Search found 54 matches
- Thu Mar 12, 2020 11:02 pm
- Forum: Administrative Questions and Class Announcements
- Topic: Final
- Replies: 2
- Views: 85
Re: Final
Professor Lavelle will release more information on the final shortly. Please stay calm and do not worry too much about it.
- Thu Mar 12, 2020 11:00 pm
- Forum: Balancing Redox Reactions
- Topic: Determing balanced rxns for a basic solution
- Replies: 5
- Views: 146
Re: Determing balanced rxns for a basic solution
I think the method you're describing works. Basically, if you need to balance hydrogens on one side of the reaction, you add water to the side that needs hydrogens and an equal amount of hydroxide to the other side of the reaction. The hydroxide will cancel out everything in the water molecule excep...
- Thu Mar 12, 2020 10:56 pm
- Forum: Arrhenius Equation, Activation Energies, Catalysts
- Topic: Activation Energy vs Free Energy of Activation
- Replies: 6
- Views: 142
Re: Activation Energy vs Free Energy of Activation
Activation energy is specific to a reaction. molecules will need to overcome an energy threshold to undergo the reaction. Free energy of activation refers to how much energy is available to cause a reaction to take place.
- Thu Mar 12, 2020 10:55 pm
- Forum: Arrhenius Equation, Activation Energies, Catalysts
- Topic: Homework question 7.1
- Replies: 2
- Views: 80
Re: Homework question 7.1
Kinetic control v thermodynamic control refers to what process is dominating the reaction process, kinetics or thermodynamics. Kinetic control infers that the fastest reaction will be taking place, whereas thermodynamic control means the reaction that is the most energy conserving, I think.
- Thu Mar 12, 2020 10:50 pm
- Forum: Student Social/Study Group
- Topic: final?
- Replies: 7
- Views: 274
Re: final?
I think Prof. Lavelle will give more details in days to come. I wouldn't worry about it too much though.
- Sun Mar 08, 2020 10:48 pm
- Forum: First Order Reactions
- Topic: How does a first order reaction "collide" with itself? [ENDORSED]
- Replies: 2
- Views: 77
How does a first order reaction "collide" with itself? [ENDORSED]
Professor Lavelle said that the order of the reaction indicates how many molecules are colliding in the reaction. How does a first order reaction work, since one molecule cannot collide with itself?
- Sun Mar 08, 2020 10:45 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: 6L.3
- Replies: 4
- Views: 109
Re: 6L.3
The right side of the diagram will be the cathode; it will be a reduction half reaction. Take whatever ions or substances are given, and make a reduction half reaction from them. The left side will be an anode; it will be an oxidation half reaction. Take whatever ions or substances are given, and ma...
- Sun Mar 08, 2020 10:42 pm
- Forum: Appications of the Nernst Equation (e.g., Concentration Cells, Non-Standard Cell Potentials, Calculating Equilibrium Constants and pH)
- Topic: Purpose of Nernst Equation
- Replies: 5
- Views: 71
Re: Purpose of Nernst Equation
The Nernst equation is used to find the cell potential of an electrochemical reaction that is not in equilibrium, but is in transit. Since you can plug in reaction quotient Q, you can determine the "weaker" cell potential, since the reaction has been going on for some time.
- Sun Mar 08, 2020 10:40 pm
- Forum: Reaction Mechanisms, Reaction Profiles
- Topic: Speed of a reaction
- Replies: 2
- Views: 58
Re: Speed of a reaction
Is there a specific problem you are asking about?
The size of the rate law will generally tell you how fast the rate is relative to other rates.
The size of the rate law will generally tell you how fast the rate is relative to other rates.
- Sun Mar 08, 2020 10:38 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: test 1
- Replies: 2
- Views: 57
Re: test 1
Use the pH to find concentration of H+ ions. That equals the concentration of conjugate base. You divide this concentration by the total concentration to get the percent ionized. To get Ka, use the formula [A-][H+]/[HA].
- Mon Mar 02, 2020 12:31 am
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Electrolysis (6.O.1)
- Replies: 3
- Views: 74
Re: Electrolysis (6.O.1)
You can always look it up on google.
- Mon Mar 02, 2020 12:30 am
- Forum: Appications of the Nernst Equation (e.g., Concentration Cells, Non-Standard Cell Potentials, Calculating Equilibrium Constants and pH)
- Topic: concentration cell
- Replies: 3
- Views: 79
Re: concentration cell
Concentration cell is a different type of cell from the galvanic cell, since the same ion is on both side. However, the due to the concentration difference, which creates a different cell potential on each side, there is a flow of electrons, a current.
