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AQA A2Thermodynamics
AQA A2 Thermodynamics
| Question | Answer |
|---|---|
| Define Enthalpy change of Formation | The enthalpy change when 1 mole of a compound is formed from its elements in their standard states under standard conditions. |
| Define Bond dissociation enthalpy | The enthalpy change when all the bonds of the same type in one mole of gaseous molecules are broken. |
| Define Enthalpy change of atomisation of an element | The enthalpy change when 1 mole of gaseous atoms is formed from an element in its standard state. |
| Define First ionisation enthalpy | The enthalpy change when one mole of gaseous 1+ ions is formed from one mole of gaseous atoms. |
| Define Second ionisation enthalpy | The enthalpy change when one mole of gaseous 2+ ions is formed from one mole of gaseous 1+ ions. |
| Define First electron affinity | The enthalpy change when one mole of gaseous 1– ions is formed from one mole of gaseous atoms. |
| Define Second electron affinity | The enthalpy change when one mole of gaseous 2– ions is formed from one mole of gaseous 1– ions. |
| Define enthalpy change of hydration | The enthalpy change when one mole of aqueous ions is formed from one mole of gaseous ions. |
| Define enthalpy change of solution | The enthalpy change when one mole of solute is dissolved in sufficient solvent that no further enthalpy change occurs on further dilution. |
| Explain why the second ionisation energy is more endothermic than the first ionisation energy | Removing an electron from a positive ion will be require more energy (not simply “difficult”) because there are more p+ than e- so the e- are more attracted to the nucleus |
| Explain why the first electron affinity is always exothermic | Energy is given out when an electron JOINs onto an atom |
| Explain why the second Electron Affinity is endothermic | Energy is required to add an electron to an already negative ion and to overcome the forces of repulsion |
| Explain why enthalpy change of hydration is exothermic | because a bond forms: an attraction between an ion and a polarised molecule |
| Define Standard conditions | 100kPa and 298 K |
| Define Pure ionic model | Ions are spherical and have charge evenly spread |
| Define Partial covalent bonding | The electrons in the negative ions are pulled towards the positive ion. |
| Explain why there is a large difference in the experimental and theoretical values? | the compound is not purely ionic, there is a covalent character |
| In which compound is there more a covalent character? NaF or AlCl3? | AlCl3 because the Al+3 is highly charged and will polarise the electron cloud of the large Cl- ion (larger than F- ion); KEYWORDS: CHARGE, SIZE, POLARISATION, ELECTRON CLOUD |
| Order the compound in increasing lattice enthalpy: LiF or NaCl or MgO or BaS? | NaCl |
| What is the Enthalpy change of solution equal to? | Lattice dissociation enthalpy + Enthalpy of hydration (of each ion) (mnemotechnic:hydration=lucozade sport) |
| What is entropy? | Entropy is the measure of the number of ways that particles can be arranged. |
| How does changing state affect entropy? | Melting or boiling increases entropy, condensing or solidifying decreases entropy. |
| How does dissolving a solid affect entropy? | Causes an increase. |
| How does number of particles affect entropy? | More particles lead to an increased entropy. |
| What is a spontaneous reaction | A reaction that does not require any external energy to occur; deltaG<0 |
| How do you work out Free energy change | ΔG = ΔH – T ΔS (Remember to convert all units to J or kJ) |
| What are the traps on a Born Haber cycle? | remember moles, moles, moles; direction of arrows |
| How do you work out the minimum temperature for a reaction to be feasible? | deltaG MUST be at least equal to 0, so T=deltaH/deltas |
| How does FreeGibbs energy fit the equation of a straight line? | deltaG=deltaH – T deltas or y =a –bx where a=deltaH and b=deltaS=gradient |
| Given the entropy of individual reactants and products, how do you work out the entropy change? | deltaS=(molesxentropy of each products – molesxentropy of reactants); REMEMBER MOLES MOLES MOLES |
| How do you work out the enthalpy change of solution in a calorimetry experiment? | deltaH=-Q/moles; ie deltaH=-m c deltaT/moles |
| Explain why. the enthalpy change of hydration of Magnesium is more exothermic than the enthalpy change of hydration of Calcium. | Both have the same charge; Magnesium is a smaller ion so will attract more the water molecule KEYWORDS: CHARGE, SIZE, ATTRACTION |
| Explain why it is difficult to predict which of Na2S or CaCl2 would have the most exothermic Lattice Enthalpy | Ca+2 is larger ion than Na+ so will attract less the anion but Ca+2 is more charged than Na+ so will attract more the anion; similarly S-2 is more charged but larger than Cl- |
| Explain why the enthalpy change of atomisation of Chlorine is more endothermic than the enthalpy change of atomisation of Bromine | Cl-Cl bond needs to be broken: as the 2 atoms of Cl are smaller so closer than the 2 atoms of Br, the bonding pair between Cl atoms is more attracted to muclei and will require more energy to be broken |
| Describe the interaction between water and a Sodium ion | the O-H bond in water is polarised as O is more electronegative than H; Sodium ion attract the partially negative oxygen atom; It is an ION-DIPOLE interaction |
| Explain why a magnesium appears to be stable in air at room temperature, despite a negative value for the Free Gibbs energy for the reaction between Magnesium and Oxygen | High activation energy (ie the reaction maybe THERMODYNAMICALLY feasible but not KINETICALLY) |
| In a graph deltaG on y-axis vs Temperature on x-axis, what does the gradient of the straight line represent? | deltaS |
| The enthalpy of solution for KCl is +17.2 kJmol–1. 5.00 g of KCl are dissolved in 20.0 g of water. Initial temperature of the water is 298 K. Calculate the final temperature of the solution. Specific heat capacity of water is 4.18 J K–1 g–1. | moles KCl = 5/74.6 = 0.067(0) mol; Heat absorbed = 17.2 × 0.0670 = 1.153 kJ Heat absorbed = mass × c × ΔT; (1.153 × 1000)= 20 × 4.18 × ΔT ; ΔT = 1.153 × 1000 / (20 × 4.18) = 13.8 K; T = 298 – 13.8 = 284(.2) K |
| What enthalpy change does this equation represent? Cl2(g)--> 2Cl(g)? | TWICE the enthalpy change of atomisation |