Ionic Bonding Basics

Ever wonder why table salt dissolves so easily in water? It's all about ionic bonding - one of the strongest ways atoms can stick together. Metal atoms lose electrons to become positive ions, while non-metal atoms gain those electrons to become negative ions.

Take magnesium oxide (MgO) as an example. Magnesium loses two electrons (Mg²⁺) and oxygen gains them (O²⁻). The electrostatic attraction between these oppositely charged ions creates the ionic bond - think of it like powerful magnets pulling together.

Ionic compounds form giant lattices - massive 3D structures where millions of ions are arranged in regular patterns. The stronger the charges and the smaller the ions, the higher the melting point. That's why MgO melts at a scorching 2852°C compared to table salt's 801°C.

Key insight: Positive ions are always smaller than their original atoms because they've lost an electron shell, while negative ions are bigger because extra electrons spread out the existing ones.

Evidence and Properties of Ionic Compounds

X-ray diffraction gives us actual proof that ions exist as separate particles. These techniques create electron density maps showing exactly where electrons hang out in compounds like sodium chloride.

The maps reveal two crucial facts: ions arrange in regular patterns (like a 3D chess board), and chloride ions are definitely larger than sodium ions. However, the maps can't show precise ion boundaries since electron density gradually fades rather than stopping abruptly.

Physical properties of ionic compounds make perfect sense once you understand the structure. They have high melting points because breaking apart all those electrostatic attractions requires massive energy. They don't conduct electricity as solids (ions can't move), but become excellent conductors when molten or dissolved (ions are free to move).

Migration experiments prove ions move independently. When you apply electricity to copper chromate solution, blue Cu²⁺ ions migrate to the negative electrode while yellow CrO₄²⁻ ions head to the positive electrode.

Lab tip: The brittle nature of ionic crystals happens because shifting layers brings like charges together - they immediately repel and the crystal splits apart.

Covalent Bonding

Covalent bonds form when atoms share electrons rather than transferring them completely. The shared electron pair sits between two nuclei, attracted to both - creating a strong electrostatic attraction that holds atoms together.

X-ray diffraction of hydrogen molecules shows high electron density right between the two nuclei. This proves the electrons spend most of their time in the gap, strongly attracted to both protons simultaneously.

Multiple bonds create interesting effects on bond strength and length. Double and triple bonds squeeze more electron density between nuclei, creating stronger attractions. This makes the bonds both shorter and stronger - triple bonds are tougher to break than single bonds.

Giant covalent structures like diamond demonstrate just how strong these bonds can be. Diamond's sky-high melting point (over 3500°C) comes from millions of strong covalent bonds throughout the entire crystal structure.

Think about it: The electron density maps show significant electron sharing between atoms in covalent compounds, unlike ionic compounds where electrons clearly belong to specific ions.

Dative Covalent Bonding

Sometimes one atom does all the sharing work - that's dative covalent bonding (also called coordinate bonding). Here, both electrons in the shared pair come from just one atom, which must have a lone pair of electrons to donate.

Ammonium ion (NH₄⁺) perfectly demonstrates this concept. Nitrogen in ammonia (NH₃) has a lone pair that bonds with a hydrogen ion (H⁺). Once formed, this dative bond behaves exactly like a normal covalent bond - you can't tell them apart.

Aluminum chloride (AlCl₃) shows dative bonding in action when two molecules join together. Each aluminum is electron-deficient, so chlorine atoms donate lone pairs to form Al₂Cl₆ dimers. The arrows in diagrams show the direction from electron donor to electron acceptor.

When predicting molecular shapes, treat dative bonds exactly like normal covalent bonds. NH₄⁺ has four bonding pairs around nitrogen, giving it a tetrahedral shape regardless of which bond is dative.

Memory trick: Draw arrows pointing from the atom giving the lone pair to the atom receiving it - this shows the direction of electron donation clearly.

Molecular Shapes

Molecular geometry depends on both bonding pairs and lone pairs of electrons around the central atom. These electron pairs repel each other and arrange themselves as far apart as possible - this is VSEPR theory (Valence Shell Electron Pair Repulsion).

Basic shapes follow predictable patterns. Two electron pairs give linear molecules (180°), three pairs create trigonal planar (120°), four pairs form tetrahedral (109.5°), five pairs make trigonal bipyramidal (90° and 120°), and six pairs create octahedral (90°).

Lone pairs affect bond angles because they occupy more space than bonding pairs. In ammonia (NH₃), the lone pair compresses the H-N-H bond angles from 109.5° to 107°. Water has two lone pairs, squashing the H-O-H angle to 104.5°.

The table shows standard shapes, but you'll encounter variations where lone pairs replace some bonding positions. For example, sulfur tetrafluoride (SF₄) starts with five electron pairs (trigonal bipyramidal) but one lone pair gives it a seesaw shape.

Pro tip: Count all electron pairs first $bonding + lone pairs$, determine the basic arrangement, then remove lone pairs to see the actual molecular shape.

Complex Molecular Shapes

More complex shapes emerge when you have five or six electron pairs with some lone pairs mixed in. These are variations of octahedral and trigonal bipyramidal arrangements where lone pairs replace some bonds.

