Search found 62 matches
- Wed Mar 13, 2019 11:28 am
- Forum: Reaction Mechanisms, Reaction Profiles
- Topic: Does reaction rate mean average reaction rate?
- Replies: 3
- Views: 495
Re: Does reaction rate mean average reaction rate?
Unless the problem specifies that it is average rate, in general, rate is instantaneous.
- Wed Mar 13, 2019 11:27 am
- Forum: Reaction Mechanisms, Reaction Profiles
- Topic: rate of disappearance
- Replies: 3
- Views: 560
Re: rate of disappearance
It would be in terms of the compound that is being consumed. For example,
A —> B + C
R = k[A]
A —> B + C
R = k[A]
- Wed Mar 13, 2019 11:26 am
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: cell diagram
- Replies: 1
- Views: 208
Re: cell diagram
Ions for both oxidation and reduction are placed closest to the salt bridge
generally in the order reactants, products
generally in the order reactants, products
- Wed Mar 06, 2019 11:45 am
- Forum: Zero Order Reactions
- Topic: General “order” question
- Replies: 6
- Views: 923
Re: General “order” question
Order is essential to calculate kr, half life, change in concentration, or time needed to get to a particular concentration. There are different equations for each order. You’ll either be given order of reaction, or if you are given elementary reactions (and need to determine order of overall reacti...
- Wed Mar 06, 2019 11:41 am
- Forum: Reaction Mechanisms, Reaction Profiles
- Topic: fast and slow elementary reactions
- Replies: 3
- Views: 490
Re: fast and slow elementary reactions
Both reactions are important in determining overall reaction. However, pertaining to rate law, the slow step (AKA the rate determining step) is the one that is used.
- Wed Mar 06, 2019 11:40 am
- Forum: Appications of the Nernst Equation (e.g., Concentration Cells, Non-Standard Cell Potentials, Calculating Equilibrium Constants and pH)
- Topic: Solubility and redox reactions
- Replies: 1
- Views: 302
Re: Solubility and redox reactions
For precipitates in general the form is: REDUCTION: Precipitate + e — ions OXIDATION: Ions — Precipitate One ion will not change charge, (for AgCl) Cl- retains an oxidation number of -1, so the other ion is the one that is undergoing oxidation or reduction (the one that is going from solid to +1) Th...
- Tue Feb 26, 2019 6:35 pm
- Forum: Balancing Redox Reactions
- Topic: Basic redox reactions
- Replies: 3
- Views: 443
Re: Basic redox reactions
First balance O with H2O.
Then balance H — add h2o equal to the number of hydrogens and for every h2o, add an oh- on opposite side
So if you have 4 extra hydrogens on one side, add four h2o on opposite side to balance, and add 4 oh- on the original side
Then balance H — add h2o equal to the number of hydrogens and for every h2o, add an oh- on opposite side
So if you have 4 extra hydrogens on one side, add four h2o on opposite side to balance, and add 4 oh- on the original side
- Tue Feb 26, 2019 6:32 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Gibbs free energy J/mol
- Replies: 1
- Views: 253
Re: Gibbs free energy J/mol
Unless the reaction specifically states for 1 mole of formation/combustion,
to my understanding, G is either in J or kJ
to my understanding, G is either in J or kJ
- Tue Feb 26, 2019 9:20 am
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Cell Diagram and Ecell [ENDORSED]
- Replies: 29
- Views: 114816
Cell Diagram and Ecell [ENDORSED]
1) With gaseous and nonconducting solid compounds, is the order Inert|Gas/solid|Chg || Chg|Gas/solid|Inert? Or does it follow the order of reactants to products? Inert|Ox Reactant|Ox Product || Red Reactant|Red Product|Inert 2) With a positive Ecell, reduction is always on the right. Is this order r...
- Fri Feb 22, 2019 1:04 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Galvanic Cells
- Replies: 2
- Views: 316
Re: Galvanic Cells
Reduction occurs at the cathode. For reduction to occur, electrons must be present at the cathode for the reaction to “pick up” electrons.
