Chemical kinetics Flashcards

(15 cards)

1
Q

What must happen for a chemical reaction to be observed (3)

A
  1. Energy is conserved (1st Law)
  2. Disorder of the Universe increases (2nd Law)
  3. The reaction rate is significant.
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2
Q

What is metastability

A

a state of a system that can be observed for a short time but is not the system’s state of least energy

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3
Q

What determines the rate of change

A

The rate of change is determined by kinetic factors, not just thermodynamics.

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4
Q

Why is the rate of change from diamond to graphite negligible (3)

A
  1. The rate of change is determined by kinetic factors, not just thermodynamics.
  2. This kinetic barrier is the reason the rate is negligible, not the value of ΔG° itself.
  3. ΔG° is negative because graphite is thermodynamically more stable than diamond under standard conditions.
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5
Q

What is activation energy (4)

A
  1. This is the minimum reactant energy required for reaction
  2. High Ea = low rate
  3. low Ea = high rate
  4. Catalysts lower Ea but don’t the affect ΔG°(which determines the equilibrium position)
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6
Q

What is reaction rate (3)

A
  1. Rate at which reactants (R) is consumed or products (P) are made
  2. Units = mol dm⁻³ s⁻¹
  3. The less negative the less reactants available
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7
Q

How is reaction rate calculated (3)

A
  1. Rate (v), can be determined from a plot of concentration versus time
  2. v = d[P]/dt = -(d[R]/dt)
  3. The less negative the less reactants available
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8
Q

What is the rate constant (2)

A
  1. The rate constant expresses rate as a function of concentration and k.
  2. k is only constant at fixed temperature and varies with temperature according to the Arrhenius equation (SM).
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9
Q

What is zero order kinetics (4)

A
  1. calculated by: v = k[A]⁰[B]⁰
  2. v = k
  3. REACTION RATE STAYS THE SAME.
  4. units = mol dm⁻³ s⁻¹
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10
Q

What is first order kinetics (5)

A
  1. Calculated by: v = k[A]¹[B]⁰
  2. v = k[A]
  3. Called ‘’first oder in A’’
  4. REACTION RATE PROPORTIONAL TO A.
  5. units = s⁻¹
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11
Q

What is second order kinetics (4)

A
  1. Second order: Two general forms
  2. v = k[B] → second order in B
  3. v = k[A][B] → first order in A and B
  4. Units = mol⁻¹ dm³ s⁻¹
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12
Q

What is overall order kinetics (5)

A
  1. general rate law is v = k[A]ᵃ[B]ᵇ
  2. and overall order is given by a + b.
  3. Units of k depend on overall oder
  4. The overall order of some complex reactions can be fractional
  5. e.g. Cl2 + CH4 → CH3Cl + HCl (via UV) is three-halves order overall, one-half order in chlorine.
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13
Q

What are complex reactions (SM) (7)

A
  1. Most reactions are complex, a series of elementary reactions (or steps) called the ‘reaction mechanism’.
  2. One step = a set of synchronous electron movements.
  3. In a haloform reaction there are 9 steps.
  4. Single step bimolecular reaction → 2nd-order
  5. But 2nd-order does NOT always mean a single step bimolecular reaction.
  6. Experiments indicate a 3-step reaction involving intermediates.
  7. The rate law always arises from the slowest step: The ‘rate limiting’ step.
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14
Q

What is molarcularity (4)

A
  1. Molecularity is the number of reactant particles involved in a step:
  2. 1 → Unimolecular
  3. 2 → Bimolecular
  4. 3 → Termolecular
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15
Q

What is negative, positive and zero free energy change

A
  1. Negative = spontaneous reaction, products are more stable than reactants
  2. Positive = non-spontaneous reactants more stable than products
  3. Zero = equal stability, no net change
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