how far 5.1.1 and 5.1.2 Flashcards

1
Q

What is rate of reaction?

A

The change in concentration of a substance per unit time.
This is used for consistency as it’s better than say change in mass per unit time.

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2
Q

Describe the following general rate equation: r = k[A]m[B]n

A

● Based on the reaction… aA + bB → products.
● Unit of r (rate) is moldm-3s-1, unit of [A] and [B] (conc. of A and
B) are moldm-3, and unit of k (rate constant) varies.
● The rate constant is ONLY dependent on temperature (i.e., it
increases with temperatures).
● The values m and n are called reaction orders and have
nothing to do with the stoichiometric coefficients in the balanced equations. They are worked out experimentally and can be 0, 1, or 2.
● The overall order is m + n.

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3
Q

What are the 3 orders of reaction with their associated rate- concentration and concentration-time graphs of the reactant(s)?

A

Zero-order reaction - rate is independent of concentration. ● First-order reaction - rate ∝ conc.
● Second-order rate - rate ∝ concX (by some factor).
The concentration-time graph for a second-order reaction isn’t required.

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4
Q

What is the half-life of a reaction? And the half-life

A

The time taken for the conc. of a reaction to half (which is constant for a first-order reaction).

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5
Q

Give 5 ways of determining the rate of a reaction

A
  1. Use a gas syringe to measure the change in volume of gas. 2. Use a top pan balance to measure the change in mass as
    gases escapes (works best with a heavy gas like CO2).
  2. Measure the time taken for a precipitate to form.
  3. Measure a change in electricity conductivity (works well if
    ions are released).
  4. Use colorimetry to measure absorbance of a wavelength by a chemical
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6
Q

What should be ensured when continually monitoring [A] and why? (in rates of reactions)

A

Having a large excess of everything else so their conc. is effectively constant ∴ its conc. won’t change much during the reaction ∴ won’t affect the reaction.

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7
Q

How can you use TLC to monitor the course of a reaction

A

By taking samples at regular intervals.

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8
Q

Give 2 ways of determining orders of reaction and state the benefit of one over the other

A
  1. Continually monitor [A] and form a concentration-time graph for many different conc.’s then use this to plot a rate- concentration graph whose shape you can use.
  2. Use a clock reaction to get a good approximation of the initial rate.
    ● Then use the initial rates method.
    ● The latter method is far less time consuming as a graph doesn’t have to be plotted each time.
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9
Q

What 3 assumptions are made during a clock reaction

A
  1. The concentration of reactant doesn’t change significantly over the timescale.
  2. Constant temperature.
  3. When the endpoint is observed, the reaction has not
    proceeded too far.
    This allows us to assume a constant rate.
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10
Q

What is the rate determining step

A

The slowest step in a reaction mechanism which determines the overall rate of reaction.

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11
Q

What things should you look out for when proposing mechanisms from overall reactions and rate equations

A
  1. A catalyst appearing in the rate equation as it will reform later.
  2. When the slowest step contains an intermediate (not a reactant). It should be replaced by substances that make up the previous step.
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12
Q

What is the Arrhenius Plot, what can it be used to find, and what does it use?

A

ln(k) = (-Ea/RT) + ln(a)
y = ln(k)
m= -Ea/R
x=1/T
c= ln(a)

Used to determine the pre-exponential factor and activation energy using a set of temperatures and rate constants.

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13
Q

What method should you use for KC questions?

A

● Initial moles.
● Change in moles.
● Equilibrium moles.

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14
Q

What are the 2 types of equilibria

A

● Homogeneous - reactants and products are in the same physical states.
● Heterogeneous - reactants and products are in different physical states

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15
Q

How do the KC and KP expressions change for heterogeneous equilibria?

A

Only gases and aqueous reactants/products are used.
E.g., Cu (s) + 2Ag+ (aq) ⇌ Cu2+ (aq) + 2Ag (s) so KC = [Cu2+] / [Ag+]2.

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16
Q

What are mole fractions and partial pressures? How do they relate

A

● Mole fraction of A - fraction of the total number of moles. ● Partial pressure of A - the pressure of A if it alone occupied
the same volume vessel alone ● p(A) = xA · Ptot
This means the total pressure is the sum of the partial pressures.

17
Q

What is KP and why do we use it?

A

● An equilibrium constant calculated from partial pressures. ● As it’s difficult to get concentrations for gases.
E.g., H2 (g) + I2 (g) ⇌ 2HI (g) so KP = p(HI)2 / p(H2)p(I2).

18
Q

What method should you use for KP questions?

A

ICE followed by XA PA.

19
Q

What is the only thing that can affect KC and KP and why not others

A

● Temperature.
● Changing the concentration/pressure of a substance won’t
have an effect as as the system restores equilibrium so it’s the SAME.