Search found 28 matches
- Sat Mar 12, 2016 8:19 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Final 2014 question 3A pikachu
- Replies: 2
- Views: 475
Re: Final 2014 question 3A pikachu
There's also a reduction reaction that utilizes the NO3 ion and that has an E of .96V. Why isn't this used?
- Fri Mar 11, 2016 9:59 pm
- Forum: Concepts & Calculations Using Second Law of Thermodynamics
- Topic: Residual Entropy of NO compared to BF3
- Replies: 3
- Views: 810
Re: Residual Entropy of NO compared to BF3
What's the difference between NO and ON?
- Sun Feb 28, 2016 2:30 pm
- Forum: *Electrophiles
- Topic: NO2+ as an electrophile
- Replies: 1
- Views: 1777
NO2+ as an electrophile
Upon drawing NO2+ or in the book +NO2 all of the elements have a complete octet. Why is it then an electrophile?
- Wed Feb 24, 2016 5:21 pm
- Forum: *Cycloalkenes
- Topic: Benzene
- Replies: 2
- Views: 480
Benzene
Benzene has a ring structure and multiple double bonds. Why isn't it called uh... 1,3,5 cyclohexatriene? I'm not sure if that's correct but at least why isn't there a cyclo - ?
- Wed Feb 24, 2016 5:06 pm
- Forum: *Electrophilic Addition
- Topic: Electrophile
- Replies: 2
- Views: 329
Re: Electrophile
A good way to remember this is that phile means 'loving' ... therefore electrophile -> electron loving (which eventually you can deduce is because they are electron deficient). This will allow you to remember that they are partial positive, attracted by electrons, etc.
- Wed Feb 24, 2016 4:58 pm
- Forum: *Electrophiles
- Topic: Transition States
- Replies: 2
- Views: 418
Re: Transition States
Additionally, the delta G is actually the difference between TS2 and the intermediate NOT the reactant. This is important!
- Fri Feb 19, 2016 5:38 pm
- Forum: *Organic Reaction Mechanisms in General
- Topic: Intermediates vs. Transition States
- Replies: 3
- Views: 3400
Re: Intermediates vs. Transition States
Per my understanding, intermediates are a sort of middle ground between reactants and products. A reactant becomes an intermediate and then this intermediate becomes a product. Transition states are HOW these these species are transforming. Transition states involve bonds IN THE PROCESS of breaking/...
- Thu Feb 11, 2016 3:05 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Cell Potential Increase/Decrease
- Replies: 2
- Views: 387
Re: Cell Potential Increase/Decrease
Cell potential increases and decreases are dictated by the parameters in the Nernst equation (mols of electron, temperature, concentration of ions in cell).
- Thu Feb 11, 2016 3:01 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Effects of Adding Reactants and Products
- Replies: 1
- Views: 326
Re: Effects of Adding Reactants and Products
Just think of it in terms of Le Chatelier's Principle. Removing a product will force the reaction to the right and encourage this forward reaction (which encourages electron production) thereby increasing E over E (naut or E standard). The same goes for removing a reactant or adding some product.
- Thu Feb 04, 2016 3:31 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Standard Reduction Potential Calculations
- Replies: 1
- Views: 266
Re: Standard Reduction Potential Calculations
Yes! You need to multiple the standard potential given by -1. Although if you multiply the entire reaction with some stoichiometric scalar (say you need 2 mols of Cu+ instead of just 1), the standard potential remains the same. This is because standard reduction potential gives the voltage differenc...
- Wed Jan 27, 2016 9:55 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: problem 8.67 b
- Replies: 1
- Views: 300
Re: problem 8.67 b
Hello! It is given in the problem as the enthalpy of sublimation.
- Thu Jan 21, 2016 3:16 pm
- Forum: Administrative Questions and Class Announcements
- Topic: Picking up the final
- Replies: 1
- Views: 628
Picking up the final
I don't have my course reader any longer; where is the office where we can pick up our fall quarter finals and when is the office open?
- Sun Jan 17, 2016 10:28 pm
- Forum: Concepts & Calculations Using First Law of Thermodynamics
- Topic: Help Breaking Down 8.25
- Replies: 1
- Views: 248
Re: Help Breaking Down 8.25
Additionally, the solution manual notes that q cal = C*deltaT... a positive value for q despite the temperature rising 7.32 degrees celsius. Does that mean the heat came from the calorimeter into the water?
- Thu Jan 14, 2016 12:01 am
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Bond Enthalpies
- Replies: 1
- Views: 365
Re: Bond Enthalpies
I was under the impression that we broke all the bonds that weren't repeated (this becomes apparent when one counts the bonds from reactants and products and see say, two X-Y bonds). If one broke all the bonds and included all of the bond formations these values would inherently cancel anyhow. I'm n...
- Wed Jan 06, 2016 3:40 pm
- Forum: Phase Changes & Related Calculations
- Topic: Steam v Water
- Replies: 4
- Views: 726
Re: Steam v Water
https://scienceisntscary.files.wordpress.com/2013/05/heating-curve.png This is the explanation in a graphical sense. If we visualize just the boiling water (the leftmost point on the red colored line), we see that the heat added which is the heat that transfers into the skin when the skin comes in ...
- Wed Dec 02, 2015 7:43 pm
- Forum: *Titrations & Titration Calculations
- Topic: Titration curve question
- Replies: 2
- Views: 595
Re: Titration curve question
I believe this point is also called the halfway point.
- Wed Dec 02, 2015 7:41 pm
- Forum: *Titrations & Titration Calculations
- Topic: What are the different names for stoichiometric point?
