How fast? rate of reaction

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29 Terms

1
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rate of reaction

speed at which a chemical reaction takes place, can be expressed as change in conc of a particular reactant/product per unit time

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calculating rate of reaction (mol dm-3 s-1 )

change in conc of reactants or products / time

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3 techniques of measuring rate

  • mass loss

  • gas production

  • colorimetry

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4 factors of collision theory

  • for a reaction between 2 particles to occur, the particles must collide with:

    • the appropriate collision geometry

    • sufficient kinetic energy

  • the minimum amount of energy required = the activation energy

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factors affecting rate of reaction

  • concentration

  • pressure

  • temperature

  • SA

  • catalysts

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concentration affecting rate

  • an increase in conc causes an increase in number of particles per unit volume

  • this causes increase in collision frequency, hence increased frequency of successful collisions

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pressure affecting rate

  • increase in pressure causes less space for particles to move in

  • number of successful collisions increases due to increased collision frequency

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temperature affecting rate

  • increase in temp cause particles to move faster as they gain KE, so collide more frequently

  • at higher temp, higher proportion of particles have the activation energy, meaning higher proportion of collisions are successful

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surface area affecting rate

  • increase in surface area means more particles are on the surface and able to collide with particles of reactant

    • means more collisions in total meaning more successful collisions

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catalyst affecting rate

  • catalyst provides reactants with alternative reaction pathway which is lower in activation energy

  • more collisions are successful

  • catalyst remains unchanged

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activation energy

  • minimum energy colliding particles need to collide successfully leading to a reaction

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homogenous & heterogenous catalyst

  • homo: catalyst is in the same phase as reactant

  • hetero: catalyst is in a different phase to the reactant

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energy profiles of catalyst reactions

knowt flashcard image
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effect of temp on maxwell boltzmann

  • when temp increases, curve flattens and the peak shifts to right

  • because higher proportion of successful collisions

<ul><li><p>when temp increases, curve flattens and the peak shifts to right</p></li><li><p>because higher proportion of successful collisions</p></li></ul>
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rate equation

  • Rate of reaction = k [A]m [B]n

  • A and B are concs of reatants

  • catalysts and products may feature

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order of reaction

  • order shows how conc affects the rate

    • the power to which the conc of the reactant is raised in the rate eqution

  • zero order

    • changing conc has no effect

  • first order

    • conc of reactant is directly proportional to rate

  • second order

    • rate is directly proportional to the square of conc of reactant

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determining rate equation from data

  • find 2 experiments where conc of 1 reactant changes but concs of others are constant

  • calculate what happens to concentration and rate

  • deduce order

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reaction orders from conc-time graphs

  • zero order

    • as time goes on, conc decreases, graph is straight line

    • rate = k

  • first order

    • conc decreases with time, graph is a curve which plateaus

  • second order

    • conc decreases more steeply with time, graph is steeper curve which plateaus

<ul><li><p>zero order</p><ul><li><p>as time goes on, conc decreases, graph is straight line </p></li><li><p>rate = k</p></li></ul></li><li><p>first order</p><ul><li><p>conc decreases with time, graph is a curve which plateaus</p></li></ul></li><li><p>second order</p><ul><li><p>conc decreases more steeply with time, graph is steeper curve which plateaus</p></li></ul></li></ul>
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reaction orders from rate-conc graphs

  • zero order

    • rate remains constant, graph is horizontal line

    • rate = k

  • first order

    • rate increases as conc increases,

    • graph is straight line

    • rate = k(A)

  • second order

    • rate increases more as conc increases, graph is curved line

    • rate = k(A)2

<ul><li><p>zero order</p><ul><li><p>rate remains constant, graph is horizontal line</p></li><li><p>rate = k</p></li></ul></li><li><p>first order</p><ul><li><p>rate increases as conc increases, </p></li><li><p>graph is straight line</p></li><li><p>rate = k(A)</p></li></ul></li><li><p>second order</p><ul><li><p>rate increases more as conc increases, graph is curved line</p></li><li><p>rate = k(A)<sup>2</sup></p></li></ul></li></ul>
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calculating the rate constant and its units

  • zero order: mol dm-3 s-1

<ul><li><p>zero order: <strong>mol dm<sup>-3</sup> s<sup>-1</sup></strong></p></li></ul><p></p>
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effect of temp on rate constant

  • increasing temp increases value of rate constant as concentration stays same

  • this is because as rate of reaction increases, rate constant increases

  • relationship is not linear though

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reaction mechanisms

  • each step in reaction is called elementary step, involves small number of particles

  • some products of an elementary step exist as intermediates and react in subsequent steps

  • sum of elementary steps must equal overall reaction equation

    • intermediates cancel out if appear on both sides

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rate determining step

  • the slowest step in the reaction

  • if reactant appears in rate determining step, conc of the reactant appears in rate equation

  • the order with respect to a reactant is the number of particles of that reactant that take part in rate-determining step

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energy profiles in single step reaction

  • when reacting molecules collide, with bond breaking/formation occurring, they will be in an unstable, high-energy state temporarily

    • transition state: higher energy state than reactants/products, corresponds to AE

<ul><li><p>when reacting molecules collide, with bond breaking/formation occurring, they will be in an unstable, high-energy state temporarily</p><ul><li><p>transition state: higher energy state than reactants/products, corresponds to AE</p></li></ul></li></ul><p></p>
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energy profiles in multi step reactions

  • the rate determining step is the step with greatest activation energy

<ul><li><p>the rate determining step is the step with greatest activation energy </p></li></ul>
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molecularity

  • number of reacting particles taking part in an elementary step

    • unimolecular: one reactant particle involved

    • bimolecular: two reactant particles involved

    • termolecular: three reactant particle involved

  • usually discussed in relation to the rate determining step

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arrhenius equation

  • k = rate constant

  • A = arrhenius factor (nature of reactants)

  • Ea= activation energy J mol-1

  • R= gas constant

  • T= temperature K

    • k and T are the only variables

    • used to describe reactions involving gases, occurring in solution, or reactions on surface of catalyst

<ul><li><p>k = rate constant</p></li><li><p>A = arrhenius factor (nature of reactants)</p></li><li><p>Ea= activation energy J mol-1</p></li><li><p>R= gas constant</p></li><li><p>T= temperature K</p><ul><li><p>k and T are the only variables</p></li><li><p>used to describe reactions involving gases, occurring in solution, or reactions on surface of catalyst</p></li></ul></li></ul><p></p>
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using the arrhenius equation

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determining Ea and the arrhenius factor

  • once k at different temperatures for a reaction has been determined, can be used to determine Ea and A

  • graph of ln k against 1/T can be plotted

    • gradient: -Ea / R

    • y intercept: ln A

  • Ea = -gradient x R

  • A = ey-intercept

<ul><li><p>once k at different temperatures for a reaction has been determined, can be used to determine Ea and A</p></li><li><p>graph of ln k against 1/T can be plotted</p><ul><li><p>gradient: -Ea / R</p></li><li><p>y intercept: ln A</p></li></ul></li><li><p>Ea = -gradient x R</p></li><li><p>A = e<sup>y-intercept</sup></p></li></ul><p></p>