Search found 60 matches
- Fri Jan 15, 2021 11:59 am
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: the different Ks
- Replies: 7
- Views: 31
Re: the different Ks
Likewise, a denotes that it is an acid, and b denotes that it is a base.
- Fri Jan 15, 2021 11:58 am
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: the different Ks
- Replies: 7
- Views: 31
Re: the different Ks
They are all the equilibrium constants, but the different subscripts can denote differences in what the equilibrium constant is for. For example, Kw is for water, so the w is for water, Kp is for when there are gases, and their measurements are in pressures, so p=pressure, and Kc is when we are deal...
- Fri Jan 15, 2021 11:55 am
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: lecture 5 question
- Replies: 13
- Views: 55
Re: lecture 5 question
I think he wants us to know the strong acids and bases that are listed in the book. In an equation, the conjugate base/acid is the base/acid once it has lost or gained a proton.
- Fri Jan 15, 2021 11:51 am
- Forum: Ideal Gases
- Topic: Question 4 Sapling [ENDORSED]
- Replies: 8
- Views: 118
Re: Question 4 Sapling [ENDORSED]
Sometimes it helps to double check your math in a computer system that solves quadratics so you can see if the math is the problem or the set up.
- Fri Jan 15, 2021 11:50 am
- Forum: Ideal Gases
- Topic: Q and K relationship
- Replies: 20
- Views: 80
Re: Q and K relationship
In terms of comparing Q and K, I use that if Q<K, I think of it as K moved left to get to Q, following the arrow of the sign, so to go back, it needs to go right, so the reaction favors the products and vice versa.
- Sun Jan 10, 2021 3:40 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: sapling week 1 #9
- Replies: 15
- Views: 174
Re: sapling week 1 #9
I'm confused on whether to use 1/kc or just kc. If I use the original kc, I get 2 positive answers for x, and when I use the reverse quotient, I get the incorrect answer for the problem. Can anyone walk me through which values they used? I used the forward reaction, and the kc value that I found fr...
- Sun Jan 10, 2021 3:22 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: sapling week 1 #9
- Replies: 15
- Views: 174
Re: sapling week 1 #9
Can we find x using either kc or 1/kc? As long as we put the respective products and reactants in their correct position depending on whether the reaction is reversed or forward?
- Thu Jan 07, 2021 2:51 pm
- Forum: Ideal Gases
- Topic: PV=nRT
- Replies: 72
- Views: 440
Re: PV=nRT
So is R the same constant as the one we used before on the equation sheet?
- Wed Jan 06, 2021 1:29 pm
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: sapling #2
- Replies: 8
- Views: 45
Re: sapling #2
I used the same steps, but when I put the numbers in my calculator I got 0.0223
- Fri Dec 11, 2020 11:05 am
- Forum: Identifying Acidic & Basic Salts
- Topic: Categorizing Salts
- Replies: 3
- Views: 35
Re: Categorizing Salts
So only the conjugate acids or bases of weak acids or bases will affect the pH?
- Fri Dec 11, 2020 11:03 am
- Forum: Polyprotic Acids & Bases
- Topic: Polyprotic Acids and Bases
- Replies: 4
- Views: 43
Re: Polyprotic Acids and Bases
Yes, so the common ones have anions with a charge of -2 or more, such as sulfate and phosphate, and these can have either one, two, or sometimes three hydrogens.
- Wed Dec 09, 2020 11:14 am
- Forum: Conjugate Acids & Bases
- Topic: Conjugates and Charge
- Replies: 8
- Views: 46
Re: Conjugates and Charge
The structure of the molecule won't change the overall charge of the molecule (formal charges must add to same overall charge), so typically if you take the acid or base, and either add a proton or remove one, it will either gain a charge or lose a charge to form the conjugate acid or base.
- Wed Dec 09, 2020 11:04 am
- Forum: Calculating pH or pOH for Strong & Weak Acids & Bases
- Topic: H3O+ versus H+
- Replies: 16
- Views: 113
Re: H3O+ versus H+
It's just the difference between specifying if the H+ ion is bonded to the water or not. I think Dr. Lavelle wants us to practice using the full hydronium ion since the proton would be binding to a water molecule.
