Reaction Rate Graphs and Applications
3. Determining Rate from Graphs
Learning outcomes
- I can calculate average rates from graphs.
- I can determine gradients from reaction graphs.
- I can estimate instantaneous rates from tangents.
- I can compare rates at different times during a reaction.
- I can interpret graphical evidence to describe reaction behavior.
Reaction Graphs Tell Us More Than What Happened
Reaction graphs do more than show how the amount of a substance changes.
They can also tell us:
how quickly the change is happening
This is the:
reaction rate
The key mathematical idea is:
gradient
A steep graph represents a rapid change.
A shallow graph represents a slower change.
A horizontal graph represents:
no net change
By calculating gradients, we can turn the shape of a graph into a numerical measurement of reaction rate.
The Basic Rate Equation
Reaction rate compares:
change in a measured quantity
with:
change in time
The general relationship is:
average rate = change in quantity ÷ change in time
This can also be written as:
Average rate = Δy / Δt
where:
- Δy = change in the quantity shown on the y-axis
- Δt = change in time
- Δ means "change in"
The quantity might be:
- concentration
- mass
- gas volume
- amount of substance
What Is Gradient?
The gradient of a graph tells us how quickly the y-value changes compared with the x-value.
For reaction graphs:
gradient = change in measured quantity / change in time
or:
gradient = Δy / Δx
Because time is normally on the x-axis:
gradient = Δy / Δt
This makes gradient extremely useful for measuring:
reaction rate
Rise Over Run
Another way to remember gradient is:
gradient = rise / run
where:
rise = vertical change
and:
run = horizontal change
For a reaction graph:
vertical change = change in concentration, mass, or volume
horizontal change = change in time
Average Rate
An average rate describes how quickly something changes over a:
time interval
Suppose a reaction produces:
60 cm³ of gas
during:
30 seconds
Average rate:
60 cm³ ÷ 30 s
= 2.0 cm³/s
Therefore:
average rate = 2.0 cm³/s
Finding Average Rate from a Graph
Consider this illustrative product-formation data:
| Time (s) | Gas Volume (cm³) |
|---|---|
| 0 | 0 |
| 10 | 28 |
| 20 | 46 |
| 30 | 57 |
| 40 | 63 |
| 50 | 66 |
| 60 | 66 |
The graph would rise rapidly at first and gradually become horizontal.
To calculate the average rate between:
10 s and 30 s
read the corresponding values:
At 10 s:
28 cm³
At 30 s:
57 cm³
Step 1: Calculate the Change in Product
Δvolume = final volume − initial volume
Δvolume = 57 − 28
Δvolume = 29 cm³
Step 2: Calculate the Change in Time
Δtime = final time − initial time
Δtime = 30 − 10
Δtime = 20 s
Step 3: Calculate the Average Rate
average rate = 29 / 20
average rate = 1.45 cm³/s
Therefore:
Average rate from 10–30 s = 1.45 cm³/s
A Common Calculation Error
Suppose we want the average rate between:
20 s and 50 s
Do not divide the product amount at 50 s by 50.
Instead, calculate the:
change between the two selected points
At 20 s:
46 cm³
At 50 s:
66 cm³
Change in product:
66 − 46 = 20 cm³
Change in time:
50 − 20 = 30 s
Therefore:
average rate = 20 / 30
= 0.67 cm³/s
approximately.
The rule is:
always calculate change in y and change in x
Units of Reaction Rate
Rate units depend on:
what the graph measures
If the graph shows:
gas volume in cm³
and:
time in seconds
then rate units are:
cm³/s
If the graph shows:
concentration in mol/L
then:
mol L⁻¹ s⁻¹
If the graph shows:
mass in grams
then:
g/s
Always derive rate units from:
y-axis unit ÷ x-axis unit
Positive Gradients
A product formation graph usually rises.
For example:
gas volume increases with time
Therefore:
Δy is positive
and:
gradient is positive
A positive gradient means the measured quantity is:
increasing
For a product graph, this usually represents:
product formation
Negative Gradients
A reactant concentration usually:
decreases
as the reaction proceeds.
Therefore, its graph may slope downward.
For example:
At 10 s:
[A] = 0.80 mol/L
At 30 s:
[A] = 0.50 mol/L
Gradient:
(0.50 − 0.80) / (30 − 10)
= −0.30 / 20
= −0.015 mol L⁻¹ s⁻¹
The negative sign tells us:
reactant concentration is decreasing
Rate of Disappearance
Although a reactant concentration graph has a negative gradient, we often report its:
rate of disappearance
as a positive magnitude.
