1) This document summarizes key concepts from a lecture on chemical kinetics including reaction rates, rate laws, reaction mechanisms, and a collision model for chemical reactions.
2) Reaction rates describe how fast concentrations of reactants and products change over time. Rate laws define the relationship between reaction rate and concentrations of reactants.
3) Reaction mechanisms involve elementary steps that may involve intermediates to ultimately form products. The rate-determining step controls the overall rate.
a detailed description of the chapter chemical kinetics (physical chemistry) including different problems by Dr. Satyabrata Si from KIIT school of biotechnology
Rate of reaction,Order of Reaction,Molecularity of Reaction,Zero Order Reactions,First Order Reactions, Half life of reactuion ,Sequential Reactions,Arrhenius Equation,Temperature Coefficient,Collision Theory of Reaction Rate,Radioactivity
GCE A LEVEL TOPIC: (A2) CHEMICAL KINETICS
PLEASE DOWNLOAD BECAUSE THERE ARE MANY ANIMATIONS THAT HIDE SOME OF THE CONTENTS (THE ANIMATIONS DO NOT PLAY DURING THE PREVIEW)
a detailed description of the chapter chemical kinetics (physical chemistry) including different problems by Dr. Satyabrata Si from KIIT school of biotechnology
Rate of reaction,Order of Reaction,Molecularity of Reaction,Zero Order Reactions,First Order Reactions, Half life of reactuion ,Sequential Reactions,Arrhenius Equation,Temperature Coefficient,Collision Theory of Reaction Rate,Radioactivity
GCE A LEVEL TOPIC: (A2) CHEMICAL KINETICS
PLEASE DOWNLOAD BECAUSE THERE ARE MANY ANIMATIONS THAT HIDE SOME OF THE CONTENTS (THE ANIMATIONS DO NOT PLAY DURING THE PREVIEW)
This unit includes: rate of a chemical reaction, graphs,, unit of rate, average rate& instantaneous rate,. factors influuncing rate of a reaction, Rate expression & rate constant, Order & molecularity of a reaction,, initiall rate method & integrated rate law equations, numerical problems,, Half life period, Pseudo first order reaction, Temperature of rate of reaction, Activation energy, collision frequency & effective collision, Collision theory, Arrhenius equation,, effect of catalyst on rate of reaction, numerical problems
Chemical kinetics, also known as reaction kinetics, is the branch of physical chemistry that is concerned with understanding the rates of chemical reactions. It is to be contrasted with thermodynamics, which deals with the direction in which a process occurs but in itself tells nothing about its rate
This unit includes: rate of a chemical reaction, graphs,, unit of rate, average rate& instantaneous rate,. factors influuncing rate of a reaction, Rate expression & rate constant, Order & molecularity of a reaction,, initiall rate method & integrated rate law equations, numerical problems,, Half life period, Pseudo first order reaction, Temperature of rate of reaction, Activation energy, collision frequency & effective collision, Collision theory, Arrhenius equation,, effect of catalyst on rate of reaction, numerical problems
Chemical kinetics, also known as reaction kinetics, is the branch of physical chemistry that is concerned with understanding the rates of chemical reactions. It is to be contrasted with thermodynamics, which deals with the direction in which a process occurs but in itself tells nothing about its rate
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
Richard's entangled aventures in wonderlandRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Nucleic Acid-its structural and functional complexity.
Chemical kinetics
1.
2. General Chemistry
Presented by: Dr Chehardoli
Department of Medicinal Chemistry,
School of Pharmacy,
Hamadan University of Medical Sciences
3. References:
Main Ref: Chemistry, Ninth Edition Steven
Zumdahl and Susan Zumdahl
Other Refs: 1- Chang General Chemistry
2- Silberberg Chemistry
3- Mortimer Chemistry
5. Section 12.1
Reaction Rates
5
Reaction Rate is:
- Change in concentration of a reactant or product per
unit time. Reaction: A B
Rate =
D[B]
Dt
Thermodynamics – does a reaction take place?
Kinetics – how fast does a reaction proceed?
Rate = -
D[A]
Dt
D[A] = change in concentration of A over
time period Dt
D[B] = change in concentration of B over
time period Dt
Because [A] decreases with time, D[A] is negative.
[A] and [B] means concentration of A and B in mol/L; A is
the reactant and B is the product.
