unit 6 Flashcards

(49 cards)

1
Q

reaction mechanism

A

sequence of bond breaking and bond making to make reactions happen
- a series of small steps

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2
Q

rate of reaction

A

describes how quickly rxn happens
- change in concentration of reactant or product in respect to time

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3
Q

the 2 ways of making a reaction occur faster

A
  • inc. # of collisions
  • inc. the fraction of effective collisions
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4
Q

how does temp affect reaction rate

A
  • temp: average kinetic energy of molecules
  • more kinetic energy=faster moving molecules-> more collisions increasing rate of reaction
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5
Q

temp increase of what to double the rate of rxn

A

10C

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6
Q

how does concentration affect reaction rate

A
  • conc: amount of material in given space
  • higher conc=inc. change that 2 molecules will collide -> inc. rate of rxn
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7
Q

how does surface area/particle size affect reaction rate

A
  • SA/particle size: a sample of matter that is able to react + visible to other particles
  • more SA=more places of contact for reactants to collide
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8
Q

how does pressure affect reaction rate (GASES)

A
  • high pressure compresses gas, inc. concentration -> inc. frequency of collisions
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9
Q

how does a catalyst affect reaction rate

A
  • can lower the amount of energy needed to break bonds
  • can also help line up reactants in the right orientation and guide collision
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10
Q

catalyst

A

substance that inc. the rate of rxn without being consumed. or consumed but reformed

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11
Q

stoichiometry in reaction rates

A
  • no indication of rates of rxn but tells us relative rate of consumption of reactants and formation of products
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12
Q

how to find rate of consumption/rate of formation when given one or the other

A
  • look at the stoichiometric ratios or use rate expression
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13
Q

rate graph: reactant concentration vs time graph

A
  • decreases quickly, then decreases slowly (exponential)
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14
Q

rate graph: product concentration vs time graph

A
  • increases quickly, then increases slowly (exponential)
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15
Q

when is the rate of reaction fastest? why

A

when t=0
- there are no products yet, so all the collisions occur bw reactants, all being successful
- more products made = higher fraction of ineffective collisions

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16
Q

what do effective collisions depend on

A
  • sufficient energy
  • correct orientation/alignment
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17
Q

what is the unstable activation complex, when does it occur

A
  • short-lived high energy, transition state where old chemical bonds break and new ones form
  • peak of activation energy barrier
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18
Q

why doe maxwell boltzmann energy distribution curves never touch the x axis (except at 0)

A
  • there is always a possibility that a molecule can have a higher average kinetic energy
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19
Q

activation energy

A

minimum collision energy required for a successful reaction
- energy required to form an activated complex from reactants

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20
Q

most probable speed vs. average speed on maxwell-boltzmann curve

A

found at the peak of the curve vs. found slightly to the right of the peak (bcus of the asymptote)

21
Q

axises of maxwell-boltzmann energy distribution graph

A

x: kinetic energy
y: number of molecules (with energy)

22
Q

how does temperature affect a maxwell-boltzmann energy distribution graph

A
  • at higher temps, peak is lower and moves to the right (molecules more distributed)
  • higher amount of molecules w enough kinetic energy to overcome activation energy barrier
23
Q

activation energy graph axises

A

x: reaction pathway
y: potential energy (kJ/mol)

24
Q

relationship bw activation energy and chemical nature of reactants

A
  • higher activation energy = less reactive (less molecules w enough Ea)
  • lower activation energy = more reactive (more molecules w enough Ea)
25
what do catalysts do
- speed up a reaction by providing an alternative lower energy pathway from reactants to products (diff mechanism/steps)
26
how to find instantaneous rate of rxn
- draw line tangent to curve at any timepoint, calculate slope
27
the only accurate data for the relationship bw concentration of reactant and reaction rate
at point where there is no product yet (t=0) - after that, it becomes uncertain
28
how to determine how concentration of reactants affects rate of rxn
- must perform multiple experiments with different initial concentrations then graph initial rates in a linear line
29
do we look at reactants or products when determining rate law equation
reactants
30
what is k
- proportionality constant (rate law constant) - different for each rxn at any given temperature
31
what does k tell us
- speed of rxn - large k = fast rxn - small k = slow rxn - units can tell overall order of rxn
32
are m and n affected by temp
- no
33
zero order rate(y)-concentration(x) curve, what it look like?
- rate is not affected by the concentration of the reactant r=k - straight horizontal line
34
first order rate(y)-concentration(x) curve, what it look like?
- rate is proportional to concentration of a reactant r=k[A] - linear line from (0,0)
35
second order rate(y)-concentration(x) curve, what it look like?
- rate is proportional to the square of the concentration of a reactant r=k[A]^2 - exponential-> starting at (0,0) increase slowly at first then quickly
36
zero order concentration(y)-time(x) curve for reactants, what it look like?
- reactants turn directly into products - linear line downwards towards x-axis
37
first order vs second order concentration(y)-time(x) curve, what it look like?
- flipped exponential line, where 1st order is steeper than 2nd order - hard to distinguish, can use integrated rate law to represent as linear lines instead - when this is done first order will have neg slope and 2nd order will have positive slope
38
name of each step in reaction mechanism
elementary step
39
reaction intermediates
- substances formed in one step and used up in another
40
rate determining step
- step with the highest activation energy (slowest step) - determines how fast a reaction can go
41
where are the reaction intermediates found on a potential energy diagram
- troughs of graph
42
molecularity
number of species involved in an elementary step
43
what can the rate determining step (RDS) help with determining
- if a proposed reaction mechanism is valid - its rate law should match the rate law for the overall rxn if valid
44
criteria for a proposed mechanism to be valid
- each step adds up to the overall balanced chemical equation - each step is reasonable/likely (unimolecular/bimolecular) - RDS rate law same as experimental rate law
45
what does the arrhenius constant represent
- aka frequency factor/pre-exponential factor - the frequency of reactions and likelihood of correct molecular orientation - number of collisions per second with the proper orientation to react
46
what does the exponential factor represent
- the fraction of the reactant particles that have enough energy to react - dimensionless (no units)
47
how does adding a catalyst affect k
increases k (suggests a faster rxn)
48
how does increasing the concentration of a reactant affect k and rate
- no effect on k (k is temp dependent not conc dependent) - increases the rate
49
how does increasing the temp affect k and rate
- increases k and rate