W3.2_Thermodynamics Flashcards

1
Q

What is thermodynamics and how are rate constants driven?

A
  • ∵ Energetic changes in components of eqm
  • ∴ Different eqm have different rates/Kc
  • Rate constant: driven by magnitude of activation energy (Ea)
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2
Q

Explain the relationship between Arrhenius equation and its Kc value.

A
  • Relationship described by Arrhenius equation: k=Ae^(-Ea/(R*T))
  • Ea directly relates to the rate of reaction (negatively)
  • Ea in reverse reaction is different
  • Kc: determined by difference in Ea between forward/reverse reaction, both passes the same stage of transition states
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3
Q

Explain the relationship between ∆G and Kc with the aid of an equation. Draw an energy profile of equilbrium.

A
  • Relationship between ∆G&Kc: Van’t Hoff equation ∆G=-RT(lnKc)
  • ∵ Difference in energy (G) between both sides, form at different rates due to Ea difference
  • ∴ Different eqm have different Kc
  • Refer to the notes
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4
Q

Explain what Gibb’s energy is and the characters of its equation. How does it relate to the feasibility of an equation and its Kc value?

A
  • ∆G=∆H-T∆S
  • ∴ Enthalpic and entropic energy contribute to magnitude of Kc
  • ∆H: heat-related, bonding environment changes energy level (-ve: exo/+ve: endo)
  • T: temperature (K)
  • ∆S: level of disorder
  • ∵ Reactions are only feasible when ∆G≼0
  • +ve ∆H, +ve ∆S: Feasible at high temperature
  • -ve ∆H, +ve ∆S: Always feasible
  • +ve ∆H, -ve ∆S: Never feasible
  • -ve ∆H, -ve ∆S: Feasible at low temperature
  • All equations above have a temperature constant (T) -> temperature affects Kc
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5
Q

Explain what would happen when an equilibrium equation is mediated by enzymes (biological/protein catalysts) in biological processes.

A
  • Ea reduced -> rate of forward and backward reactions increased (refer to Arrhenius equation)
  • ∆G remains unchanged -> Kc does not change (refer to Van’t Hoff equation)
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