Search found 69 matches
- Sat Jan 23, 2021 10:04 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: How to fill in 2nd row of ICE table?
- Replies: 25
- Views: 65
Re: How to fill in 2nd row of ICE table?
In general, if the first row has a "0", then the second row will be adding x or 2x, etc But for a more formal look at this, you should compare Q and K. If Q < K, then the reaction needs more products, and will proceed to the right. So the products will have a +x or +2x etc while the produc...
- Sat Jan 23, 2021 10:00 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Exothermic and Endothermic Reactions
- Replies: 9
- Views: 33
Re: Exothermic and Endothermic Reactions
Catie Donohue 2K wrote:So just to clarify what's already been said, catalysts control the speed of endothermic and exothermic reactions, but do not affect the change in enthalpy of the reaction?
Yes, that is correct :)
- Sat Jan 23, 2021 9:59 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Standard State
- Replies: 11
- Views: 29
Re: Standard State
Standard states are at 1 atm and 25 degrees Celsius. When trying to find the standard state of a molecule, if you cant look it up, I think we should just go with what we have seen in this class, like in previous problems in example. For example, N2 would be N2(g) and H would be H2(g), as these are w...
- Sat Jan 23, 2021 9:56 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: standard states
- Replies: 6
- Views: 33
Re: standard states
Hello! I think the ones he mentioned in class were He(g), Ar(g), N2(g), O2(g), F2(g), H2(g), Cl2(g), B2(l), I2(s), most stable form of carbon is graphite. I think in general we should just do what "feels right" or what we have seen before when trying to figure out the standard state in a p...
- Sat Jan 23, 2021 9:54 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Exothermic and Endothermic Reactions
- Replies: 9
- Views: 33
Re: Exothermic and Endothermic Reactions
Catalyst speed up a chemical reaction by lowering the activation energy.
Enthalpy is a state property, so it does not depend on the path taken. Therefore, lowering the activate energy will not effect the net enthalpy.
Enthalpy is a state property, so it does not depend on the path taken. Therefore, lowering the activate energy will not effect the net enthalpy.
- Sat Jan 23, 2021 9:53 pm
- Forum: Phase Changes & Related Calculations
- Topic: Steam causing severe burns
- Replies: 19
- Views: 68
Re: Steam causing severe burns
Yes! I think that since the steam first comes into contact with the air, and the system involving the steam is much hotter than the surrounding, the system naturally loses heat to the surroundings before it hits your face. Also, I feel that this would have to do with diffusion of this extremely hot ...
- Fri Jan 15, 2021 11:34 am
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: Temperature
- Replies: 45
- Views: 123
Re: Temperature
For endothermic Rxn (delta H is greater than 0, the forward reaction requires energy): increase temperature--> increases K --> the forward reaction is favored (reaction shifts to the right) decrease temperature --> decrease K --> reverse reaction is favored For exothermic reaction (delta H is negati...
- Fri Jan 15, 2021 11:31 am
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: Sapling #4
- Replies: 7
- Views: 64
Re: Sapling #4
Yes, that is correct!
Now, you set the Kp expression you provided equal to the given K value. Also, set up an ice table with initial, change, and equilibrium concentrations to attain your quadratic, solve for x, and then you can find the equilibrium pressures for all species.
Now, you set the Kp expression you provided equal to the given K value. Also, set up an ice table with initial, change, and equilibrium concentrations to attain your quadratic, solve for x, and then you can find the equilibrium pressures for all species.
- Fri Jan 15, 2021 11:29 am
- Forum: Non-Equilibrium Conditions & The Reaction Quotient
- Topic: Q and K on and reactant/product concentrations
- Replies: 8
- Views: 27
Re: Q and K on and reactant/product concentrations
Q = [P] / [R], so if Q<K, there is no way that the reactant concentration could be greater than the products and Q be <K.
- Fri Jan 15, 2021 11:27 am
- Forum: Ideal Gases
- Topic: Ice method
- Replies: 14
- Views: 68
Re: Ice method
I= initial concentration C= change in concentration E= equilibrium concentration. For a balanced reaction, you have the initial concentrations of each species (given, or 0). Many times you have the equilibrium conc of one of the species, with which you can find the change in concentration for each s...
