Reaction Kinetics Notes
Reaction Kinetics Notes
Reaction Kinetics Notes
in general: rate = amount (a reactant or product) time Note: A time unit is always in the denominator of a rate equation. eg.) Zn(s) + 2HCl(aq) H2(g) + ZnCl2(aq) r= mass of Zn time volume H2 time r = [ HCl ] time (note: [ ] = molar concentration)
r=
Note - some rxs, when written in ionic form show that some ions dont change concentration. eg. Mg(s) + 2HCl(aq) H2(g) + MgCl2(aq)
NOTE: To write an equation in IONIC FORM, dissociate all the aqueous (aq) compounds:
Page 1 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes Calculations Involving Reaction Rates When doing calculations involving rate, amount (grams, moles, Litres etc.) use the general equation:
Rate = amount (g, mol, L) time (s, min) or time = amount Rate
or
WHEN YOU USE ONE OF THESE FORMULAS, MAKE SURE YOUR UNITS CAN CANCEL OUT PROPERLY!
to help solve for what you need. ALWAYS use conversion factors to cancel units you dont want and replace them with ones you do want! Eg.) 0.020 mol = min. ? mol s 1 min = 3.3 x 10-4 mol 60 s s
The 60 in 60 s/1min is an exact number by definition. Therefore, we dont consider it using significant digits. The 0.020 has 2 sig. digs., therefore the answer has 2.
Solution:
You also must use molar mass to go grams moles. Eg.) 0.26 mol Zn min = ? g of Zn s 0.28 g of Zn s
You would use 22.4 L for conversions moles L (STP) for gases. 1 mol eg.) 0.030 mol O2 /s = Solution: 0.030 mol O2 x 1s L/s (STP) 22.4 L mol = 0.67 L O2 s
(The 0.030 has 2 sig digs so the answer must have 2 sig. digs.)
NOTE: This conversion is only used for gases at STP!
Page 2 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes Try this problem: The rate of a reaction is 0.034 g of Mg per second. Calculate the number of moles of Mg used up in 6.0 minutes.
Comparing rates using balanced equations -use coefficient ratios - only proportional to mol /s (not to g/s) eg.) ethane 2C2H6 + 7O2 4CO2 + 6H2O
consumed produced
eg.) if ethane is consumed at a rate of 0.066 mol /s, calculate the rate of consumption of O2 in mol /s Solution: 0.066 mol C2H6 x 7 mol O2 = 0.23 mol O2 s 2 mol C2H6 s if ethane is consumed at a rate of 0.066 mol /s calculate rate of production of CO2 Solution: 0.066 mol C2H6 x 4 mol CO2 s 2 mol C2H6 = 0.13 mol CO2 s
- when other units used you must use moles to (go over the mole bridge) (you may go from L L of one gas to another at STP) eg.) given: 2Al + 3Br2 2AlBr3 if 67.5 g of Al are consumed per second - calculate the rate of consumption of Br2 in g/s. Solution: 67.5 g Al x 1 mol Al x 3 mol Br2 s 27.0 g Al 2 mol Al x 159.8 g Br2 = 599 g Br2 1 mol Br2 s
You may have to use a few conversions and the rate equation to arrive at an answer. As you did in Chem. 11, make a plan first and make sure your units all cancel the correct way! Heres an example on the next page Chemistry 12Unit 1-Reaction KineticsNotes Page 3 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes An experiment is done to determine the rate of the following reaction: 2Al(s) + 6 HCl (aq) 3 H2(g) + 2 AlCl3 (aq) It is found that the rate of production of H2(g) is 0.060 g/s. Calculate the mass of Aluminum reacted in 3.0 minutes.
CaCO3(s) + 2H+(aq) + 2Cl-(aq) H2O(l) + CO2(g) + Ca2+(aq) + 2Cl-(aq) CaCO3(s) + 2H+(aq) H2O(l) + CO2(g) + Ca2+(aq)
in an open system CO2(g) escapes
Page 4 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes - as CO2 escapes, mass of the rest of the system will _____________________________ - so rate could be expressed as.. . r = mass of container and contents (open system) time Note rate = slope of amount. vs. time graph (disregard sign of slope. Slope will be negative if something is being consumed and positive if something is being produced. Rate is just the amount/time )
Slope = rise (g) run (s)
Mass of Container and Contents (g) rise (g) run (s)
Time (s)
Note - for a changing rate (slope) which is more realistic -rate could be expressed over a certain interval
100.
