator, as it contains no metal atoms to carry a current. — A student who decides conductivity from the elements present picks this. Conductivity depends on mobile charged particles, not on metal atoms: graphite contains no metal and conducts, and magnesium oxide contains a metal but does not conduct as a solid.
  2. It softens on heating, as the covalent bonds in its chains break apart. — A student who thinks softening breaks covalent bonds picks this. Heating overcomes the intermolecular forces between chains; the C–C and C–H bonds within the chains stay intact.
  3. It is an electrical insulator, as all of its valence electrons are in localized bonds. — Poly(ethene) consists of chains of C–C and C–H covalent bonds. Every valence electron is held in a bond between two particular atoms, and there are no ions, so there are no mobile charged particles to carry a current.
  4. It does not biodegrade, as synthetic substances cannot be broken down by organisms. — A student who thinks being synthetic is the reason picks this. Poly(ethene) persists because its long chains of strong, non-polar C–C and C–H bonds are not broken down by microorganisms; some synthetic polymers, such as poly(lactic acid), do biodegrade.

Syllabus statement S2.4.4 · Read this in Learn

4 A section of an addition polymer is –CH₂–C(CH₃)₂–CH₂–C(CH₃)₂–CH₂–C(CH₃)₂–. Which is the monomer?

Answer and reasoning
  1. (CH₃)₃CH — A student who thinks the bonds do not change on polymerization gives a monomer with the same single bonds as the chain. An alkane has no C=C to break, so it cannot form an addition polymer; the monomer must be the alkene (CH₃)₂C=CH₂.
  2. CH₂=CHCH₂CH₃ — A student who puts every carbon into the main chain reads the four carbons of each unit as a straight chain. The CH₃ groups are side groups on one main-chain carbon, so the monomer is branched: (CH₃)₂C=CH₂. But-1-ene would give –CH₂–CH(CH₂CH₃)–.
  3. (CH₃)₃COH — A student who thinks addition polymerization releases water adds H₂O to the repeating unit. No small molecule is lost in addition polymerization; the monomer has the same atoms as the repeating unit, C₄H₈.
  4. (CH₃)₂C=CH₂ — The repeating unit is –CH₂–C(CH₃)₂–: a two-carbon unit of the main chain with two CH₃ side groups on one carbon. Restoring the C=C between the two main-chain carbons gives (CH₃)₂C=CH₂. The monomer has exactly the same atoms as the repeating unit.

Syllabus statement S2.4.5 · Read this in Learn

5 Nylon-6,6 forms from hexane-1,6-diamine, H₂N(CH₂)₆NH₂ (M_r = 116.24), and hexanedioyl dichloride, ClOC(CH₂)₄COCl (M_r = 183.04). Using A_r values H 1.01, C 12.01, N 14.01, O 16.00 and Cl 35.45, what is the M_r of one repeating unit of the polymer? HL

Answer and reasoning
  1. 299.3 — A student who thinks no atoms are lost adds the two monomers: 116.24 + 183.04 = 299.28. Each amide link forms with the release of HCl, so two HCl must be subtracted per repeating unit.
  2. 263.2 — A student who assumes the small molecule is always water subtracts 2 × 18.02: 299.28 − 36.04 = 263.24. With an acyl chloride, the H from –NH₂ and the Cl from –COCl leave as HCl (M_r = 36.46), not H₂O.
  3. 226.4 — Each repeating unit contains one residue of each monomer, and two amide links form per unit, each releasing HCl: 116.24 + 183.04 − 2 × 36.46 = 226.36. The repeating unit is –NH(CH₂)₆NHCO(CH₂)₄CO–, C₁₂H₂₂N₂O₂.
  4. 114.2 — A student who takes the repeating unit from the diamine alone, –NH(CH₂)₆NH– (C₆H₁₄N₂), gets 114.22. The repeating unit contains one residue of each monomer, –NH(CH₂)₆NHCO(CH₂)₄CO–.

Working Repeating unit: –NH(CH₂)₆NHCO(CH₂)₄CO– = C₁₂H₂₂N₂O₂. M_r = 12 × 12.01 + 22 × 1.01 + 2 × 14.01 + 2 × 16.00 = 144.12 + 22.22 + 28.02 + 32.00 = 226.36 ≈ 226.4. Check from the monomers: two amide links form per repeating unit, each releasing HCl (M_r = 1.01 + 35.45 = 36.46): 116.24 + 183.04 − 2 × 36.46 = 226.36.

