OCR A-Level Chemistry: Module 3 - Periodic Table and Energy
This flashcard set explores atomic structure and bonding trends across the periodic table. It covers ionisation energy differences, metallic bonding strength, and the impact of molecular size on intermolecular forces and melting points.
Why does Xenon have a lower first ionisation energy than neon? (3)
Xe has a bigger atomic radius
Xe has more shielding
Lower nuclear attraction
Key Terms
Why does Xenon have a lower first ionisation energy than neon? (3)
Xe has a bigger atomic radius
Xe has more shielding
Lower nuclear attraction
Na melting point: 98°C
Mg melting point: 639°C
Explain the difference in melting point (3)
Mg ions have a greater charge
Mg has more electrons
Mg has greater attraction between ions and electrons
Sulphur exists as S8 molecules, and chlorine as Cl2. Explain why S has a higher melting point than Cl (2)
S8 and Cl2 have intermolecular forces
S8 has stronger intermolecular forces than Cl2
Why does atomic radius decrease across a period? (3)
Nuclear charge increases
Shielding remains the same
Greater attraction
Why does first ionisation energy increase across a period? (3)
Atomic radius decreases
Nuclear charge increases
Shielding remains the same
Define first ionisation energy (3)
Energy change when each atom in 1 mole of gaseous atoms loses an electron
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| Term | Definition |
|---|---|
Why does Xenon have a lower first ionisation energy than neon? (3) | Xe has a bigger atomic radius |
Na melting point: 98°C | Mg ions have a greater charge |
Sulphur exists as S8 molecules, and chlorine as Cl2. Explain why S has a higher melting point than Cl (2) | S8 and Cl2 have intermolecular forces S8 has stronger intermolecular forces than Cl2 |
Why does atomic radius decrease across a period? (3) | Nuclear charge increases |
Why does first ionisation energy increase across a period? (3) | Atomic radius decreases |
Define first ionisation energy (3) | Energy change when each atom in 1 mole of gaseous atoms loses an electron |
Explain why first ionisation energy of B is less than that of Be (2) | In B, electron being removed is at a higher energy An s electron is lost in Be and a p electron is lost in B |
Explain why first ionisation energy of O is less than that of N (2) | In N, all 2p electrons are unpaired In O, 2p electron removed is paired so has repulsion that makes removal easier. |
Describe what would be seen when a magnesium ribbon is added to excess dilute HCl (2) | Effervescence Mg dissolves |
Describe the difference between Mg and Sr reacting with HCl (1) | Sr would be a quicker reaction |
Predict the formulas of: Barium oxide and barium nitride (2) |
Ba3N2 |
Describe and explain the trend down group 2 of reactivity with water (5) | Reactivity increases down the group Atomic radii increase More shielding Nuclear attraction decreases Easier to remove outer electrons |
A student reacts calcium exactly with HCl in solution. After adding more calcium it still reacts, explain this (2) | Calcium reacts with water producing calcium hydroxide Ca(s) + H2O(l) -> Ca(OH)2(aq) + H2(g) |
Explain why samples of magnesium oxide become contaminated with magnesium carbonate over time (1) | MgO reacts with CO2 |
CO2 can be prepared by which reaction of carbonates (1) | Thermal decomposition |
How do indigestion tablets containing CaCO3 work? (2) | CaCO3 neutralises HCl CaCO3 + 2HCl → CaCl2 + H2O + CO2 |
Write the equation and conditions for chlorine reacting with sodium hydroxide to form bleach (2) | 2NaOH + Cl2 -> NaCl + NaClO + H2O Cold and dilute NaOH |
Define disproportionation (1) | The simultaneous oxidation and reduction of the same element |
Which reagent would need to be added to calcium iodide to prove it contained iodide ions? (1) | Silver nitrate |
A solution contains CaBr2 and CaCl2, along with silver nitrate, which other reagent is added to prove iodide ions are present? (1) | Concentrated NH3 |
Which reaction type is forming AgCl from adding silver nitrate to chloride ions? (1) | Precipitation |
Use bond breaking and bond making to explain why some reactions are exothermic (2) | Bond breaking absorbs energy and bond making releases energy More energy released then absorbed |
Suggest three reasons why standard enthalpy changes of combustion are lower experimentally than theoretically (3) | Heat released to the surroundings |
Define enthalpy change of combustion (2) | The enthalpy change for the complete combustion of 1 mol of a substance |
What are standard conditions? (1) | 101kPa and 298K |
Why is it difficult to determine enthalpy change of formation for hydrocarbons? (1) | Many different hydrocarbons would form |
Why do bond enthalpies have positive values? | Bond breaking is endothermic |
Define enthalpy change of formation (2) | Change in enthalpy when 1 mole of substance is formed from its elements |
Define bond enthalpy (2) | Energy required to break 1 mole of bonds in the substance in the gaseous state |
Explain why increasing the temperature increases reaction rate (Boltzmann distribution) (1) | More molecules have energy above activation energy |
CO(g) + 2H2(g) -> CH3OH(g) ∆H = –91 kJ mol–1 | Why would high pressure and low temperature give maximum yield? (2) | High pressure as fewer moles of gas on RHS | Low temperature as forward reaction is exothermic |
Why is high pressure and low temperature often not used in chemical industry for reaction conditions? (2) | Too expensive to use a high pressure | Too slow to use a low temperature |
Suggest two ways in which catalyst use in industry makes processes more sustainable (4) | Reactions take place at lower temperatures Catalyst not used up in reaction |
State le Chatelier's principle (2) | When a system in dynamic equilibrium is subjected to an external change, the system readjusts itself to minimise the effect of that change |
Describe the effect on equilibrium of adding a catalyst (2) | No change in equilibrium position | Catalyst speeds up forward and reverse reactions by same amount |
Give two features of a reversible reaction, when a dynamic equilibrium has been set up (2) | Rate of forward reaction = rate of reverse reaction | Concentrations remain constant |
What is meant by a catalyst? (1) | A substance that lowers the activation energy by providing an alternative route |
What is the difference between homogeneous and heterogeneous catalysts? (2) | Homogeneous: catalyst in same state as reactants |
State the pressure and temperature used in the Haber process (2) | Pressure: 200 atm |
Describe and explain why the conditions of the Haber process are a compromise between rate and equilibrium (9) | Increased pressure increases rate because molecules are closer together |