- Replies: 1
- Views: 421
Re: What are the different names for stoichiometric point?
Stoichiometric and equivalence points are synonymous. I believe the halfway point refers to weak/strong titrations and the actual point occurs when pH=pkA/pkB. I believe it is halfway to the stoichiometric point.
- Mon Nov 30, 2015 2:49 pm
- Forum: *Making Buffers & Calculating Buffer pH (Henderson-Hasselbalch Equation)
- Topic: Buffers
- Replies: 2
- Views: 504
Re: Buffers
I believe strong acids and bases are poor buffers because their respective conjugate bases/acids are extremely weak. In order to be an effective buffer, both the acid and its conjugate base have to be relatively weak. Check this picture out for a graphical representation: http://forums.studentdoctor...
- Sat Nov 14, 2015 7:07 pm
- Forum: Shape, Structure, Coordination Number, Ligands
- Topic: EDTA binding sites
- Replies: 1
- Views: 1043
EDTA binding sites
http://www.chemgapedia.de/vsengine/media/width/247/height/178/vsc/de/ch/16/biochem/grafik/edta.svg.jpg Looking at the 4 oxygens with a - and the two nitrogens with one lone pair makes EDTA have six lone pair binding sites. Why are we not taking into account the oxygens that are double bonded, don't...
- Sat Nov 14, 2015 6:58 pm
- Forum: Shape, Structure, Coordination Number, Ligands
- Topic: How to determine monodentate or bidentate?
- Replies: 3
- Views: 3857
Re: How to determine monodentate or bidentate?
In this case Dr. Lavelle, why is it that CO3 (2-) can be bidentate. Considering that H2O has angles of 109.5 between the lone pairs and can only form 1 binding site how come the 120 degrees (> than 109.5) in CO3 (2-) can form two binding sites despite being wider than water?
- Sat Nov 14, 2015 6:47 pm
- Forum: Naming
- Topic: Bisoxalato vs. Dioxalato
- Replies: 1
- Views: 1099
Bisoxalato vs. Dioxalato
For ligands such as ethylene DI amine(en) or ethylene DI amine TETRA acetato (EDTA), I understand that we have to use bis, tris, tetrakis when referring to multiple of these ligands. For oxalato in question 17.31D, oxalato is referred to as bisoxalato. Why not dioxalato for this ligand considering t...
- Fri Nov 13, 2015 8:32 am
- Forum: Sigma & Pi Bonds
- Topic: Identifying the composition of bonds/hybridizations notation
- Replies: 2
- Views: 572
Re: Identifying the composition of bonds/hybridizations nota
Given a lewis structure we'll know the number of sigma/pi bonds just given the number of single/double/triple bonds. Sigma for all single bonds and pi bonds for anything above so (doubles are 1 sig 1 pi, triples are 1 sig 2 pi). As for that hybridization notation we'll have to figure out which orbit...
- Sat Oct 31, 2015 10:55 pm
- Forum: *Molecular Orbital Theory (Bond Order, Diamagnetism, Paramagnetism)
- Topic: Bonding Molecular Orbital Energies
- Replies: 1
- Views: 220
Bonding Molecular Orbital Energies
Why is it that sigma bonds are lower energy than pi bonds but in atoms with z>8, their anti bonding counterparts are higher nrg than the pi bonds. What exactly is an anti bonding orbital? We can see the sigma and pi bonds in a molecules 3D bond representation but can we see the anti bonding orbitals?
- Fri Oct 30, 2015 1:46 am
- Forum: Dipole Moments
- Topic: Dipole moments with vectors
- Replies: 1
- Views: 408
Dipole moments with vectors
The debye was introduced in the course reader; for molecules such as CCl3F, how do we know if the dipole is towards the Cls or towards the F. We know that the F-C difference is greatest and its individual dipole will be the strongest but if we add the dipole moments as vectors with units debye, are ...
- Sun Oct 18, 2015 10:29 pm
- Forum: Polarisability of Anions, The Polarizing Power of Cations
- Topic: Polarisability
- Replies: 1
- Views: 326
Polarisability
Assuming different elemental sizes, why is it that the cation charge (+2 or +3 etc.) is such a big determinant of an element's polarizing power. For example, I understand that Be2+ is much smaller than Sr2+ but the high powered nucleus of Strontium isn't enough to overcome the electron repulsions an...
- Sat Oct 10, 2015 1:19 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: Penetration
- Replies: 2
- Views: 522
Penetration
The book in chapter 2.5 describes inner-shell electrons as having a "penetrating effect." This is also seen in question #2.37 which states that electrons in an s-orbital are more effective than those in other orbitals at shielding from the nuclear charger because an electron in an s-orbita...
- Wed Oct 07, 2015 5:44 pm
- Forum: Heisenberg Indeterminacy (Uncertainty) Equation
- Topic: Heisenberg Indeterminacy Experiment
- Replies: 1
- Views: 255
Heisenberg Indeterminacy Experiment
In the experiment that led to Heisenberg's Indeterminacy equation, a major point was that the distance that the electron traveled could not be calculated with certainty because we weren't sure how much it had been deflected off of its path. Hypothetically speaking, if we were to set up a pair of sen...
- Thu Oct 01, 2015 12:07 am
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: How many photos of infrared radiation?
- Replies: 1
- Views: 335
How many photos of infrared radiation?
In 1.0 s, a 60 W bulb emits 11 J of energy in the form of infrared radiation (heat) of wavelength 1850 nm. What is the energy per photon of light emitted? How many photons of infrared radiation does the lamp generate in 1.0 s? So I understand how to do the first part of the problem but I'm not reall...