S2 Fulton L1-4 Flashcards

(51 cards)

1
Q

What is the RDS

A

The rate determining step, the slowest step in a multistep process

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2
Q

What is the rate law

A

The rate law is an algebraic equation which describes the dependence of the reaction rate upon the concentration of compounds involved

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3
Q

What is the rate constant

A

The rate constant is the proportionality constant on the rate law. It allows us to put a number on how fast or slow a process goes.

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4
Q

What are we measuring when we measure kinetics

A

When we measure kinetics we are measuring how concentrations of reactions and/or products change as a reaction proceeds

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5
Q

What does the study of reaction kinetics allows us to do

A
  • determine rate law, these rate laws leads to an understanding of molecularity
  • measure rate constants
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6
Q

Define molecularity

A

The number of molecules that come together to form an activated complex (unimolecular or bimolecular)

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7
Q

What does measuring rate constants allows us to do

A

This allows us to relate the changes in solvent, structure, catalyst to the rate of reaction

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8
Q

What is a kinetic profile

A

A kinetic profile describes how the concentrations of reactants and products change over time during a chemical reaction.

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9
Q

How can we obtain reaction kinetics

A

Measure changes in concentration of reagents and/or products by UV, FTIR, NMR spectroscopy (either continuously or by taking aliquots of reactions)

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10
Q

How would decreasing reagents starting concentration affect the reaction kinetics

A

Decreasing the starting concentration of reactants the slower the reaction will become

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11
Q

What do we use the kinetic data for

A

We use the kinetic data to test a rate law

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12
Q

How would we know the rate law is first order

A

If plot of rate vs concentration is linear, shows rate is first order in that reagent/products

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13
Q

How would we know the rate law is second order

A

If rate vs concentration is not linear, then plot rate vs concentration^2: a straight line shows rate is second order

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14
Q

Describe the difference between reaction order and molecularity

A

Reaction order is the exponent in an algebraic equation that relates rate of a reaction to concentration of reagents. It can be zero, integer or fractional. Molecularity is the number of species involved in an elementary process. It can only be 1 or 2.

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15
Q

How can we use integrated rate laws to interpret kinetic profiles

A

If plot of ln[A] vs t is linear then the reaction is first order. If plot of 1/[A] vs t is linear reaction is second order

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16
Q

What is an important thing to note when we talk about proposed reaction mechanisms

A

Note that rate laws cannot prove a reaction mechanism: they can support a proposed mechanism, and they can also be used to discount a proposed mechanism

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17
Q

What are labelling experiments

A

Labelling experiments allow us to correlate atoms in products with starting material, information which can provide mechanistic insight

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18
Q

What are the common labels for H 12C and 16O

A

D for H
13C for 12C
18O for 16O

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19
Q

Describes the labels for labelling experiments

A

All labels are non-radioactive. Easy to spot their incorporation by mass spectrometry, and 13C and D can be detected by NMR spectroscopy

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20
Q

What is a crossover experiment

A

A crossover experiment uses labelled and unlabelled versions of reactants mixed together to see if mixed (crossover) products form, which indicates intermolecular exchange or reaction.

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21
Q

What is a double labelling experiment

A

A double labelling experiment involves tagging two different atoms or positions in a molecule with labels to observe two variables at once.

22
Q

What is a single labelling experiment

A

A single labelling experiment involves tagging one atom or molecular position with a detectable label to trace its movement, transformation, or role in a chemical system.

23
Q

Why type of labelling experiments are generally the most useful

A

Double labelling experiment are more useful

24
Q

What is the Hammett equation

A

Log kx/kH = pσx

25
What is the Hammett relationship
The Hammett relationship allows us to gain insight into the nature of a transition state by qualifying the effects electron donating or electron withdrawing groups have on the course of a reaction.
26
What is σx
The substituent constant, in effect we are measuring how electron-donating/withdrawing a substituent X is relative to an H substituent
27
What does it mean if σ=0
If σ=0 the substituent has the same electron-donating/withdrawing ability as H
28
What does it mean if σ>0
If σ>0 the substituent is electron-withdrawing relative to H
29
What does it mean σ<0
If σ<0 the substituent is electron-donating relative to H
30
Give examples of electron donating groups
-OCH3 -CH3
31
Give examples of electron withdrawing groups
-Br -COCH3 -NO2
32
What is kx/kH
The rate constants, in the Hammett relationship this serve to quantify how a substituent affects the rate of a chemical reaction
33
What does the Hammett relationship focus on
Focus is only on meta and para substituted species
34
How do we measure/determine the rate constant
Substituents effects the reactivity of the reaction centre and hence alters the value of kx. We measure the value of kx for different substituents. Hammett found it is best to consider rate (kx) relative to reaction when H is substituted i.e kx/kH
35
How do we draw a Hammett plot for a given reaction
1) run the reaction with a wide variety of substituent ax 2) measure rate constants in kx and divide by rate constant when H is substituent kx 3) calculate log kx/kH 4) plot these values vs substituent constants σ X axis log(kx/kH) Y axis
36
What is the gradient of the line in the Hammett plot
The gradient of the line is the reaction constant p
37
What is p in the Hammett relationship
P is the reaction constant and the value of p indicates how sensitive a reaction is to substituent effects
38
What does a positive value of p mean
A positive value of p means development of negative charge or disappearance of positive charge at reaction centre
39
What does a negative value of p means
A negative value of p means development of positive change or disappearance of negative charge at reaction centre.
40
What does the magnitude of p reflect
The magnitude of p reflects change in charge density at reaction centre during formation of TS
41
What does it mean if p is -5 or -6
Positive charge on ring or delocalised round aromatic ring
42
What does it mean if p is -2 to -4
Electrons flow out of transition states
43
What does it mean when p is between -1 to +1
No electron change
44
What does it mean when p is between +2 and +4
Electrons flow into transition state
45
What does it mean when p is between +5 and +6
Negative charge on ring or delocalised round aromatic ring
46
What are the common reactions when p is between -5 to -6
Electrophilic aromatic substitution
47
What are the common reactions when p is between -2 to -4
SN1 reactions
48
What are the common reactions when p is between -1 to +1
SN2
49
What are the common reactions when p is between +2 and +4
Base catalysed ester hydrolysis
50
What are the common reactions when p is between +5 to +6
Nucleophilic aromatic substitution
51
What does it mean when Hammett plot is not linear
Hammett plot is not linear indicates a change in mechanism