Search found 29 matches
- Tue Mar 13, 2018 10:30 pm
- Forum: Kinetics vs. Thermodynamics Controlling a Reaction
- Topic: Increasing Tempt
- Replies: 2
- Views: 475
Re: Increasing Tempt
Increasing temperature increases the energy of the atoms or molecules that are participating in a reaction, so it makes them collide more frequently and with higher energy. Because they collide more often and with higher energy, they overcome the activation energy barrier more often, so the reaction...
- Tue Mar 13, 2018 10:28 pm
- Forum: Kinetics vs. Thermodynamics Controlling a Reaction
- Topic: mechanisms
- Replies: 3
- Views: 642
Re: mechanisms
Mechanisms need to support the orders shown in the rate law- so if the rate law says that something is second order, then there should be two molecules used up in the slow step of its elementary reaction. However, mechanisms can only provide possible answers to the rate law, not prove one, and there...
- Tue Mar 13, 2018 10:26 pm
- Forum: Arrhenius Equation, Activation Energies, Catalysts
- Topic: Catalysts
- Replies: 2
- Views: 370
Re: Catalysts
Catalysts don't show up in the rate law because they are usually 0th order. Because they are not used up in a reaction, their concentration doesn't change the rate of a reaction and so it doesn't show up in the rate law.
- Mon Mar 05, 2018 2:43 pm
- Forum: Reaction Mechanisms, Reaction Profiles
- Topic: Molecularity
- Replies: 3
- Views: 356
Re: Molecularity
Molecularity affects the order of the reaction as well- bimolecular reactions are second order, unimolecular is first order, etc.
- Mon Mar 05, 2018 2:41 pm
- Forum: General Rate Laws
- Topic: 3rd order, 4th order, etc.
- Replies: 5
- Views: 1906
Re: 3rd order, 4th order, etc.
You can derive all of the half life reactions, but since third and fourth order reactions aren't likely, we don't need to know them really.
- Mon Mar 05, 2018 2:40 pm
- Forum: General Rate Laws
- Topic: Order?
- Replies: 3
- Views: 433
Re: Order?
You could also look at the slow step of a reaction and figure out it's molecularity. If it's A->B, then first order, A+A->B, second order, and so on.
- Mon Mar 05, 2018 2:39 pm
- Forum: Kinetics vs. Thermodynamics Controlling a Reaction
- Topic: Catalyst in a Equilibria
- Replies: 2
- Views: 355
Re: Catalyst in a Equilibria
Yes, the catalyst increases the rate of both the forward and the reverse reaction.
- Sun Mar 04, 2018 8:45 pm
- Forum: Arrhenius Equation, Activation Energies, Catalysts
- Topic: Homogenous vs. Heterogenous Catalyst and Rate Law
- Replies: 2
- Views: 613
Re: Homogenous vs. Heterogenous Catalyst and Rate Law
I think that since heterogeneous catalysts are usually used in the solid phase, their appearance in the rate law would depend on the phases of the other reactants and products.
- Sun Mar 04, 2018 8:43 pm
- Forum: First Order Reactions
- Topic: K constant
- Replies: 3
- Views: 499
Re: K constant
When we graph K, we make it negative, because the reaction is using up reactants (at least initially). K itself is usually positive.
- Sun Mar 04, 2018 8:41 pm
- Forum: General Rate Laws
- Topic: catalytic reaction
- Replies: 5
- Views: 675
Re: catalytic reaction
Enzymes are examples of catalytic reactions, where one molecule that isn't used up helps to facilitate the reaction of another set of molecules.
- Fri Feb 23, 2018 6:46 pm
- Forum: General Rate Laws
- Topic: Rate Constant K [ENDORSED]
- Replies: 4
- Views: 658
Re: Rate Constant K [ENDORSED]
Essentially, at different temperatures and activation energies, K changes. You calculate it the same way, using concentrations, but you're going to get a different value at different states. We don't have a way to calculate new K's based on old ones yet, but we might learn one.
- Tue Feb 13, 2018 4:22 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: delta G vs. standard Gibbs free energy
- Replies: 1
- Views: 245
Re: delta G vs. standard Gibbs free energy
They're almost the same thing! ∆G° is just defined in terms of the standard molar Gibbs energies of the reactants and products; it's the difference in energy between the pure products and the pure reactants that won't change as the reaction proceeds.
- Tue Feb 13, 2018 4:17 pm
- Forum: Concepts & Calculations Using Second Law of Thermodynamics
- Topic: Reversible vs Irreverisble
- Replies: 1
- Views: 300
Re: Reversible vs Irreverisble
For anything besides entropy (where it doesn't matter if something is reversible or irreversible), you should be told whether or not it's reversible or irreversible. If the problem just says volume changes from 2L to 5L, you assume it's irreversible. If it says something along the lines of "thr...
- Tue Feb 13, 2018 4:12 pm
- Forum: Entropy Changes Due to Changes in Volume and Temperature
- Topic: Entropy equation
- Replies: 2
- Views: 374
Re: Entropy equation
This depends on which C you're using. When you have to multiply C by n, it means that C is the specific heat per mole of substance, and when you don't, it's just specific heat. You can also tell if you look at the units; specific heat per mole will be in J/mol, while specific heat will just be J.