Average slope between 0 and 30 s is shown by a straight line drawn from time 0 to time 30 s on the graph.
or (g) rate at a certain point in time is the slope of the tangent that point. Slope = rise =at 100.g 20.g = 80. g
20. 0.0 10. 20. 30. Time (s)
Mass
run
30. s 0.0 s
30. s
= 2.7 g s
100.
tangent
Rate at t =22 seconds is the slope of the tangent to the curve at time = 22 seconds.
Page 5 of 40 pages
[ do ex.6 on page 3 of SW.] [Read page 11 and do ex. 18-19 on p. 11 SW.] [ do experiment on measuring rx. rates]
1.)
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2.)
Temp changes
- in exothermic reaction temperature of surroundings will ____________________ - in endothermic reaction temperature of surroundings will ____________________ - measured in insulated container (calorimeter) rate = temp time 3.) Pressure changes (constant volume or sealed container)
- if more moles of gas (coefficient) in products pressure will go up Zn(s) + 2HCl(aq) H2(g) + ZnCl2(aq) O m.o.g. 1 m.o.g. - If more MOG in reactants - pressure will __________________________ rate = pressure time (constant volume)
- If equal MOG, pressure will not change: NO2(g) + CO(g) 2 m.o.g. 4.) Volume change CO2(g) + NO(g) 2 m.o.g.
eg.) if more gas is produced, volume of balloon will increase rate = volume time 5.) Mass changes - if only one solid is used up - could remove periodically and weigh it: Mg(s) + 2HCl(aq) H2(g) + MgCl2(aq)
(periodically remove Mg and weigh what is left)
(constant pressure)
Page 7 of 40 pages
- if one gas is produced and escapes, measure mass of whats left in container (mass of container and contents) eg) heat + CaCO3(s) CaO(s) + CO2(g) rate = mass of container & contents time
Only CO2 gas escapes. So as CO2 escapes, the mass of the container and contents will decrease.
Note: its not practical to measure masses of (aq) substances separately since they are mostly water. eg) Ca(s) + 2HNO3(aq) H2(g) + Ca(NO3)2(aq) mass of HNO3(aq) time 6.) Changes in molar concentration of specific ions eg) Mg(s) + 2HBr(aq) H2(g) + MgBr2(aq) ionic form: Mg(s) + 2H+(aq) + 2Br -(aq) H2(g) + Mg2+(aq) + 2Br -(aq) - could monitor [ H+] - it will ______________crease eg.) rate = [Mg2+] [ Mg2+] - will ______________crease time Note: Does the [Br -] change? _______________ Explain. - the concentration of a specific ion can be measured: - using spectrophotometer - periodic samples taken and titrated to measure conc. 7.) Changes in Acidity - special case of #6 rate = [H+] time pH is a measure of acidity pH 0 7 14 Page 8 of 40 pages [H+] not acceptable
Chemistry 12Unit 1-Reaction Kinetics--Notes <----------------- ------------------> more acidic more basic (less basic) (less acidic) if H+ is a reactant (or any acid HCl, HNO3 etc.) [H+] will decrease so pH will INCREASE! (less acidic) rate = pH time
Measured with a pH meter
- Do Hand-In Assignment on Reaction Rates - Do expt 18-B (or A) To look at factors affecting rx rates. - Factors affecting reaction rates - 2 kinds of reactions: Homogeneous reactions - all reactants are in the same phase (don't consider products) eg.) 3H2(g) + N2(g) 2NH3(g) (both gases) Ag+(aq) + Cl-(aq) AgCl(s) ( both (aq) )
Heterogeneous Reactions - more than one phase in reactants. eg.) Zn(s) + 2HCl(aq) H2(g) + ZnCl2(aq) (2 diff. phases) eg.) C(s) + O2(g) CO2(g) (2 diff. phases)
Page 9 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes 3.) Pressure - affects reactions with gases in reactants. eg.) C(s) + O2(g) ---> CO2(g) - as pressure increases, rate _____________________________ Note: a decrease in the volume of reaction container increases the pressure (therefore rate) 4.) Nature of reactants -rate depends on how strong & how many bonds in reactants need to be broken. in general covalent bonds are strong and slow to break. C3H8(g) + 5O2(g) 3CO2(g) + 4H2O(g) (slow at room temp)
H H H H H H
H- C-C -C-H
strong covalent bonds between C-C and C-H atoms + 2MnO4- + 16H+ 10CO2 + 8H2O
eg.)
