Search found 22 matches
- Fri Mar 11, 2016 8:36 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Homework 14.15C
- Replies: 1
- Views: 241
Homework 14.15C
(For homework 14.15c) In the solution manual it lists KOH (aq) as one of the aqueous species. I am confused as to why this is there. Is this a typo?
- Mon Mar 07, 2016 12:37 pm
- Forum: *Alkanes and Substituted Alkanes (Staggered, Eclipsed, Gauche, Anti, Newman Projections)
- Topic: Gauche vs Anti Stability
- Replies: 1
- Views: 1072
Gauche vs Anti Stability
The energy diagram in the book shows that gauche and anti configurations are not equally stable for 1,2-dibromoethane. Why is the anti configuration the most stable while the gauche is sightly less stable? Is this because of torsional or steric strain? or both?
Thanks
Thanks
- Mon Mar 07, 2016 12:25 am
- Forum: Administrative Questions and Class Announcements
- Topic: Video Competition
- Replies: 66
- Views: 28534
Re: Video Competition
First Order Rate Law
Created by-
Ian Hurst
Lovelyn Edillo
Vinay Sharma
Hope you guys enjoy!
Created by-
Ian Hurst
Lovelyn Edillo
Vinay Sharma
Hope you guys enjoy!
- Sun Mar 06, 2016 1:42 am
- Forum: *Alkanes and Substituted Alkanes (Staggered, Eclipsed, Gauche, Anti, Newman Projections)
- Topic: Sawhorse vs Newman Projection
- Replies: 1
- Views: 589
Sawhorse vs Newman Projection
I understand that sawhorse projections are drawn at an angle for the best representation of a structure while Newman projections utilize line intersections to represent carbon bonds. Are there situations where one is preferred over the other? In what situation is optimal to use a sawhorse projection...
- Sat Feb 27, 2016 6:28 pm
- Forum: *Alkanes
- Topic: Determining Priority
- Replies: 2
- Views: 446
Determining Priority
How do we determine which functional group has priority? Do we just have to memorize the list and just know, for example, that carboxylic groups have higher priority than alcohol groups? Is there another way to figure it out by looking at atomic mass or something? Also, for (E)-4-methlycyclopent-2-e...
- Sun Feb 21, 2016 10:53 pm
- Forum: Arrhenius Equation, Activation Energies, Catalysts
- Topic: Homogeneous and Heterogeneous Catalysts
- Replies: 3
- Views: 1003
Re: Homogeneous and Heterogeneous Catalysts
In the course reader (page 78), it explains that reactants sit on the surface of the catalyst in a reaction (and this is known as adsorption). Although it may look like a typo, adsorption is actually a term that refers to a substance that sticks to the surface (so in a reaction, reactants sticking t...
- Sun Feb 14, 2016 1:43 pm
- Forum: Arrhenius Equation, Activation Energies, Catalysts
- Topic: Catalyst and Activation Energy
- Replies: 1
- Views: 432
Catalyst and Activation Energy
How do catalysts lower the activation energy of a reaction if they are not consumed in the process? If they increase the speed of a reaction and cause more products to be formed, shouldn't they be consumed?
- Sun Feb 07, 2016 10:34 pm
- Forum: Work, Gibbs Free Energy, Cell (Redox) Potentials
- Topic: Standard G
- Replies: 1
- Views: 514
Standard G
I know that delta G= standard G + RTln(Q) and that if the reaction is at standard conditions then delta G goes to 0 but I do not understand why. Can someone explain to me why delta G = 0 when Q=K?
- Sun Jan 31, 2016 10:04 pm
- Forum: Balancing Redox Reactions
- Topic: Work in Electrochemistry
- Replies: 1
- Views: 407
Re: Work in Electrochemistry
I believe the direction of the electron flow is dependent on how you set up the beakers. Regardless of how you set up the beakers, the solution that will be reduced will be on the "right" and the solution that is oxidized will be on the "left." This is in reference to the equatio...
- Mon Jan 25, 2016 8:08 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: Giffs Free Energy Definition
- Replies: 1
- Views: 540
Giffs Free Energy Definition
I understand that Gibbs free energy is a state function (meaning it doesn't matter how you got there) and that if it's positive you know it is describing a spontaneous reaction (meaning the reaction will go forward without external influence). In the course reader it says that this energy is "f...
- Sun Jan 17, 2016 5:06 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Bond Enthalpies vs. Mean Bond Enthalpy
- Replies: 2
- Views: 2616
Bond Enthalpies vs. Mean Bond Enthalpy
Can someone explain to me why bonds have an enthalpy and a mean bond enthalpy? (What is the mean bond enthalpy an average of?) Also, which one do we use when solving problems?
