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SingaporeChemistrySyllabus dot point

How do the type of bonding and the shape of a molecule arise from electron arrangement, and how do they control physical properties?

Describe ionic, covalent (including dative) and metallic bonding, predict molecular shapes and bond angles using VSEPR, account for bond polarity and overall polarity, and relate intermolecular forces (van der Waals, hydrogen bonding) to physical properties

A focused answer to the H2 Chemistry learning outcome on bonding and shape. Ionic, covalent, dative and metallic bonding, using VSEPR to predict shapes and bond angles, bond and molecular polarity, and how van der Waals forces and hydrogen bonding govern boiling points and solubility.

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  1. What this dot point is asking
  2. The answer
  3. Examples in context
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What this dot point is asking

SEAB wants you to describe the three primary bonding types (ionic, covalent including dative, and metallic), use VSEPR theory to predict shapes and bond angles, judge whether a molecule is polar overall, and connect intermolecular forces to measurable properties such as boiling point and solubility. Shape prediction and the explanation of anomalous boiling points are perennial exam staples.

The answer

The three bonding types

Ionic bonding is the electrostatic attraction between oppositely charged ions formed by electron transfer (typically metal to non-metal). It gives giant ionic lattices: high melting points, brittle, conduct when molten or aqueous.

Covalent bonding is a shared pair of electrons between two atoms. A dative (coordinate) bond is a covalent bond where both electrons come from the same atom, as in NH4+\text{NH}_4^+ or the donor bond in H3O+\text{H}_3\text{O}^+.

Metallic bonding is the attraction between a lattice of positive ions and a sea of delocalised valence electrons. It explains electrical conductivity, malleability, and high melting points.

VSEPR: predicting shape

Valence Shell Electron Pair Repulsion theory says electron pairs around a central atom arrange themselves to minimise repulsion. The repulsion order is:

lone pair-lone pair>lone pair-bond pair>bond pair-bond pair\text{lone pair-lone pair} > \text{lone pair-bond pair} > \text{bond pair-bond pair}

Count the electron pairs (regions of electron density), choose the geometry, then account for any lone pairs:

Bond pairs Lone pairs Shape Angle Example
2 0 linear 180180 CO2\text{CO}_2
3 0 trigonal planar 120120 BF3\text{BF}_3
4 0 tetrahedral 109.5109.5 CH4\text{CH}_4
3 1 trigonal pyramidal 107\approx 107 NH3\text{NH}_3
2 2 bent 104.5\approx 104.5 H2O\text{H}_2\text{O}
6 0 octahedral 9090 SF6\text{SF}_6

Each lone pair compresses bond angles by roughly 2.52.5 degrees because of its greater repulsion.

Bond polarity and overall polarity

A bond is polar if the two atoms differ in electronegativity, giving partial charges. A molecule is polar overall only if the bond dipoles do not cancel by symmetry:

  • CO2\text{CO}_2 has two polar C=O bonds but is linear, so the dipoles cancel; it is non-polar.
  • H2O\text{H}_2\text{O} is bent, so the dipoles do not cancel; it is polar.

Intermolecular forces

Three types, increasing in strength:

  1. Instantaneous dipole-induced dipole (dispersion) forces. Present in all molecules; strengthen with more electrons (larger MrM_r) and larger surface contact.
  2. Permanent dipole-dipole forces between polar molecules.
  3. Hydrogen bonding, the strongest, occurs when H is bonded to N, O or F and there is a lone pair on a neighbouring electronegative atom.

These control boiling point, melting point, viscosity, and solubility. Like dissolves like: polar and hydrogen-bonding solutes dissolve in polar solvents.

The boiling-point anomalies

Down a group the hydrides should boil higher (more electrons, stronger dispersion forces), and they mostly do. But H2O\text{H}_2\text{O}, HF\text{HF} and NH3\text{NH}_3 boil anomalously high because of hydrogen bonding. Water is the standout: each molecule has two H atoms and two lone pairs, so it forms an extensive hydrogen-bonded network.