- Mon Mar 02, 2020 12:29 am
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: cell diagrams
- Replies: 1
- Views: 22
Re: cell diagrams
In a cell diagram, you always put the cathode on the right side of the double lines, and the anode on the left side of the double lines. any phase change is separated by a single line. If there is no phase change, use commas.
- Mon Mar 02, 2020 12:27 am
- Forum: Appications of the Nernst Equation (e.g., Concentration Cells, Non-Standard Cell Potentials, Calculating Equilibrium Constants and pH)
- Topic: Nernst Equation Use
- Replies: 3
- Views: 109
Re: Nernst Equation Use
Use the Nernst equation to calculate cell potential in nonstandard conditions. Also, while the redox reaction is taking place.
- Mon Mar 02, 2020 12:26 am
- Forum: Appications of the Nernst Equation (e.g., Concentration Cells, Non-Standard Cell Potentials, Calculating Equilibrium Constants and pH)
- Topic: Nernst
- Replies: 10
- Views: 177
Re: Nernst
Remember that Q is the reaction quotient. (quo-tee-ent)
- Mon Feb 24, 2020 12:00 am
- Forum: Third Law of Thermodynamics (For a Unique Ground State (W=1): S -> 0 as T -> 0) and Calculations Using Boltzmann Equation for Entropy
- Topic: surroundings
- Replies: 4
- Views: 168
Re: surroundings
When the reaction is reversible expansion, delta S total is zero. Thus, delta S surroundings = negative delta S system.
When reaction is irreversible free expansion, delta S total equals delta S of system, and delta S of surroundings is zero.
When reaction is irreversible free expansion, delta S total equals delta S of system, and delta S of surroundings is zero.
- Sun Feb 23, 2020 11:58 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Electron Transfer
- Replies: 3
- Views: 61
Re: Electron Transfer
Electrons are too small and fast moving to be quantified, so they cannot be directly counted.
- Sun Feb 23, 2020 11:57 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: gibbs free energy
- Replies: 15
- Views: 235
Re: gibbs free energy
You can think of Gibbs free energy as the energy level of reactants/products. If you think of a reaction curve where the reactants sit at a certain G and the products sit at another G, the difference between those energies will be delta G. If the reactants G are lower than products G then it will re...
- Sun Feb 23, 2020 11:55 pm
- Forum: Balancing Redox Reactions
- Topic: Tips for Balancing Reactions
- Replies: 3
- Views: 64
Re: Tips for Balancing Reactions
Also, just adding onto the above point, if the solution is basic, then you can add OH- to the reactants. If acidic, you can add H+. It's really just trial and error until you make it work.
- Sun Feb 23, 2020 11:49 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: cell potential
- Replies: 3
- Views: 62
Re: cell potential
Concentration tells you what direction the reaction will go in. If it is not going forward, then the cell will not be going forward.
- Sun Feb 23, 2020 11:46 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: salt bridge
- Replies: 9
- Views: 140
Re: salt bridge
Adding on, the salt bridge consists of salts that will balance out the building charge of the anion and cation.
- Sun Feb 23, 2020 11:45 pm
- Forum: Appications of the Nernst Equation (e.g., Concentration Cells, Non-Standard Cell Potentials, Calculating Equilibrium Constants and pH)
- Topic: conducting solids
- Replies: 5
- Views: 101
Re: conducting solids
Examples of conducting solids are all transition metals and some metalloids. Non conducting solids are everything that is not in those two categories.
- Sun Feb 16, 2020 1:47 pm
- Forum: Balancing Redox Reactions
- Topic: Number of electrons
- Replies: 5
- Views: 86
Re: Number of electrons
Just adding on, for the overall redox reaction, you usually wouldn't write the electrons, but in the reduction and oxidation half reactions you would.
- Sun Feb 16, 2020 1:36 pm
- Forum: Administrative Questions and Class Announcements
- Topic: about the Midterm...
- Replies: 8
- Views: 193
Re: about the Midterm...
Hi Janet, I'm sorry you felt that way about the midterm. Honestly, sometimes tests are more about test taking than knowing the material. I know you probably did a lot of practice tests, but the only advice I can give is to do practice test. Finding previous midterms can be difficult, but is possible...
- Sun Feb 16, 2020 1:32 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: relationship between delta G and K
- Replies: 2
- Views: 36
Re: relationship between delta G and K
at equilibrium, delta G = -RTlnK
- Sun Feb 16, 2020 1:31 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: signs of G with different values of K
- Replies: 3
- Views: 40
Re: signs of G with different values of K
For the delta G equation at equilibrium, you take the natural log of K. If K is less than 1 but greater than 0 (so a fraction) then the value of the natural log will be a negative number. That's why it will be negative.
