This document provides an overview and review of topics for the CHEM 111 exam. It outlines basic concepts from CHEM 101 like moles, molarity, and Lewis structures that will be important. Example problems are provided for calculating moles and experimental techniques like acid-base titrations, determining cations and anions, gas laws, and drawing Lewis structures are reviewed. The document concludes by advising students on effective exam preparation strategies.
Presentation given by Dr David Vega-Maza from University of Aberdeen on "Vapour-Liquid and Solid-Vapour-Liquid Equilibria of the System (CO2 + H2) at Temperatures Between (218 and 303) K and at Pressures up to 15 MPa" in the Effects of Impurities Technical Session at the UKCCSRC Biannual Meeting - CCS in the Bigger Picture - held in Cambridge on 2-3 April 2014
Presentation given by Dr David Vega-Maza from University of Aberdeen on "Vapour-Liquid and Solid-Vapour-Liquid Equilibria of the System (CO2 + H2) at Temperatures Between (218 and 303) K and at Pressures up to 15 MPa" in the Effects of Impurities Technical Session at the UKCCSRC Biannual Meeting - CCS in the Bigger Picture - held in Cambridge on 2-3 April 2014
THE PHASE RULE
phase rule
degree of freedom in mixture
one component system
two component system
pressure temperature diagram sulfur hydrogen
eutectic eutectoid mixture
By using the anharmonic correlated einstein model to define the expressions o...Premier Publishers
By using potential effective interaction in the anharmonic correlated Einstein model on the basis of quantum statistical theory with phonon interaction procedure, the expressions describing asymmetric component (cumulants) and thermodynamic parameters including the anharmonic effects contributions and by new structural parameters of cubic crystals have been formulated. These new parameters describe the distribution of atoms. The expansion of cumulants and thermodynamic parameters through new structural parameters has been performed. The results of this study show that, developing further the anharmonic correlated Einstein model it obtained a general theory for calculation cumulants and thermodynamic parameters in XAFS theory including anharmonic contributions. The expressions are described through new structural parameters that agree with structural contributions of cubic crystals like face center cubic (fcc), body center cubic (bcc).
THE PHASE RULE
phase rule
degree of freedom in mixture
one component system
two component system
pressure temperature diagram sulfur hydrogen
eutectic eutectoid mixture
By using the anharmonic correlated einstein model to define the expressions o...Premier Publishers
By using potential effective interaction in the anharmonic correlated Einstein model on the basis of quantum statistical theory with phonon interaction procedure, the expressions describing asymmetric component (cumulants) and thermodynamic parameters including the anharmonic effects contributions and by new structural parameters of cubic crystals have been formulated. These new parameters describe the distribution of atoms. The expansion of cumulants and thermodynamic parameters through new structural parameters has been performed. The results of this study show that, developing further the anharmonic correlated Einstein model it obtained a general theory for calculation cumulants and thermodynamic parameters in XAFS theory including anharmonic contributions. The expressions are described through new structural parameters that agree with structural contributions of cubic crystals like face center cubic (fcc), body center cubic (bcc).
Catalyst Education 2020Enthalpy of Dissolution and NeutrMaximaSheffield592
Catalyst Education 2020
Enthalpy of Dissolution and Neutralization
Objectives
• Use simple calorimetry apparatus to determine the molar enthalpies of three different
reactions.
• Understand that in a closed system, the heat of a reaction is equal in magnitude but opposite
in sign to the change in heat of the surroundings.
• Directly determine the molar enthalpy of dissolution of NaOH(s) in water and use Hess’s
Law to indirectly determine the same thermodynamic value from two different reactions.
Compare molar enthalpy results with literature values using a percent error calculation and
compare the molar enthalpy of dissolution as determined by two different methods using a
percent difference calculation.
• Use mass and molarity as needed to mathematically determine the limiting reactant for
each reaction so enthalpy per mole can be determined.
Introduction
This week the enthalpy due to both physical and chemical transformations will be
investigated. The first experiment will involve a physical transformation, the reorganization of
molecules in forming a solution. The resulting enthalpy in kJ/mol will be called the molar enthalpy
of dissolution, DHm,dissolution, since NaOH will be dissolving in water. The second experiment will
determine the molar enthalpy from the chemical neutralization of an acid with a base,
DHm,neutralization, again in kJ/mol.
