4 - Inorganic chemistry and the periodic table Flashcards
Trend in ionisation energy down group 2?
- decreases as you go down the group
- atomic radii increases
- number of shells increases, greater shielding effect.
- energy of the outermost electrons increases,
- so ionisation energy decreases down a group.
What type of bonding is present in group 1 and 2 elements?
metallic bonding
Trend in metallic bonding down group 1 and 2?
- decreases
- although nuclear charge increases
- atomic radius increases
- distance between the positive nuclei and delocalised electrons increases.
- shielding effect from inner electron shells also increases
- force of attraction between positive nuclei and delocalised electrons decreases.
Trend in reactivity down group 2?
- increases
- although nuclear charge increases
- atomic radii increases
- shielding effect increases
- attraction between nucleus and outer electrons decreases.
- easier to remove outer electrons, easier to form cations.
group 2 metal + oxygen
metal oxide.
- bright flame
- high melting points (ionic bonding)
2M + O2 -> 2MO
Group 2 metal + chlorine
metal chloride
- misty fumes
- white solid
M + Cl2 -> MCl2
Group 2 metal + water (warm)
metal hydroxide
- bubbles form
- fizzing
- metal dissolving
- solution heats up
^^(more vigorous, faster, more heat, down the group due to increase in reactivity).
- calcium, white precipitate. (Less precipitate forms down the group)
M + 2H2O(l) -> M(OH)2(aq) + H2
Calcium is exception:
Ca + 2H2O(l) -> Ca(OH)2(s) + H2
calcium hydroxide is only slightly soluble in water, precipitate forms, solution becomes cloudy.
Group 2 metal + water (steam)
metal oxide and hydrogen
- bright flame
M + H2O(g) -> MO(s) + H2
What type of reactant is a metal oxide classified?
Base
Group 2 oxide + water
metal hydroxide
MO(s) + H2O(l) -> M(OH)2(aq)
simplified (no change in Mg2+ ion):
O2- + H2O -> 2OH-
What type of reaction occurs when group 2 oxides AND hydroxides react with dilute acids?
BAWS
- neutralisation reaction.
MO + H2SO4 -> MSO4 + H2O
M(OH)2 + H2SO4 -> MSO4 + 2H2O
M(OH)2 + 2HCl -> MCl2 + 2H2O
Trend in solubility of group 2 sulfates down the group?
- decreases down the group.
- magnesium sulfate soluble
- calcium sulfate slightly soluble
- strontium and barium sulfate insoluble.
How is the insolubility of a certain group 2 sulfate used to test for the presence of sulfate ions?
- sample solution is acidified with dilute hydrochloric acid (to remove carbonate impurities).
- barium chloride solution is added.
- If sulfate ions are present, the sulfate ions in the solution will react with the barium ions in the BaCl2 to form BaSO4. BaSO4 is insoluble and will show as a white precipitate.
Trends in solubility of group 2 hydroxides down the group?
- increases down the group.
- magnesium hydroxide has very low solubility in water.
- barium hydroxide has high solubility in water.
What is the formula for limewater?
Calcium hydroxide
Ca(OH)2.
reasonably soluble in water.
What is the test for CO2?
- lime water is used.
- CO2 reacts to form CaCO3 which is a white precipitate.
- CaCO3 is insoluble in water
- limewater turns cloudy.
Trend in thermal stability of group 1 and 2 carbonates and nitrates down the group?
- thermal stability increases down the group.
- cation size increases
- polarising ability of the cation on the anion decreases.
- bond strength increases between cations and anions.
- thermal stability increases
Do group 1 carbonates decompose?
No, except lithium carbonate.
- group 1 cations have a 1+ charge which means that the polarising ability of group 1 cations are too small.
- Lithium ion is small enough to have a polarising ability on the carbonate anion.
- group 1 carbonates are all thermally stable except lithium.
Polarising effect compare between group 1 and group 2 cations
group 2 cations have a greater polarising effect because they have a 2+ charge.
the 1+ charge on the group 1 ions means they have a too little charge density to have a polarising ability. (group 1 carbonates cannot decompose except lithium).
What is polarising ability of a cation?
The ability of a cation to distort the electron cloud around the anion.