So if:
gradient = −0.015 mol L⁻¹ s⁻¹
we may say:
rate of disappearance = 0.015 mol L⁻¹ s⁻¹
The negative gradient describes:
direction of change
The positive magnitude describes:
how quickly the reactant disappears
Straight-Line Graphs
If a reaction graph is a straight line, its gradient is:
constant
This means the measured quantity changes at a:
constant rate
For example:
0 s → 0 cm³
10 s → 20 cm³
20 s → 40 cm³
30 s → 60 cm³
Every 10 seconds:
20 cm³ more product forms
Therefore:
rate = 20 / 10 = 2 cm³/s
throughout that interval.
Curved Reaction Graphs
Most reaction graphs are not perfectly straight.
They are:
curved
A curved graph means:
the gradient is changing
Therefore:
the reaction rate is changing
This is why we need to distinguish between:
average rate
and:
instantaneous rate
Average Rate vs Instantaneous Rate
Average Rate
Measures the rate over:
a time interval
For example:
average rate between 10 s and 30 s
Instantaneous Rate
Measures the rate at:
one particular moment
For example:
rate at exactly 20 s
These are different quantities.
Why Do We Need Instantaneous Rate?
Imagine driving a car.
Your average speed during a one-hour journey might be:
60 km/h
But at one particular moment, your speedometer might show:
85 km/h
Reaction rates work similarly.
An average rate tells us about:
an interval
An instantaneous rate tells us about:
one moment
Finding Instantaneous Rate
For a curved graph, we cannot simply use the gradient of the entire curve.
Instead, we draw:
a tangent
at the point we want to investigate.
A tangent is a straight line that touches the curve at that point and follows its direction there.
The gradient of the tangent estimates:
the instantaneous rate
How to Draw a Tangent
Suppose you want to find the reaction rate at:
30 seconds
Step 1
Find:
30 s
on the x-axis.
Step 2
Find the corresponding point on the reaction curve.
Step 3
Draw a straight line that:
just touches the curve at that point
and follows the direction of the curve.
Step 4
Extend the tangent so that you can select:
two widely separated points
on the tangent.
Step 5
Calculate:
gradient = Δy / Δt
The result estimates the:
instantaneous rate at 30 s
Use Points on the Tangent
This is extremely important.
When calculating instantaneous rate:
use points on the tangent
not necessarily points on the original curve.
The tangent is a:
straight line
so its gradient can be calculated accurately.
Use a Large Triangle
When finding the gradient of a tangent, choose points that are:
far apart
on the tangent.
Why?
A larger gradient triangle generally reduces the effect of:
small reading errors
So instead of choosing two points very close together:
use as much of the tangent as practical
Worked Example: Instantaneous Rate
Suppose a tangent drawn at 20 s passes through:
(10 s, 25 cm³)
and:
(30 s, 55 cm³)
Change in product:
55 − 25 = 30 cm³
Change in time:
30 − 10 = 20 s
Gradient:
30 / 20
= 1.5 cm³/s
Therefore:
instantaneous rate at 20 s ≈ 1.5 cm³/s
The approximation symbol is useful because the tangent itself is:
an estimate
Comparing Rates at Different Times
A reaction often begins quickly and then slows.
Suppose the instantaneous rates are:
At 10 s:
2.8 cm³/s
At 30 s:
1.4 cm³/s
At 50 s:
0.3 cm³/s
We can conclude:
reaction rate decreases with time
The graph becomes progressively:
less steep
Why Does Rate Decrease?
As the reaction proceeds:
reactants are consumed
Therefore:
reactant concentrations decrease
There are fewer reactant particles available for:
successful collisions
As a result:
successful collision frequency decreases
and:
reaction rate decreases
This produces the typical curved shape.
Connecting Gradient to Collision Theory
The relationship can be summarized:
high reactant concentration
↓
frequent successful collisions
↓
fast reaction
↓
steep graph
As the reaction proceeds:
lower reactant concentration
↓
fewer successful collisions
↓
slower reaction
↓
shallower graph
Comparing Early and Late Gradients
Consider a product graph.
Near the beginning:
large gradient
Later:
smaller gradient
Finally:
gradient ≈ 0
This corresponds to:
fast → slower → no further net product formation
The gradient therefore provides a mathematical description of:
reaction progress
The Gradient at Completion
When a product graph becomes horizontal:
Δy = 0
Therefore:
gradient = 0 / Δt
and:
gradient = 0
For a simple irreversible reaction, this means:
no additional product is being formed
The reaction has effectively:
reached completion
Reaction Graph Regions
A typical reaction graph can be interpreted in three regions.
