Periodic Table

Cards (46)

  • Atomic radius is half the distance between the centres of 2 adjacent atoms in the structure of the element
  • Metallic radius is half the distance between the centres of 2 adjacent atoms in a metal
  • covalent radius is half the distance between the centres of 2 adjacent atoms that are covalently bonded
  • van der Waal’s radius is half the distance between the centres of 2 adjacent atoms which are not chemically bonded
  • Across the period, atomic radii decreases
    • number of protons increases, nuclear charge increases
    • same number of inner shell electrons, shielding effect approximately constant
    • increase in effective nuclear charge
    • increase in electrostatic forces of attraction between nucleus and valence electrons
  • ionic radii decreases
    • nuclear charge increases
    • same inter-electronic repulsion (same number of electrons)
    • stronger electrostatic forces of attraction
  • Anions bigger than cations
    • anions have one more filled principal quantum shell
    • valence electrons further from nucleus
    • weaker electrostatic forces of attraction
  • 1st IE increases across the period:
    • nuclear charge increases
    • shielding effect approximately constant
    • increase in effective nuclear charge
    • increase in electrostatic forces of attraction
    • more energy needed to remove valence electron
  • 1st IE of Al (grp 13) lower than Mg (grp 2)
    • 3p electron is at higher energy level
    • less energy needed to remove
  • 1st IE of S (grp 16) lower than P (grp 15)
    • inter-electronic repulsion between paired electron of the same orbital in S
    • less energy needed to remove
  • Melting point of giant metallic lattice structure
    • high due to large amount of energy needed to overcome strong metallic bonds
    • as number of delocalised electrons increase, smaller cationic radius --> higher charge density, more energy needed to overcome strong electrostatic forces of attraction between metal cations and sea of delocalised electrons
  • Electrical conductivity of giant metallic lattice structure
    • sea of delocalised electrons as mobile charge carriers
  • Melting point of giant molecular structure
    • large amount of energy needed to overcome strong and extensive covalent bonds between atoms
  • Melting point of simple molecular structures
    • low, small amount of energy needed to overcome weak id-id interactions
    • melting point increases with increase in number of electrons, increase in polarisability of electron cloud and thus more energy needed to overcome stronger id-id
  • across the period, oxidation numbers increases
    • number of valence electrons available increases
  • P and S can exhibit multiple oxidation numbers
    • presence of vacant and energetically accessible d orbitals, can be used for bonding through expansion of octet structure
  • sodium oxide dissolves completely in water to form sodium hydroxide (pH14 solution)
    magnesium oxide dissolves partially in water due to high lattice energy (pH9 solution)
    • basic O2- ion reacts with H2O by accepting H+ to form hydroxide ion (forms 2 hydroxide ions)
  • aluminium oxide does not dissolve in water due to extremely high lattice energy, large amount of energy needed to break strong ionic bonds (pH7 solution)
  • Silicon dioxide is a giant molecular structure, does not dissolve in water due to strong and extensive covalent bonds between Si and O atoms
  • P4O10 and SO3 dissolves in water to give phosphoric acid and sulfuric acid
    • S=O and P=O bond reacts with H2O to give P/S-O-H bonds, then dissociate to give H+
  • Group 2 elements atomic and ionic radius increases down the group
    • both nuclear charge and shielding effect increase, valence electrons located further away from the nucleus
    • weaker electrostatic forces of attraction between nucleus and valence electrons
  • group 2 elements first IE decreases down the group
    • nuclear charge and shielding effect increase, valence electrons located further away from the nucleus
    • weaker electrostatic forces of attraction betw nucleus and valence electrons, less energy needed to remove
  • group 2 elements electronegativity decreases down the group
    • weaker electrostatic forces of attraction between nucleus and electron pair in covalent bond
  • group 2 elements melting point decreases down the group
    • size of cations increases, charge density decreases (charge remains the same)
    • weaker electrostatic forces of attraction between cations and sea of delocalised electrons
    • less energy needed to overcome
  • Group 17 elements (halogens) structure and bonding
    • simple molecular structure
    • weak Id-id between non-polar molecules
  • group 17 elements boiling point increases down the group
    • number of electrons increase
    • polarisability of electron cloud increase
    • more energy needed to overcome stronger id-id
  • structure and bonding of hydrogen halides (HX)
    • simple molecular structure
    • weak id-id and pd-pd between polar molecules
  • Boiling point of hydrogen halides increases down the group
    • number of electrons increases
    • polarisability of electron cloud increases
    • more energy needed to overcome stronger id-id
  • thermal stability of hydrogen halides decrease down the group
    • size of halogen atom increases
    • effectiveness of orbital overlap decreases
    • bond strength decreases
    • less energy required to break bond
  • Basic oxides: sodium oxide, magnesium oxide
  • Amphoteric oxide: aluminium oxide
  • acidic oxides: phosphorus pentoxide, sulfur trioxide
  • sodium chloride undergoes complete hydration, but does not undergo hydrolysis
  • magnesium chloride undergoes:
    • hydration, forms hydrated metal ions (complex ion) and chloride ions
    • slight hydrolysis, metal cation has high charge density, polarises electron cloud of surrounding water molecules, break O-H bond to release H+ (results in acidic solution, pH 6.5)
    • dissolves completely in water
  • aluminium chloride:
    • undergoes hydration, forms hydrated metal ions (complex ion) and chloride ions
    • slight hydrolysis, metal cation has high charge density (aluminium higher than magnesium), polarises electron cloud of surrounding water molecules, can break O-H bonds, release H+ (results in acidic solution, pH 3)
    • dissolves completely in excess water
  • Metal ions that form complexes: magnesium, aluminium
    • water molecules form dative bonds with cation
    • metal ion uses 1 empty 3s, 3 3p, 2 3d orbitals to form 6 hybrid orbitals, accepts 6 lone pairs from 6 water molecules
  • Aluminium chloride in limited water:
    • complete hydrolysis, has vacant and energetically accessible 3p orbital, can accept lone pair from water molecules to form dative bonds
    • reacts vigorously, white solid of aluminium hydroxide/aluminium oxide forms, white fumes of HCl
    • pH 3
  • silicon tetrachloride:
    • does not undergo hydration
    • complete hydrolysis, has vacant and energetically accessible 3d orbitals, can accept lone pair from water molecules, form dative bond
    • reacts vigorously with water, forms white solid (silicon dioxide), white fumes of HCl
    • pH 2
  • phosphorus pentachloride:
    • does not undergo hydration
    • complete hydrolysis, P has vacant and energetically accessible 3d orbitals, can accept lone pair from water molecules, forms dative bond
    • reacts vigorously with water, white fumes of HCl
    • pH 2
  • down group 17:
    • atomic radius increases, lower tendency to accept electrons
    • lower tendency for atom to be reduce to anion
    • oxidising power of halogens decreases down the group, E value becomes less positive (smaller tendency to be reduced, weaker OA)