Square planar molecules like XeF₄ start with six electron pairs (octahedral arrangement). Xenon contributes 8 electrons, four fluorines add 4 more, giving 12 electrons total. That's 4 bonding pairs and 2 lone pairs, creating the square planar shape with 90° bond angles.

T-shaped molecules like ClF₃ begin with five electron pairs (trigonal bipyramidal). Chlorine has 7 outer electrons, three fluorines contribute 3 more, totaling 10 electrons. With 3 bonding pairs and 2 lone pairs, you get the distinctive T-shape.

Seesaw shapes appear in molecules like SF₄ and IF₄⁺. For IF₄⁺, iodine starts with 7 electrons, four fluorines add 4, but remove 1 for the positive charge. That gives 10 electrons (4 bonding, 1 lone pair) in a trigonal bipyramidal arrangement.

Strategy: Always start by counting total electrons, divide by 2 for electron pairs, then work out how many are bonding vs. lone pairs to predict the final shape.

Electronegativity and Polar Bonds

Electronegativity measures how strongly atoms attract electrons in covalent bonds. Fluorine tops the scale at 4.0, with oxygen, nitrogen, and chlorine also being highly electronegative. This concept explains why some bonds behave more like ionic bonds.

Trends are predictable across the periodic table. Electronegativity increases across periods (more protons pulling electrons) and decreases down groups (electrons further from nucleus with more shielding). These patterns determine bond polarity.

Polar covalent bonds form when electronegativity differences range from 0.3 to 1.7. The more electronegative atom becomes slightly negative (δ-) while the other becomes slightly positive (δ+). In H-Cl, chlorine is more electronegative, so it's the negative end.

Molecular polarity depends on shape, not just individual bond polarity. Carbon tetrachloride (CCl₄) has four polar C-Cl bonds, but the tetrahedral shape makes them cancel out - the molecule is non-polar. However, CHCl₃ is polar because the shape isn't perfectly symmetrical.

Real-world test: Polar liquids are attracted to charged rods due to dipole alignment, while non-polar liquids show no deflection - a simple way to test molecular polarity.

Intermolecular Forces - London Forces

London forces (also called van der Waals forces) exist between all molecules and atoms, even noble gases. They're much weaker than chemical bonds but crucial for determining physical properties like boiling points.

These forces arise from temporary dipoles created by constantly moving electrons. When electrons bunch up on one side of a molecule, it becomes temporarily negative. This induces opposite dipoles in neighbouring molecules, creating weak attractions.

Electron count directly affects London force strength. More electrons mean higher chances of temporary dipoles forming, creating stronger intermolecular attractions. This explains why iodine (I₂) is solid while chlorine (Cl₂) is gas - iodine has way more electrons.

Molecular shape also matters for London forces. Long, straight-chain alkanes have larger surface contact areas than branched alkanes, allowing more London force interactions. That's why straight-chain molecules often have higher boiling points than their branched counterparts.

Pattern recognition: The steady increase in boiling points down the halogen group (F₂, Cl₂, Br₂, I₂) perfectly demonstrates how electron count affects London force strength.

Permanent Dipole and Hydrogen Bonding

Permanent dipole-dipole forces occur between polar molecules and are stronger than London forces. Molecules with C-Cl, C-F, or C=O bonds often show these interactions because the electronegativity differences create permanent charge separations.

Hydrogen bonding represents the strongest intermolecular force, occurring when hydrogen bonds to nitrogen, oxygen, or fluorine. The massive electronegativity difference creates highly polar bonds, and the small hydrogen atom allows close approach between molecules.

Hydrogen bond geometry is crucial - bonds should be linear (180°) for maximum strength. Water molecules can form two hydrogen bonds each because oxygen has two lone pairs. This extensive hydrogen bonding network gives water its unusually high boiling point.

Real-world effects of hydrogen bonding appear everywhere. Alcohols have higher boiling points than similar alkanes due to hydrogen bonding. Ice floats because hydrogen bonds hold water molecules further apart in the solid state, reducing density.

Key insight: The anomalously high boiling points of H₂O, HF, and NH₃ compared to their period neighbours (like H₂S, HCl, PH₃) clearly show hydrogen bonding's extra strength.

Solubility and Intermolecular Forces

Solubility depends on the balance between energy needed to break existing bonds and energy released forming new interactions. The rule "like dissolves like" reflects how similar intermolecular forces promote mixing.

Ionic dissolution in water involves hydration - water molecules surround ions with their polar ends. Positive ions attract the negative oxygen end of water molecules, while negative ions attract the positive hydrogen ends. Higher charge density increases hydration strength.

Alcohol solubility decreases as carbon chains get longer. Small alcohols like methanol and ethanol dissolve completely in water because they can form hydrogen bonds with water molecules. However, longer hydrocarbon chains become increasingly water-repelling.

Non-polar substances like hexane can't form hydrogen bonds with water, making them insoluble. Even polar molecules without hydrogen bonding capability (like halogenoalkanes) remain largely insoluble in water.

Practical application: Understanding solubility helps predict everything from which cleaning products work best to how drugs are absorbed in your body.