- Wed Dec 09, 2020 11:02 am
- Forum: Identifying Acidic & Basic Salts
- Topic: Salt Acidic Ions
- Replies: 3
- Views: 23
Re: Salt Acidic Ions
I was confused about some of the salt stuff too. In this case, isn't NH3 a weak base, and the resulting acid is just a conjugate acid?
- Wed Dec 09, 2020 10:59 am
- Forum: Calculating pH or pOH for Strong & Weak Acids & Bases
- Topic: Sapling Week 10 question
- Replies: 6
- Views: 58
Re: Sapling Week 10 question
I notice that all the problems above are labeled to be at 25 degrees Celsius. How would the temperature affect the pH of substances? I think that when the temperature changes, it can change the rate of reaction, but I think 25 degrees Celsius is about room temperature, so it is specifying that. Som...
- Wed Dec 09, 2020 10:54 am
- Forum: Acidity & Basicity Constants and The Conjugate Seesaw
- Topic: pH vs pKa
- Replies: 9
- Views: 104
Re: pH vs pKa
So pKa is the -log(Ka)?, which dictates what the pH is? Or is there a different equation for pKa?
- Sun Dec 06, 2020 4:53 pm
- Forum: Amphoteric Compounds
- Topic: How to know if a molecule is amphoteric
- Replies: 9
- Views: 100
Re: How to know if a molecule is amphoteric
How can we identify if a molecule is amphoteric or not? Other than water being a common one?
- Sun Dec 06, 2020 4:50 pm
- Forum: Conjugate Acids & Bases
- Topic: Conjugate acids vs conjugate base
- Replies: 12
- Views: 74
Re: Conjugate acids vs conjugate base
So the acid gives a proton and the base accepts it, so the conjugate base of an acid would lose an H+ ion, and the conjugate acid of a base would gain an H+ ion?
- Sun Dec 06, 2020 4:48 pm
- Forum: Properties & Structures of Inorganic & Organic Acids
- Topic: Effect of Electronegativity on the Strength of Acids
- Replies: 4
- Views: 50
Re: Effect of Electronegativity on the Strength of Acids
Is the acid itself being more electronegative make it a stronger acid or is it the conjugate base ?
- Sun Nov 29, 2020 7:06 pm
- Forum: Hybridization
- Topic: Sapling #12
- Replies: 27
- Views: 176
Re: Sapling #12
I always make sure that the number of regions of electron density match up with the number of hybridized orbitals. Sometimes I try to read the hybridized orbitals as s1p1, s1p2, s1p3... etc rather than just sp or sp2. This makes it clearer when I add it up so that I don't miss that s counts as one o...
- Sun Nov 29, 2020 7:03 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Sapling #20
- Replies: 5
- Views: 64
Re: Sapling #20
Always check to see if there are unnecessary formal charges on atoms, and if there are any that can be zero by adding or removing a bond in place of a lone pair!
- Sun Nov 29, 2020 7:02 pm
- Forum: Hybridization
- Topic: Lecture #23
- Replies: 13
- Views: 115
Re: Lecture #23
Are electrons only delocalized when the shape is a ring or can it happen with any molecules that have resonance structures?
- Sun Nov 29, 2020 7:01 pm
- Forum: Hybridization
- Topic: Sapling #18
- Replies: 10
- Views: 100
Re: Sapling #18
I believe this is figured out by looking at pi bonding. whenever you have an even number there are enough pi bonds to lock the carbon into a single plane. This is because the pi bond does not allow for rotation. Every pi bond is formed at a 90 degree Angle to the other, so even numbers would go bac...
- Sun Nov 29, 2020 6:58 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: sigma vs pi bonds
- Replies: 33
- Views: 185
Re: sigma vs pi bonds
Do pi bonds only occur in double and triple bonds? Or can be somewhere else where there are orbitals side by side?