Enthalpy of Dissolution
When a solid is dissolved in a liquid, the solid is usually referred to as the solute and the
liquid is referred to as the solvent. In order for solvation (for the compound to dissolve) to occur,
the solvent molecules must rearrange to allow room for the solute. Similarly, the solute- solute
interactions must be broken apart and allow the solvent to surround individual solute molecules.
Finally, the interaction of the solute-solvent will be different than the solute- solute and solvent-
solvent interactions. All these changes in interactions involve energy, often detected in the form
of heat exchange. If the system gives off heat during these reactions, it is said to be exothermic,
and if the system takes in heat, it is said to be endothermic. If the system is exothermic, it will
transfer heat to the surroundings and the temperature of the surroundings will increase. If the
system is endothermic, it will absorb heat from its surroundings and the temperature of the
surroundings will decrease.
Catalyst Education 2020
Enthalpy of Dissolution
2
An example of the dissolving process can be illustrated when solid sodium hydroxide,
NaOH(s), is placed in water (Eq. 1)
NaOH(s)
!!"(⎯* Na#(aq) + OH$(aq)
Equation 1
This reaction is an exothermic process so an increase in temperature of the solution is
observed. A coffee cup calorimeter does a fairly good job of isolating the reaction. Assuming no
heat loss through the insulating walls of the calorimeter cup, then, because of conservation of
energy, the sum of th ...
Arizona State University 1 School of Molecular Sciences .docxjustine1simpson78276
Arizona State University 1 School of Molecular Sciences
How Can the Thermodynamics of
Dissolution be Defined?
Introduction:
The Gibbs-Helmholtz equation expresses the relationship between the free-energy
change, the enthalpy change, and the entropy change at constant temperature and
pressure:
∆G = ∆H - T∆S Equation 1
From knowing the value of ∆G, you may predict whether a process/reaction will be
spontaneous at a certain temperature. A process is spontaneous if ∆G is negative (∆G <
0), nonspontaneous if ∆G is positive (∆G > 0), and at equilibrium if ∆G = 0.
The enthalpy change, ∆Hrxn, is the heat gained or lost by a system during a reaction
carried out at constant pressure. Most reactions occur in several steps, with energy
required (endothermic, positive ∆H) because energy is needed to break bonds, and
energy released (exothermic, negative ∆H) because energy is released as new bonds
are formed. ∆Hrxn represents the total change in heat energy or enthalpy over the course
of the reaction. In this experiment, you will use a coffee-cup calorimeter to determine the
heat absorbed or released during the dissolution of ammonium chloride and the
dissolution of calcium chloride. From observing the contents of the coffee-cup calorimeter,
you will decide whether the dissolution processes are spontaneous or nonspontaneous.
You will also calculate values of ∆Grxn to check your prediction.
From the law of conservation of energy (energy is conserved) the total energy for the
dissolution process is:
qsystem + qsurroundings = 0 or qsystem = - qsurroudnings Equation 2
where qsystem (or qrxn) represents the heat gained or lost by dissolving the solid (the
system), and qsurroundings (or qsolution) is the heat gained or lost by the solution in the
calorimeter (the surroundings). Thus, heat energy is essentially transferred between the
dissolving solid and the solution in the calorimeter. (For this experiment, the heat
absorbed by the cup, probe, and surroundings can be considered as negligible, so it is
not included in the expression above.)
The heat absorbed or released by the contents of the calorimeter is given by:
q = (mass solution)*(specific heat of solution)*(change in temperature)
q = m· Cs · T, where T=Tfinal-Tinitial Equation 3
The mass of the solution is the sum of the masses of the water and solid placed in the
calorimeter. (Recall that the density of water is1.00 g/mL.) Because the solution is very
Arizona State University 2 School of Molecular Sciences
dilute, the specific heat of the solution is basically equal to that of water, which is 4.184
J/gºC. To calculate change (∆) for a variable it is always final minus initial. The value of
qsurr can be calculated.
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Interested in deploying notification automations for Bonterra Impact Management? Contact us at sales@sidekicksolutionsllc.com to discuss next steps.
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The modern software delivery process (or the CI/CD process) includes many tools, distributed teams, open-source code, and cloud platforms. Constant focus on speed to release software to market, along with the traditional slow and manual security checks has caused gaps in continuous security as an important piece in the software supply chain. Today organizations feel more susceptible to external and internal cyber threats due to the vast attack surface in their applications supply chain and the lack of end-to-end governance and risk management.