- Fri Jan 15, 2021 11:24 am
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: lecture 5 question
- Replies: 13
- Views: 56
Re: lecture 5 question
Yes, there are trends (like group 1 and 2 metal oxides/hydroxides are strong bases) and also specific strong acids and bases you should memorize, found in the textbook. When an acid protonates, it forms is conjugate base. When a base accepts the H+, it forms its conjugate acid. Heres an example: HCl...
- Fri Jan 15, 2021 11:21 am
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: Le Chatelier's Principle
- Replies: 19
- Views: 103
Re: Le Chatelier's Principle
Le Chatelier's principle holds that when a change is exerted on a system (like changing the concentration or pressure by changing the volume), the system will respond in a way that will minimize that change and return to "normal" Example: For the reaction A+ B --> C. Assume this reaction i...
- Fri Jan 08, 2021 11:01 am
- Forum: Ideal Gases
- Topic: Units of Temperature
- Replies: 82
- Views: 288
Re: Units of Temperature
We always use Kelvin for temperature in PV=nRT. This is simply because the units cancel out with the units of the other species in the equation.
- Fri Jan 08, 2021 11:00 am
- Forum: Ideal Gases
- Topic: Ideal vs real gases
- Replies: 12
- Views: 59
Re: Ideal vs real gases
I believe in lecture Dr. Lavelle said that an ideal gas is defined as a gas that does not undergo a phase change to a liquid when it is cooled. I believe that for this class, we assume all gases (assuming that they are a gas for a specific T and not a liquid that was cooled) are ideal and we can use...
- Fri Jan 08, 2021 10:58 am
- Forum: Ideal Gases
- Topic: Bars to atm [ENDORSED]
- Replies: 35
- Views: 173
Re: Bars to atm [ENDORSED]
One bar is about equal to one atm. There is a slight difference, but for the purpose of this class, you can use the two terms interchangeably.
- Fri Jan 08, 2021 10:56 am
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: ICE tables
- Replies: 11
- Views: 66
Re: ICE tables
I= initial concentration. This is the concentration of each reactant and product (mol/L) that you start off with C= change in concentration. The reactant usually will have a decrease in concentration that is proportional to the increase in concentration in the product. If there is one mol of a react...
- Fri Jan 08, 2021 10:52 am
- Forum: Non-Equilibrium Conditions & The Reaction Quotient
- Topic: names for reaction quotient Q
- Replies: 19
- Views: 68
Re: names for reaction quotient Q
Q can mean either Qp or Qc. Qp uses the partial pressures of each species (raised to a certain power if necessary), and is when all the elements in the equation are all gases, as solids and liquids can't exert partial pressure. Qc uses molar concentrations of each reactant and product (exclude solve...
- Fri Jan 08, 2021 10:50 am
- Forum: Ideal Gases
- Topic: Ideal Gas Law Question
- Replies: 11
- Views: 57
Re: Ideal Gas Law Question
T is constant because the temperature does not change when you are using PV=nRT. Although temperature in general can change, when we use PV=nRT we assume a certain set of conditions, in which Temperature is a set value.
- Sat Dec 12, 2020 4:06 pm
- Forum: Octet Exceptions
- Topic: Clarification on Expanded Octets
- Replies: 3
- Views: 15
Re: Clarification on Expanded Octets
Expanded octet just means that an atom utilizes its d block to hold more than 8 electrons in the valence, which is not possible with only s and p orbitals. The common expanded octets are P, S, Cl. Any atom in row 3 of the periodic table (in the p block) and below, can have an expanded octet because ...
- Sat Dec 12, 2020 4:04 pm
- Forum: Hybridization
- Topic: sp3 orbitals
- Replies: 6
- Views: 52
Re: sp3 orbitals
The number in front is the energy level (n), or the principle quantum number. This specifies the different shells that the valence electrons are in.