7. Section 12.1
Reaction Rates
Br2 (aq) + HCOOH (aq) 2Br- (aq) + 2H+ (aq) + CO2 (g)
time
13.1
time
Reaction between bromine and formic acid: An example
8. Br2 (aq) + HCOOH (aq) 2Br– (aq) + 2H+ (aq) + CO2 (g)
= –
[Br2]final – [Br2]initial
tfinal - tinitial
13.1
slope of
tangent
slope of
tangent slope of
tangent
average rate = –
D[Br2]
Dt
= –
[Br2]final – [Br2]initial
tfinal - tinitial
Instantaneous rate
11. Section 12.2
Rate Laws: An Introduction
Rate Law
Decomposition of nitrogen dioxide: An example
For the decomposition of nitrogen dioxide:
2NO2(g) → 2NO(g) + O2(g)
Rate = k[NO2]n:
k = rate constant
n = order of the reactant
11
13. Section 12.2
Rate Laws: An Introduction
Rate Law
2NO2(g) → 2NO(g) + O2(g)
Rate = k[NO2]n
The concentrations of the products do not appear in the
rate law. [NO] [O2]
13
14. Section 12.2
Rate Laws: An Introduction
Rate Law
Rate = k[NO2]n
The value of the exponent n must be determined by
experiment; it cannot be written from the balanced
equation.
14
15. Section 12.2
Rate Laws: An Introduction
×
The order of a reactant is not related to the
stoichiometric coefficient of the reactant in the
balanced chemical equation.
F2 (g) + 2ClO2 (g) 2FClO2 (g)
rate = k [F2][ClO2]
1
16. Section 12.3
Determining the Form of the Rate Law
Overall Reaction Order is:
The sum of the exponents in the reaction rate equation.
Rate = k[A]n[B]m
reaction is nth order in A
reaction is mth order in B
Overall reaction order = n + m
k = rate constant
[A] = concentration of reactant A
[B] = concentration of reactant B
16
aA + bB cC + dD
17. 17
Determine the rate law and calculate the rate constant for
the following reaction from the following data:
S2O8
2– (aq) + 3I– (aq) 2SO4
2– (aq) + I3
– (aq)
Experiment [S2O8
2 – ] [I – ]
Initial Rate
(M/s)
1 0.08 0.034 2.2 x 10–4
2 0.08 0.017 1.1 x 10–4
3 0.16 0.017 2.2 x 10–4
rate = k [S2O8
2–]x[I–]y
Double [I–], rate doubles (experiment 1 & 2) 2y=2 y = 1
y = 1
Double [S2O8
2–], rate doubles (experiment 2 & 3) 2x=2 x = 1
x = 1
k =
rate
[S2O8
2–][I–]
=
2.2 x 10–4 M/s
(0.08 M)(0.034 M)
= 0.08/M•s
rate = k [S2O8
2–][I–]
×2 ×2
×2 ×2
18. Section 12.3
Determining the Form of the Rate Law
c. What is the overall reaction order? = 3
×2 ×4
×2 ×2
Rate= k[NO]2[Cl2]
0.18= k[0.1]2[0.1]= 180
19. 1) First-Order Reaction:
Rate = k[A]1
Integrated
ln[A] = –kt + ln[A]o
[A] = concentration of A at time t
k = rate constant
t = time
[A]o = initial concentration of A
19
Relation Between Reactant Concentrations and Time
D[A]
Dt
= k [A]Differential: –
A product
[A] = [A]0exp(–kt)
20. 1) First-Order Reaction: Plots
20
Relation Between Reactant Concentrations and Time
ln[A] = –kt + ln[A]o
[A] = [A]0exp(–kt)
21. Compare: ln[A] = –kt + ln[A]o With Y=mX + b
Relation Between Reactant Concentrations and Time
1) First-Order Reactions:
Straight line
Negative slope
Tangent = -k =
Δy
Δx
23. The reaction 2A B is first order in A with a rate constant of
2.8 x 10–2 s–1 at 800C. How long will it take for A to decrease
from 0.88 M to 0.14 M ?
ln[A]t = ln[A]0 – kt
kt = ln[A]0 – ln[A]
t =
ln[A]0 – ln[A]
k
= 66 s
[A]0 = 0.88 M
[A]t = 0.14 M
ln
[A]0
[A]
k
=
ln
0.88 M
0.14 M
2.8 x 10–2 s–1
=
24. 1) First-Order Reaction:
Time required for a reactant to reach half its original concentration. Its
application is used in medicine to predict the concentration of a substance
over time. It means that even though we can calculate and predict the
probability that any drug may decrease in the target during a certain interval of
time (sec, minute, day,etc.).