Region 1 — Steep
large gradient
The reaction is:
fast
Region 2 — Curving
decreasing gradient
The reaction is:
slowing
Region 3 — Plateau
gradient ≈ 0
There is:
no further net change
Comparing Two Reactions
Suppose Reaction A and Reaction B are plotted on the same graph.
Reaction A has a steeper initial slope.
Reaction B has a shallower initial slope.
We can conclude:
Reaction A has a greater initial rate
provided the graphs show comparable measured quantities and scales.
Same Final Amount, Different Rates
Suppose both reactions eventually produce:
80 cm³ of gas
but:
Reaction A reaches 80 cm³ in 40 s
while:
Reaction B reaches 80 cm³ in 90 s
Reaction A is:
faster
but both produce:
the same final amount
This demonstrates:
gradient → rate
while:
plateau height → final amount
Different Rates at the Same Time
Suppose at 20 s:
Reaction A has a tangent gradient of:
2.0 cm³/s
Reaction B has a tangent gradient of:
1.1 cm³/s
Therefore, at 20 s:
Reaction A is producing gas more rapidly
This is a comparison of:
instantaneous rates
Different Rates Within the Same Reaction
We can also compare the reaction with:
itself
at different times.
For example:
At 10 s:
rate = 3.0 cm³/s
At 30 s:
rate = 1.5 cm³/s
At 50 s:
rate = 0.4 cm³/s
This tells us:
the reaction is slowing down
Percentage Decrease in Rate
Sometimes we can quantify how much the rate changes.
Suppose:
Initial rate:
2.0 cm³/s
Later rate:
0.5 cm³/s
Decrease:
2.0 − 0.5 = 1.5 cm³/s
Percentage decrease:
1.5 / 2.0 × 100
= 75%
The rate has decreased by:
75%
Product Graphs
For a product formation graph:
positive gradient → product forming
large positive gradient → rapid product formation
small positive gradient → slow product formation
zero gradient → no further net product formation
The gradient generally decreases as the reaction progresses.
Reactant Graphs
For a reactant concentration graph:
negative gradient → reactant being consumed
steep negative gradient → rapid reactant consumption
shallow negative gradient → slower consumption
zero gradient → concentration no longer changing
Mass-Loss Graphs
Some reactions release gas.
If the gas escapes from the reaction vessel:
measured mass decreases
For example:
acid + carbonate → salt + water + carbon dioxide
As CO₂ escapes:
mass decreases
The graph therefore slopes:
downward
The magnitude of the gradient tells us:
how quickly mass is being lost
Gas Volume Graphs
If the gas is collected instead:
gas volume increases
The graph slopes:
upward
Even though one graph decreases and the other increases, both can measure the rate of:
the same reaction
This is why you must always read:
the axes
before interpreting the graph.
Units from Different Graphs
| Graph | Typical Rate Unit |
|---|---|
| Gas volume vs time | cm³/s |
| Mass vs time | g/s |
| Concentration vs time | mol L⁻¹ s⁻¹ |
| Amount vs time | mol/s |
The units come directly from:
y-axis units ÷ x-axis units
Graph Scale Matters
Two graphs can look very different simply because they use:
different axis scales
A visually steeper curve does not automatically mean a faster reaction if the graphs use different scales.
For reliable comparisons:
- check the x-axis scale
- check the y-axis scale
- check the units
- calculate gradients when necessary
Never compare graph steepness without first checking:
the axes
Worked Example 1: Average Rate
A gas-producing reaction gives:
| Time (s) | Gas Volume (cm³) |
|---|---|
| 0 | 0 |
| 20 | 40 |
| 40 | 64 |
| 60 | 76 |
| 80 | 80 |
Calculate the average rate from:
20 s to 60 s
Change in volume:
76 − 40 = 36 cm³
Change in time:
60 − 20 = 40 s
Rate:
36 / 40
= 0.90 cm³/s
Worked Example 2: Overall Average Rate
Using the same data, calculate the average rate from:
0 to 80 s
Change in volume:
80 − 0 = 80 cm³
Change in time:
80 − 0 = 80 s
Average rate:
80 / 80
= 1.0 cm³/s
Notice that this does not mean the reaction rate was:
1.0 cm³/s at every moment
It is only the:
average over the entire interval
Worked Example 3: Reactant Concentration
A reactant concentration decreases from:
1.20 mol/L
at 10 s to:
0.60 mol/L
at 40 s.