- Sat Dec 12, 2020 4:02 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Seesaw vs. trigonal pyramidal
- Replies: 22
- Views: 150
Re: Seesaw vs. trigonal pyramidal
See saw is AX4E , while trigonal pyramidal is AX3E
- Sat Dec 12, 2020 4:01 pm
- Forum: Shape, Structure, Coordination Number, Ligands
- Topic: Heme Complex Coordination Compound
- Replies: 3
- Views: 46
Re: Heme Complex Coordination Compound
I think we just know that its square planar because Dr. Lavelle told us in class. Otherwise, theres no way to tell if somethings square planar vs tetrahedral if you cant see the Lone pairs. We know that only one O2 can bind to hemoglobin/the heme complex because the Fe is bonded to 4 N's and a hista...
- Sat Dec 12, 2020 3:57 pm
- Forum: Acidity & Basicity Constants and The Conjugate Seesaw
- Topic: Textbook Problem 6C.17
- Replies: 2
- Views: 13
Re: Textbook Problem 6C.17
I was also confused about this explanation the textbook gave. I do not think we have the memorize the pKA values or anything, I think that they were just provided in the textbook and we were supposed to reference them. Assuming we were not given the pKA values, I said that BrO- would be the stronger...
- Sat Dec 05, 2020 10:39 am
- Forum: Biological Examples
- Topic: chelates
- Replies: 8
- Views: 70
Re: chelates
The quick answer is that whenever you see a compound with at least one polydenate ligand, that compound is a chelate. A chelate is a compound that is a ring-like structure, in which the polydenate ligand(s) form a ring which locks in the central TM atom. An example of a chelate is the heme complex. ...
- Sat Dec 05, 2020 10:36 am
- Forum: Hybridization
- Topic: How to find the hybridization
- Replies: 14
- Views: 93
Re: How to find the hybridization
Find the regions of electron density around that atom. Electron density refers to a Lone pair of electrons, or a bond (single, double, triple bonds all count as one region of electron density) If there is one region of e density - only uses s orbital two regions of e density- sp hybridization three ...
- Sat Dec 05, 2020 10:33 am
- Forum: Lewis Acids & Bases
- Topic: Water
- Replies: 62
- Views: 492
Re: Water
Water can act as an acid or base, it just depends. This makes sense if you think about Dr. Lavelle's discussion about how molecules do not just "choose" to be an acid or a base, and it depends on their chemical environment.
- Sat Dec 05, 2020 10:31 am
- Forum: Naming
- Topic: Polydentate
- Replies: 8
- Views: 58
Re: Polydentate
Polydenate means that the ligand binds with the TM more than once. So, polydendate ligands have at least 2 lone pairs, and they have to be long enough to stretch/bend in order to make 2/more coordinate covalent bonds with the TM. There needs to be single (Sigma) bonds that allow for this rotation. T...
- Sat Dec 05, 2020 10:17 am
- Forum: Naming
- Topic: Naming Order
- Replies: 16
- Views: 62
Re: Naming Order
For the chemical formula, the order does not really matter. Just make sure that you put the transition metal first, followed by all of the other ions and atoms.
- Sat Nov 28, 2020 4:07 pm
- Forum: Hybridization
- Topic: Question about Hybridized Orbitals
- Replies: 5
- Views: 35
Re: Question about Hybridized Orbitals
Hybridization is a "mixing" of atomic orbitals in terms of energy. So, the hybridized orbital sp^3 is a mixing of one s and 3 p orbitals in terms of energy. Since this is true, the sp^3 hybrid orbital will have more energy than an unhybridized s orbital and less energy than a hybridized p ...
- Sat Nov 28, 2020 4:05 pm
- Forum: Hybridization
- Topic: e density
- Replies: 30
- Views: 138
Re: e density
Yes, every bond is considered a region of electron density. Remember that a double bond and triple bond are bond considered one region of electron density, even though there is more than one bond.