Oxidation occurs at the anode. Oxidation thus releases electrons at the anode, which are then transported to cathode.
Oxidation occurs at the anode. Oxidation thus releases electrons at the anode, which are then transported to cathode.
- Fri Feb 22, 2019 1:02 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Salt Bridge
- Replies: 5
- Views: 579
Re: Salt Bridge
At the anode, oxidation occurs, which leads to the buildup of positively charged ions. At the cathode, reduction occurs, which leads to the buildup of negatively charged ions. As Lorena said, the buildup of these charges will eventually stop e- flow from anode to cathode. To maintain this flow, the ...
- Fri Feb 22, 2019 12:18 pm
- Forum: Balancing Redox Reactions
- Topic: oxidation state of MnO4-
- Replies: 3
- Views: 402
Re: oxidation state of MnO4-
Mn is determined by the oxidation state of oxygen as well as the overall charge of the compound.
Oxygen = -2
Because there are 4 Oxygens and overall charge is -1, we need a +7 to balance it out.
Thus, Mn is +7
Oxygen = -2
Because there are 4 Oxygens and overall charge is -1, we need a +7 to balance it out.
Thus, Mn is +7
- Fri Feb 15, 2019 11:50 am
- Forum: Thermodynamic Definitions (isochoric/isometric, isothermal, isobaric)
- Topic: Isobaric
- Replies: 12
- Views: 1727
Re: Isobaric
That also means that you must use the Cv value for ideal gases
MONOATOMIC: 3/2*R
LINEAR: 5/2*R
NONLINEAR: 7/2*R
MONOATOMIC: 3/2*R
LINEAR: 5/2*R
NONLINEAR: 7/2*R
- Fri Feb 15, 2019 11:45 am
- Forum: Calculating Standard Reaction Entropies (e.g. , Using Standard Molar Entropies)
- Topic: Cv vs. Cp
- Replies: 6
- Views: 1050
Re: Cv vs. Cp
When calculating change in entropy for systems that have a change in both volume and temperature: S = nRln(V2/V1) + nCvln(T2/T1) Because entropy is a state function: you can add change in volume to change in temperature. For change in temperature, you use Cv. Cv and Cp can also be found for linear a...
- Fri Feb 15, 2019 11:39 am
- Forum: Calculating Work of Expansion
- Topic: Reversible vs Irreversible
- Replies: 4
- Views: 484
Re: Reversible vs Irreversible
^^ Adding onto Faith’s answer:
For reversible, the question will also state that system is isothermal.
Also, Ssys is the same for irreversible and reversible work.
The only difference is Ssurr.
For reversible, the question will also state that system is isothermal.
Also, Ssys is the same for irreversible and reversible work.
The only difference is Ssurr.
- Fri Feb 08, 2019 12:43 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: Knowing which one to use
- Replies: 3
- Views: 619
Re: Knowing which one to use
Heat capacity (neither specific nor molar) is used if no mass/moles are given.
An example is using a calorimeter calibration.
q = Ccal * delta T
Then plug in Ccal to determine q for a different reaction.
An example is using a calorimeter calibration.
q = Ccal * delta T
Then plug in Ccal to determine q for a different reaction.
- Fri Feb 08, 2019 12:39 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Delta H
- Replies: 7
- Views: 1251
Re: Delta H
You can also use bond enthalpies to determine delta H:
Delta H = H bonds broken (reactants - H bonds formed (products)
But this is not always accurate, as it uses average enthalpy values for the bonds.
Delta H = H bonds broken (reactants - H bonds formed (products)
But this is not always accurate, as it uses average enthalpy values for the bonds.
- Fri Feb 08, 2019 12:36 pm
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: How to know which gas constant to use
- Replies: 2
- Views: 327
Re: How to know which gas constant to use
8.314 J/K*mol
.082 L*atm/K*mol
^^ Like Josephine said, it depends on the units in the question.
