U1.2: Energy Cycles in Reactions Flashcards

1
Q

Define bond enthalpy

A
  • The amount of energy needed to break one mole of bonds in gaseous molecules under standard conditions
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2
Q

Define average bond enthalpy

A
  • The amount of energy needed to break one mole of bonds in gaseous molecules under standard conditions
  • averaged over a range of similar compounds
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3
Q

How to calculate bond enthalpy?

A

Sum of bonds broken in Endo + Sum of bonds formed in Exo
( + becomes - in actual calculations )

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4
Q

What is true about Ozone regarding its decomposition rate

A

Ozone decomposes faster than O2

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5
Q

State Hess’s Law

A

The enthalpy change for a reaction is independent of the pathway between the initial and final states

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6
Q

How does the Hess’ Law energy cycle look like (REP)

A

R –>P : Arrow is Delta Hr
E—>R: Arrow is Delta H(1) [usually positive]
E—>P: Arrow is Delta H(2) [usually negative]

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7
Q

Formula for Hess’s Law?

A

Delta H1 = Delta H2 + Delta H3

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8
Q

What to do if reactants and products switch in Hess’s Cycle

A

Sign of Delta H also changes

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9
Q

Define Standard Enthalpy changes of formation

A
  • The enthalpy change when 1 mole of a compound forms from its constitute elements under standard conditions
  • All reactants and products are in standard states
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10
Q

Equation for Standard Enthalpy changes of formation?

A

ΔHr ⦵ = SUM (ΔHf ⦵ products - ΔHf ⦵ reactants)

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11
Q

Outline the enthalpy of formation for elements and why

A
  • 0
  • this is because no energy was required to make them in their natural state
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12
Q

Define Standard Enthalpy changes of combustion

A
  • The enthalpy change when 1 mole of a SUBSTANCE is completely burned in Oxygen under standard conditions.
  • All reactants and products are in their standard conditions
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13
Q

What state is water in its standard conditions

A

Liquid

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14
Q

Equation for Standard Enthalpy changes of combustion?

A

ΔHr ⦵ = SUM (ΔHc ⦵ reactants - ΔHc ⦵ products)

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15
Q

For Standard enthalpy of combustion reactions, if the data is given for the enthalpy of formation, how do we approach these types of questions

A
  • Use ΔHf formula
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16
Q

How else can we find the Standard Enthalpy of combustion reactions (other than formation and combustion values from the data booklet)

A
  • Use bond enthalpy values as it is also calculated as Bonds broken in reactants - bonds formed in products
17
Q

Define lattice enthalpy

A

Enthalpy change when 1 mole of an ionic compound’s broken apart into its constituent gaseous ions in standard states

18
Q

Define enthalpy of atomisation

A

Enthalpy change when 1 mole is formed from an element

19
Q

Define bond association energy (E)

A

Energy required to break 1 mole of bonds in gaseous states

20
Q

Define 1st Electron A*ffinity (always exo –> favourable) and state the equation

A

Enthalpy change when one e- is A*dded to each atom in 1 mole of gaseous atoms
- X(g) + e- –> X(g)-

21
Q

Define 2nd Electron A*ffinity (always endo–> unfavourable) and state the equation

A

Enthalpy change when the 2nd e- is A*dded
- X(g)- + e- –> X(g)2-

22
Q

Define 1st Ionisation energy (endo) and state the equation

A

Enthalpy change when 1 e- is removed from each atom in 1 mole of gaseous atoms
- M(g) –> M(g)+ + e-

23
Q

Define 2nd Ionisation energy (endo) and state the equation

A

Enthalpy change when a 2nd e- is removed from each atom in 1 mole of gaseous atoms
- M(g) –> M(g)2+ + e-

24
Q

State the formula for the Born Haber Cycle

A

Hlat + Hf = 2(Hat - metal and nonmetal) + HIE + HEA

25
Q

What is true about the ionic character of compounds when considering experimental and theoretical lattice enthalpies?

A
  • Most compounds dont have 100% ionic character theoretically but we assume 100% ionic character experimentally
26
Q

Describe the pattern for covalent character across and a period and down a group

A

Covalent character increases down a group and across a period as:
- The difference between experimental and theoretical values of lattice enthalpy increases (there is a greater discrepancy %)

27
Q

Describe the relationship between the discrepancy and covalent character

A

The greater the discrepancy in a compound, the more covalent character the element has and thus, the more purely ionic a compound (crystal) is

28
Q

State what hydrogenation is

A

The addition of H2

29
Q

Suggest why it may be useful to use Hess’s law to determine the heat of formation

A
  • In some cases, the heat of formation is impossible to measure directly
  • Hess’s law helps us break a reaction or process into a series of small steps