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3.1 The periodic table: Classification of elements

Understanding Points
Structure 3.1.1—The periodic table consists of periods, groups and blocks.
Structure 3.1.2—The period number shows the outer energy level that is occupied by electrons.
Elements in a group have a common number of valence electrons.
Structure 3.1.3—Periodicity refers to trends in properties of elements across a period and down a
group.
Structure 3.1.4—Trends in properties of elements down a group include the increasing metallic
character of group 1 elements and decreasing non-metallic character of group 17 elements.
Structure 3.1.5—Metallic and non-metallic properties show a continuum. This includes the trend
from basic metal oxides through amphoteric to acidic non-metal oxides.
Structure 3.1.6—The oxidation state is a number assigned to an atom to show the number of
electrons transferred in forming a bond. It is the charge that atom would have if the compound
were composed of ions.
The periodic table
Elements on the periodic table go from left to right in increasing atomic number by 1
Z and # of e- increase by 1 as you move from left → right
Period number = outer energy level occupied by electrons
Group number = number of valence electrons
The periodic table consists of:
7 Periods (rows)
n of the outermost energy level occupied by e-
Elements in the same period have varying chemical/physical properties
18 groups (columns)
# of valence electrons in outermost energy level
Elements in the same group have similar chemical/physical properties
4 blocks (s, p, d, f)
Elements which have occupied subshells orbitals
Metal, non-metal, and metalloid regions
From left → right, metallic character ↓
Groups 1, 2, and d, f, block contain metals, right-most part of p block contain non-metals, and the in between contain metalloids
Element Groups
Group 1 Alkali metals
Group 17 Halogens
Group 18 Noble gases
D-block Transition metals
F-block 1st row Lanthanoids
F-block 2nd row Actinoids
Periodicity: repeating pattern of physical and chemical properties across a period /down a group
Trends in Physical Properties
Comparison of Physical and Chemical Properties
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Physical Properties
Across Period
Down Group
파일
Effective nuclear charge (Zeff) Nuclear charge experienced by the valence e-s Number of protons - number of non-valence e-s due to shielding
Same
Atomic radius Half the distance b/w nuclei of two neighbouring atoms (distance b/w nucleus and outermost e-)
↓ ˙.˙ effective nuclear charge ↑ ElectrostaticDistance ↓ “Atomic shrinkage” “Results in valence shell being pulled more strongly to the nucleus”
↑ ˙.˙  no. e- shells ↑ DistanceElectrostatic ↓ “Atomic/ionic expansion”
Ionic radius Half the distance b/w nuclei of two neighbouring ions (distance b/w nucleus and outermost e-) *No value for Group 18 Ionic vs atomic radii (same nuclear charge & different no. of valence e-s) *For group 1 to 14,  ionic < atomic radius ˙.˙ of loss of an e- shell & same no. of protons pulling lower no. of e-s *For group 14 to 17,  ionic > atomic radius ˙.˙ of more no. of e- and e--e- repulsion caused expansion/same no. of protons pulling higher no. of e-s (e.g. Cl vs Cl-)
(different nuclear charge & same no. of valence e-s) ↓ from group 1 to 14 ˙.˙ Nuclear charge ↑ ElectrostaticDistance ↓ “Ionic shrinkage” Jump ˙.˙ a new e- shell is introduced ↓ from group 4 to 7 ˙.˙ Nuclear charge ↑ ElectrostaticDistance ↓ “Ionic shrinkage” *Original vs X large doughnut & 8 different weighted consumer analogy*
Ionization energy Energy required to remove 1 mole of e-s from 1 mole of gaseous atoms (kJ mol-1) X(g) → X+(g)+ e– “Endothermic as bond broken between removed e- and nucleus”
*Staircase analogy* Overall ↑ ˙.˙ effective nuclear charge ↑Atomic radius ↓ Electrostatic ↑ Very high value for Group 18 ˙.˙ noble gases do not want to lose full octet
↓ ˙.˙  no. e- shells ↑ DistanceElectrostatic ↓ “Easier to remove e-”
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Electron Affinity Energy change when 1 mole of electrons is added to 1 mole of gaseous atoms X(g) + e– → X–(g) *No value for Group 18 (do not form -ve ion)  “Exothermic as bond formed between new e- and nucleus”