5C2O42-
(slow)
Many bonds have to be broken and many new bonds have to form. So this reaction is slow at room temperature. Eg.) H2(g) + Cl2(g) Cl - Cl slow at room temp. 2HCl(g) ( H2 and Cl2 are diatomic)
H-H +
Fast reactions at room temperature: -simple electron transfer (no bonds broken) eg.) Sn2+ + Te4+ Sn4+ + Te2+ (2 electrons have been transferred from _____ to _____ ) fast at room temp . -precipitation reactions: Chemistry 12Unit 1-Reaction KineticsNotes Page 10 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes eg.) Fe2+(aq) + S2-(aq) FeS(s) fast at room temp. both reactants (aq) - no bonds to break.
-acid base (proton transfers) ProtonTransferAnimation -intermediate in rate eg.) NH4+ + SO32- NH3 + HSO3- Do ex. 10 p.7 SW. Also, do this question:
5.)
Catalysts - a substance which can be added to increase the rate of a rx. without being consumed itself. (reactants are consumed) Demo with H2O2 + MnO2 2H2O2(l) 2H2O(l) + O2(g) MnO2 2H2O2(l) 2H2O(l) + O2(g) uncatalyzed - slow catalyzed - fast
Inhibitors - a substance which can be added to reduce the rate of a reaction. (can combine with a catalyst or a reactant & prevent it from reacting) -eg. poisons (cyanide) - organophosphates (diazinon) -antibiotics -antidepressants (serotonin uptake inhibitors) -sunscreens
Page 11 of 40 pages
Factor which affects only heterogeneous reactions (more than one phase)
6.) Surface area -when 2 different phases react, reaction can only take place on surface. solid
liquid
solid
liquid gas
gas
increase surface area by cutting solid into smaller pieces (liquids in smaller droplets)
These "inside" surfaces are added
- do lycopodium powder demo - In general - reactants with solids are slow (except powdered) - gaseous reactants are faster (but watch for diatomic bonds!) - reactants in ionic solution. are fastest if no bonds to break eg. pptn Ag+(aq) + Cl-(aq) AgCl (s)
(aqueous ions are mobile (unlike in a solid ) and more concentrated than molecules in a gas ) - Read pages 5-9 SW. - do ex. 12-14 SW. (page 8) Some points 1.) Temperature affects rate of all reactions Chemistry 12Unit 1-Reaction KineticsNotes Page 12 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes 2.) Pressure (or volume) affect reactions with gaseous reactants 3.) Concentration only affects (aq) or (g) reactants 4.) Surface area - affects only heterogeneous reactions. - do ex. 15-17 p. 9-10 SW. Pay close attention to the graphs in question 17!
- Cooking
Page 13 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes - if too hot causes burning and productions of carcinogens (benzopyrenes) - Food preservation - lower temperature - anti-oxidants (eg. ascorbic acid) - keep from O2 (sealing) - preservatives (nitrates, nitrites) Think of more!
Collision theory
- explains rates on the molecular level http://chem.salve.edu/chemistry/temp2a.asp Basic idea (basic premise)
http://www.chem.iastate.edu/group/Greenbowe/sections/projectfolder/animations/NO+O3singlerxn.html
I2
2HI
+
first later still successful collision ( reaction ) later
Effect of concentration
(slow reaction)
(faster reaction)
Effect of temperature
- when molecules move faster more collisions per unit time faster rate - also - when they move faster they collide with more kinetic energy. (hit harder) [Read page 12 SW. Do Ex. 20-22 on page 12 of SW.]
Page 14 of 40 pages
Enthalpy (H) & enthalpy change ( ) - the heat content of a substance or - the total KE & PE of a substance at const. pressure. Chemists interested in enthalpy changes ( )
H+H Heat is released to surroundings. Exothermic H is negative (-) H2
Enthalpy
Enthalpy (H)
Reaction Proceeds O + O
Enthalpy (H) O2
Reaction Proceeds
H2 + S ---> H2S = - 20 KJ ( -ive means exothermic) 6C + 3H2 ---> C6H6 = + 83 KJ ( +ive means endothermic)
Thermochemical equations: (Heat Term is right in the equation. NO shown beside the equation!) - heat term shown on left side of arrow - endothermic (it uses up heat like a reactant) eg. CH3OH + 201KJ C(s) + 2H2(g) + O2(g)
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Chemistry 12Unit 1-Reaction Kinetics--Notes -heat term shown on right side of arrow -exothermic ( it gives off heat like a product) eg. S(g) + O2(g) ---> SO2(g) + 296 kJ
Read page 13-16 in SW. Do ex. 24-28 on page 16 of SW. -now back to collision theory...