- Tue Feb 06, 2018 3:08 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: Spontaneity and the Direction of a Reaction
- Replies: 2
- Views: 370
Re: Spontaneity and the Direction of a Reaction
When delta G is negative, it means that the products are at a lower energy level than the reactants, and thus the reaction moves toward them. When it's positive, however, the reactants are at a lower energy level than the products, and so the reaction moves toward them.
- Tue Feb 06, 2018 3:06 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: Irreversible Vs. Reversible Expansion
- Replies: 2
- Views: 389
Re: Irreversible Vs. Reversible Expansion
However, entropy is a state function, so regardless of whether it's irreversible or reversible expansion, it's going to have the same entropy at the end, and you can use the same formulas.
- Tue Feb 06, 2018 3:03 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: Calculating deltaG
- Replies: 2
- Views: 297
Re: Calculating deltaG
You use them based on the information you're given, and depending on what is being changed (Is value constant, pressure, etc.).
- Wed Jan 31, 2018 11:33 am
- Forum: Concepts & Calculations Using Second Law of Thermodynamics
- Topic: Definition of Entropy
- Replies: 10
- Views: 1415
Re: Definition of Entropy
The more moles of gas there are in the system, the greater the entropy because W=number of possible states^number of molecules, and when you increase the number of moles in a system you also increase the number of molecules.
- Wed Jan 31, 2018 11:28 am
- Forum: Concepts & Calculations Using Second Law of Thermodynamics
- Topic: 9.5
- Replies: 5
- Views: 613
Re: 9.5
Whenever heat is leaving something, the amount of possible spaces (W) that the molecules can take up decreases, so entropy does as well.
- Wed Jan 31, 2018 11:27 am
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: Relationship between ΔG⁰ AND K
- Replies: 2
- Views: 366
Re: Relationship between ΔG⁰ AND K
The K here is also a constant for all equations, and doesn't change with each reaction/molecule being used.
- Sun Jan 28, 2018 5:25 pm
- Forum: Thermodynamic Definitions (isochoric/isometric, isothermal, isobaric)
- Topic: gas with 2x positions
- Replies: 2
- Views: 409
Re: gas with 2x positions
The equation is the number of possible states (In this case, 2) raised to the number of particles. If there were three possible states, it would be 3^n, and so on.
- Sun Jan 28, 2018 5:23 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: Gas atoms
- Replies: 4
- Views: 506
Re: Gas atoms
Gas molecules will never go back to a smaller volume because it would decrease the entropy, or amount of states, of that system. In a smaller volume, there are less possible organizations for the molecules. Objects always want to go to a state of greater entropy, and moving to a smaller volume would...
- Sun Jan 28, 2018 5:21 pm
- Forum: Entropy Changes Due to Changes in Volume and Temperature
- Topic: Entropy [ENDORSED]
- Replies: 4
- Views: 547
Re: Entropy [ENDORSED]
Yes, entropy is a state function, because the it describes the equilibrium state of a system, regardless of how it got to that state.
- Thu Jan 18, 2018 10:00 am
- Forum: Phase Changes & Related Calculations
- Topic: Thermochemistry Sections in Ch 8
- Replies: 2
- Views: 365
Re: Thermochemistry Sections in Ch 8
In class, I think we started with 8.11, which is the enthalpy of physical change.
- Wed Jan 17, 2018 11:14 pm
- Forum: Thermodynamic Systems (Open, Closed, Isolated)
- Topic: Heating/Cooling A System
- Replies: 4
- Views: 603
Re: Heating/Cooling A System
Because an open system is connected to its surroundings, any heat added would be dispersed throughout its surroundings, so the total E of the system would remain the same. Therefore, it wouldn't work as a way to add energy to a system.
- Wed Jan 17, 2018 11:11 pm
- Forum: Thermodynamic Systems (Open, Closed, Isolated)
- Topic: Radiation vs. Convection
- Replies: 3
- Views: 437
Re: Radiation vs. Convection
Radiation doesn't require the use of a medium- think of the Sun, for example, which heats us despite there being nothing directly connecting us. Convection requires a medium- when you put something less hot in something hot, the heat moves from the hot thing to the less hot thing.
- Fri Jan 12, 2018 3:21 pm
- Forum: Phase Changes & Related Calculations
- Topic: Heat Enthalpies We Need to Know
- Replies: 3
- Views: 249
Heat Enthalpies We Need to Know
In the reading for Chapter 8, it says that we should include table 8.2, which is a list of some the heat enthalpies. Do we need to memorize these for the test, or will they be provided?
- Fri Jan 12, 2018 3:18 pm
- Forum: Administrative Questions and Class Announcements
- Topic: Homework grading
- Replies: 6
- Views: 728
Re: Homework grading
I think this depends on your TA- a friend of mine took 14A last quarter and her TA understood that since most people have or have access to the solutions manual, we usually have the right answers, and just graded the homework on completion. Regardless, though, you should probably just check your ans...
- Fri Jan 12, 2018 3:15 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: What type of system is a Bomb Calorimeter?
- Replies: 4
- Views: 2409
Re: What type of system is a Bomb Calorimeter?
To figure out if something is a closed system, you should first try to figure out what the system is. In a bomb calorimeter, the system is what is inside, the inner chamber. Because this system can't exchange heat or energy with its surroundings, it's a closed system.