Overall ↑ (more exothermic) ˙.˙ effective nuclear charge ↑ Electrostatic ↑ Energy released ↑ Jump b/w 1 & 2 (endothermic) ˙.˙ added e- is placed at p orbital that is further away from nucleus (shielding)  Attraction b/w e- and nucleus is weaker Less energy released/exothermic (actually endothermic) Jump b/w 14 & 15 ˙.˙ e- added to an already half-filled orbital new e- is pushed further away from nucleus due to e- - e- repulsion Attraction b/w e- and nucleus is weaker Less energy released/exothermic *N/A for Group 18 *2nd e- affinity is endothermic ˙.˙ energetically unfavourable to remove e- from -ve ion
↓ ˙.˙  no. e- shells ↑ DistanceElectrostatic ↓ “Difficult to gain e-”
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Electronegativity 1. Ability of an atom to pull a shared pair of e-s to its nucleus 2. Effective nuclear charge experienced by a shared pair of e-s
↑ ˙.˙ effective nuclear charge ↑ Electrostatic
↓ ˙.˙  no. e- shells ↑ DistanceElectrostatic
Metallic and non-metallic behaviour
↓ ˙.˙ I.E. ↑ .˙. Less likely to be oxidised (ionised)
↓ ˙.˙  Ionic radius ↓ More easily oxidised (ionised)
Repeating Tags
distance b/w nucleus and valence e-  electrostatic attraction b/w nucleus and valence e-
Group 1 and 17
Down Group
Group 1 Alkali Metals
Group 17 Halogens
Melting Point
↓ ˙.˙ delocalised e- is further away from nucleus Metallic bonding ↓ M.P. ↓ “Electrostatic attraction b/w cations and delocalised e-s”
↑ ˙.˙ molecular size ↑ London dispersion force ↑  M.P. ↑  “Electrostatic attraction temporary b/w non-polar molecules with temporary induced dipoles (due to random shift in e- position)”
Reactivity
Ionisation energy ↓ ˙.˙ valence e- being ionised is further away from nucleus More easily lost and ionised to form ionic compound
electronegativity ↓ ˙.˙ e- being accepted is further to nucleus Less easily accepted to ionise to form ionic compound
Reactions of Group 1 with water
Reaction with Water
Reactivity
Product
Observation
Li
Slow
Alkaline solution (LiOH, NaOH, KOH) + H2 gas
Floats on water
Na
Vigorous
Melts into a small ball (large heat)
K
V. Vigorous
Hydrogen gas ignites into lilac flame
Group 1 with halogens
Group 17 - Displacement reaction
“Salt production”
2NaBr(aq) + Cl2(g) -> NaCl(aq) + Br2(g) Cl2 is more reactive than Br2 and displaces Br from Na *Observation - Solution turns colourless to orange/brown
Period 3 Oxides
Na2O(s)
MgO(s)
Al2O3(s)
SiO2(s)
P4O10(s)
SO3(g)
Acid-base character
Basic Na2O(s) + H2O(l) → 2NaOH(aq)  MgO(s) + H2O(l) → Mg(OH)2(aq)
Amphoteric (Insoluble)
Insoluble
Acidic P4O10(s) + 6H2O(l) → 4H3PO4(aq) SO3(g) + H2O(l) → H2SO4(aq) NO2(g) + H2O(l) → HNO3(aq)
Oxidation state
Represents the charge on an atom in a compound if it were composed of ions
Describes the number of electrons shared or transferred when forming a bond
Oxidation state rules:
1.
All elements in their natural form have O.S.= 0
2.
For a given ion with only one atom, O.S.=charge of the ion
a.
e.g. Na+ → +1, Cu2+ → +2, O2- → -2
3.
For a polyatomic ion, the sum of the O.S. of the atoms in the ion = charge of the ion
4.
For a neutral compound, the sum of O.S. of the atoms = 0
5.
Metal O.S. in a compound
a.
Group 1 metals have O.S= +1 in a compound
b.
Group 2 metals have O.S.= +2 in a compound
c.
Transition metals can have varying O.S.
6.
O.S. to know for common atoms in a compound:
a.
Hydrogen O.S. = +1
i.
except when in metal hydrides where O.S.= -1 (e.g. KH, O.S. of H = -1)
b.
Fluorine O.S.= -1
c.
Oxygen O.S. = -2
i.
Except when in OF2 (O.S. of O= +1) and in peroxides (e.g. H2O2, O.S. of O = -1)
d.
Halogens O.S. = -1
i.
Except when in compounds with O, F where O.S. >0
Transition metals have variable O.S. → expressed as roman numerals in parentheses
Compound
Oxidation state
Name (oxidation numbered)
FeO
Fe (+2)
iron(II) oxide
Fe2O3
Fe (+3)
iron(III) oxide
Cu2O
Cu (+1)
copper(I) oxide
CuO
Cu (+2)
copper(II) oxide
MnO2
Mn (+4)
manganese(IV) oxide
MnO4– *
Mn (+7)
manganate(VII) ion
K2Cr2O7*
Cr (+6)
potassium dichromate(VI)
Cr2O3
Cr (+3)
chromium(III) oxide
NO
N (+2)
nitrogen(II) oxide
NO2
N (+4)
nitrogen(IV) oxide
no. of valence e-s with assumption that shared electron pair in a covalent bond belongs entirely to a more electronegative element, e.g. in S2O32-, 0 & +4 or -2 & +6 O.S. for average value of of +2