# of Molecules
See the next page for the Kinetic Energy Distribution at a low and a high temperature
Page 16 of 40 pages
# of Molecules
Kinetic Energy NOTICE: -That at the higher temperature, there are less slow (low KE) molecules and more fast (high KE) molecules -That the curve is more spread out at the higher temperature. -The TOTAL AREA UNDER THE CURVE is the same for the high temperature as for the low temperature.
Activation Energy
-minimum energy needed in a collision before a reaction take place. - it can also be defined as the minimum energy colliding particles must have in order to have a successful collision (ie. one that results in a reaction.) (SW p.19 called M.E.) A Collision in which the molecules have sufficient energy for a reaction to take place is called a SUCCESSFUL COLLISION. SEE THE GRAPH ON THE NEXT PAGE....
Page 17 of 40 pages
# of Molecules
Kinetic Energy
This shaded region represents the molecules which have sufficient energy for a successful collision
NOTE: - area under curve is proportional to # of molecules with that range of K.E. - on the graph above - a small fraction of the molecules (~ 1/10 - 1/15) (fraction of shaded area compared to total area under curve) have enough energy to react therefore it is a slow reaction
Page 18 of 40 pages
Number of Molecules
Kinetic Energy
At Temperature T1
molecules also With the higher temperature, a have KE which is > or =have the Ea. th th sufficient energy for a In this case about 1/5 to 1/6 of the molecules have sufficient KE. successful collision th th (the shaded region is about 1/5 to 1/6 the total area under the Temperature T2 curve)
(lower temp.), only these molecules have sufficient energy for a greatersuccessful fraction collision of the molecules
At Temperature T2
Rule of thumb -if the activation energy (threshold) is near the tail of the curve: - if the temperature is increased by 10oC reaction rate will about double. (ie. about twice the number of molecules have sufficient KE for a successful collision.)
Page 19 of 40 pages
Number of Molecules
Here the Activation Energy is near the tail of the curve Curve at Lower Temp. (T1)
Curve at Temp. T1 + 10 oC
Kinetic Energy
At Temperature T1
(lower temp.), only these molecules have sufficient energy for a successful collision
At Temperature T1 + 10oC
On the graph above, temperature T2 is about 10C higher that T1. Notice that the area under the T2 curve to the right of the Activation Energy is about twice the area under the T1 curve. This means that the number of molecules with sufficient KE at T2 is about double the number of molecules with sufficient KE at T1. Note - if Activation Energy or ME is near the middle of the curve (or left side) - reaction is already fast, so an increase in temperature has a less drastic effect on the reaction rate.
See the graph on the next page, where Ea is a lot lower (NOT near the tail of the curve)
Page 20 of 40 pages
Number of Molecules
Ea
Curve at T1 Curve at T1 + 10 oC
Kinetic Energy
When the Ea is low, there is not a great difference between the areas under each curve with energies greater than Ea. So when Ea is low, an increase in temperature has less effect.
Activation energies
(back to collision theory.....)
http://www.wwnorton.com/chemistry/tutorials/ch14.htm
+
e
Repulsive Force
Page 21 of 40 pages
- as colliding molecules approach the repulsion slows them down so kinetic energy decreases. - as they push against the repulsive force potential energy increases (like compressing a spring) - so: KE + Kinetic Energy PE =
is converted to
Potential Energy
Potential
Energy
(kJ)
Progress of Reaction
Molecules form a temporary, unstable species called the ACTIVATED COMPLEX Activated Complex rearranges to form the PRODUCT molecules
REACTANTS
(High KE, Low PE)
PRODUCTS
Page 22 of 40 pages
Think of this as a barrier which must be overcome before the reaction can take place
ACTIVATED COMPLEX
PRODUCTS
Reaction Proceeds
If colliding molecules dont have enough KE to convert to PE to make it over the Activation Energy Barrier, it is an UNSUCCESSFUL collision and there is NO reaction. The molecules will just bounce off of each other unchanged.