Examples in context

Example 1. Comparing boiling points of isomers. A Paper 2 question compares the boiling points of butan-1-ol and diethyl ether, both C4H10OC_4H_{10}O. Butan-1-ol has an O-H group and forms hydrogen bonds between molecules, so it boils much higher (about 118 degrees Celsius) than diethyl ether (about 35 degrees Celsius), which can only accept hydrogen bonds (no O-H) and relies mainly on dipole-dipole and dispersion forces. This shows that the functional group, not the molecular formula, sets the dominant intermolecular force.

Example 2. Explaining solubility. Ethanol is fully miscible with water because its O-H group hydrogen bonds with water, while hexane is immiscible because it is non-polar and can only form dispersion forces, which cannot disrupt water's hydrogen-bonded network. This like-dissolves-like reasoning is exactly what SEAB expects in solubility explanations.

Try this

Q1. Predict the shape and bond angle of (a) BF3\text{BF}_3 and (b) PCl3\text{PCl}_3. [2+2 marks]

  • Cue. (a) Trigonal planar, 120120 degrees, no lone pairs. (b) Trigonal pyramidal, about 107107 degrees, one lone pair on P.

Q2. State and explain whether CCl4\text{CCl}_4 is polar. [2 marks]

  • Cue. Tetrahedral and symmetric; the four polar C-Cl dipoles cancel, so CCl4\text{CCl}_4 is non-polar.

Q3. Place CH4\text{CH}_4, NH3\text{NH}_3 and H2O\text{H}_2\text{O} in order of increasing boiling point and explain. [3 marks]

  • Cue. CH4<NH3<H2O\text{CH}_4 < \text{NH}_3 < \text{H}_2\text{O}. CH4\text{CH}_4 has only dispersion forces; NH3\text{NH}_3 and H2O\text{H}_2\text{O} hydrogen bond, and water forms more hydrogen bonds per molecule (two H and two lone pairs).

Exam-style practice questions

Practice questions written in the style of SEAB exam questions on this dot point, with worked answer explainers. The year tag is the paper they imitate, not the source.

Specimen (9729)5 marksPredict and explain the shape and bond angle of (a) NH3 and (b) the ion NH4+. Account for any difference between them.
Show worked answer →

Count electron pairs (bonding and lone) around the central nitrogen, then apply VSEPR.

(a) NH3: N has 5 valence electrons; 3 are shared in N-H bonds and one lone pair remains. Total 4 electron pairs, so the electron-pair geometry is tetrahedral. With one lone pair the molecular shape is trigonal pyramidal.

Lone pair-bond pair repulsion is greater than bond pair-bond pair repulsion, so the bond angle is compressed from 109.5 to about 107 degrees.

(b) NH4+: the lone pair has formed a dative (coordinate) bond to H+. Now there are 4 bond pairs and no lone pairs. The shape is tetrahedral with a bond angle of 109.5 degrees.

The difference arises because the lone pair in NH3 is replaced by a bonding pair in NH4+, removing the extra lone-pair repulsion.

Markers reward the electron-pair count, the named shapes, the angle values, and the lone-pair repulsion argument.

2022 (style)4 marksExplain why water (Mr = 18) has a much higher boiling point than hydrogen sulfide (Mr = 34), even though H2S has a larger relative molecular mass.
Show worked answer →

Identify the intermolecular forces in each.

H2O molecules form hydrogen bonds: O is highly electronegative and bonded to H, and O has lone pairs. Each water molecule can form on average two hydrogen bonds.

H2S has only weaker van der Waals (permanent dipole-dipole and instantaneous dipole-induced dipole) forces, because S is not electronegative enough for significant hydrogen bonding.

Hydrogen bonds are much stronger than the van der Waals forces in H2S, so more energy is needed to separate water molecules.

Therefore water boils at a much higher temperature, despite its smaller Mr.

Markers reward naming hydrogen bonding in water, the requirement (electronegative atom with H, plus lone pair), the weaker forces in H2S, and the link to energy needed to boil.

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