Half–Life for a first-order reaction:
k = rate constant
For a first-order reaction: Half–life does not depend on the
concentration of reactants.
24
1
2
0.693
=t
k
Relation Between Reactant Concentrations and Time
Half-Life (t½ ) of First-Order Reactions
t½ = t when [A] = [A]0/2
ln
[A]0
[A]0/2
k
=t½
ln2
k
=
0.693
k
=
25. Half-Life of a First-Order Reaction
The half-life of a first-order reaction stays the same.
As you can see, the time to reach one-half the starting
concentration in a first-order reaction does not depend
on what that starting concentration is.
1
2
0.693
=t
k
26. What is the half-life of N2O5 if it decomposes with a rate
constant of 5.7 x 10–4 s–1?
t½
ln2
k
=
0.693
5.7 x 10–4 s–1
=
How do you know decomposition is first order?
= 1200 s = 20 minutes
units of k = s-1
27. 2) Second-Order Reaction:
Rate = k[A]2
[A] = concentration of A at time t
k = rate constant
t = time
[A]o = initial concentration of A
27
0
1 1
= +
A A
kt
Relation Between Reactant Concentrations and Time
A product
D[A]
Dt
= k [A]2Differential: – Integrated:
28. Compare: With Y=mX + b
Relation Between Reactant Concentrations and Time
2) Second-Order Reactions:
Straight line
Positive slope
Tangent = k =
Δy
Δx
0
1 1
= +
A A
kt
29. 2) Second-Order reaction:
Half–Life:
k = rate constant
[A]o = initial concentration of A
Half–life gets longer as the reaction progresses and the
concentration of reactants decrease.
Each successive half–life is double the preceding one.
29
1
2
0
1
=
A
t
k
Relation Between Reactant Concentrations and Time
Half-Life (t½ ) of Second-Order Reactions
31. The combination of iodine atoms to form molecular iodine is a
second-order kinetics and has the high rate constant
7.03×109/M.s at room temperature : I(g) + I(g) I2(g)
a) If the initial concentration of I was 0.068 M, calculate the
concentration after 3.5 min.
b) Calculate the half-life of the reaction if the initial
concentration of I is 0.53 M. c) and if it is 0.39 M.
1
[A]
=
1
0.068 M
+ 7.03×109/M.s (3.5 min×60 s/1 min)
1
[A]
=
1
[A]0
+ kt
[A]= 6.8×10-13 M
a)
b) For [I]0= 0.53 M
1
2
0
1
=
A
t
k
=
1
7.03×109/M.s (0.53 M)
= 2.7×10-10 s
c) For [I]0= 0.39 M = 3.7×10-10 s
32. 3) Zero-Order Reaction:
Rate = k[A]0 = k
Integrated: [A] = –kt + [A]o
[A] = concentration of A at time t
k = rate constant
t = time
[A]o = initial concentration of A
32
Relation Between Reactant Concentrations and Time
A product
D[A]
Dt
= kDifferential: –
33. Compare: [A] = –kt + [A]o With Y=mX + b
Relation Between Reactant Concentrations and Time
3) Zero-Order Reactions:
Straight line
Negative slope
Tangent = -k =
Δy
Δx
34. 3) Zero-Order Reaction:
34
Relation Between Reactant Concentrations and Time
Half-Life (t½ ) of Second-Order Reactions
Half–Life:
k = rate constant
[A]o = initial concentration of A
Half–life gets shorter as the reaction progresses and the
concentration of reactants decrease.
0
1
2
A
=
2
t
k
35. Half-Lives of a Zero-Order Reaction
Each half-life is ½ the time of the previous half-life.
37. Section 12.5
Reaction Mechanisms
Reaction Mechanism
Most chemical reactions occur by a series of elementary
steps. The sequence of elementary steps that leads to
product formation is the reaction mechanism.
