Chapter 23 (Part 1) Energetics Flashcards

1
Q

Lattice Enthalpy. (2)

A
  • a measure of the strength of forces between the ions in an ionic solid
  • the greater the lattice enthalpy, the stronger the forces
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2
Q

Lattice Formation Enthalpy

A
  • enthalpy change when one mole of an ionic lattice is formed from its isolated gaseous ions
  • highly exothermic
  • strong electrostatic attraction btw oppositely-charged ions
  • always negative
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3
Q

Lattice Dissociation Enthalpy

A
  • enthalpy change when one mole of an ionic lattice dissociates into isolated gaseous ions
  • highly endothermic
  • strong electrostatic attraction btw oppositely-charged ions
  • always positive
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4
Q

Factors affecting lattice enthalpy

A
  • charge density
  • ionic radius
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5
Q

Charge Density

A
  • the strength of the bond between the ions of opposite charge in an ionic compound
  • depends on charges on the ion & the distance btw the centres of ions when they pack to form a crystal
  • greater charge = greater force = lattice energies more exothermic
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6
Q

Ionic Radius

A
  • smaller ionic radius = greater attraction between ions because of greater charge density
  • increased lattice enthalpies, increased melting points
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7
Q

Electron affinity

A
  • energy change when 1 mole of electron is added to 1 mole of gaseous atom to form a negatively-charged ion
  • X (g) + e- –> X- (g)
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8
Q

Why is 1st EA exothermic & 2nd, 3rd etc. EA endothermic?

A

2nd EA onwards:
- electron repels the anion
- energy absorbed to overcome repulsion between electron & anion

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9
Q

Steps for Simple Hess Cycle.

A
  1. Write out balanced H f & H LE.
  2. Atomise.
  3. Ionise. Metals must always be ionised before non-metals because electrons are needed for the non-metal.
  4. Ions come together to form solid.
    - refer to class discussion
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10
Q

Steps for constructing Born Haber Cycle.

A
  • Big arrow upwards for energy (E).
  • Arrow upwards = endothermic / enthalpy change +ve
  • Arrow downwards = exothermic / enthalpy change -ve
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11
Q

Enthalpy of atomisation.

A
  • Enthalpy change when 1 mole of gaseous atoms is formed from the element in its standard state, under standard conditions.
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12
Q

Bond enthalpy (ΔHBe)

A
  • Energy required to break a particular covalent bond in 1 mole of molecule in a gaseous state
  • 1/2 Cl2 (g) –> Cl (g)
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13
Q

Carbonate anion dot-&-cross

A
  • Refer to class discussion
  • 2 single, 1 double
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14
Q

Nitrate anion dot-&-cross

A
  • Refer to class discussion
  • 1 double, 1 single, 1 dative
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15
Q

Explain delocalisation on carbonate & nitrate ions.

A
  • pi bond on C=O & lone pairs overlaps with delocalised pi system
    -anion is polarised due to attraction towards G2 cation (think of dipole)
  • under heating, weakest (polarised) bond breaks
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16
Q

Thermal stability of G2 carbonates & nitrates.

A

Going down G2:
- ionic radius increase
- charge density decrease
- anion is less polarised
- more heat needed to decompose
- thermal stability increase

17
Q

Enthalpy change of solution (ΔH Sol)

A
  • Enthalpy change when 1 mole of solute is dissolved in water to form infinitely dilute solution under standard conditions.
  • Soluble compounds = exothermic, -ve
  • Insoluble compounds = endothermic, +ve
18
Q

Enthalpy change of hydration (ΔH Hyd)

A
  • Enthalpy change when 1 mole of gaseous ion dissolves in water to give infinitely dilute solution.
  • Mg2+ (g) –> Mg2+ (aq)
  • exothermic (ALWAYS)
19
Q

Variation of G2 sulfates down the group.

A
  • ΔH LE & ΔH hyd become less exothermic
  • ionic radius increases, charge density decreases
  • ΔH hyd decreases more than ΔH LE
  • ΔH Sol becomes more endothermic (more energy required)
  • Solubility of G2 sulfates decreases
20
Q

Variation of G2 hydroxides down the group.

A
  • ΔH LE & ΔH hyd become less exothermic
  • ionic radius increases, charge density decreases
  • ΔH LE decreases more than ΔH Hyd
  • ΔH Sol becomes more exothermic
  • Solubility of G2 hydroxides increases
21
Q

ΔH Sol = ?

A
  • ΔH LE (formation) + ΔH Hyd