Search found 30 matches
- Sat Mar 17, 2018 10:24 pm
- Forum: Concepts & Calculations Using Second Law of Thermodynamics
- Topic: Concept of Second Law of Thermodynamics
- Replies: 6
- Views: 966
Re: Concept of Second Law of Thermodynamics
deltaS = q + w
- Sat Mar 17, 2018 10:20 pm
- Forum: Phase Changes & Related Calculations
- Topic: Standard States
- Replies: 2
- Views: 485
Re: Standard States
It's in standard state if the substance is at 25 C and 1 atm.
- Sat Mar 17, 2018 10:14 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Friday Section Test 2
- Replies: 2
- Views: 415
Friday Section Test 2
For #6 on the test, why is the reducing agent O2?
The galvanic cell given is:
O3/O2, OH- and O3, H+/O2.
The galvanic cell given is:
O3/O2, OH- and O3, H+/O2.
- Sun Mar 11, 2018 10:24 pm
- Forum: First Order Reactions
- Topic: Equation variations
- Replies: 9
- Views: 1227
Re: Equation variations
The equations will give you the same thing; the second is just rearranged using log rules.
- Sun Mar 11, 2018 10:20 pm
- Forum: Second Order Reactions
- Topic: the slope
- Replies: 12
- Views: 1604
Re: the slope
The integrated zero-order rate law is [A] = -kt so the slope would be -k.
The integrated first-order rate law is ln[A] = ln[A]0 - kt, so the slope would be -k.
The integrated second-order rate law is 1/[A] = 1/[A]0 + kt, so the slope is k.
The integrated first-order rate law is ln[A] = ln[A]0 - kt, so the slope would be -k.
The integrated second-order rate law is 1/[A] = 1/[A]0 + kt, so the slope is k.
- Sun Mar 11, 2018 10:14 pm
- Forum: Second Order Reactions
- Topic: Half life
- Replies: 6
- Views: 986
Re: Half life
If you're talking about finding the time for when the concentration is 1/16 of the initial concentration, you would use the integrated second-order rate law which is: 1/{A] = 1/[A] 0 + kt [A] = (1/16)[A] 0 Subbing that into the 1/[A] part would give you 1/((1/16)[A] 0 ), and if you reorganize it, yo...
- Sun Mar 04, 2018 2:16 pm
- Forum: General Rate Laws
- Topic: Integrated Rate Laws when a =/= 1
- Replies: 4
- Views: 582
Re: Integrated Rate Laws when a =/= 1
Because to find the first order integrated rate law, we integrate (-1/a)d[A]/dt = -k[A], where a is the coefficient of the reactant.
- Sun Mar 04, 2018 2:13 pm
- Forum: General Rate Laws
- Topic: How to know when to use which formula?
- Replies: 2
- Views: 410
Re: How to know when to use which formula?
I'm not really sure what you're trying to ask, but here are some hopefully helpful points. Zero-order integrated rate law: [A] = - kt + [A] 0 First-order integrated rate law: ln[A] = -kt + ln[A] 0 Second-order integrated rate law: 1/[A] = kt + 1/[A] 0 These can be found on the constants and equation...
- Fri Mar 02, 2018 1:24 pm
- Forum: General Rate Laws
- Topic: Integrated Rate Laws when a =/= 1
- Replies: 4
- Views: 582
Integrated Rate Laws when a =/= 1
For a reaction like 2H 2 O 2 --> 2H 2 O + O 2 , should we integrate a rate law using a = 2 or just use the ones given to us on the constant sheet? I know that the integrated first-order rate law for this would be ln[A] = ln[A] 0 - 2kt, but I remember being told to just use the a = 1 rate law. Can so...
- Sun Feb 25, 2018 11:40 pm
- Forum: General Rate Laws
- Topic: Differential rate law
- Replies: 3
- Views: 488
Re: Differential rate law
For a reaction aR --> bP, the initial reaction rate is k[R]n. I believe in class we used this to compare two or more initial rates, but there could be more uses discovered later on in lecture.