.082 L*atm/K*mol
^^ Like Josephine said, it depends on the units in the question.
- Thu Jan 31, 2019 7:36 am
- Forum: Heat Capacities, Calorimeters & Calorimetry Calculations
- Topic: Comparing SHC
- Replies: 3
- Views: 495
Re: Comparing SHC
Not necessarily: Water SHC = 4.184 Benzene SHC = 1.74 Benzene has more atoms than water, yet its SHC is less than water. SHC depends on the types of bonds, not necessarily the amount of atoms. Molar heat capacity is dependant on amount of each substance, but again, the types of bonds mostly determin...
- Thu Jan 31, 2019 7:29 am
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Phase changes
- Replies: 2
- Views: 268
Re: Phase changes
^^ Like Gwyn said, heat is not only needed to raise the temperature of the substance, but it is needed to convert it from solid to liquid and liquid to gas. Heat is applied in order to break the intermolecular forces between molecules. Since more heat is required to completely sever bonds (liquid to...
- Thu Jan 31, 2019 7:23 am
- Forum: Thermodynamic Systems (Open, Closed, Isolated)
- Topic: Perfect system
- Replies: 3
- Views: 876
Re: Perfect system
A perfect system would involve no loss of energy to surroundings. This by definition is an isolated system, which though exists in theory, there is no completely isolated system in reality.
- Wed Jan 23, 2019 11:20 am
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: All products are solids
- Replies: 3
- Views: 361
Re: All products are solids
Equilibrium constant would be equal to
1/[r] — if concentrations are given or reactants are aqeous
1/(Pr) — if reactants are gases
1/[r] — if concentrations are given or reactants are aqeous
1/(Pr) — if reactants are gases
- Wed Jan 23, 2019 11:16 am
- Forum: Ideal Gases
- Topic: atm vs. bar?
- Replies: 25
- Views: 2997
Re: atm vs. bar?
Different units of measurement
Thus entails use of different value for R constant.
Thus entails use of different value for R constant.
- Wed Jan 23, 2019 11:14 am
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: 5% Rule
- Replies: 5
- Views: 517
Re: 5% Rule
The 5% approximation technique can be used for any K calculation, provided
K < 10-3 — Very little product formed, R-x = R
K > 103 — Very little reactant remaining, P+x = P
K < 10-3 — Very little product formed, R-x = R
K > 103 — Very little reactant remaining, P+x = P
- Wed Jan 16, 2019 2:32 pm
- Forum: Acidity & Basicity Constants and The Conjugate Seesaw
- Topic: Pka and Acidty
- Replies: 2
- Views: 439
Re: Pka and Acidty
Small Ka = high pKa = weak acid
Big Ka = low pKa = strong acid
Big Ka = low pKa = strong acid
- Wed Jan 16, 2019 2:30 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: Leveled
- Replies: 2
- Views: 230
Re: Leveled
I believe a substance can be leveled by a solvent.
So in the case of a strong acid, if it is dissolved with a solvent that is a strong base, it is “leveled off.”
Both solute and solvent become more neutral
So in the case of a strong acid, if it is dissolved with a solvent that is a strong base, it is “leveled off.”
Both solute and solvent become more neutral
- Wed Jan 16, 2019 1:49 pm
- Forum: Non-Equilibrium Conditions & The Reaction Quotient
- Topic: 5% approximation for weak acids/bases
- Replies: 2
- Views: 298
Re: 5% approximation for weak acids/bases
The 5% approximation can be used for values of K that are very large or very small.
If K is large — P+x = P
If K is small — R-x = R
But the verification must be computed after calculating equilibrium values.
If K is large — P+x = P
If K is small — R-x = R
But the verification must be computed after calculating equilibrium values.
