Unit 3 -PPQ Flashcards
Explain why enthalpy of hydration is always exothermic [2]
bonds form between polar water molecules and charged ions
- reduces kinetic energy of system of which is given out as heat
Why is lattice energy of Mg(OH)2 more exothermic than that of Ba(OH)2? [3]
atomic radius of Ba2+»_space; radius of Mg2+
- strength of ionic bonding in Mg(OH)2 is greater as ions in lattice are closer together
- as lattice forms, more energy released
HCOOH + H20 ⇌ H3O+ + HCOO-
Explain how this, with sodium methanoate acts as a buffer solution [4]
on adding acid: added H+ ions mopped up by available HCOO- ions. Eqm shifts to left. [H+] remains fairly constant, as does pH.
on adding alkali: added OH- reacts w/ H+ to form water. Eqm shifts to right. More HCOOH dissociates to replace H+ ions removed. [H+] remains fairly constant, as does pH
Reaction is exothermic. State the effect, if any, on Kp of increasing the temperature at constant pressure [1]
Eqm shifts in endothermic direction, favouring reactants, decreasing Kp
Give 2 equations to show how PbO exhibits amphoteric character [2]
PbO(s) + 2HNO3(aq) -> Pb(NO3)2(aq) + H2O(l)
PbO(s) + 2NaOH(aq) -> Na2Pb(OH)4(aq)
Give an equation to show why solutions of CO2 in water are acidic [1]
CO2 + H2O⇌ H2CO3⇌2H+ + CO32-
When a metal is placed in a solution of its ions, the electrode potential set u between metal and solution can’t be measured without using a reference electrode. Explain why this is so [1]
It’s not possible to make electrical contact between ions in solution and voltmeter
State how metallic character of G4 elements change with an increase in atomic number. jUstify your answer [2]
Metallic character increases down group
- Carbon: diamond (electrical insulator)
- Lead: Metallic lattice (electrical conductor)
Stability of +2 oxidation state increases down G4. What’s the reason for this?
An increasing tendency for outer pair of s electrons not to become involved in bonding i.e. only pair of p electrons involved. +2 state becomes more stable
CCl4 and SiCl4 behave in different ways when added to water. State how each chloride behaves and explain the difference [5]
CCl4: no hydrolysis occurs. 2 immiscible liquid layers form. C has filled outer quantum shell of electrons. No vacant orbitals that can be attacked by lone pairs of O on H2O
SiCl4: rapid hydrolysis occurs. Evolution of misty white fumes + formation of faint white suspension occurs. Has empty 3d orbitals into which lone pairs from H2O can donate to
SiCl4 + 2H2O -> SiO2 + 4HCl
What types of bonding exist in Al2Cl6? [2]
Single covalent bonding between 1x Al and 3xCl
Dative covalent bonding between 1x Al and 1x Cl
Van der Waals beween Al2Cl6 dimer units
Give the expression for the ionic product of water [1]
Kw= [H3O+][OH-]
When HCl is added to aqueous ammonia, explain why a buffering effect occurs where a mixture of NH3(aq) and NH4Cl(aq) is present [3]
NH4+ ⇌ NH3 + H+
NH3 reacts w/ added acid to form NH4+
NH4+ dissociates as H+ reacts w/ added alkali
State the function performed by the salt bridge in an electrochemical cell [2]
completes circuit between electrode solutions
allows movements of ions without mixing of solution
Explain why the 2H+ + 2e- ⇌ H2 electrode has an electrode potential of 0 [1]
used as a standard
State 1 disadvantage of using hydrogen fuel cells to power vehicles [1]
difficult to store enough hydrogen
State 1 advantage of using hydrogen fuel cells compared to combustion of petrol [2]
Doesn’t release CO2 which is a greenhouse gas
Both BN and C form hexagonal graphite-type structures. Explain why:
BN and C both adopt same hexagonal structure
Both exhibit lubricating properties
C is an electrical conductor by BN is an insulator at room temp [6]
BN and C = isoelectronic; can form 3 bonds w/ 1 unbounded p orbital
Both have layer structures; weak VdW forces allow slippage of layers
In C, delocalisation of electrons allows for conduction of electricity; in BN each N has full unbounded p orbital whereas each b has empty unbounded p orbital; N is more electronegative than B, so electron density not evenly spread
Explain why most Cu2+ compounds are coloured in presence of water [4]
3d orbitals split by water ligands into high energy doublet and low energy triplet
electrons absorb energy allowing for d-d transition
blue colour due to non-absorbed frequencies
Explain why most Cu+ compounds are colourless/white [1]
3d sub-shell is full
- d-d transition can’t occur
Explain why lead forms solid chloride PbCl2 but CCl2 and SiCl2 are too unstable to exist [2]
In PbCl2, Pb2+ ion stabilised due to inert pair effect
CCl2 and SiCl2 instable because:
- +4 oxidation state more stable that +2 at top of G4
- covalent bonding more stable than ionic at top of group and 4 bonds needed for outer octet
State what is meant by amphoteric [1]
Reacts with both acids and bases
Aluminium chloride is a compound of amphoteric Al whilst magnesium chloride contains non-amphoteric Mg. Explain how NaOH can be used to distinguish between these 2 solutions [3]
add NaOH drop-wise until there’s excess
white ppt forms w/ Mg but doesn’t redissolve
white ppt forms w/ Al which redissolved in excess
Explain why 2 AlCl3 monomers join together [2]
Al is electron deficient and Cl has lone pairs which it donates, to form dative covalent bond
2N2O5(g) -> 4NO2(g) + O2(g)
colourless brown colourless
Suggest 2 methods of studying kinetics of this reaction [2]
colorimetry
- measure intensity of brown colour over time
measure pressure/volume over time
State what is meant by transition metal [1]
partially filled d orbitals in atom/when they form ions
Write the overall equation when ion is extracted from Fe2O3 in blast furnace using CO [1]
Fe2O3 + 3CO -> 2Fe + 3CO2
Explain why CO can be used as a reducing agent but PbO can’t [2]
Stable oxidation state of C is +4 but for Pb it’s +2
- due to inert pair effect becoming more significant down group