- Sun Feb 25, 2018 11:22 pm
- Forum: General Rate Laws
- Topic: Reaction Rates [ENDORSED]
- Replies: 2
- Views: 360
Reaction Rates [ENDORSED]
I know that even if a reactant is decreasing, we should write the rate as positive. Why do we want to work with positive reaction rates?
- Sun Feb 25, 2018 9:17 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Cell Diagrams
- Replies: 4
- Views: 657
Cell Diagrams
How do you know what goes in what order for a cell diagram? For example, for #14.13 part c, the question gives
Cl2 (g) --> 2Cl- (aq) and
2H+ (aq) --> H2 (g).
Cl2 (g) --> 2Cl- (aq) and
2H+ (aq) --> H2 (g).
- Mon Feb 19, 2018 12:02 am
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: The Daniell Cell
- Replies: 4
- Views: 583
Re: The Daniell Cell
What makes the Daniell cell different from a general galvanic cell?
- Sun Feb 18, 2018 5:37 pm
- Forum: Balancing Redox Reactions
- Topic: Add H+ or OH-
- Replies: 2
- Views: 2165
Add H+ or OH-
In Example 14.1 in the book, the solution adds H+ to balance the extra H+ from the H2O. In Example 14.2, the solution adds OH- instead. How do you know whether to add H+ or OH-?
- Tue Feb 13, 2018 7:19 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Heat
- Replies: 1
- Views: 311
Heat
Why is heat not a state function?
- Sat Feb 10, 2018 11:13 am
- Forum: Calculating Standard Reaction Entropies (e.g. , Using Standard Molar Entropies)
- Topic: 9.75 [ENDORSED]
- Replies: 1
- Views: 482
Re: 9.75 [ENDORSED]
I'm not sure if there's any mathematical way of discerning the number of microstates there are, but I usually just visualize and count the different orientations a molecule can have. To explain, imagine cis -MX 2 Y 4 replacing all the X atoms with Y atoms. There's only one microstate because M must ...
- Sat Feb 10, 2018 10:51 am
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: 9.63
- Replies: 2
- Views: 418
Re: 9.63
The book gives definitions for thermodynamically stable/unstable compounds. A stable compound has a negative standard Gibbs free energy, meaning the reaction goes toward the compound. An unstable compound has a positive standard Gibbs free energy, meaning the reaction goes toward the elements. The q...
- Sat Feb 10, 2018 1:06 am
- Forum: Balancing Redox Reactions
- Topic: Midterm Topics [ENDORSED]
- Replies: 2
- Views: 356
Midterm Topics [ENDORSED]
I know that chapters 8, 9 and 11 will be covered for the midterm, but will chapter 14 (electrochemistry) be on it? I noticed the constants sheet has stuff from electrochemistry.
- Thu Feb 01, 2018 11:41 pm
- Forum: Calculating Standard Reaction Entropies (e.g. , Using Standard Molar Entropies)
- Topic: Mass and molar entropy
- Replies: 3
- Views: 1136
Re: Mass and molar entropy
The heavier the molecules are, the more vibrational energy levels they have available. The more energy levels they have, the greater the entropy.
- Thu Feb 01, 2018 11:32 pm
- Forum: Entropy Changes Due to Changes in Volume and Temperature
- Topic: Entropy change
- Replies: 4
- Views: 486
Re: Entropy change
Yes, entropy is always increasing because even if an endothermic reaction occurs, the energy had to have come from somewhere in order to perform the reaction.
- Thu Feb 01, 2018 11:06 pm
- Forum: Entropy Changes Due to Changes in Volume and Temperature
- Topic: The value of Cp
- Replies: 8
- Views: 1543
Re: The value of Cp
The Cp and Cv values can be found on page 281 in the textbook. Cp is the heat capacity of the system at constant pressure while Cv is the heat capacity at constant volume. R is the ideal gas constant, and you would typically use R in the form 8.3145 J*K-1*mol-1 for these calculations.