- Fri Jan 11, 2019 12:28 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: liquids in equilibrium
- Replies: 2
- Views: 245
Re: liquids in equilibrium
The change in concentration of pure liquids and solids are insufficient — they essentially remain constant.
Thus, they are not included in equilibrium calculations.
Thus, they are not included in equilibrium calculations.
- Fri Jan 11, 2019 12:24 pm
- Forum: Ideal Gases
- Topic: Pressure and volume
- Replies: 4
- Views: 492
Re: Pressure and volume
Pressure and volume are inversely related, according to Boyle’s law.
Thus increasing pressure implies a decrease in volume.
Decreasing volume causes reaction to move to side with fewer moles of gas.
So increasing pressure causes reaction to move to side with fewer moles of gas.
Thus increasing pressure implies a decrease in volume.
Decreasing volume causes reaction to move to side with fewer moles of gas.
So increasing pressure causes reaction to move to side with fewer moles of gas.
- Thu Jan 10, 2019 9:27 am
- Forum: Ideal Gases
- Topic: Algebra
- Replies: 5
- Views: 348
Re: Algebra
Concentration is n (mol) / V (L)
Given the ideal gas law: PV = nRT
We write P = (n/V)RT
Thus P = (Conc)RT
Then to determine concentration, we divide P by RT
And get P/RT = Conc
Given the ideal gas law: PV = nRT
We write P = (n/V)RT
Thus P = (Conc)RT
Then to determine concentration, we divide P by RT
And get P/RT = Conc
- Wed Dec 05, 2018 1:33 pm
- Forum: Bronsted Acids & Bases
- Topic: J.9
- Replies: 2
- Views: 561
Re: J.9
KOH + HC2H3O2 >> KC2H3O2 + H2O
Net ionic: OH- + HC2H3O2 >> H2O + C2H3O2-
Acetic acid donates a proton, which makes the conjugate base C2H3O2-
KOH is a base, which means it accepts a proton to form water,
Because KOH is a strong base and acetic acid is a weak acid: the salt is basic.
Net ionic: OH- + HC2H3O2 >> H2O + C2H3O2-
Acetic acid donates a proton, which makes the conjugate base C2H3O2-
KOH is a base, which means it accepts a proton to form water,
Because KOH is a strong base and acetic acid is a weak acid: the salt is basic.
- Wed Dec 05, 2018 1:26 pm
- Forum: Electronegativity
- Topic: Electronegativity
- Replies: 2
- Views: 655
Re: Electronegativity
Electronegativity follows a diagonal trend: increasing towards the upper right: however, period is more important than group. This is because a lower period is associated with fewer energy shells, and thus a higher Zeff. Higher Zeff implies greater electronegativity: because the stronger the nuclear...
- Wed Dec 05, 2018 1:22 pm
- Forum: Lewis Acids & Bases
- Topic: Difference between Bronsted and Lewis Acids
- Replies: 2
- Views: 15086
Re: Difference between Bronsted and Lewis Acids
Bronsted acids are more specific than Lewis acids. Bronsted acids are compounds that can donate a proton, where Lewis acids are electron pair acceptors. So all Bronsted acids are Lewis acids, but not all Lewis acids are Bronsted acids.
- Sat Dec 01, 2018 11:05 am
- Forum: Naming
- Topic: Neutral ligand
- Replies: 2
- Views: 311
Re: Neutral ligand
One way of determining charge of complex is through the presence of anions or cations outside []. Basically, the overall charge of the complex equals the charge on the anion or cation present.
- Sat Dec 01, 2018 11:01 am
- Forum: Acidity & Basicity Constants and The Conjugate Seesaw
- Topic: Equilibrium Constants
- Replies: 2
- Views: 327
Re: Equilibrium Constants
From my understanding, we do not need to do calculations involving weak acids or bases. In general, however, the value of the constant remains the same: the concentrations of the conjugate acids and bases will decrease. This is because for weak acids and bases, there is incomplete disassociation, he...
