Chapter 18 - Rates of Reaction

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Last updated 3:27 PM on 2/8/26
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19 Terms

1
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rate of reaction

change in concentration of a reactant/product per unit time

equation = change in conc/time

units = mol dm-3 s-1

2
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order of a reactant

the power to which the concentration of a reactant is raised by in rate equation e.g. [A]x

-can only be 0, 1 or 2

rate α [A]x [B]y

3
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zero order with respect to reactant

-changing the concentration of reactant has no effect on rate of reaction e.g. ‘as [A] is doubled, the rate of reaction remains constant

rate α [A]0

<p>-changing the concentration of reactant has <strong>no effect on rate</strong> of reaction e.g. ‘as [A] is doubled, the rate of reaction <span style="color: red;">remains constant</span><span>’</span></p><p>rate <strong><span>α </span></strong><span>[A]</span><span style="color: red;"><strong><sup><span>0</span></sup></strong></span></p>
4
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first order with respect to reactant

-the rate of reaction is directly proportional to concentration of reactant e.g. ‘as [A] is doubled, the rate of reaction is doubled

rate α [A]1

<p>-the rate of reaction is <strong>directly proportional</strong> to concentration of reactant e.g. ‘as [A] is <span style="color: blue;">doubled</span>, the rate of reaction is <span style="color: blue;">doubled</span><span>’</span></p><p><span>rate </span><strong><span>α </span></strong><span>[A]</span><span style="color: blue;"><strong><sup><span>1</span></sup></strong></span></p>
5
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second order with respect to reactant

-the rate of reaction will equal to concentration of reactant squared e.g. ‘as [A] is doubled, the rate of reaction is quadrupled

rate α [A]2

<p>-the rate of reaction will equal to <strong>concentration </strong>of reactant <strong>squared </strong>e.g. ‘as [A] is <span style="color: green;">doubled</span>, the rate of reaction is <span style="color: green;">quadrupled</span><span>’</span><span style="color: green;"> </span></p><p><span>rate </span><strong><span>α </span></strong><span>[A]</span><span style="color: green;"><strong><sup><span>2</span></sup></strong></span></p>
6
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rate equation + constant

rate = k [A]x [B]y [C]z

k = constant that links rate of reaction with order of reactants

7
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overall order

-sum of individual orders in reaction equation

e.g. x + y + z

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calculating k and units

-rearrange rate equation to work out k

-work out units the same as Kc, mol dm-3 s-1

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measuring rate of reactions 

-measuring pH changes in titrations

-measure volume of gaseous product with gas syringe

-monitor colour changes using colorimeter

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half life t1/2

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

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concentration-time graph for ZERO ORDER (draw graph)

has no effect on rate so also no effect on half life

<p>has no effect on rate so also <strong>no effect</strong> on half life </p>
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concentration-time graph for FIRST ORDER (draw graph)

half life remains constant/the same over time

<p>half life remains <strong>constant/the same </strong>over time</p>
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equation for k using HALF LIFE

k = ln2 / t1/2

14
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plotting RATE-CONCENTRATION graphs

x-axis = concentration, y-axis = rate

gradient = rate constant k

15
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clock reaction

-method to measure initial rate of reaction

initial rate α 1/t

examples = visual colour change, formation of ppt increases over time, time taken for ppt depends on conc of reactants

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rate determining step

the slowest step in a reaction mechanism

-determines the rate as it is the slowest

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how to work out rate determining step 

-given overall chemical equation

-then given rate equation - reactant in equation is the only species present in rate determining step

-first equation uses reactant and forms products then used in second equation 

-then cancel out species present on both sides to gain chemical equation 

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example of rate determining step

CH3Br + OH- → CH3OH + Br-

rate = k [CH3Br]

1) CH3Br → CH3+ + Br-

2) CH3+ + OH → CH3OH

then cancel out CH3+

19
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Arrhenius equation - taking logs

k = Ae-Ea/RT

k = rate constant, Ea = activation energy, T = temp in Klevin, A = pre-exponential factor, R= gas constant,

ln k = (-Ea/R x 1/T) + ln A

y = m x + c - y = ln k, m = -Ea/R, x = 1/T, c = ln A

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