- Sat Nov 28, 2020 4:03 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: H2O VSEPR
- Replies: 27
- Views: 147
Re: H2O VSEPR
it would be bent
there are 4 total electron density regions, with two being lone pair electrons and 2 being bonds
there are 4 total electron density regions, with two being lone pair electrons and 2 being bonds
- Sat Nov 28, 2020 4:01 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Polarity and Shape
- Replies: 13
- Views: 93
Re: Polarity and Shape
A molecule is polar if the dipoles on the diagram do not cancel out. So, the bonds themselves must be polar (there must be an electronegativity difference between the 2 atoms) and the bonds cannot cancel out, so there is a charge separation element too.
- Sat Nov 28, 2020 4:00 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Delocalized Pi Bond
- Replies: 7
- Views: 38
Re: Delocalized Pi Bond
delocalized pi bonds occur when the molecule with the pi bond has resonance. Remember that resonance structures have atoms that all have the same bond lengths. For a resonance structure with double and single bonds, the actual bond length is in between double and single. Because all bond lengths hav...
- Sat Nov 28, 2020 3:51 pm
- Forum: Hybridization
- Topic: Hybridization Explanation
- Replies: 6
- Views: 73
Re: Hybridization Explanation
Hybridization is a mathematical model that can be thought as a "mixing" of several orbitals in terms of energy. For ex, sp^2 hybridization creates a hybrid orbital that is a "mix" of one "s" and 2 "p" orbitals to create an sp^2 orbital that has an energy level...
- Thu Nov 19, 2020 3:58 pm
- Forum: Coordinate Covalent Bonds
- Topic: Identifying Lewis Acid and Lewis Base
- Replies: 3
- Views: 57
Re: Identifying Lewis Acid and Lewis Base
Lewis bases- donate an electron pair in coordinate covalent bond. For atoms without a charge, look for lone pairs on the atoms which can be easily donated. Lewis acids- accept a lone pair of electrons in a coordinate covalent bond. For atoms without a charge, look for atoms like B that do not have a...
- Thu Nov 19, 2020 3:57 pm
- Forum: Electronegativity
- Topic: Periodic trend
- Replies: 17
- Views: 150
Re: Periodic trend
Electronegative, electron affinity, and ionization energy all have the same trends. They increase across a period, and decrease down a group. ionization energy has one exception- O has a lower ionization energy than N for electron-electron repulsion reasons (N has 3 unpaired e's in its p subshell wh...
- Thu Nov 19, 2020 3:54 pm
- Forum: Polarisability of Anions, The Polarizing Power of Cations
- Topic: Polarizability vs Polarizing Power in anions/cations & bonding
- Replies: 10
- Views: 65
Re: Polarizability vs Polarizing Power in anions/cations & bonding
Polarizability pertains to the anion. It is a measure of how easily their electrons can be distorted (and moved into the shared region, which is on the internuclear axis between two atoms in a bond). Larger anions have more electrons that are not as closely held to the nucleus, so they are more pola...
- Thu Nov 19, 2020 3:51 pm
- Forum: Formal Charge and Oxidation Numbers
- Topic: Best Formal Charge Equations
- Replies: 24
- Views: 133
Re: Best Formal Charge Equations
The best way to calculate formal charge is (number of valence electrons) - (dots) - (lines). Professor Lavelle covered another formula in class, but the formula I provided gives the same answer and is a lot faster.
- Thu Nov 19, 2020 3:49 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: bond angles
- Replies: 16
- Views: 260
Re: bond angles
We can predict the bond angles using VSPR, which is based on electron electron repulsion between lone pair electrons and bonding pair electrons. In terms of finding the exact value of the bond angles, this may not be always known, as many times the angles are described as being "less than"...
- Sat Nov 14, 2020 9:20 pm
- Forum: Resonance Structures
- Topic: bond length
- Replies: 6
- Views: 25
Re: bond length
Look at the trends Bond length depends on the number of bonds (double, single, triple) and the size of the atoms You cant look at the periodic table for the number of bonds, but you can look for the size of the atoms atomic radius increases down a group (higher energy levels occupied with more elect...
