The periodic table Flashcards
Periodicity
a regular periodic variation of properties of elements with atomic number and position in the periodic table
First ionisation energy-
energy required to remove 1 electron from each atom in 1 mole of gaseous atoms to form 1 mole of gaseous 1+ ions
Factors affecting ionisation energy
-atomic radius- larger atomic radius, the lower nuclear attraction, therefore lower ionisation energy
-nuclear charge- higher nuclear charge, larger nuclear attraction
-electron shielding- the more shells, the larger the shielding, so less nuclear attraction
1st, 2nd and 3rd ionisation energy equations for Li
Li-> e- + Li+
Li+ -> e- + Li2+
Li2+-> e- + Li3+
Successive ionisation energies
-electrons removed, less repulsion between remaining electrons, so drawn closer nucleus
-positive nuclear charger outweighs the negative charge every time an electron is removed
-as the distance of each electron to the nucleus decreases, nuclear attraction increases, causing ionisation energy to increase
Draw ionisation graph for nitrogen (7)
graph
Ionisation energy trend across period
-general increase because:
-higher nuclear charge as more protons
-electrons added to same shell, which is drawn closer to nucleus
-same number of inner shells, so no change in shielding
8 elements that don’t follow ionisation energy trend
Be-> B and Mg-> Al
-both decrease in ionisation energy even though they’re further along period
-this is because B and Al have their outer electron in a P orbital whereas Be and Mg outer electron is in an S orbital
-P orbitals have higher energy and therefore further from the nucleus
-this therefore decreases nuclear attraction, meaning lower ionisation energy
N->O P->S decrease ionisation energies even though they’re along the period
-because in N and P, each p orbital only contains one electron
-in O and S, the p orbital has 2 electron in = spin paired
-spin paired electrons experience some repulsion and therefore are easier to remove
Ionisation energy trends down a group
-first ionisation energies decrease
-more shells, so more shielding
-larger atomic radius
-nuclear charge increases, but its effects are outweighed by atomic radius and shielding
Metallic bonding
electrostatic forces of attraction between positive ions and delocalised electrons
Giant metallic lattice structure
-delocalised electrons spread throughout
-electrons free to move
-over whole structure, charges balance
Properties of giant metallic lattices
-high MP and BP- attraction between ions and electrons are very strong so high temp required to overcome electrostatic forces
-electrical conductors- delocalised electrons free to move and can carry charge
-ductile- can be drawn out/ stretched eg. wires
-malleable- can be hammered into different shapes
Types bonding across elements in period 2 + 3
Giant metallic:
-Li, Be
-Na, Mg, Al
Giant covalent
-B, C
- Si
Simple molecular
-N2, O2, F2, Ne
-P4, S8, CL2, Ar
Trend melting points in metals
-across the period, MP increases
-this is because ionic charge increases, ionic size decreases
-therefore attraction between ions and electrons increase, so more energy required to disrupt the lattice
Group 2 properties
-high MP + BP
-light metals, low densities
-white compounds