- Sun Feb 16, 2020 1:29 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: maximum work
- Replies: 5
- Views: 138
Re: maximum work
That's my understanding of it. Max work only occurs in a theoretical scenario, as does most of thermodynamics and chemistry, because real life situations are too complicated.
- Sun Feb 09, 2020 9:16 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: Heat capacity
- Replies: 2
- Views: 29
Re: Heat capacity
Basically, you don't have to worry about the process of determining the heat capacity. Just worry about the heat capacity itself, which usually functions as a constant.
- Sun Feb 09, 2020 9:14 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: constant p
- Replies: 4
- Views: 43
Re: constant p
This is the equation for change in enthalpy at constant pressure. At constant pressure, delta H is equal to the heat.
- Sun Feb 09, 2020 9:14 pm
- Forum: Ideal Gases
- Topic: Gas constant
- Replies: 10
- Views: 189
Re: Gas constant
It depends on the units of the other measurements given.
- Sun Feb 09, 2020 9:13 pm
- Forum: Thermodynamic Systems (Open, Closed, Isolated)
- Topic: problem 4A9
- Replies: 2
- Views: 77
Re: problem 4A9
So the q of the copper is equal to the - q of the water. Just set them equal to each other, then plug in all the variables you know. Since you don't know the final temperature, plug that in as a variable. Since the final temperature will be the same for both materials, you use -q(cu) = q(h2o) to sol...
- Sun Feb 09, 2020 9:11 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: Is heat capacity an extensive or intensive property?
- Replies: 2
- Views: 32
Re: Is heat capacity an extensive or intensive property?
Heat capacity is intensive. It does not matter what quantity is there, the heat capacity stays the same.
- Sun Feb 02, 2020 10:13 pm
- Forum: Calculating Work of Expansion
- Topic: Integral Calculations
- Replies: 3
- Views: 61
Re: Integral Calculations
You're right, integrals are used to quickly find the sum of an infinite number of sums. I don't think Lavelle has given us any problems that require us to use it yet...
- Sun Feb 02, 2020 10:12 pm
- Forum: Phase Changes & Related Calculations
- Topic: Pressure in an Open Beaker
- Replies: 10
- Views: 108
Re: Pressure in an Open Beaker
If it says the surroundings are at standard temp and pressure it would be 1atm. If it's not specified, then you probably don't need the specific pressure to solve the problem.
- Sun Feb 02, 2020 10:08 pm
- Forum: Calculating Work of Expansion
- Topic: Enthalpy
- Replies: 5
- Views: 31
Re: Enthalpy
State functions can be contrasted with path functions, where the pathway to the current state does matter. Compared to those, state functions do not rely on the pathway, so yes, can be added or subtracted simply.
- Sun Feb 02, 2020 9:59 pm
- Forum: Third Law of Thermodynamics (For a Unique Ground State (W=1): S -> 0 as T -> 0) and Calculations Using Boltzmann Equation for Entropy
- Topic: Degeneracy
- Replies: 4
- Views: 35
Re: Degeneracy
Degenerate describes states that have the same energy level, but different positions/configurations. For example, the three p-orbitals of a given energy level are degenerate. Calculating it is complicated because it depends on the number of particles and the types of particles in the system.
- Sun Feb 02, 2020 9:55 pm
- Forum: Phase Changes & Related Calculations
- Topic: Pressure in an Open Beaker
- Replies: 10
- Views: 108
Re: Pressure in an Open Beaker
An open beaker has constant pressure because you are assuming the only pressure acting upon it is air pressure, which will be uniform on the contents of the beaker.
- Sun Jan 26, 2020 5:21 pm
- Forum: Phase Changes & Related Calculations
- Topic: State Properties
- Replies: 3
- Views: 57
Re: State Properties
It's any quantity that is independent of how the substance was prepared.
- Sun Jan 26, 2020 5:20 pm
- Forum: Phase Changes & Related Calculations
- Topic: State Properties
- Replies: 3
- Views: 57
Re: State Properties
Pressure, volume, temperature, enthalpy.
- Sun Jan 26, 2020 5:19 pm
- Forum: Non-Equilibrium Conditions & The Reaction Quotient
- Topic: Kw Equations
- Replies: 10
- Views: 175
Re: Kw Equations
Also, keep in mind that although:
[Ka][Kb] = Kw and [H3O+][OH-] = Kw
[Ka] != [H3O+] and [Kb] != [OH-]
[Ka][Kb] = Kw and [H3O+][OH-] = Kw
[Ka] != [H3O+] and [Kb] != [OH-]
- Sun Jan 26, 2020 5:15 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Bond Enthalpies
- Replies: 2
- Views: 21
Re: Bond Enthalpies
Yes, if 2 bonds of C-H were formed, multiply by 2. Coefficients do matter, a lot. Make sure the equation is balanced.