ACTIVATED COMPLEX
PRODUCTS
Chemistry 12Unit 1-Reaction Kinetics--Notes ACTIVATION ENERGY (Ea) http://chem.salve.edu/chemistry/temp2a.asp - The minimum energy required for a successfull collision. (or) The minimum energy reacting molecules must have in order to form the Activated Complex. The Activated Complex can be defined as a very short-lived, unstable combination of reactant atoms that exists before products are formed. NOTE: The Activation Energy (Ea) is fixed by the nature of the reactants (#s and strengths of bonds in reactants.) Ea is NOT affected by temperature or concentration.! 100 90 80 70 60 50 40 30 20 10
PRODUCTS REACTANTS
Ea = 85 - 50 = 35 kJ
Number of Molecules
Progress of Reaction Temperatures role - the temperature determines how many (or what fraction of the) molecules will have energy > Ea (to make it over the barrier & have a successful collision)
Kinetic Energy
At Temperature T1 (lower temp), the molecules 12Unit 1-Reaction KineticsNotes represented by this area do NOT have sufficient KE for a successful collision At Temperature T1
Chemistry
(lower temp.), only 24 Page these molecules have sufficient energy for a successful collision
of 40 pages
Potential Energy
REACTANTS
PRODUCTS
Progress of Reaction Notice in the diagrams on the previous page and above, that only a small fraction of the molecules had enough energy to overcome the Activation Energy barrier. Now, at a Higher Temperature: Activation Energy (Ea)
Curve at Higher Temp. (T2) Number of Molecules
Kinetic Energy
At a higher Temperature (T2), there are less molecules which dont have enough KE for a 12Unit 1-Reaction KineticsNotes successful collision.
Chemistry
At Temperature T2
Page 25 of 40 pages (higher temp.), there are more molecules which have sufficient energy for a
At the higher temperature, a greater fraction of the molecules have sufficient energy to make it over the Activation Energy barrier. (ie. a greater fraction of the molecules posses enough energy to form the Activated Complex):
Potential Energy
REACTANTS
PRODUCTS
Progress of Reaction Looking at the diagram above, you can see that at a higher temperature, a greater fraction of the molecules have sufficient energy to make it over the barrier. Therefore the reaction is faster. So if you study the graphs on the previous pages, you will see that: Increasing the temperature increases the fraction of molecules which have sufficient energy to form the Activated Complex (ie. sufficient energy to make it over the activation energy barrier.) This is one reason that increasing the temperature will INCREASE the rate of reaction. Also, NOTICE that a change in temperature does NOT change the Potential Energy diagram at all. Temperature does NOT affect the Activation energy or the !! Review the difference between Activated Complex and Activation Energy on the top of page 21 of SW.
Page 26 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes See: The 3 Cases on Page 21 of SW. Also study the diagram at the bottom of page 21, where it compares the KE distribution and the PE diagram
PRODUCTS
90 80 Ea 70 60 50 40 REACTANTS 30 20 10
PRODUCTS
Collision Geometry
eg. for the rx. A2 +
the above collision has unfavourable alignment (need higher energy for collision to be effective) A + A B A B A B A B A + B B
Page 27 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes In the above collision, the reactants have favourable alignment (less energy needed for an effective collision) Potential energy diagram
Route with UNFAVOURABLE Collision Geometry (Alignment) POTENTIAL ENERGY Route with FAVOURABLE Collision Geometry (Alignment) Products
Reactants
REACTION PROCEEDS
To Summarize Collision Theory so far: For any successful collision (one resulting in a reaction): 3 Requirements: 1.) - particles must collide 2.) - they must collide with sufficient energy > Ea 3.) - they need to have correct alignment (collision geometry) (to keep Ea as low as possible)
ACTIVATED COMPLEX
Page 28 of 40 pages
ACTIVATED COMPLEX
PRODUCTS
Progress of Reaction
Using the graph above, find: Ea (forward rx.) = _________kJ (forward rx. ) = _________kJ
ACTIVATED COMPLEX
( reverse rx.)