- Sat Dec 01, 2018 10:56 am
- Forum: Sigma & Pi Bonds
- Topic: Number of Sigma and Pi Bonds
- Replies: 6
- Views: 1006
Re: Number of Sigma and Pi Bonds
Sigma bonds refer to overlap of s orbitals: since there is only one s orbital, there can only be one sigma bond. Pi bonds, on the other hand, refer to overlap of p orbitals. Since there are multiple p orbitals, multiple pi bonds can form.
- Thu Nov 22, 2018 7:18 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: 7th Edition Question 2E. 29
- Replies: 2
- Views: 128
Re: 7th Edition Question 2E. 29
Because the two chlorines are closer together on the first molecule, they create a strong negative pull. In the second molecule, they are a bit farther apart, and because of this the negative pull created by the individual chlorines partially cancel each other, creating a weaker overall pull.
- Thu Nov 22, 2018 7:10 pm
- Forum: Hybridization
- Topic: Hybridization and drawing
- Replies: 3
- Views: 424
Re: Hybridization and drawing
Hybridization depends on regions of electron density. While VSEPR does help visualize these regions, it is not necessary to determine hybridization.
- Thu Nov 22, 2018 7:08 pm
- Forum: Octet Exceptions
- Topic: Expanded Octets
- Replies: 1
- Views: 463
Re: Expanded Octets
A bond is only formed if it is energetically favorable, meaning that electrons in a bond have a lower energy then free electrons. Thus, it is more energetically favorable to fill 1 d orbital and have all electrons in a bond, as opposed to having electrons in a free orbital.
- Sat Nov 17, 2018 11:43 am
- Forum: Shape, Structure, Coordination Number, Ligands
- Topic: Sigma bond and Pi bonds
- Replies: 2
- Views: 522
Re: Sigma bond and Pi bonds
Sigma bonds = overlap of two s orbitals, overlap of s and one lobe of p, overlap of 2 p orbitals (one lobe only)
Pi bonds = both lobes of p orbitals overlap — atoms cannot rotate
Single bonds = sigma bond
Double bond = sigma and pi bond
Triple bond = sigma and 2 pi bonds
Pi bonds = both lobes of p orbitals overlap — atoms cannot rotate
Single bonds = sigma bond
Double bond = sigma and pi bond
Triple bond = sigma and 2 pi bonds
- Sat Nov 17, 2018 11:40 am
- Forum: Interionic and Intermolecular Forces (Ion-Ion, Ion-Dipole, Dipole-Dipole, Dipole-Induced Dipole, Dispersion/Induced Dipole-Induced Dipole/London Forces, Hydrogen Bonding)
- Topic: Instantaneous dipole equation
- Replies: 1
- Views: 324
Re: Instantaneous dipole equation
By instantaneous interactions, I assume you are referring to induced dipole interactions. Polarazability (the amount an electron field can be distorted) is directly proportional to atomic radius: the larger the radius, the more distortion, Greater polarizability allows for stronger induced dipole in...
- Sat Nov 17, 2018 11:34 am
- Forum: Hybridization
- Topic: Electron promotion
- Replies: 2
- Views: 357
Re: Electron promotion
Electron promotion allows for bond formation. In most cases, forming bonds equates a lower energy state. Lower energy states are most favorable: Pauli Exclusion Principle is less favorable.
- Thu Nov 08, 2018 12:42 pm
- Forum: Resonance Structures
- Topic: Resonance Structures
- Replies: 3
- Views: 385
Re: Resonance Structures
If there is an equivalent Lewis structure that can be formed (overall formal charge value remains the same)
simply by exchanging positions of atoms — then a molecule has resonance.
simply by exchanging positions of atoms — then a molecule has resonance.