The software team must secure its software delivery process to avoid vulnerability and security breaches. This needs to be achieved with existing tool chains and without extensive rework of the delivery processes. This talk will present strategies and techniques for providing visibility into the true risk of the existing vulnerabilities, preventing the introduction of security issues in the software, resolving vulnerabilities in production environments quickly, and capturing the deployment bill of materials (DBOM).
Speakers:
Bob Boule
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JMeter webinar - integration with InfluxDB and GrafanaRTTS
Watch this recorded webinar about real-time monitoring of application performance. See how to integrate Apache JMeter, the open-source leader in performance testing, with InfluxDB, the open-source time-series database, and Grafana, the open-source analytics and visualization application.
In this webinar, we will review the benefits of leveraging InfluxDB and Grafana when executing load tests and demonstrate how these tools are used to visualize performance metrics.
Length: 30 minutes
Session Overview
-------------------------------------------
During this webinar, we will cover the following topics while demonstrating the integrations of JMeter, InfluxDB and Grafana:
- What out-of-the-box solutions are available for real-time monitoring JMeter tests?
- What are the benefits of integrating InfluxDB and Grafana into the load testing stack?
- Which features are provided by Grafana?
- Demonstration of InfluxDB and Grafana using a practice web application
To view the webinar recording, go to:
https://www.rttsweb.com/jmeter-integration-webinar
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Let me take this questions and provide you a short journey through existing deployment models and use cases for AI software. On practical examples, we discuss what cloud/on-premise strategy we may need for applying it to our own infrastructure to get it to work from an enterprise perspective. I want to give an overview about infrastructure requirements and technologies, what could be beneficial or limiting your AI use cases in an enterprise environment. An interactive Demo will give you some insides, what approaches I got already working for real.
2. BASIC THINGS YOU NEED
TO KNOW FOR MOST
EXPERIMENTS
MAKE SURE YOU STUDY &
REVIEW
BASIC THINGS FROM CHEM 101
SUCH AS
Moles / Molarity / Molecular
Weight
Bond types / Valence Electrons
Electronegativity / Lewis
Structures
3. HOW TO CALCULATE THE NUMBER OF
MOLES
If you have a solution (therefore the volume and the
molarity/concentration of the solution is known)
n n
C n CV V
V C
Where C: the molarity/concentration of you solution (mol/L)
n: the number of moles (mol)
V: the volume of the solution in L (L)
If you have a solid compound (therefore the mass and the
molecular weight is known)
m
n m MW n
MW
Where n: the number of moles (mol)
m: the mass of your solid
Mw: the molecular weight of your solid
4. They might as well ask you something
more complicated:
Calculate the number of moles in 50g of HCl
solution, if d=1.048 kg/L and C=6M.
From the density I know that I have 1.048 kg HCl
per Liter. Notice that kg/L is the same as g/mL
Hence I can calculate the volume of my solution:
m m 50gHCl
d V V V 47.71mLHCl
V d gHCl
1.048
mLHCl
5. Now you have the Volume and the Molarity and
you can calculate the number of moles.
DON’T FORGET TO CHANGE THE VOLUME IN L!
47.71mLHCl
47.71mLHCl LHCl 0.04771LHCl
1000mLHCl
n molHCl
C n CV N 6 0.04771LHCl 0.28626molHCl
V LHCl
6. Calculate the number of moles in 50g of
10% w/w HCl solution.
Step 1:
The HCl solution is 10% w/w,
meaning that in 100 kg (or g) of the solution
I have 10 kg (or g) of HCl acid.
Therefore my solution contains:
10gHCl
50gSolution 5gHCl
100gSolution
7. Step 2:
Now you have the mass of the HCl acid (5g) and
you can easily calculate the Molecular weight:
gHCl
MW AW (H ) AW (Cl) 1 35.45 36.45
molHCl
Step 3:
Now you are ready to calculate the number of
moles:
m 5gHCl
n n n 0.137molHCl
MW gHCl
36.45
molHCl
9. Experiments / Exercises
The chemistry of recycling
The graphical depiction of Scientific Data
Acid Base Chemistry
Project 2 (cations, anions and unknown)
Enthalpy determination
Gas Laws
Scientific Literature
From Atoms to molecules
10. Chemistry of Recycling
Balance chemical equations
Write net ionic equations
Write total ionic equations
Figure out the type of the
reaction
Calculate the theoretical yield
Calculate the percent yield
11. Graphical Depiction of Scientific
Data
You should be able to determine what type of
chart you should use every time
Remember:
in chemistry, we don’t use pie charts and bar/column charts
often, because it is common to have correlation between the
quantities measured.