- Fri Jan 26, 2018 12:12 am
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: Question regarding 8.39 homework question
- Replies: 5
- Views: 629
Re: Question regarding 8.39 homework question
When ice is melting, the temperature doesn't change until it is fully melted. That means you can only calculate the change from 0C to 20C until the ice is fully melted and becomes water. Therefore, you have to use the specific heat capacity of water. Now, if the ice were at -10C, then you would calc...
- Thu Jan 25, 2018 11:43 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: Calculating heat (q)
- Replies: 4
- Views: 2156
Re: Calculating heat (q)
Whether you use mCsdeltaT or nCmdeltaT is dependent on what's given initially. mCsdeltaT is used when your information is in terms of grams while nCmdeltaT is used when you information is in terms of moles.
- Thu Jan 25, 2018 10:05 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: What are the types of calorimeters we learned about/ covered in class?
- Replies: 4
- Views: 484
Re: What are the types of calorimeters we learned about/ covered in class?
I believe that the system would be whatever's inside the calorimeter and the surroundings would be the calorimeter itself since the calorimeter is absorbing the heat.
- Sat Jan 20, 2018 4:55 pm
- Forum: Calculating Work of Expansion
- Topic: Formula for reversible expansion
- Replies: 2
- Views: 194
Re: Formula for reversible expansion
The ideal gas constant from PV = nRT is given as 0.08206 (L*atm)/(mol*K). For R to be more applicable to w = -nRT*ln(Vfinal/Vinitial), they rewrote it with the conversion 101.325 J = 1 L*atm to get 8.3145 J/(K*mol).
- Sat Jan 20, 2018 4:46 pm
- Forum: Calculating Work of Expansion
- Topic: Irreversible and Reversible Processes
- Replies: 4
- Views: 509
Irreversible and Reversible Processes
I understand that a reversible process is one that can be reversed by an infinitely small change and an irreversible process is expansion against an external pressure that differs by a finite amount from the system's pressure. Can someone give examples for these two processes?
- Sat Jan 20, 2018 4:42 pm
- Forum: Thermodynamic Systems (Open, Closed, Isolated)
- Topic: Difference between Closed and Isolated
- Replies: 10
- Views: 13376
Re: Difference between Closed and Isolated
Closed systems are able to exchange energy with their surroundings, but they cannot exchange matter. Isolated systems cannot exchange energy or matter. For example, if you were to put hot water in a normal bottle, the water will start to cool down to room temperature. However, if you put hot water i...
- Sun Jan 14, 2018 10:50 am
- Forum: Phase Changes & Related Calculations
- Topic: Irreversible process vs reversible process
- Replies: 4
- Views: 317
Re: Irreversible process vs reversible process
An irreversible process is expansion against an external pressure such that an infinitesimal change in the external pressure does not reverse the direction. A reversible process is expansion that can be reversed by an infinitesimal change. For example, in an irreversible process, a piston can only m...
- Sun Jan 14, 2018 10:32 am
- Forum: Phase Changes & Related Calculations
- Topic: Expansion and change in pressure
- Replies: 4
- Views: 388
Re: Expansion and change in pressure
Volume and pressure are inversely related only if there are no other factors in play. However, because of the temperature change, you cannot only consider volume change when trying to figure out whether pressure increases or decreases. The answer given makes sense because as temperature drops, molec...
- Sun Jan 14, 2018 10:17 am
- Forum: Phase Changes & Related Calculations
- Topic: Heat Capacity vs. Specific Heat Capacity
- Replies: 3
- Views: 4582
Re: Heat Capacity vs. Specific Heat Capacity
Heat capacity is defined as the amount of energy needed to raise the temperature of a substance by 1°C. Specific heat capacity is defined as the amount of energy needed to raise the temperature of ONE GRAM of a substance by 1°C. As you can see, the specific heat capacity can be applied to all amount...