- Sat Nov 14, 2020 9:18 pm
- Forum: Polarisability of Anions, The Polarizing Power of Cations
- Topic: increasing polarizability
- Replies: 5
- Views: 48
Re: increasing polarizability
Agreeing with what everyone has said, you look at the atomic radius (larger atomic radius means the electrons are less tightly held and more easily distorted). In terms of looking at this on the periodic table, Cl- is clearly the largest atom of all the ones on the list (because its on a lower perio...
- Sat Nov 14, 2020 9:12 pm
- Forum: Dipole Moments
- Topic: Textbook discrepancy
- Replies: 6
- Views: 45
Re: Textbook discrepancy
Hi, I was also confused about this. But, since in lecture and all of the peer review sessions they have the arrow pointing to the more electronegative atom, I think that we should use this as the standard. It makes sense because the arrow represents the pulling of the electrons, and the more electro...
- Sat Nov 14, 2020 9:10 pm
- Forum: Lewis Structures
- Topic: Recognizing lowest formal charge
- Replies: 11
- Views: 50
Re: Recognizing lowest formal charge
I dont think there is any set rule, but I like to draw the lewis structure with the lowest formal charge that I can think of and then quickly draw some other options just to make sure that it does in fact have the lowest possible formal charge. Helpful tips would be to make sure that the most electr...
- Sat Nov 14, 2020 9:08 pm
- Forum: Octet Exceptions
- Topic: Octet Exceptions Rules
- Replies: 3
- Views: 23
Re: Octet Exceptions Rules
The exceptions are: less than an octet: H, He- 2 electrons (usually) Li, Be - 4 electrons usually Al and Boron- won't always have less than an octet, but if they do they'll usually have 6 electrons in the valence radicals (7 valence e's) In terms of explaining this, it makes sense that H and He have...
- Sun Nov 08, 2020 11:47 am
- Forum: Formal Charge and Oxidation Numbers
- Topic: Why do we use formal charge?
- Replies: 14
- Views: 116
Re: Why do we use formal charge?
Usually, we are looking to draw a lewis structure with a formal charge equal to zero, because this is the most stable form. Many times there are many different possible ways we can bond atoms in a molecule via a lewis structure, so considering formal charge is the way to figure out the "correct...
- Sun Nov 08, 2020 11:44 am
- Forum: Resonance Structures
- Topic: Bond lengths
- Replies: 20
- Views: 143
Re: Bond lengths
I don't think that you have to do that, at least for this class! However, I know that a double bond is stronger than a single bond, so that may be why you draw the double bonds as shorter in some cases.
- Sun Nov 08, 2020 11:43 am
- Forum: Formal Charge and Oxidation Numbers
- Topic: Formal Charge
- Replies: 11
- Views: 347
Re: Formal Charge
It doesn't matter if its an electron, formal charge is the # of valence e's - (# dots) - (#lines) to put it simply. So if you get -1 when you do this, the Formal Charge would be -1.
- Sun Nov 08, 2020 11:42 am
- Forum: Lewis Structures
- Topic: Atom in the middle of a lewis structure
- Replies: 7
- Views: 40
Re: Atom in the middle of a lewis structure
Lower ionization energy (and thus lower electronegativity) has more space to accept bonds/electrons. So, it goes in the middle because this atom generally has the highest number of bonds in the atom
- Sun Nov 08, 2020 11:39 am
- Forum: Ionic & Covalent Bonds
- Topic: Atomic Radius
- Replies: 38
- Views: 224
Re: Atomic Radius
As you move right across a period, the number of protons increases (positive charge). This positive charge "pulls in" the negative electrons, so the electrons are closer to the nucleus (where the protons are). Because the electrons are more pulled closer to the nucleus as the number of pro...
- Fri Oct 30, 2020 9:36 am
- Forum: Quantum Numbers and The H-Atom
- Topic: Energy Level Excited
- Replies: 8
- Views: 69
Re: Energy Level Excited
For an electron to be excited, it has to absorb a photon of light with a frequency (v) that matches the specific energy difference between two energy levels/shells. After the electron is excited, it will eventually come back down to the lower energy state, emitting a photon with the same frequency/e...
