Search found 52 matches
- Sun Mar 18, 2018 4:09 pm
- Forum: General Rate Laws
- Topic: 15.85 Drawing structures for activated complex
- Replies: 3
- Views: 894
Re: 15.85 Drawing structures for activated complex
The activated complex refers to the transition state. Based on reactants and products as given, the transition state can be figured out (which atom should be linked to which atom etc.)
- Sun Mar 18, 2018 4:06 pm
- Forum: Reaction Mechanisms, Reaction Profiles
- Topic: Catalyst and Intermediate
- Replies: 7
- Views: 1076
Re: Catalyst and Intermediate
If a molecule is produced and consumed in the next step, it's an intermediate.
If a molecule appears on the reactant side and the product side, it's a catalyst.
If a molecule appears on the reactant side and the product side, it's a catalyst.
- Sun Mar 18, 2018 4:03 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: Heat Capacity of Water
- Replies: 4
- Views: 779
Re: Heat Capacity of Water
Heat capacity of water is high because the hydrogen bonds that make up water are considered strong bonds. They are hard to break.
- Mon Mar 12, 2018 3:49 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Why is entropy extensive?
- Replies: 5
- Views: 5397
Re: Why is entropy extensive?
Entropy is a extensive property because it depends on the number of moles involved ( involves mass, size )
- Mon Mar 12, 2018 3:35 pm
- Forum: *Enzyme Kinetics
- Topic: Catalysts
- Replies: 18
- Views: 2537
Re: Catalysts
Yes, because catalyst lowers the activation energy which works in both the forward and reverse reactions.
- Thu Mar 08, 2018 7:06 pm
- Forum: General Rate Laws
- Topic: Stoichiometric coefficients and order
- Replies: 5
- Views: 1149
Re: Stoichiometric coefficients and order
You cannot determine the rate law by justing looking at the balanced equation unless it is an elementary step.
- Thu Mar 08, 2018 7:05 pm
- Forum: General Rate Laws
- Topic: Integrated Rate Laws
- Replies: 6
- Views: 823
Re: Integrated Rate Laws
I would say it will be helpful to know how to derive those equations.
- Thu Mar 08, 2018 6:58 pm
- Forum: Reaction Mechanisms, Reaction Profiles
- Topic: Intermediate [ENDORSED]
- Replies: 7
- Views: 922
Re: Intermediate [ENDORSED]
Intermediate can be determined by looking at the separate steps of a reaction. If one molecule is produced in one step and consumed in the following step, then the molecule can be considered an intermediate.
- Mon Mar 05, 2018 1:56 am
- Forum: Method of Initial Rates (To Determine n and k)
- Topic: Units of k
- Replies: 8
- Views: 1442
Re: Units of k
You can calculate the unit of k based on the rule that the rate of reaction has an unchanging unit which is mol*L-1*s-1
- Mon Mar 05, 2018 1:51 am
- Forum: Second Order Reactions
- Topic: Half-life of second order reactions
- Replies: 2
- Views: 415
Re: Half-life of second order reactions
Half life of a second order reaction is dependent on the initial concentration since the the half life equals to 1/k[Ao]
- Mon Mar 05, 2018 1:46 am
- Forum: First Order Reactions
- Topic: Half-life of first order reactions
- Replies: 3
- Views: 465
Re: Half-life of first order reactions
Yes and it not only works for first order reactions. It is the case for all reactions.
- Sun Feb 25, 2018 11:36 pm
- Forum: Kinetics vs. Thermodynamics Controlling a Reaction
- Topic: The rate of a reaction
- Replies: 5
- Views: 771
Re: The rate of a reaction
Yes! I think in class, it is put as rate of constant k depends of temperature and activation energy.
- Sun Feb 25, 2018 11:31 pm
- Forum: Work, Gibbs Free Energy, Cell (Redox) Potentials
- Topic: Dissolving [ENDORSED]
- Replies: 3
- Views: 544
Re: Dissolving [ENDORSED]
To see if a metal will dissolve in the solution, you need to list out the corresponding cathode and anode reaction. In this way, the overall cell potential can be calculated. If the overall cell potential is positive, then the medal will dissolve in the solution.
- Sun Feb 25, 2018 11:14 pm
- Forum: Work, Gibbs Free Energy, Cell (Redox) Potentials
- Topic: Cell potential calculation
- Replies: 4
- Views: 612
Re: Cell potential calculation
There are two ways to calculate the cell potential. 1st: list out the anode and cathode reaction and copy the corresponding cell potential to these two reaction. Cell potential of this reaction equals to cell potential of the cathode reaction minus the cell potential of the anode reaction. 2nd: list...