Progress of Reaction
Page 29 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes Ea (reverse rx.) = _________kJ (reverse rx. ) = _________kJ
This reverse reaction is ______thermic Answers Given the following Potential Energy Diagram for the Reaction: A 2 + B2
50 45
POTENTIAL ENERGY
2AB
A2B2
40 35 30 25 20 15 10 5 2 AB
A 2 + B2
Progress of Reaction
a) b) c) d) e) f)
Ea (forward) =
KJ KJ KJ
Energy needed to break bonds in A2 & B2 A-A B-B Ea (reverse) = KJ Energy needed to break bonds in AB (A-B) Which has the stronger bonds A2 & B2 or 2AB? On a PE diagram, species with stronger bonds (more stable) are (low/high)__________________er on the graph
g)
Which set of species (A2 & B2, A2B2, or 2AB) have the weakest bonds? . This species is the most stable. It is called the
__________________________ ______________________________
Page 30 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes h) Which set of species has the highest PE?_________________________ i) j) Which set of species has the highest KE?_________________________ Draw a graph of KE vs. reaction proceeds for the same forward rx.
KINETIC ENERGY
Progress of Reaction
Read
pages 20-22 and 24-25 in SW Answers Do Ex. 33-45 on pages 23 - 25 of SW Do Worksheet 1-2 (Potential Energy Diagrams)
Reaction Mechanisms
every long journey begins with a ______________________________ -Car building analogy lada In a chemical rx. eg.) 5C2O42- + 2MnO4- + 16H+ involves 23 reacting particles -chances of this taking place in one step are almost 0 even a 3 particle collision 2H2(g) + O2(g) probably doesnt take place in a single step. (1,000 times less probable than a 2 particle collision) Chemistry 12Unit 1-Reaction KineticsNotes Page 31 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes Most reactions (other than simple 2 particle collisions eg. Ag+ + Cl- AgCl(s) ) take place in a series of simple steps. each step depends on the others before it Reaction Mechanism - the series (sequence) of steps by which a reaction takes place. cannot be determined by just looking at overall reaction. deduced through much study and research (up to years) you will not be asked to come up with mechanism from scratch. some mechanisms are known, many are yet to be discovered. Example (known mechanism) for the overall reaction: 4HBr + O2 2H2O + 2Br2
5 reactant particles. Doesnt take place in a single step! Mechanism (determined from lots of research) Diagrams step 1: step 2: step 3: HBr + O2 HOOBr (found to be slow) see p. 26 for AC & products (fast) see page 27 SW (very fast)
2HOBr
H2O + Br2
- Each step is called an Elementary Process Rate determining step - the slowest step in the mechanism. the overall reaction can never be faster than the RDS the only way to speed up an overall reaction is to speed up the RDS (eg. by increasing. the concentration of a reactant in the RDS) eg.) in this case, increasing [HBr] or [O2] would speed up Step 1 (the RDS) and hence the overall rate. - speeding up a fast step (not RDS) will have no effect on the overall rate. (eg. adding HOOBr or HOBr has no effect)
Page 32 of 40 pages
Determining overall reaction given steps (mechanism) - cancel stuff which is identical on both sides - add up whats left. eg.) 1.) 2.) 3.) overall rx: eg.) 1.) 2.) 3.) HBr O2 HOOBr HBr + HOOBr 2HOBr 2HBr + 2HOBr 2H2O + 2Br2 +
_____________________________________________________________________
_____________________________________________________________________
overall rx:____________________________________________ Question the following reaction occurs in a 3 step mechanism: 2A4+ + B+ 2A3+ + B3+ step 1: A4+ + C2+ C3+ + A3+ step 2: A4+ + C3+ C4+ + A3+ step 3: ? find step 3.