- Fri Oct 30, 2020 9:31 am
- Forum: *Shrodinger Equation
- Topic: The Hamiltonian
- Replies: 8
- Views: 126
Re: The Hamiltonian
The Hamiltonian of the wave function is equal to the energy of the wave function. Since the wave function is sin theta/cos theta, the Hamiltonian is taking the double derivative of the wave function (sin theta), which gives you back sin theta. because of this fact, you are given back the wave functi...
- Fri Oct 30, 2020 9:28 am
- Forum: Trends in The Periodic Table
- Topic: In class question
- Replies: 8
- Views: 62
Re: In class question
I believe that the measure of the atomic radius still exists, but at least for our purposes, we cannot calculate it from just a lone atom, only when it is interaction with another.
- Fri Oct 30, 2020 9:27 am
- Forum: Wave Functions and s-, p-, d-, f- Orbitals
- Topic: Nodal Plane Importance
- Replies: 9
- Views: 50
Re: Nodal Plane Importance
The position of a nodal plane also further differentiates an orbital from another (px, py, pz for example). The position of the nodal plane implies how the orbital is shaped and oriented.
- Fri Oct 30, 2020 9:25 am
- Forum: Quantum Numbers and The H-Atom
- Topic: quantum number 4
- Replies: 6
- Views: 67
Re: quantum number 4
I think the biggest reason for knowing the fourth quantum number is to understand that no 2 electrons can have the same 4 quantum numbers in an atom. The fourth quantum number provides the direction of spin.
- Sun Oct 25, 2020 10:16 am
- Forum: Properties of Light
- Topic: Wavelength
- Replies: 14
- Views: 91
Re: Wavelength
The equations will give you the wavelength in meters (as long as all of the values you plug in are in SI units). However, you can give the answer in m or nm, but since our midterm is multiple choice, it should be clear which one they are asking for.
- Sun Oct 25, 2020 10:14 am
- Forum: Heisenberg Indeterminacy (Uncertainty) Equation
- Topic: Question about the Delta X and what it stands for
- Replies: 6
- Views: 53
Re: Question about the Delta X and what it stands for
When it says delta x is equal to 10 m/s + or - 3, then the uncertainty in x would be 6
when it says delta x is 1% of the radius (or anything along these lines), take 1% of the specified value
When an electron or something is confined to the atom, the uncertainty is the diameter of the atom
when it says delta x is 1% of the radius (or anything along these lines), take 1% of the specified value
When an electron or something is confined to the atom, the uncertainty is the diameter of the atom
- Sun Oct 25, 2020 10:12 am
- Forum: DeBroglie Equation
- Topic: Light and momentum
- Replies: 7
- Views: 58
Re: Light and momentum
Hi! Confirming what has already been said, light has momentum in the form of energy even though it does not have a mass. So, photons do have momentum but because they do not have mass, you cannot use the debroglie equation for a photon/EMR
- Sun Oct 25, 2020 10:10 am
- Forum: Properties of Electrons
- Topic: intensity vs energy
- Replies: 29
- Views: 254
Re: intensity vs energy
I went to a UA session about this, and the statement technically depends on whether light is acting like a wave or a particle. If light is acting like a particle, increasing intensity increases the amplitude of the wave, so it would increase energy. If light is acting like a wave, increasing intensi...
- Sun Oct 25, 2020 10:08 am
- Forum: Photoelectric Effect
- Topic: Intensity vs. Frequency
- Replies: 22
- Views: 140
Re: Intensity vs. Frequency
For a particle-model, increasing intensity means increasing the amplitude, which increases the energy. This refers to increasing the intensity (brightness) of the light For a wave-like model, increasing intensity does not increase the energy because the EMR is acting like a particle and not a wave. ...
- Fri Oct 16, 2020 4:56 pm
- Forum: Einstein Equation
- Topic: E=hv vs E=pc?
- Replies: 8
- Views: 325
Re: E=hv vs E=pc?
Both equations are valid for calculating the energy of the photon. You would use either equation depending on what variables you are given.