- Sun Nov 29, 2020 6:57 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: #13 Sapling Week 8
- Replies: 18
- Views: 98
Re: #13 Sapling Week 8
Since each carbon atom has four bonded regions, that would make it tetrahedral!
- Sun Nov 29, 2020 6:56 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Linear Shape and Lone Pairs
- Replies: 8
- Views: 79
Re: Linear Shape and Lone Pairs
Another common example is nitrogen triple bonded to a central atom, having two lone pairs on the opposite end of the atom. I think if there are two regions of electron density (whether bonded or lone pairs), it can be linear
- Mon Nov 23, 2020 12:51 pm
- Forum: Formal Charge and Oxidation Numbers
- Topic: Formal Charge and Ions
- Replies: 7
- Views: 81
Re: Formal Charge and Ions
When the formal charges are added, they should equal the overall charge of the molecule, and they favor the structure that has the most atoms with a formal charge of 0.
- Mon Nov 23, 2020 12:50 pm
- Forum: Ionic & Covalent Bonds
- Topic: Polar/ Nonpolar
- Replies: 23
- Views: 167
Re: Polar/ Nonpolar
Are there dipole moments between all atoms with a difference in electronegativity or just the polar bonds?
- Mon Nov 23, 2020 12:48 pm
- Forum: Lewis Structures
- Topic: Week 8 Sapling Homework #18
- Replies: 2
- Views: 25
Re: Week 8 Sapling Homework #18
For larger molecules like these, is the order that the formula is written in the same order of the molecules in its structure? At least for the most part?
- Mon Nov 23, 2020 12:47 pm
- Forum: Hybridization
- Topic: Sigma vs Pi Bonds
- Replies: 10
- Views: 64
Re: Sigma vs Pi Bonds
How do we tell which way the internuclear axis is lined up?
- Mon Nov 16, 2020 6:56 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: Textbook Problem 2A.5
- Replies: 2
- Views: 35
Textbook Problem 2A.5
Give the ground-state electron configuration expected for each of the following ions: (a) Cu+
I was doing this problem and was confused as to why the answer was [Ar]3d10 instead of [Ar]4s2 3d8? Does it fill up the 3d block before the 4s block?
I was doing this problem and was confused as to why the answer was [Ar]3d10 instead of [Ar]4s2 3d8? Does it fill up the 3d block before the 4s block?
- Thu Nov 12, 2020 3:27 pm
- Forum: Coordinate Covalent Bonds
- Topic: Lewis Acid Identification
- Replies: 3
- Views: 52
Re: Lewis Acid Identification
If Lewis acids are always electron deficient, can they always form coordinate covalent bonds? Or is that only in certain cases where the base has a lone pair to contribute?
- Thu Nov 12, 2020 3:25 pm
- Forum: Polarisability of Anions, The Polarizing Power of Cations
- Topic: Distortion
- Replies: 8
- Views: 61
Re: Distortion
Is an anion always the atom that is polarizable and the cation is what can have high polarizing ability?
- Thu Nov 12, 2020 3:22 pm
- Forum: Polarisability of Anions, The Polarizing Power of Cations
- Topic: Polarizability
- Replies: 6
- Views: 45
Re: Polarizability
Between two anions in the same row, would an anion with a -2 charge be more or less polarizable than an anion with a -1 charge?
- Thu Nov 12, 2020 3:20 pm
- Forum: Dipole Moments
- Topic: Sapling #17
- Replies: 7
- Views: 59
Re: Sapling #17
Are london dispersion forces present in all nonpolar molecules?
- Thu Nov 12, 2020 3:17 pm
- Forum: Dipole Moments
- Topic: Sapling Question #13
- Replies: 5
- Views: 54
Re: Sapling Question #13
So other hydrogen atoms can form hydrogen bonds to any N,O, or F molecule that has unpaired electrons in the valence shell? Or do they need to be N,O, and F atoms that are already bonded with a hydrogen?
- Mon Nov 09, 2020 11:47 am
- Forum: Bond Lengths & Energies
- Topic: Bond Length
- Replies: 22
- Views: 353
Re: Bond Length
So shorter bond lengths have higher energies right? Since they are stronger the energy of the bond is more negative, but is it still considered higher energy?
