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Chapter 18 Rates of reactants Flashcards

(44 cards)

1
Q

Define rate of reaction.

A

Time taken for concentration of reactants to decrease and products to increase

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2
Q

Define order.

A

This is the power in which individual reactants are raised in the rate equation

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3
Q

Define overall order.

A

The sum of individual orders present on the rate equation

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4
Q

Define rate constant.

A

The constant that links the rate of reaction with the concentrations of the reactants raised to the powers of their orders in the rate equation.

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5
Q

Define half-life

A

The time taken for the concentration of a reactant to decrease by half.

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6
Q

Define rate-determining step.

A

The slowest step in the reaction mechanism of a multi-step reaction

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7
Q

How do you calculate units from a rate equation.

A

Right down all units present
Cancel out the units that are repeated
Bring the units from the bottom to the top
Change the sign to its opposite

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8
Q

Name the order of this concentration-time graph.

A

0

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9
Q

Name the order of this concentration-time graph.

A

1st

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10
Q

Name the order of this concentration-time graph.

A

2nd

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11
Q

Name the order of this rate-concentration graph.

A

0

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12
Q

Name the order of this rate-concentration graph.

A

1st

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13
Q

Name the order of this rate-concentration graph.

A

2nd

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14
Q

what are the units for rate?

A

mol dm-3 s-1

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15
Q

Can orders be determined from a balanced chemical equation?

A

NO

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16
Q

How are orders calculated?

A

From experimental results.

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17
Q

A + B + 2C → D + 2E

when calculating order wrt A keep ___ and ___ constant.

A

B and 2C

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18
Q

what do you do when calculating orders and you cannot keep the other concentrations constant?

A

us the orders you know and substitute like an equation, if rate can be calculated and the order can be deduced as 1 or 2, if not it must be 0.

19
Q

calculate the overall order:

rate = k[X]2 [Y]2 [Z]0

20
Q

what does k equal?

A

rate constant

21
Q

how do you calculate k?

rate = k[NO2] [O3]

A

rearrange:

k = rate /

[NO2] [O3]

22
Q

describe the half-life of a first order reaction from a conc-time graph.

23
Q

what technique can be used to calculate concentrations of solutions?

24
Q

what two methods are used for continuous monitoring of rate?

A
  • gas collection
  • mass loss
25
what does exponential decay refer to?
the pattern of 1st order reactions (c-t) having a constant half-life.
26
after a tangent is drawn hoe can you show constant half-life?
the times taken for concentration to half and half should both be equal eg. 0.5 → 0.25 = 100s 0. 25 → 0.125 = 100s
27
how do you calculate k from t½?
* k* = ln 2 / * t*1/2
28
how do you calculate k(rate constant) from the rate on a conc-time graph?
- rearrange rate equation - substitute in rate( gradient change in y/x) and concentration (point where tangent is drawn(touching the line))
29
how do you calculate reaction constant of first order from a rate conc graph?
gradient = change in y / x
30
how do you calculate reaction constant of first order from a conc-time graph?
draw tangent at conc wanted and calculate gradient
31
What does a balanced equation show when calculating RDS?
the number of molecules of each species after cancelling the intermediates
32
If Ea is large k is …
SMALL and therefore rate is slow
33
If k is large Ea is …
SMALL
34
what do the two parts in the Arrhenius equation represent? k = *A e-Ea /RT*
* A = pre-exponential factor (FREQUENCY of collision with correct orientation)* * e-Ea /RT *= exponential factor (proportion of molecules that exceed Ea and correct temperature)
35
what do they stand for and units? k = *A e-Ea /RT *
k-rate constant A- Arrhenius constant Ea- activation energy **J/mol** R- gas constant 8.314 **J mol-1 K-1** T- temperature **Kelvin**
36
A plot of ____ against ____ .
**ln k** (logarithm) against **1/T**
37
A plot of ln.k again 1/T gives a straight line with …
gradient = -Ea/R y-intercept = ln A on y axis
38
what sign will the gradient ALWAYS be. (hint ; exo)
**NEGATIVE**
39
if y-intercept = ln A how do you work out A?
A = e value at y-intercept
40
increase in A = ______ in k(rate constant)
INCREASE
41
increase in Ea = ______ in k(rate constant) and why
DECREASE less molecules have sufficient energy to exceed Ea and collide.
42
increase in T = ______ in k(rate constant) and why?
INCREASE more collisions when temperature increase
43
if gradient= -Ea/R how do you work out Ea?
Ea= gradient(negative value) x R(8.314)
43
if gradient= -Ea/R how do you work out Ea?
Ea= gradient(negative value) x R(8.314)