Gradient:
(0.60 − 1.20) / (40 − 10)
= −0.60 / 30
= −0.020 mol L⁻¹ s⁻¹
Therefore:
gradient = −0.020 mol L⁻¹ s⁻¹
and the average rate of disappearance is:
0.020 mol L⁻¹ s⁻¹
Worked Example 4: Tangent
A tangent drawn at 25 s passes through:
(10 s, 18 cm³)
and:
(40 s, 60 cm³)
Change in volume:
60 − 18 = 42 cm³
Change in time:
40 − 10 = 30 s
Gradient:
42 / 30
= 1.4 cm³/s
Therefore:
instantaneous rate at 25 s ≈ 1.4 cm³/s
Worked Example 5: Comparing Rates
Reaction A has an initial gradient of:
2.4 cm³/s
Reaction B has an initial gradient of:
1.6 cm³/s
Difference:
2.4 − 1.6 = 0.8 cm³/s
Therefore, Reaction A initially produces product:
0.8 cm³/s faster
than Reaction B.
Worked Example 6: Rate at Completion
A product graph becomes horizontal after:
70 seconds
What is the gradient after 70 seconds?
Because the product amount remains constant:
Δy = 0
Therefore:
gradient = 0
For a simple irreversible reaction:
no further product is being formed
Experimental Data and Scatter
Real experimental results rarely produce perfectly smooth curves.
Data may contain:
scatter
Small variations may occur because of:
- measurement uncertainty
- timing uncertainty
- temperature fluctuations
- reading errors
- limitations of equipment
Scientists therefore often draw:
a smooth curve of best fit
rather than connecting every data point with straight lines.
Tangents and Experimental Data
When using experimental data:
- Draw an appropriate curve of best fit.
- Identify the required time.
- Draw a tangent to the curve.
- Choose two widely separated points on the tangent.
- Calculate the gradient.
This provides an estimate of:
instantaneous reaction rate
Why Tangent Rates Are Estimates
A tangent drawn by hand will not be:
perfectly exact
Two students may draw slightly different tangents and calculate slightly different rates.
This is acceptable if:
- the tangent is reasonable
- a large gradient triangle is used
- calculations are correct
- units are included
Therefore, instantaneous rates obtained graphically are often reported as:
approximate values
Interpreting Graphical Evidence
Calculations are only part of graph analysis.
You should also be able to explain:
what the graph tells us about the reaction
For example:
The curve is steepest during the first 10 seconds, indicating the greatest reaction rate. The gradient decreases with time as reactants are consumed. After approximately 60 seconds, the graph becomes horizontal, showing that there is no further net product formation.
This combines:
observation + calculation + chemical explanation
A Strong Graph Analysis Structure
Use:
Observe → Quantify → Explain
Observe
Describe what the graph does.
"The curve becomes less steep."
Quantify
Use numbers or gradients.
"The rate decreases from approximately 2.5 cm³/s to 0.6 cm³/s."
Explain
Use chemistry.
"Reactants are being consumed, so successful collisions become less frequent."
This creates a much stronger scientific response.
Comparing Reaction Conditions
Suppose two curves represent the same reaction:
Curve A: higher temperature
Curve B: lower temperature
If Curve A has a greater initial gradient:
higher temperature produced a faster initial reaction
This can be explained because particles have:
greater kinetic energy
and a larger fraction of collisions can overcome:
activation energy
Catalyst Graphs
Suppose two experiments differ only by the presence of a catalyst.
The catalyzed reaction generally has:
a greater gradient
and reaches the plateau:
sooner
If both experiments contain the same reactant amounts and reach the same completion:
final product amount remains the same
The catalyst changes:
rate
not the stoichiometric amount of product available.
Concentration and Graph Gradient
Higher reactant concentration usually increases:
collision frequency
Therefore, the initial gradient may be:
greater
A graph can therefore provide evidence about how concentration affects:
reaction rate
Surface Area and Graph Gradient
For reactions involving solids:
greater surface area
means more particles are exposed.
This increases collision opportunities.
Therefore:
greater surface area → greater initial gradient
For example:
powdered calcium carbonate
will generally react faster than the same mass of:
large calcium carbonate pieces
under otherwise identical conditions.
Common Misconception: Rate Is the Height of the Graph
Rate is not determined by:
how high the graph is
Rate is determined by:
gradient
A graph can be very high but completely horizontal.
In that case:
rate of change = 0
Remember:
height → amount
gradient → rate
Common Misconception: Use y ÷ x for Every Gradient
This only works if your interval begins at:
(0,0)
For any two general points, you must calculate:
(y₂ − y₁) / (x₂ − x₁)
Always use:
change in y ÷ change in x
Common Misconception: Use Curve Points to Calculate a Tangent Gradient
For instantaneous rate:
draw the tangent first
Then select two points:
on the tangent
They do not have to be points on the original reaction curve.