- Mon Nov 09, 2020 11:45 am
- Forum: Octet Exceptions
- Topic: Expanded Octets
- Replies: 6
- Views: 27
Re: Expanded Octets
I know that the elements in the 3d block and also the 3p block can have expanded octets, but how many additional electrons can they fit? Is it only one more orbital (making 10) for p-block, and more for d block?
- Mon Nov 09, 2020 11:43 am
- Forum: Dipole Moments
- Topic: Dispersion/London/Van der Waals/Induced Dipole-Induced Dipole
- Replies: 6
- Views: 55
Re: Dispersion/London/Van der Waals/Induced Dipole-Induced Dipole
What types of molecules are capable of inducing a dipole moment?
- Sun Nov 01, 2020 3:04 pm
- Forum: Ionic & Covalent Bonds
- Topic: Strength of bonds
- Replies: 13
- Views: 90
Re: Strength of bonds
Does it matter if the covalent bond is polar or nonpolar in terms of its strength?
- Sun Nov 01, 2020 3:02 pm
- Forum: Trends in The Periodic Table
- Topic: Oxygen and Ionization Energy
- Replies: 9
- Views: 43
Re: Oxygen and Ionization Energy
Are we supposed to know all of the exceptions to the periodic trends, or is it sufficient to understand the trends and why there are a few atoms that don't follow these rules?
- Sun Nov 01, 2020 2:59 pm
- Forum: Wave Functions and s-, p-, d-, f- Orbitals
- Topic: Orbital vs. Subshell
- Replies: 13
- Views: 93
Re: Orbital vs. Subshell
So there are only 4 possible subshells, which would be s, p, d, and f?
- Tue Oct 27, 2020 12:49 pm
- Forum: *Shrodinger Equation
- Topic: Wave function
- Replies: 8
- Views: 97
Re: Wave function
Hi. I am still a bit confused about this. Is it correct to say that the Hamiltonian value represents the probability of finding the electron while the energy wave function represents the orbital itself? It would be great if someone could explain what exactly the equation is representing with the tw...
- Tue Oct 27, 2020 12:45 pm
- Forum: *Shrodinger Equation
- Topic: Shrodinger Equation on Midterm 1
- Replies: 3
- Views: 78
Re: Shrodinger Equation on Midterm 1
I was under the impression we would only have to know the first part (H times the wave function = E times the wave function), however I was also curious if we needed to know the other pieces that are on the equation sheet.
- Fri Oct 23, 2020 11:02 am
- Forum: *Shrodinger Equation
- Topic: Wave function
- Replies: 8
- Views: 97
Re: Wave function
Right now, can we consider the wave function to just be simplified to the version where we treat it like a sine function?
- Fri Oct 23, 2020 11:01 am
- Forum: Photoelectric Effect
- Topic: Intensity vs. Frequency
- Replies: 22
- Views: 140
Re: Intensity vs. Frequency
So just to clarify: an increase in frequency increases the energy of the wave and the number of photons, but not the energy per photon? And this is what the photoelectric effect is? That the waves have particle like properties where only one photon interacts with an electron, and therefore changing ...
- Fri Oct 23, 2020 10:58 am
- Forum: Photoelectric Effect
- Topic: Sapling HW Weeks 2, 3, 4 Question #9
- Replies: 10
- Views: 104
Re: Sapling HW Weeks 2, 3, 4 Question #9
What is the difference between the question asking what the maximum wavelength is and just simply the wavelength? Does it change how we need to solve it?
- Fri Oct 23, 2020 10:57 am
- Forum: Heisenberg Indeterminacy (Uncertainty) Equation
- Topic: Midterm 1
- Replies: 18
- Views: 206
Re: Midterm 1
I think Dr. Lavelle specifically changed the order of questions on the Sapling homework so that problems 1-19 were wat would be on the midterm, so I would study those topics to the extent they are talked about in the homework.