Syllabus statement S2.4.6 · Read this in Learn

6 Ethane-1,2-diol, HOCH₂CH₂OH, and hexanedioic acid, HOOC(CH₂)₄COOH, react to form a polyester. Which option gives the repeating unit and describes it correctly? HL

Answer and reasoning
  1. –OCH₂CH₂OOC(CH₂)₄CO–, with two H₂O lost per unit — Each –OH of the diol reacts with a –COOH of the acid to form an ester link, –COO–, releasing H₂O. The repeating unit contains one residue of each monomer: the diol has lost the H of each –OH and the acid the –OH of each –COOH, because each unit forms one ester link inside it and one to the next unit. Two H₂O are lost per unit, leaving C₈H₁₂O₄ with 4 O atoms.
  2. –OCH₂CH₂OOC(CH₂)₄COOH, with one H₂O lost per unit — A student who counts only the ester link inside the unit removes one H₂O and leaves the –COOH at the end intact. That group must also react to link the unit to the next one, so it loses its –OH: two ester links and two H₂O per repeating unit, giving –OCH₂CH₂OOC(CH₂)₄CO–.
  3. –O(H)CH₂CH₂O(H)C(O)(OH)(CH₂)₄C(O)(OH)–, with no atoms lost — A student who thinks the monomers simply add together, losing no atoms, keeps every H and OH. Each link O would then form three bonds and each link C five. At each ester link H₂O is released, so the unit has two H₂O fewer than the two monomers.
  4. –OCH₂CH₂O–, with each unit made from a single monomer — A student who takes the repeating unit from one monomer only, as for an addition polymer, gives the diol residue alone. The diol and acid residues alternate along the chain, so the smallest unit that repeats contains one residue of each: –OCH₂CH₂OOC(CH₂)₄CO–.

Syllabus statement S2.4.6 · Read this in Learn

7 Hexane-1,6-diamine, H₂N(CH₂)₆NH₂, and decanedioic acid, HOOC(CH₂)₈COOH, react to form the polyamide nylon-6,10. Which option gives the repeating unit and describes it correctly? HL

Answer and reasoning
  1. –NH(CH₂)₆NHCO(CH₂)₈CO–, with two H₂O lost per unit — Each –NH₂ of the diamine reacts with a –COOH of the acid to form an amide link, –CONH–, releasing H₂O. The repeating unit contains one residue of each monomer: each N has lost one H and each C=O carbon its –OH, with two amide links (two H₂O) per unit, giving C₁₆H₃₀N₂O₂.
  2. –NH(CH₂)₆NHCO(CH₂)₈COOH, with one H₂O lost per unit — A student who counts only the amide link inside the unit leaves the second –COOH unreacted. That group must also react to join the unit to the next diamine residue, so it loses its –OH: two amide links and two H₂O per repeating unit.
  3. –NH₂(CH₂)₆NH₂C(O)(OH)(CH₂)₈C(O)(OH)–, with no atoms lost — A student who thinks the monomers add together without losing atoms keeps every H and OH, giving each link N four bonds and each link C five. Each amide link forms with the release of H₂O, so the unit has two H₂O fewer than the two monomers.
  4. –NH(CH₂)₆NH–, with a single monomer in each unit — A student who takes the repeating unit from one monomer only gives the diamine residue alone. The diamine and diacid residues alternate, so the repeating unit contains one of each: –NH(CH₂)₆NHCO(CH₂)₈CO–.

Syllabus statement S2.4.6 · Read this in Learn

You're done here

That was your twenty minutes. Real practice on S2.4 is past-paper questions marked against the mark scheme.

Paper 1A tests it as multiple choice; Paper 1B through data you have not seen before; Paper 2 with short answers and, at HL, extended responses. Look for the command words — outline, explain, compare, evaluate — and give exactly what each asks for.

← S2.3 The metallic model S3.1 The periodic table: Classification of elements →

Compiled from the IB Chemistry guide (first assessment 2025) and our question bank · Specialist review in progress. How these pages are made · Free, no account ·