Common Misconception: A Steep Downward Graph Means a Slow Reaction
A steep downward slope has a:
large negative gradient
Its magnitude is large.
Therefore, it represents:
rapid decrease
For a reactant:
steep downward slope = rapid reactant consumption
Common Misconception: Negative Rate Means the Reaction Is Going Backward
A negative gradient usually means:
the measured quantity is decreasing
For example:
reactant concentration decreases
or:
mass decreases because gas escapes
It does not automatically mean the chemical reaction is:
running backward
Common Misconception: Average Rate Equals Rate at Every Moment
If the graph is curved:
rate changes continuously
The average rate describes the entire selected interval.
It does not necessarily equal the rate at:
any particular moment
Common Misconception: The Steepest-Looking Graph Is Always Fastest
Before comparing curves on different graphs, check:
- axis scales
- units
- quantities measured
- time intervals
Visual appearance alone can be:
misleading
Calculating gradients provides stronger evidence.
Graph Interpretation Checklist
When given a reaction graph, ask:
1. What is on the x-axis?
Usually:
time
2. What is on the y-axis?
Concentration? Mass? Gas volume?
3. Is the graph increasing or decreasing?
This tells you the:
direction of change
4. How steep is the graph?
This tells you the:
rate
5. Does the gradient change?
This tells you whether the reaction:
speeds up or slows down
6. Does the graph become horizontal?
This indicates:
no further net change in the measured quantity
Check Your Understanding
1. What does the gradient of a reaction graph represent?
2. A reaction produces 48 cm³ of gas in 24 s. Calculate the average rate.
3. Product volume increases from 30 cm³ at 10 s to 70 cm³ at 30 s. Calculate the average rate between these times.
4. A reactant concentration decreases from 0.90 mol/L to 0.50 mol/L over 20 s. Calculate the gradient.
5. Why is the gradient of a reactant concentration graph usually negative?
6. Explain the difference between average rate and instantaneous rate.
7. Describe how a tangent can be used to estimate instantaneous reaction rate.
8. Why should two widely separated points be selected when calculating a tangent gradient?
9. A reaction graph is steep at 10 s but almost horizontal at 50 s. What does this tell you about how the reaction rate has changed?
10. Explain why reaction graphs often become less steep as the reaction proceeds.
Key Terms
- Reaction rate: Measure of how quickly reactants are consumed or products are formed.
- Gradient: Change in the y-value divided by the corresponding change in the x-value.
- Average rate: Rate calculated over a specified time interval.
- Instantaneous rate: Rate at one particular moment.
- Initial rate: Reaction rate at the beginning of a reaction.
- Tangent: Straight line touching a curve at a particular point and following its direction there.
- Rate of formation: Speed at which a product is produced.
- Rate of disappearance: Speed at which a reactant is consumed.
- Positive gradient: Gradient produced when the measured quantity increases.
- Negative gradient: Gradient produced when the measured quantity decreases.
- Plateau: Horizontal region where the measured quantity remains approximately constant.
- Curve of best fit: Smooth curve representing the overall pattern of experimental data.
- Collision theory: Model explaining reaction rates through collisions between reacting particles.
- Successful collision: Collision that results in a chemical reaction.
- Activation energy: Minimum energy required for a successful reaction.
Key Takeaways
- Reaction rates can be determined from the gradients of reaction graphs.
- Average rate = change in measured quantity ÷ change in time.
- Always calculate Δy ÷ Δt, not simply y ÷ t unless the interval begins at the origin.
- Rate units depend on the quantities shown on the graph.
- Gas-volume graphs may give rates in cm³/s.
- Concentration graphs may give rates in mol L⁻¹ s⁻¹.
- Mass graphs may give rates in g/s.
- Product formation graphs usually have positive gradients.
- Reactant concentration graphs usually have negative gradients.
- The magnitude of a gradient indicates how quickly the measured quantity is changing.
- Steep gradient = rapid change.
- Shallow gradient = slow change.
- Horizontal graph = zero net change in the measured quantity.
- A curved graph indicates that reaction rate is changing.
- Average rate describes a time interval.
- Instantaneous rate describes one particular moment.
- Instantaneous rate can be estimated by drawing a tangent to the curve.
- Calculate the gradient using two widely separated points on the tangent.
- Tangent-based rates are estimates and should usually be treated as approximate.
- Reaction rates often decrease with time because reactants are consumed.
- Lower reactant concentrations generally lead to fewer successful collisions.
- Different reaction rates can be compared using gradients at the same time or over equivalent intervals.
- Graph scales and units must be checked before comparing curves.
- Graph height tells us amount; graph gradient tells us rate.
- Strong graph analysis uses Observe → Quantify → Explain.