- Fri Oct 23, 2020 10:55 am
- Forum: Heisenberg Indeterminacy (Uncertainty) Equation
- Topic: Problem 1B.25
- Replies: 3
- Views: 69
Re: Problem 1B.25
If we manipulate other equations based on the values given, and we set the two equal to each other, does it matter that the one equation has a greater than or equal to symbol? For example, if we have delta p = m(delta v), and delta p is greater than or equal to h/(delta x)(4pi), can we still substit...
- Sun Oct 18, 2020 5:20 pm
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: 1.A.15 on Homework
- Replies: 6
- Views: 48
Re: 1.A.15 on Homework
I also get confused about the n1 and n2 terms. Is n1 the final energy level and n2 is the initial? I thought it was the other way around but problem 8 on the sapling homework has it that way.
- Sun Oct 18, 2020 5:18 pm
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: Rydberg Equation and Empirical Equation
- Replies: 4
- Views: 28
Re: Rydberg Equation and Empirical Equation
I think that Dr. Lavelle said we wouldn't be working with the equations that are used for other atoms that aren't hydrogen, but it is possible to tweak the equation so that it would work in other scenarios.
- Wed Oct 14, 2020 11:58 am
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: 1.A.15 on Homework
- Replies: 6
- Views: 48
Re: 1.A.15 on Homework
Can't we also just look at the figure that shows the wavelengths and series? Since it is in the UV series, the final energy level =1, and since it is the second line in the series, it goes from level 3 to 1? The first line represents it going from 2 to 1, so just add one each time?
- Wed Oct 14, 2020 11:21 am
- Forum: Properties of Light
- Topic: Photoelectric spectrum
- Replies: 24
- Views: 163
Re: Photoelectric spectrum
Oh wait I meant shorter wavelength, but thank you!
- Wed Oct 14, 2020 11:02 am
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: Atomic Spectra Lecture question
- Replies: 5
- Views: 50
Atomic Spectra Lecture question
When Dr. Lavelle was explaining that each atom will only absorb/emit a specific frequency of light, does this also mean that each atom requires a different amount of energy to excite an electron from its ground state to the next level?
- Wed Oct 14, 2020 10:25 am
- Forum: Properties of Light
- Topic: Photoelectric spectrum
- Replies: 24
- Views: 163
Re: Photoelectric spectrum
Adding on to memorizing the wavelengths, are we also supposed to know things like the frequencies or energy of each one, or can we just understand that higher frequency correlates with longer wavelength and more energy?
- Fri Oct 09, 2020 10:27 am
- Forum: Limiting Reactant Calculations
- Topic: Limiting reactants in all chemical rxns?
- Replies: 18
- Views: 148
Re: Limiting reactants in all chemical rxns?
If you had the perfect amount of two reactants for them to react with one another and there to be no excess of anything after, would you say this equation has two limiting reactants or none?
- Wed Oct 07, 2020 12:21 pm
- Forum: Empirical & Molecular Formulas
- Topic: Fundamental F. 17
- Replies: 6
- Views: 75
Re: Fundamental F. 17
For formulas with C,H, and O, I think they follow that order, but outside of carbon being first and hydrogen second, I've never seen a formal description of what order to write them in.
- Wed Oct 07, 2020 12:18 pm
- Forum: Molarity, Solutions, Dilutions
- Topic: G.21 Homework Problem
- Replies: 7
- Views: 73
Re: G.21 Homework Problem
For the textbook readings and exercises: we do these for practice, but we don't turn it in online? Or is there somewhere we are supposed to upload our work to?
- Wed Oct 07, 2020 12:16 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)
So are we supposed to know how to write a formula for a given molecule based on its prefixes and ending? Should I review the difference between endings such as -ide vs -ate, and things like that?
- Wed Oct 07, 2020 12:13 pm
- Forum: Significant Figures
- Topic: When are sig figs applied?
- Replies: 12
- Views: 104
Re: When are sig figs applied?
I agree with all of these! I've always done it at the end, as long as you note at the beginning what number of sig figs you should round to at the end. I find it easier to do that when I first read the problem so that I don't get confused later on.