A D
Elementary steps: A B C D
An intermediate is formed in one step and used up in a
subsequent step and thus is never seen as a product in
the overall balanced reaction.
Intermediate: B and C
37
38. Section 12.5
Reaction Mechanisms
A Molecular Representation of the Elementary Steps in the Reaction
of NO2 and CO
NO2(g) + CO(g) → NO(g) + CO2(g)
38
NO2 NO2 NO3 NO
NO3
NO2
CO2CO
Intermediate
39. Section 12.5
Reaction Mechanisms
Elementary Steps (Molecularity)
Unimolecular – reaction involving one molecule; first
order.
Bimolecular – reaction involving the collision of two
species; second order.
Termolecular – reaction involving the collision of three
species; third order. This type is very rare.
39
A products rate = k [A]
A + A products
A + B products
rate = k [A]2
rate = k [A][B]
40. Section 12.5
Reaction Mechanisms
Rate-Determining Step
A reaction is only as fast as its slowest step.
The rate-determining step (slowest step) determines the
rate law and the molecularity of the overall reaction.
A C
1) A B Rate-Determining Step: Rate=k[A]
2) B C
40
Fast
Slow
41. The experimental rate law for the reaction between NO2
and CO to produce NO and CO2 is rate = k[NO2]2. The
reaction is believed to occur via two steps:
Step 1: NO2 + NO2 NO + NO3
Step 2: NO3 + CO NO2 + CO2
What is the equation for the overall reaction?
NO2+ CO NO + CO2
What is the intermediate?
NO3 (unstable)
What can you say about the relative rates of steps 1 and 2?
rate = k[NO2]2 is the rate law for step 1 so
step 1 must be slower than step 2
13.5
Step 1: Stable molecules
converted to unstable particle
Step 2: Unstable particle
converted to stable products
42. Section 12.6
A Model for Chemical Kinetics
Collision Model
Molecules must collide to react.
Main Factors:
Activation energy, Ea
Temperature
Molecular orientations
42
43. Section 12.6
A Model for Chemical Kinetics
Activation Energy, Ea
Energy that must be overcome to produce a chemical
reaction.
43
44. Section 12.6
A Model for Chemical Kinetics
Transition States and Activation Energy
44
45. Section 12.6
A Model for Chemical Kinetics
Change in Potential Energy
45
Example: 2BrNO 2NO + Br2
46. Section 12.6
A Model for Chemical Kinetics
For Reactants to Form Products
Collision must involve enough energy to produce the
reaction (must equal or exceed the activation energy).
Relative orientation of the reactants must allow
formation of any new bonds necessary to produce
products.
46
48. Arrhenius Equation
k = rate constant
A = frequency factor (represents the frequency of
collisions between reactant molecules)
Ea = activation energy (J/mol)
R = gas constant (8.3145 J/K·mol)
T = temperature (in K)
48
/
=
a
E RT
k Ae
Temperature Dependence of the Rate Constant
49. Section 12.6
A Model for Chemical Kinetics
Linear Form of Arrhenius Equation
49
a
E 1
ln( ) = ln
R T
k + A
For Two Temperatures:
= ( - )
Ea
R
1
T2
1
T1
Ln( )
k2
k1Ea is the activation energy (J/mol)
R is the gas constant (8.314 J/K•mol)
T1 is the initial temperature
T2 is the final temperature
k1 is the rate constant in T1
k2 is the rate constant in T2
50. At 550 0C the rate constant for the below reaction is 1.1 L/mol.s, and at
625 0C the rate constant is 6.4 L/mol.s. Using these values, calculate
Ea for this reaction.
CH4(g) + 2S2(g) CS2(g) + 2H2S(g)
= ( - )
Ea
R
1
T2
1
T1
Ln( )
k2
k1
( - ) = 1.4 × 105 J/molLn( ) =
6.4
1.1
Ea
8.314 J/K.mol
1
898 k
1
823 K
51. Section 12.7
Catalysis
Catalyst
A substance that speeds up a reaction without being
consumed itself.
Catalyst provides a new pathway for the reaction with a
lower activation energy.
51
52. Section 12.7
Catalysis
Energy Plots for a Catalyzed and an Uncatalyzed Pathway
for a Given Reaction
52
ratecatalyzed > rateuncatalyzed
Ea < Ea