UNIT 5 - Energetics And Thermochemistry Flashcards

1
Q

State the heat of formation of pure element in standard state.

A

Equal to 0.

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2
Q

Define entropy [S].

A

Measure of disorder in the system
but also distribution of available energy among the particles.

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3
Q

State the second law of thermodynamics in terms of entropy.

A

The total entropy of a system either increases or remains constant in any spontaneous process it never decreases.

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3
Q

State the factors entropy depends on.

A
  • temperature
  • pressure
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3
Q

State the formula for lattice enthalpy.

A

∆H= K (constant dependent on geometry) *
n (magnitude of charges on the ions) * m (magnitude of charges of the ions) / Rn+Rm (ionic radii).

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3
Q

Determine with reason the feasibility of a reaction depending on the temperature (entropy, Gibbs).

A

Feasible at high temperature - all reaction with ∆S system because the ∆G is almost equal -T∆S, making ∆H negligible.

Feasible at low temperature - all exothermic reactions because at low temp the T∆S is almost equal to 0 thus making the ∆G=∆H

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3
Q

Define lattice enthalpy.

A

Enthalpy change that occurs when one mole of a solid ionic compound is separated into gaseous ions under standard conditions.

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3
Q

Define energy.

A

Measure of the ability to do work.

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3
Q

State when does exothermic reaction occur in terms of entropy.

A

If the change of entropy of the system can compensate for the negative entropy change of the surroundings (as heat flows from the surrounding to the system).

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3
Q

State how lattice enthalpy changes.

A

Decreases with increasing ion radius.

Increases with increasing ion charge.

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3
Q

Define the enthalpy of combustion.

A

Energy change upon complete combustion of one mole of a substance.

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3
Q

Define the specific heat capacity.

A

The amount of heat needed to raise the temperature of a unit mass of pure substance by 1C or 1K.

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3
Q

State the formula for heat [q].

A

q = m * ∆T * C

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3
Q

Define the enthalpy of atomization.

A

Enthalpy change that occurs when one mole of gaseous atoms is formed from the elements in their STP.

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3
Q

State the 1st law of thermodynamics.

A

Energy cannot be neither created nor destroyed only converted.

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3
Q

State the formula for entropy change of the reaction.

A

∆S =∑∆S prod - ∑∆S reactants

3
Q

State the formula for enthalpy change of a reaction using heat of formation.

A

∆H = ∑∆Hf products - ∑∆Hf substrates

3
Q

State the most ordered and most disordered state.

A

most ordered - solid state
most disorder - gaseous state

3
Q

Define enthalpy.

A

A measure of the amount of heat energy contained in a substance.

4
Q

State the formulae for the Gibbs free energy change of the reaction.

A

∆G = ∑∆G products - ∑∆G substrates

5
Q

List the possible systems and their definitions.

A
  • open system - can exchange energy and matter with the surroundings
  • closed system - can only exchange energy but not matter
  • isolated system - perfect one no exchange of anything (neither energy nor matter)
6
Q

Define hydration enthalpy.

A

Strength of interaction between the polar water molecules and the separated ions.

7
Q

Define a system in terms of thermodynamics.

A

The area of interest.

8
Q

State the Hess law.

A

The enthalpy change for any chemical reaction is independent of the route, providing the starting, final conditions and reactants, products are the same.

9
Q

State the formulae and define the Gibbs free energy.

A

Potential of a system to do work.

∆G = ∆H - T∆S

10
Q

Define an enthalpy change of solution.

A

Enthalpy change when one mole of a solute is dissolved in a solvent to infinite dilution under STP.

11
Q

Determine spontaneity of a reaction depending on the values of ∆H, ∆S, ∆G and T.

A
  • ∆H>0, ∆S>0

∆G < 0, T high - spontaneous
∆G > 0, T low - non-spontaneous

  • ∆H>0, ∆S<0

∆G>0 - non-spontaneous

  • ∆H<0, ∆S<0

∆G < 0, T low - spontaneous
∆G > 0, T high - non-spontaneous

  • ∆H<0, ∆S>0

∆G < 0 - spontaneous

12
Q

State the formulae for enthalpy change using the enthalpies of combustion.

A

∆H = ∑∆Hc substrates - ∑∆H products

13
Q

State the formulae for enthalpy change in a reaction using bond enthalpy.

A

∆H = ∑E bonds broken - ∑E bonds formed

14
Q

State the spontaneity of the reaction depending on the value of Gibbs free energy.

A

∆G<0 - spontaneous (exothermic usually)
∆G>0 - non-spontaneous (endothermic)
∆G=0 - equilibrium

15
Q

List the factors the increase in temperature when heated depends on.

A
  • mass of object
  • heat added
  • nature of the substance
16
Q

Define the surroundings in terms of thermodynamics.

A

Everything else (except for the system) in the universe.

17
Q

List the standard conditions for enthalpy changes.

A
  • pressure of 100kPa
  • concentrations of 1 mol/dm3 for all
  • all substances in their standard states (298K,10^5Pa)
18
Q

Define the enthalpy change of formation.

A

The energy change upon a formation of one mole of substance from elements in their standard states and conditions.

19
Q

Define bond enthalpy.

A

Energy required to break one mole of bonds in covalent, gaseous molecules under STP, is an average for every molecule.

20
Q

State the formulae for heat capacity [C].

A

C = ∆heat/∆T