- Thu Nov 08, 2018 12:30 pm
- Forum: Interionic and Intermolecular Forces (Ion-Ion, Ion-Dipole, Dipole-Dipole, Dipole-Induced Dipole, Dispersion/Induced Dipole-Induced Dipole/London Forces, Hydrogen Bonding)
- Topic: Potential Energy of London interactions
- Replies: 2
- Views: 623
Re: Potential Energy of London interactions
In terms of bond strength: type of bond is more important than size of molecule A larger radius, as you said, implies greater electron distortion Greater distortion of electrons means that the atom is more easily polarizable: will more easily form a dipole Since LDF forces are based on the formation...
- Thu Nov 08, 2018 12:12 pm
- Forum: Dipole Moments
- Topic: Van Der Waal vs Hydrogen Bons
- Replies: 2
- Views: 325
Re: Van Der Waal vs Hydrogen Bons
Hydrogen bonding and Van der Waal forces are both intermolecular forces. VDW forces are present in all molecules H-bonding is typically characterized by H-NOF bonds From my understanding, because VDW forces is a bond between induced dipoles (which arise from a “temporary” dipole formation), hydrogen...
- Thu Nov 01, 2018 5:06 pm
- Forum: Resonance Structures
- Topic: Radicals and "damaging"
- Replies: 5
- Views: 411
Re: Radicals and "damaging"
Taking antioxidants (vitamins) can help offset some of the damage.
- Thu Nov 01, 2018 4:56 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: 1E.25
- Replies: 1
- Views: 257
Re: 1E.25
Alkali — (no d electrons) s1
Grp 15 — if period 3+: (n-1)d10ns2np3
Grp 5 — (n-1)d3ns2
Coinage metals — acheive greater stability with a partially or completely filled d subshell
(n-1)d5ns1 OR (n-1)d10ns1
n = principal quantum number
Grp 15 — if period 3+: (n-1)d10ns2np3
Grp 5 — (n-1)d3ns2
Coinage metals — acheive greater stability with a partially or completely filled d subshell
(n-1)d5ns1 OR (n-1)d10ns1
n = principal quantum number
- Thu Nov 01, 2018 4:51 pm
- Forum: Resonance Structures
- Topic: Delocalized electrons
- Replies: 2
- Views: 324
Re: Delocalized electrons
Delocalized electrons are electrons spread over multiple atoms: they do not belong to a single atom. This usually occurs in double bonds or triple bonds.
- Thu Oct 25, 2018 7:42 pm
- Forum: Photoelectric Effect
- Topic: Work Function
- Replies: 14
- Views: 2274
Re: Work Function
It depends on information given. If given kinetic energy and energy/wavelength/frequency of incoming light, you can just subtract the energy of the incoming light from the value of kinetic energy to obtain the work function. Another way is if you are given the value of energy of photon at 0KE (maxim...
- Thu Oct 25, 2018 7:39 pm
- Forum: Wave Functions and s-, p-, d-, f- Orbitals
- Topic: Quantum Numbers n, l, and m
- Replies: 5
- Views: 386
Re: Quantum Numbers n, l, and m
n = principle energy level (shell), l is angular momentum (subshell), and ml = magnetic quantum (orbital).
The highest value of l is equal n-1
Values of l correspond to subshells: 0-s, 1-p, 2-d, 3-f
The highest value of l is equal n-1
Values of l correspond to subshells: 0-s, 1-p, 2-d, 3-f
- Thu Oct 25, 2018 7:36 pm
- Forum: *Shrodinger Equation
- Topic: Help on how to find l, ml, and ms
- Replies: 6
- Views: 60915
Re: Help on how to find l, ml, and ms
l is angular momentum quantum number.