You should be able to tell if the trendline given
represents the data accurately or not (and how
this reflects on the R-squared value)
You should be able to tell the relationship
between two quantities, when the graph (with or
without the trendline) is given
12. Acid-Base Chemistry
You should know the most common acids and bases
that we used in the Lab. (eg you should know that
NaOH is a base and HNO3 is an acid etc)
Different types of titration
The importance of the indicator and the difference
between the final and the equivalence point
Review the mustard experiment
13. Project 2 : Determination of
an unknown ionic
compound
FROM PART I (CATIONS)
You should remember the most obvious (and easy)
things in the lab. For example that K+ didn’t precipitate
at any point, or that Cu2+ had the easiest flame test or
that Zn+ is the only amphoteric one.
Remember that the tests are based on the differences
in solubility between the cations
You should remember the two different elimination tests
that we performed & the confirmation test (flame test)
14. FROM PART II (ANIONS)
You should remember the most obvious (and easy)
things in the lab. For example that Cl- didn’t dissolve at
any point.
Remember that the confirmation tests are different for
each anion this time
You should remember the two distinct branches of the
logic tree
15. FROM PART III (UNKNOWN)
You should remember that the first thing you had
to do was to dissolve your compound
You should be able to figure at least one reason
for getting a false positive or negative result in
ANY case.
16. IN GENERAL
They might give you a logic tree and
observations and ask you to follow down the
tree.
They might give you a list with observations and
ask YOU to draw the logic tree
You should be able to go from data to logic tree
and back
17. Enthalpy Determination
Energy neither created or destroyed
Closed or open system
Heat flow of a system
Enthalpy of a chemical reaction
Memorize the basic relationships
MAKE SURE YOU KNOW HOW YOU DEFINE THE
SYSTEM AND HOW YOU DEFINE THE
SURROUNDINGS EVERY TIME
18. Heat flow & Molar enthalpy change
q mc
0 qP
n
First Law of Thermodynamics
quniverse qsystem qsurroundings 0
qsurroundings qsystem
19. Gas Laws: P, V, T
Ideal Gas Law
PV nRT
P = Pressure
V = Volume
n = number of moles
T = Temperature
R = ideal or universal Gas Constant
MAKE SURE YOU USE THE SAME UNITS
EVERYWHERE AND YOU USE THE CORRECT
VALUE FOR R (ACCORDING TO THE UNITS)
20. From the Ideal Gas Law you can determine
EVERYTHING! (REALLY E V E R Y T H I N G!!!)
Therefore you should know the relationship between
Pressure and Volume
Pressure and Temperature
Volume and Temperature
What happens to a system when you heat it up?
(Consider the kinetic energy of the system)
How can you calculate one of them when you are given
the rest of them?
How can you calculate one of them GRAPHICLY?
21. It is possible that they will combine this
experiment with exercise 2.
You might be given different graphs and asked
to calculate something or to determine the
relationship between the two quantities.
You might be asked whether a given graph can
accurately describe the relationship between
two quantities.
22. Scientific Literature
Make sure you know what Peer-Reviewed
Sources are.
Make sure you know how to read a reference
Author(s)
Title
Year or date of the publication
Title of the journal where it was published
Volume and number (or issue) where the article was
printed
Page number
23.
24. From Atoms to Molecules
Find the number of Valence electrons each time
Consider the charge of the molecule (if any)
Draw a “draft” Lewis structure
Consider the electronegativity of each one of the atoms
Assign partial charges accordingly
Figure out the molecular geometry
Draw a final Lewis structure (don’t forget the total
charge!)
Consider if there is an overall dipole or not
Remember if a molecule is more likely to intercalate or
bind to DNA
25.
26.
27. A word of advice!
Don’t pull an all-nighter the day BEFORE the exam. It’s
not helpful if you’re sleepy!
Don’t assume that your exam will be the same as the
day before, because it WON’T
If you have absolutely NO CLUE about a problem don’t
try to guess; however if you know how to approach the
problem but you don’t know how to get to the final
answer go for it!
Eat something sweet before taking your exam (you
think it’s not working but .. It’s chemistry!)
Good luck !!