- Sun Jan 26, 2020 5:14 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Bond Enthalpies
- Replies: 2
- Views: 21
Re: Bond Enthalpies
Enthalpies should be given. It is hard to determine them on your own. And you will need to know number of bonds broken and formed for the second method that Dr. Lavelle mentioned in class.
- Sun Jan 26, 2020 5:13 pm
- Forum: Phase Changes & Related Calculations
- Topic: Combustion vs. Cellular Respiration
- Replies: 5
- Views: 80
Re: Combustion vs. Cellular Respiration
Technically, since energy is conserved, the change in overall free energy would be the same. However, there are many other factors that come into play, such as entropy.
- Sun Jan 26, 2020 5:05 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Standard enthalpy of solids and liquids
- Replies: 2
- Views: 30
Re: Standard enthalpy of solids and liquids
Enthalpy of formation will depend on the substance you are working with. But yes, it is standard for each substance.
- Sun Jan 19, 2020 11:06 pm
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: Conjugates
- Replies: 2
- Views: 48
Re: Conjugates
Conjugates are also good to know for weak acids and bases; the conjugates tell you which reactant/products are related in the equation.
- Sat Jan 18, 2020 5:27 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: Acids and Bases Ice Box
- Replies: 5
- Views: 70
Re: Acids and Bases Ice Box
In summary of the above comments, using Ka or Kb is situational. However, many times the question will give you the constant that you need to answer the question.
- Sat Jan 18, 2020 5:25 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: 6B. 9 Solutions Typo
- Replies: 1
- Views: 29
Re: 6B. 9 Solutions Typo
The solution manual is correct for these. Make sure you are using the equation 1.0 x 10^-14 = [H3O+][OH-]
- Sat Jan 18, 2020 5:20 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: 6D. 7
- Replies: 3
- Views: 46
Re: 6D. 7
I'm not really sure what this question is asking, but I don't think you need Ka or Kb. It looks like the questions just wants you to convert pH into concentration of [H3O+].
- Thu Jan 16, 2020 3:09 am
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: Endothermic/Exothermic Rxns and Delta H
- Replies: 3
- Views: 119
Re: Endothermic/Exothermic Rxns and Delta H
As for the first part of the question, photosynthesis is not an exothermic reaction in the forward direction, because exothermic implies that the reaction is spontaneous, and the products have a lower free energy than the reactants. However, CO2 and H2O have less free energy than a large molecule li...
- Sun Jan 12, 2020 5:28 pm
- Forum: Non-Equilibrium Conditions & The Reaction Quotient
- Topic: Reaction Q
- Replies: 7
- Views: 135
Re: Reaction Q
To clarify further upon Anna's comment, when the forward reaction is favored, more products will be created, and the concentration of products will grow. If the reverse reaction is favored, more reactants will be created, and the concentration of reactants will increase. Q is relevant because it com...
- Sun Jan 12, 2020 5:24 pm
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: Le Chatelier's Principle
- Replies: 5
- Views: 121
Re: Le Chatelier's Principle
Le Chatelier's Principle applies fundamentally to changes in temperature, pressure, or concentration. Changing other physical parameters will matter when they affect these three factors. For example, changing the volume of the container in which the reaction takes place effects the concentration of ...
- Wed Jan 08, 2020 11:47 am
- Forum: Non-Equilibrium Conditions & The Reaction Quotient
- Topic: N2O4 <--> 2NO2, color?
- Replies: 3
- Views: 57
N2O4 <--> 2NO2, color?
Professor Lavelle mentioned this reaction in class. Apparently, nitrogen dioxide is the gas that gives smog its yellowish color, because as a gas it appears yellow to brown. Interesting!
- Tue Jan 07, 2020 4:38 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: 5G.11
- Replies: 3
- Views: 65
Re: 5G.11
For substances that are aqueous (aq), simply plug the concentration (n/V) of that substance at equilibrium into the equation for K.
- Mon Jan 06, 2020 7:13 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: Equilibrium constant v. Reaction quotient
- Replies: 3
- Views: 64
Equilibrium constant v. Reaction quotient
What exactly is the difference between an equilibrium constant and a reaction quotient? The textbook said that the reaction quotient can be used for any stage of the reaction, and it accounts for free energy, but I am confused as to how exactly it does this.