It is the number of subshells per principal energy level
l = n-1
ml is magnetic quantum number, and refers to the number of orbitals per subshell
ml = 2l + 1
ms is spin quantum number, and refers to spin of electron. It is either positive or negative one half
It is the number of subshells per principal energy level
l = n-1
ml is magnetic quantum number, and refers to the number of orbitals per subshell
ml = 2l + 1
ms is spin quantum number, and refers to spin of electron. It is either positive or negative one half
- Sun Oct 21, 2018 1:31 pm
- Forum: Wave Functions and s-, p-, d-, f- Orbitals
- Topic: Electron Configuration [ENDORSED]
- Replies: 1
- Views: 153
Re: Electron Configuration [ENDORSED]
Atoms prefer to be in the lowest energy state possible. A half-filled or fully-filled d-subshell has a lower energy, which is why electron configurations that should be written as 3d4-4s2 or 3d9-4s2 are instead written 3d54s1 and 3d104s1
- Sun Oct 21, 2018 1:27 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: Effective Nuclear Charge
- Replies: 3
- Views: 402
Re: Effective Nuclear Charge
Nuclear charge refers to the strength of nuclear pull on electrons of an atom. However, the presence of more electrons creates shielding, which lowers the nuclear pull. Z-eff refers to the value of nuclear charge - shielding.
- Sun Oct 21, 2018 1:25 pm
- Forum: Properties of Electrons
- Topic: Atomic Spectra: absorption vs emission
- Replies: 3
- Views: 204
Re: Atomic Spectra: absorption vs emission
I believe frequencies in absorption and emission spectra would be different. For example, if red light is absorbed, green light would be given off, and red and green have different frequencies.
- Sat Oct 13, 2018 10:02 pm
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: H-Atom Emperical Equation
- Replies: 2
- Views: 225
Re: H-Atom Emperical Equation
Since other atoms have more than one electron, determining energy would depend on both distance from nucleus and electron-electron repulsion.
- Sat Oct 13, 2018 9:56 pm
- Forum: Photoelectric Effect
- Topic: Intensity — Photoelectric Effect
- Replies: 1
- Views: 294
Intensity — Photoelectric Effect
Is there a way of mathematically calculating intensity/amplitude via the photoelectric effect equation:
KE electron = Energy of photon - Threshold energy?
KE electron = Energy of photon - Threshold energy?
- Sat Oct 13, 2018 9:25 pm
- Forum: Photoelectric Effect
- Topic: Work Function
- Replies: 4
- Views: 246
Re: Work Function
More information would need to be provided, unless the problem specifies kinetic energy is 0 (i.e. longest wavelength). In this case, set threshold energy equal to energy of photon (velocity does not need to be calculated).
- Sat Oct 13, 2018 8:42 pm
- Forum: Photoelectric Effect
- Topic: Work Function
- Replies: 4
- Views: 246
Re: Work Function
More information would need to be provided, unless the problem specifies kinetic energy is 0 (i.e. longest wavelength). In this case, set threshold energy equal to energy of photon (velocity does not need to be calculated).
- Wed Oct 10, 2018 4:53 pm
- Forum: Significant Figures
- Topic: Repeating Decimal
- Replies: 3
- Views: 2507
Repeating Decimal
When we have a repeating decimal number, such as 1/3, do we simply follow “normal” (lowest decimal point value for addition/subtraction and lowest number of sig figs for multiplication/division)? Or are there special rules? Also, how does rounding work?
- Thu Oct 04, 2018 8:35 am
- Forum: Empirical & Molecular Formulas
- Topic: Molar mass and molecular weight
- Replies: 3
- Views: 497
Molar mass and molecular weight
Technically, don’t molar mass and molecular weight refer to the same concept: the total weight (in grams) of the molecular formula?
- Wed Oct 03, 2018 11:33 pm
- Forum: Empirical & Molecular Formulas
- Topic: Definition of Empirical Formula
- Replies: 8
- Views: 659
Re: Definition of Empirical Formula
Theoretically, doesn’t it also refer to mass percent composition of the molecule?
- Wed Oct 03, 2018 10:41 pm
- Forum: Empirical & Molecular Formulas
- Topic: Definition of Empirical Formula
- Replies: 8
- Views: 659
Definition of Empirical Formula
Does the empirical formula represent the relative number of atoms of a compound or the relative mass ratio of the atoms in a compound?