- Sun Feb 18, 2018 10:51 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: 14.37
- Replies: 1
- Views: 229
14.37
Hey guys, I'm having trouble solving question 14.37a.
Determine the potential of the following cell: Pt(s)|H2 (g. 1.0 bar) | HCl (0.075M)||HCl(1.0 mol\L) |H2(1.0 bar)|Pt(s)
Can someone please tell me how to put in the data. Thanks!
Determine the potential of the following cell: Pt(s)|H2 (g. 1.0 bar) | HCl (0.075M)||HCl(1.0 mol\L) |H2(1.0 bar)|Pt(s)
Can someone please tell me how to put in the data. Thanks!
- Sun Feb 18, 2018 7:27 pm
- Forum: Balancing Redox Reactions
- Topic: 14.5d
- Replies: 2
- Views: 393
14.5d
Hey guys, I'm having trouble getting the right answer for question 14.5d. A little clarification would be helpful. Thanks!
P4=H2PO2- + PH3 under basic condition.
P4=H2PO2- + PH3 under basic condition.
- Mon Feb 12, 2018 3:42 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: practice test 6A&6B
- Replies: 1
- Views: 272
practice test 6A&6B
The question states that 'We expect a reaction to be spontaneous if it is exothermic at a very low temperature.' I wonder if we need to know the sign of ∆S to figure out if the ∆G is negative.For the next true or false question, it said that We can expect an endothermic reaction to be favorable at a...
- Mon Feb 12, 2018 12:05 am
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: delta H
- Replies: 4
- Views: 556
Re: delta H
Both endothermic and exothermic reactions involve forming bonds but exothermic reactions are favored because even though it is forming bonds, the energy of the products is lower than the energy of the reactants.
- Mon Feb 12, 2018 12:00 am
- Forum: Thermodynamic Definitions (isochoric/isometric, isothermal, isobaric)
- Topic: Entropy
- Replies: 6
- Views: 921
Re: Entropy
Diatomic atoms have more entropy than monatomic molecules because there are more possible states to be occupied and the rotational and vibrational energy contribute to the greater entropy.
- Sun Feb 11, 2018 7:53 pm
- Forum: Administrative Questions and Class Announcements
- Topic: Practice Midterm Winter 2018
- Replies: 10
- Views: 3149
Re: Practice Midterm Winter 2018
Hey, do you know where are the simple answers posted?
- Sun Feb 04, 2018 7:11 pm
- Forum: Calculating Standard Reaction Entropies (e.g. , Using Standard Molar Entropies)
- Topic: standard states
- Replies: 3
- Views: 472
Re: standard states
I think the standard pressure is 1bar but because 1atm is so close to 1bar, we consider 1atm the standard pressure as well.
- Sun Feb 04, 2018 7:04 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: delta G
- Replies: 3
- Views: 420
Re: delta G
I think what you are asking what is the minimum temperature when the reaction is spontaneous? The reason that ∆G is 0 because when ∆G is negative, the reaction is spontaneous, therefore, to figure out the minimum temperature, we set the limit:∆G=0, so any temperature above the limit will have a ∆G a...
- Thu Feb 01, 2018 12:40 am
- Forum: Concepts & Calculations Using Second Law of Thermodynamics
- Topic: ∆S=q/T
- Replies: 2
- Views: 461
∆S=q/T
Can someone explain why ∆S=q/T=nR ln(V2/V1)? I know that ∆S=klnW2/W1, so does nR equals k then?
- Mon Jan 29, 2018 1:24 am
- Forum: Thermodynamic Definitions (isochoric/isometric, isothermal, isobaric)
- Topic: Microstates [ENDORSED]
- Replies: 3
- Views: 636
Re: Microstates [ENDORSED]
I think the easy way the understand it is the possible arrangement atoms can have under specific environments.
- Fri Jan 26, 2018 10:31 pm
- Forum: Concepts & Calculations Using Second Law of Thermodynamics
- Topic: reversible and irreversible reactions
- Replies: 4
- Views: 607
reversible and irreversible reactions
I'm confused about how can we find out if a reaction is reversible or not. Are we gonna be given information about it?
- Fri Jan 26, 2018 10:15 pm
- Forum: Concepts & Calculations Using Second Law of Thermodynamics
- Topic: Entropy of gas vs liquid vs solid
- Replies: 7
- Views: 8944
Re: Entropy of gas vs liquid vs solid
When the molecules are in gas phase, there are many more possible states they can occupy compared to the possible states molecules can occupy when they are in liquid phase or solid phase. With more possible states, the entropy will be higher.