- Fri Jan 08, 2016 10:47 am
- Forum: Phase Changes & Related Calculations
- Topic: Heat Capacity and Phase Change
- Replies: 2
- Views: 487
Heat Capacity and Phase Change
I understand that higher heat capacities lead to lower slopes (and vise versa for lower heat capacities) on heat supplied vs. temperature diagrams because the substance can store more energy. Does the heat capacity of a substance also effect how much energy is needed in a phase change (for example a...
- Fri Dec 04, 2015 1:03 am
- Forum: *Titrations & Titration Calculations
- Topic: Strong Acid Vs Weak Base Titrations
- Replies: 1
- Views: 528
Strong Acid Vs Weak Base Titrations
I remember in class Professor Lavelle explained that in weak acid- strong base titrations, strong bases "dominate" weak acids. This means that after the equivalence point there should be a higher concentration of OH- ions. How do you know how to set up a reaction (equilibrium) for chemistr...
- Sun Nov 29, 2015 10:22 pm
- Forum: Lewis Acids & Bases
- Topic: Acids and Bases
- Replies: 1
- Views: 471
Re: Acids and Bases
A polyprotic acid is a compound that can donate more than one proton. Common polyprotic acids are Sulfuric acid (H2SO4) and carbonic acid (H2CO3). You can look at the deprotonation of these compounds as a series of steps. For example, in the first deprotonation, H2CO3 will react with water and form ...
- Sun Nov 22, 2015 4:55 pm
- Forum: Properties & Structures of Inorganic & Organic Acids
- Topic: Strong Vs. Weak Acids
- Replies: 1
- Views: 504
Strong Vs. Weak Acids
I read that as the strength of acids increases as you go down the halogen group on the periodic table (HF --> HI). Why is it that even though the molecules are becoming less polar (and have a lower difference in electronegativity) they are increasing in acidic strength?
- Sat Nov 14, 2015 11:19 pm
- Forum: Ideal Gases
- Topic: PV=nRT
- Replies: 2
- Views: 1183
Re: PV=nRT
According to the Ideal Gas Law, pressure increases as temperature increases, and temperature increases as volume increases. Then why doesn't it make sense for pressure to increase as volume to increase? Think of the PV= nRT formula like this (for comparing temperature and volume)--> P= (nRT)/V. If y...
- Sun Nov 08, 2015 11:36 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: K Constant
- Replies: 3
- Views: 713
Re: K Constant
K (the equilibrium constant) is derived from the division of products by reactants. (K= [Products]/[Reactants]) A large K (greater than 10^3) means that the reaction favors the formation of products ("equilibrium is shifted to the right"). A small K (less than 10^-3) means that, at equilib...
- Sun Nov 01, 2015 10:18 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Distinct DIfference between Linear and Bent
- Replies: 2
- Views: 6411
Re: Distinct DIfference between Linear and Bent
In determining the shape of a compounds and molecules, I always find it best to draw out and write out the generic formula ( A for the central atom, X for the number of atoms surrounding the central atom, and E for the number of lone pairs on the central atom). Note that bent refers to the AX2E2 and...
- Sun Oct 25, 2015 10:52 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: BF3 VSEPR Shape
- Replies: 1
- Views: 849
BF3 VSEPR Shape
I have a question regarding the molecular structure of BF3. In the book (page 110) it shows a Boron as the central atom, with 3 Fluorines attached with single bonds. In this structure all of the formal charges are 0, however, the central Boron atom only has 6 electrons and does not satisfy the octet...
- Sun Oct 18, 2015 6:38 pm
- Forum: Ionic & Covalent Bonds
- Topic: Ionic Bond Structure
- Replies: 1
- Views: 426
Ionic Bond Structure
I am confused about the "crystal structure" that forms in ionic bonds. Do all ionic bonds have a crystal structure with cations and anions alternating down a row (Figure 3.5)? And does "lattice energy" only refer to ionic bonds with this structure (or to all crystal structures)?
- Sat Oct 10, 2015 1:12 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: Ionic radius
- Replies: 1
- Views: 627
Re: Ionic radius
First, lets look at the periodic trends for atomic radius. As you go down the periodic table (from top to bottom), you go from 1s --> 2s -- 3s.. etc... the atomic radius INCREASES (there are more electrons, and each orbital can only hold two electrons, so the more electrons in an element, the bigger...
- Sun Oct 04, 2015 3:07 pm
- Forum: *Black Body Radiation
- Topic: Black body [ENDORSED]
- Replies: 3
- Views: 1221
Re: Black body [ENDORSED]
To understand planck's constant (and his hypothesis), the formula it is used with (E=hv), and its importance, you must first understand that light rays push and pull on an electron. This creates the "wave" picture that is shown by figure 1.7 in the book. How fast the cycles (created by the...