this is the overall reaction
Another Example: Consider the following reaction for the formation of HCl in the presence of light. Cl2 + CHCl3 HCl + CCl4 The following is the proposed reaction mechanism: Step 1: Cl2 Cl + Cl Step 2: Step 3: Cl + CCl3 CCl4 Chemistry 12Unit 1-Reaction KineticsNotes Page 33 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes Determine Step 2 of the reaction mechanism. Step 2: ________________________________________________________
Reaction intermediate
-a species (atom, molecule or ion) which is produced in one step and used up in a later step. (appears on right & also lower on left) eg.) 1) 2) 3) For the mechanism: HBr + O2 HOOBr HBr + HOOBr 2HOBr 2HBr + 2HOBr 2H2O + 2Br2 intermediates are Notes: an intermediate doesnt accumulate (like a product) because as soon as it is formed, it gets used up again (like money) intermediates are not necessarily unstable. (in other circumstances, they may last a while) an activated complex is very unstable and short-lived. It doesnt usually obey bonding rules. (see diagrams p. 26 & 27) (very high PE, temporary arrangement) Read pages 26-27 in SW Do ex. 46-53 p.28 of SW. ___ & ______________
PE
STEP 1
STEP 3
H2O + Br2
Chemistry 12Unit 1-Reaction Kinetics--Notes each bump is a step the higher the bump, (greater Ea) the slower the step the highest bump (from the reactants level) is for the RDS ACs at top of bumps, intermediates in middle valleys, products in the final valley the Ea for the forward overall rx. is vertical distance from reactants to top of highest bump. On the diagram for this mechanism on the previous page, label the Rate Determining Step. Draw an arrow to show the Ea (overall reaction) . Label it. Draw another labeled arrow to show the Ea for Step 1. Draw a labeled arrow to show for the overall reaction.
PE
Ea (Overall Rx.)
REACTION PROCEEDS
PE
Ea (Overall Rx.)
REACTION PROCEEDS
In each of the reactions in the diagram above, the Ea for the overall forward reaction is the difference in energy between the reactants and the top of the highest peak. Chemistry 12Unit 1-Reaction KineticsNotes Page 35 of 40 pages
Question: Given the following Potential Energy Diagram for a reaction mechanism:
PE (KJ) 80 70 60 50
Reaction Proceeds
steps
kJ
5. The overall rx. is 7. for reverse rx. = 9. RDS for reverse rx. is step
kJ
Draw a Potential Energy Diagram for a reaction mechanism with 2 steps. The first step is fast and the second step is slow. The overall reaction is exothermic. With labeled arrows show the overall Activation Energy (Ea) and the for the forward reaction.
PE
Page 36 of 40 pages
Reaction Proceeds
catalyst- an introduced substance which produce an alternate mechanism with a lower activation energy.
PRODUCTS
Progress of Reaction
Look on the next page to see the PE diagram showing the uncatalyzed and the catalyzed routes for the same reaction.
Page 37 of 40 pages
Ea (catalyzed rx.)
PRODUCTS
Progress of Reaction
Notes energy required (Ea) is less with the catalyst, so at the same temperature, more molecules can make it over the barrier so reaction rate speeds up (eg. lower standards for a pass, eg. 30% will let more students pass!) catalyzed reactions usually involve more steps but its highest Ea (highest bump) is never as high as the uncatalyzed reaction a catalyst NEVER changes the PE of reactants of products - only the route between them. (no change in ! ) uncatalyzed reaction still continues at its own slow rate when a catalyst is added. (usually insignificant compared to catalyzed rate) if catalyst speeds up forward reaction, it also speeds up (reduces Ea for) the reverse reaction.
Page 38 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes Study the PE diagram on the next page which compares the Eas for the forward and reverse uncatalyzed and catalyzed reactions
Ea(f) (catalyzed)
Ea (r)
(Uncatalyzed )
PRODUCTS
Progress of Reaction
Ea (r)
(Catalyzed )
providing a surface whose spacing of atoms is just right to break a reactant molecule and hold it for an attack from another reactant.
helping to form an intermediate which can react more easily to form products. eg.) 2H2O2(l) 2H2O(l) + O2(g) (very slow uncatalyzed) Page 39 of 40 pages
Chemistry 12Unit 1-Reaction Kinetics--Notes -add some KI (I-) Demonstration Catalyzed Mechanism: step 1) H2O2 + I- ---> H2O + OI- (The catalyst I- is put in.) step 2) H2O2 + OI- ---> H2O + O2 + I- (The catalyst I- is regenerated.) overall rx. 2H2O2 ---> 2H2O + O2 See the example in the textbook on p. 32-33. In the diagrams on page 33, the Activated Complexes are also shown in the square brackets. Also compare the PE diagram for the uncatalyzed reaction (bottom of p. 32 SW.) and the PE diagram for the catalyzed reaction (middle of p. 33 SW.) OCl_IMechanism Read pages 30-36 in SW. Do ex. 56-61 on page 34 SW See Examples of real Catalysts p.34-36 SW. Get hand-out on catalysts from teacher Do ex. 62 & 63 on page 36 of SW . Do Worksheet 1-3 (Reaction Mechanisms) Do Provincial Questions on Unit 1
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