- Sun Jan 21, 2018 12:26 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: 8.31
- Replies: 3
- Views: 287
Re: 8.31
It means that when a gas is working as an ideal gas, its Cv and Cp will be 3/2R and 5/2R. It can be found on the equation sheet.
- Fri Jan 19, 2018 11:24 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: PV=nRT
- Replies: 4
- Views: 925
Re: PV=nRT
As we know, change in internal energy equals w+q and w=-q*∆V. For gases, when it's under constant pressure and there is a net change in the number of moles, there will be a change in the volume. According to PV=nRT, P∆V=∆nRT. Therefore, when a reaction under constant pressure and has a net change in...
- Thu Jan 18, 2018 10:16 pm
- Forum: Calculating Work of Expansion
- Topic: units for calculating work
- Replies: 6
- Views: 599
Re: units for calculating work
I'll say use liter for volume and atm for pressure.
- Wed Jan 17, 2018 7:44 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: 8.31
- Replies: 3
- Views: 256
Re: 8.31
Hey, how do you know the molar heat capacity is 5/2R and 3/2R ? Can you explain a little bit?
- Wed Jan 17, 2018 7:31 pm
- Forum: Calculating Work of Expansion
- Topic: 8.17 Work done by a system
- Replies: 6
- Views: 702
Re: 8.17 Work done by a system
Hey, if a work is done by the system, it is considered negative because the system as a whole is losing energy. Since condensation requires energy, work has to be done to the system so that condensation can occur. Hope that helps.
- Wed Jan 17, 2018 7:24 pm
- Forum: Thermodynamic Definitions (isochoric/isometric, isothermal, isobaric)
- Topic: Enthalpy Equation
- Replies: 3
- Views: 524
Re: Enthalpy Equation
Hey, P∆V represents work done to the system. Since w=FxD and F=PxA D (distance) and A (area), we can get the equation w=P ∆V.
Hope it helps.
Hope it helps.
- Sun Dec 10, 2017 5:21 pm
- Forum: Shape, Structure, Coordination Number, Ligands
- Topic: Ligands [ENDORSED]
- Replies: 1
- Views: 253
Re: Ligands [ENDORSED]
Hey, I believe ligand is what is attached to the transition metal and the coordination complex is the metal with the ligands.
- Sun Dec 10, 2017 2:47 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: shape [ENDORSED]
- Replies: 2
- Views: 511
shape [ENDORSED]
Hey guys, on the final there was a question that asks for the shape ( not electron density) of nitrogen atoms.What does the shape mean??
- Tue Dec 05, 2017 9:25 pm
- Forum: Calculating the pH of Salt Solutions
- Topic: negative pH
- Replies: 2
- Views: 635
Re: negative pH
Hey, I think professor Lavelle mentioned in class that solution can have negative pH when it is superacid.... Hope it helps.
- Tue Dec 05, 2017 9:23 pm
- Forum: Lewis Acids & Bases
- Topic: 12.29
- Replies: 2
- Views: 623
Re: 12.29
Hey, there are two hydroxide ion per Ba(OH)2 because if we write out the balanced equation: Ba(OH)2----Ba2+ + 2OH-, for every Ba(OH)2 molecule ionized, two hydroxide ions is produced. That's why you need to multiply it by 2. Hope it helps.
- Thu Nov 30, 2017 8:23 pm
- Forum: Shape, Structure, Coordination Number, Ligands
- Topic: TM cations in solutions
- Replies: 2
- Views: 293
Re: TM cations in solutions
Hey, I believe in class, professor Lavelle said that species like NH3, NaCl are electron rich, so they will replace H2O ligands and form coordination compounds. Hope it helps.
- Thu Nov 30, 2017 8:13 pm
- Forum: Shape, Structure, Coordination Number, Ligands
- Topic: Dipole moments
- Replies: 2
- Views: 448
Re: Dipole moments
Hey, dipole moment is resulted from an uneven distribution of electrons between atoms. When the electronegativity difference between the atom is big, the dipole moment will be big and when the electronegativity difference is small, the dipole moment will be small. Hope it helps.
- Tue Nov 21, 2017 11:58 am
- Forum: Shape, Structure, Coordination Number, Ligands
- Topic: Homework question 17.33
- Replies: 4
- Views: 463
Re: Homework question 17.33
For ion CO3 2-, I think it is bidentate because if you draw the lewis structure of it, you will see that two out of the three oxygen have lone pairs around them and do not have a formal charge of 0. So for these two oxygen atoms, they would want to form bonds. For water molecule, if you draw out the...
- Tue Nov 21, 2017 11:43 am
- Forum: Hybridization
- Topic: 4.95
- Replies: 3
- Views: 368
Re: 4.95
The number is related to the number on the periodic table because the number represents which orbital the valence electron is, for example, H1s, the valence electron of hydrogen atom is in the 1s orbital. Hope that helps.
- Thu Nov 16, 2017 12:31 pm
- Forum: Hybridization
- Topic: the number of pi bonds
- Replies: 3
- Views: 603
the number of pi bonds
I have a question about how many pi bonds are formed in benzene. In class, professor Lavelle said that there are three pi bonds formed in benzene because there are three double bonds formed between C-C, but what about the unhybridized 2p electrons, don't they also form pi bonds with each other? Do w...
- Thu Nov 16, 2017 12:23 pm
- Forum: Hybridization
- Topic: HW 4.33
- Replies: 1
- Views: 433
Re: HW 4.33
Yeah, for questions about hybridization, you need to find out the number of electron densities around the central atom by drawing the Lewis structure. After you find out the number of electron density around the central atom, you can figure out the hybridization because regions of electron density e...
- Sun Nov 12, 2017 5:27 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Tetrahedral vs Trigonal Pyramid
- Replies: 2
- Views: 4952
Re: Tetrahedral vs Trigonal Pyramid
Tetrahedral is when the central atom has only four bonds around it(no lone pairs) and trigonal pyramid is when the central atom has three bonds and one lone pair around it. Hope it helps.
- Sun Nov 12, 2017 4:22 pm
- Forum: Lewis Structures
- Topic: atomic structure of HOCO
- Replies: 8
- Views: 1216
Re: atomic structure of HOCO
In these kinds of questions I always assume the way the molecule is written as the way it is bonded.
- Sun Nov 05, 2017 7:30 pm
- Forum: Polarisability of Anions, The Polarizing Power of Cations
- Topic: Highly Polarizable
- Replies: 4
- Views: 763
Re: Highly Polarizable
Hey, highly distorted electron means the electron is loosely held by the atom or ion, therefore it can easily be distorted. Ions that cause large distortions are described as having high polarizing power, in this case, small highly charged ions. Hope it helps.
- Sun Nov 05, 2017 7:24 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Lewis Structures
- Replies: 6
- Views: 787
Re: Lewis Structures
I think the 3d diagrams are the actual shape of the electron orbitals because they are based on mathematical equations. Hope it helps.
- Thu Nov 02, 2017 12:36 am
- Forum: Octet Exceptions
- Topic: Octet Exceptions
- Replies: 4
- Views: 623
Re: Octet Exceptions
I think it depends on what the central atoms are. Like we said before, if the central atom is P, S, or Cl, they can have extra electrons around them because they do have a d orbital. And if there are two central atoms, they still have have more electrons depending on what they are. Hope it makes sen...
- Wed Oct 18, 2017 9:17 pm
- Forum: Heisenberg Indeterminacy (Uncertainty) Equation
- Topic: Heisenberg Uncertainty Equation
- Replies: 7
- Views: 748
Re: Heisenberg Uncertainty Equation
Well, 4pi must have come from some kind of experiment or something. For now, I don't think we are able to understand how scientists derived the specific function, but maybe we will, in the future.
- Wed Oct 18, 2017 8:56 pm
- Forum: Quantum Numbers and The H-Atom
- Topic: Quantum Numbers
- Replies: 4
- Views: 745
Re: Quantum Numbers
To the question about d orbital, 3d orbital comes after 4s orbital. About where different orbitals are, you can refer to the energy level of different orbitals on page 43. About why electron spin is +-1/2, I believe the values are derived from experiment... but exactly why +- 1/2, I have no idea :(
- Fri Oct 13, 2017 12:43 pm
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: why is Bohr Frequency equation negative
- Replies: 4
- Views: 1868
why is Bohr Frequency equation negative
Can somebody please tell me why there is a negative sign in the equation ∆E=-hR/n2. I didn't quite get that in the class and why n approaches infinity the energy of the electron will be 0? Doesn't it have to receive a ton of energy to be excited to the outer levels?? I'm so confused.
- Wed Oct 11, 2017 11:23 pm
- Forum: Photoelectric Effect
- Topic: Photoelectric Effect Module Question 18 [ENDORSED]
- Replies: 3
- Views: 668
Re: Photoelectric Effect Module Question 18 [ENDORSED]
I think this question is asking for all the conditions that apply to the situation. Since electrons can be ejected when the energy of the photon is equal or greater than the energy needed to remove the electron which is work function, so choice B and C both are correct.
- Mon Oct 09, 2017 4:49 pm
- Forum: Properties of Light
- Topic: Amplitude of the wave [ENDORSED]
- Replies: 7
- Views: 1443
Re: Amplitude of the wave [ENDORSED]
So if the amplitude of the light is higher, does the light become brighter?