- Fri Oct 16, 2020 4:54 pm
- Forum: Properties of Light
- Topic: "Intensity"
- Replies: 20
- Views: 134
Re: "Intensity"
Here are the general rules: Light can have both wave and particle properties, both are valid, but we just refer to light as a wave or particle depending on the situation. When we say light is acting like a wave, increasing intensity means increasing the amplitude of the wave, which increases energy ...
- Fri Oct 16, 2020 4:46 pm
- Forum: DeBroglie Equation
- Topic: Question about post-module assessment
- Replies: 5
- Views: 95
Re: Question about post-module assessment
This is correct. Every day objects do not demonstrate diffraction patterns because their masses are large, so the value of their wavelength from the equation wavelength=h/momentum yields an extremely small wavelength. Because their wavelengths are so extremely small, we cannot measure/notice wavelik...
- Fri Oct 16, 2020 4:43 pm
- Forum: Properties of Electrons
- Topic: Electron Transition
- Replies: 7
- Views: 36
Re: Electron Transition
An electron transition means that an electron is either absorbing a photon (absorption) and going to a higher energy level (a higher n). An electron transition to a lower energy level entails the electron emitting a photon of light. The energy required or released for an electron to make an energy t...
- Fri Oct 16, 2020 4:40 pm
- Forum: Photoelectric Effect
- Topic: photoelectric effect
- Replies: 17
- Views: 135
Re: photoelectric effect
yes, the threshold energy is the same as the work function. remember that this is equal to the amount of energy that is required to remove from electron from a certain element/atom (ejecting it so that the electron is no longer associated with the atom).
- Wed Oct 07, 2020 10:15 pm
- Forum: Accuracy, Precision, Mole, Other Definitions
- Topic: Writing a Formula Based Off of Compound Name (E.9)
- Replies: 6
- Views: 71
Re: Writing a Formula Based Off of Compound Name (E.9)
I also had this question. Fundamentals D (Nomenclature), which is part of the optional reading, is all about naming compounds and all the rules. It was very helpful and I would recommend looking at sections 1-4 if you're having difficulty because it really cleared it up for me!
- Wed Oct 07, 2020 10:06 pm
- Forum: Accuracy, Precision, Mole, Other Definitions
- Topic: E21 (molecules vs formula units)
- Replies: 3
- Views: 50
E21 (molecules vs formula units)
E.21 Calculate the amount (in moles) and the number of molecules and formula units (or atoms, if indicated) in (a) 10.0 g of alumina, Al 2 O 3 ; (b) 25.92 mg of hydrogen fluoride, HF HF; (c) 1.55 mg of hydrogen peroxide, H 2 O 2 ; (d) 1.25 kg of glucose, C 6 H 12 O 6 ; (e) 4.37 g of nitrogen as N N ...
- Wed Oct 07, 2020 9:55 pm
- Forum: Molarity, Solutions, Dilutions
- Topic: Solute versus solvent
- Replies: 5
- Views: 78
Re: Solute versus solvent
Hi, like others have said, the solute is the substance that is dissolved in the solvent. Just a tip to remember when dealing with dilution problems- the moles/amount of solute stays the same before and after you dilute a solution, only the concentration of the solute changes. The solute concentratio...
- Wed Oct 07, 2020 9:53 pm
- Forum: Significant Figures
- Topic: Which number determines sig figs of the answer?
- Replies: 26
- Views: 179
Re: Which number determines sig figs of the answer?
Supporting what others have said, the number of sig figs depends. For multiplication and division, use the smallest number of overall sig figs. For addition and subtraction, you look at the smallest number of decimal places and
- Wed Oct 07, 2020 9:49 pm
- Forum: Significant Figures
- Topic: intermediate calculations with sig figs
- Replies: 8
- Views: 75
intermediate calculations with sig figs
I know the rules of sig figs, but when we have problems that requires multiple steps/calculations, should we follow the rules of sig figs for each step, or should we have numbers with more sig figs than what is technically allowed and just make sure the final answer has the correct number of sig figs?