Historical development of the periodic table, groups and periods, electronic configuration and position, trends in Group II and Group VII, trends across Period 3, and predicting properties from position.
The periodic table organises every known element in a way that reveals patterns. Once you understand why elements are arranged as they are, you can predict the behaviour of unfamiliar elements without memorising individual facts.
Several scientists contributed to the periodic table before its modern form was established.
Johann Döbereiner (1817–1829) observed that certain elements could be grouped into sets of three, called triads, where the middle element had properties and an atomic mass approximately halfway between the other two. For example, lithium (7), sodium (23), and potassium (39) form a triad: the average of 7 and 39 is 23, matching sodium. This was an early indication that element properties followed a pattern, but the system only worked for a handful of groups.
Dmitri Mendeleev (1869) arranged elements in order of increasing atomic mass, placing elements with similar properties in the same vertical column. He left deliberate gaps where undiscovered elements should fit and predicted their properties. When those elements were later found, his predictions proved largely correct, which established the table's credibility.
Henry Moseley (1914) demonstrated that elements should be ordered by increasing atomic number (proton number) rather than atomic mass. This resolved anomalies in Mendeleev's arrangement and produced the modern periodic law: the physical and chemical properties of elements are periodic functions of their atomic numbers.
The modern periodic table organises elements into:
The group number tells you the number of valence electrons; the period number tells you how many electron shells are occupied.
Magnesium has the configuration 2,8,2:
Chlorine has the configuration 2,8,7:
Do not confuse group and period. Group = number of valence electrons = vertical column. Period = number of occupied shells = horizontal row.
Group II elements — beryllium, magnesium, calcium, strontium, barium — all have 2 valence electrons and form 2+ ions.
Ionisation (removal of valence electrons) becomes easier going down Group II. As atomic radius increases down the group, the outer electrons are further from the nucleus and more shielded from its attraction by inner shells. Less energy is therefore needed to remove them.
All Group II metals burn in oxygen to form metal oxides. Reactivity increases down the group:
Magnesium reacts very slowly with cold water but burns vigorously in steam:
Calcium reacts steadily with cold water, producing calcium hydroxide and hydrogen gas:
Moving down the group, reactivity with cold water increases progressively.
Magnesium and calcium both react with dilute hydrochloric acid to produce a salt and hydrogen gas. The reaction rate increases down the group:
The overall trend in Group II: reactivity increases going down because valence electrons are held less tightly as atomic radius increases and shielding from inner shells increases.
Group VII — fluorine, chlorine, bromine, iodine, astatine — all have 7 valence electrons. They gain one electron to form −1 ions and are the most reactive non-metals.
| Element | Formula | State | Colour |
|---|---|---|---|
| Fluorine | F₂ | Gas | Pale yellow |
| Chlorine | Cl₂ | Gas | Yellow-green |
| Bromine | Br₂ | Liquid | Red-brown |
| Iodine | I₂ | Solid | Grey-black |
Moving down the group, the molecules become heavier and intermolecular forces between them strengthen, raising melting and boiling points.
Halogens are oxidising agents — they gain electrons from other substances. Oxidising power decreases going down Group VII. Fluorine is the strongest oxidising agent of all known elements; iodine is considerably weaker.
As atomic radius increases down the group, the outer shell is further from the nucleus and more shielded by inner shells. The ability to attract an incoming electron weakens.
A more reactive halogen displaces a less reactive one from a solution of its salt, which directly demonstrates the relative oxidising powers:
Chlorine displaces bromine because it is a stronger oxidising agent. Bromine can displace iodine for the same reason, but bromine cannot displace chlorine.
In Group VII, reactivity decreases down the group — the opposite direction to Group I and Group II. This is because halogens react by gaining electrons, not losing them, and the ability to attract electrons weakens as atomic size increases.
Period 3 contains eight elements: Na, Mg, Al, Si, P, S, Cl, and Ar. Moving from left to right, the elements change from metals through a metalloid to non-metals:
| Element | Symbol | Z | Type | Valence electrons |
|---|---|---|---|---|
| Sodium | Na | 11 | Metal | 1 |
| Magnesium | Mg | 12 | Metal | 2 |
| Aluminium | Al | 13 | Metal | 3 |
| Silicon | Si | 14 | Metalloid | 4 |
| Phosphorus | P | 15 | Non-metal | 5 |
| Sulfur | S | 16 | Non-metal | 6 |
| Chlorine | Cl | 17 | Non-metal | 7 |
| Argon | Ar | 18 | Noble gas | 8 |
As nuclear charge increases across the period (more protons, same number of shells), atomic radius decreases and ionisation energy generally rises, making it progressively harder to remove electrons. This shift produces the transition from metallic to non-metallic character.
The type of oxide formed by each element also changes systematically:
| Element | Oxide | Character |
|---|---|---|
| Na | Na₂O | Basic |
| Mg | MgO | Basic |
| Al | Al₂O₃ | Amphoteric (reacts with both acids and bases) |
| Si | SiO₂ | Weakly acidic |
| P | P₄O₁₀ | Acidic |
| S | SO₃ | Acidic |
| Cl | Cl₂O₇ | Acidic |
Basic oxides react with acids; acidic oxides react with bases; amphoteric oxides (aluminium oxide) react with both. This trend from basic to amphoteric to acidic directly mirrors the transition from metal to non-metal across the period.
Once the group and period of an element are known, many of its properties follow:
An unknown element X is in Group II, Period 4. Expected properties: