Search found 64 matches
- Fri Mar 15, 2019 8:31 am
- Forum: Second Order Reactions
- Topic: integrating equations
- Replies: 2
- Views: 570
Re: integrating equations
on the unit outlines, some bullet points do state that we should know how to derive certain equations (like integrated rate laws). I would know it just in case; Dr. Lavelle went over the process several times in lecture so it could definitely be something we're tested on.
- Fri Mar 15, 2019 8:29 am
- Forum: Reaction Mechanisms, Reaction Profiles
- Topic: Rate constants at equilibrium
- Replies: 5
- Views: 646
Re: Rate constants at equilibrium
no, although K=k1/k1' that doesn't mean that k1=k1'
- Wed Mar 13, 2019 9:38 am
- Forum: Arrhenius Equation, Activation Energies, Catalysts
- Topic: Arrhenius Equation
- Replies: 1
- Views: 251
Re: Arrhenius Equation
The "A" is known as the frequency factor, or the pre-exponential factor. This represents the amount of times a collision between molecules happens at the correct orientation.
- Tue Mar 12, 2019 8:05 am
- Forum: First Order Reactions
- Topic: first order intergrated rate laws
- Replies: 2
- Views: 364
Re: first order intergrated rate laws
Usually, if you're given components of the integrated rate law (such as initial concentration, final concentration, k or time) and told to solve for one variable, you can plug it into the equation and solve. As far as key words go, the question will have to tell you that the reaction is first order....
- Sun Mar 10, 2019 10:25 am
- Forum: Zero Order Reactions
- Topic: Deeming what Order a molecule is
- Replies: 2
- Views: 270
Re: Deeming what Order a molecule is
When NO is doubled and the rate increases by 4, you have the equation 2^n=4. the 2^n represents the concentration of NO to the power of the order (n), and the 4 represents the rate. Therefore, n=2 and the NO is second order. When both NO and O2 are doubled and the rate of the reaction increases by 8...
- Wed Mar 06, 2019 9:02 am
- Forum: General Rate Laws
- Topic: Unit for reaction rates
- Replies: 4
- Views: 490
Re: Unit for reaction rates
The rate of the reaction will always be in terms of mol/L•s, but the units for k changes based on the overall order of the reaction. If order=1, the unit for k is s^-1. If order=2, the unit for k is L/mol•s. If order=3, the unit for k is L^2/mol^2•s.
- Mon Mar 04, 2019 2:32 pm
- Forum: General Rate Laws
- Topic: 7th Ed. 7A.15
- Replies: 2
- Views: 328
Re: 7th Ed. 7A.15
To calculate the order for C, I used experiments 1 and 4. I divided experiment 1 ([A]=10^x, [B]=100^y, [C]=700^z) by experiment 4 ([A]=10^x, [B]=100^y, [C]=400^z). The rates for exp 1/exp 4 are 2/2=1 (so your order for C will have to result in a rate of 1). [A] and [B] cancel out, so you're left wit...
- Sat Mar 02, 2019 11:28 am
- Forum: General Rate Laws
- Topic: Point of equilibrium
- Replies: 5
- Views: 524
Re: Point of equilibrium
When the graphs of reactants and products have leveled off and remain at a constant concentration, the system has reached equilibrium.
- Sat Mar 02, 2019 9:01 am
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Order of Cell Diagrams
- Replies: 13
- Views: 1609
Re: Order of Cell Diagrams
The solid should always come first, then aqueous and gas substances. The solid stands for the anode/cathode, so it should always go on the ends. As for the order of aqueous/gas solutions, I'm not too sure if there's any particular way to write them; Dr. Lavelle hasn't specified so I would think it d...
- Fri Mar 01, 2019 4:07 pm
- Forum: Method of Initial Rates (To Determine n and k)
- Topic: Gas phase products
- Replies: 3
- Views: 530
Re: Gas phase products
no, but it is safe to assume that the reverse reaction is very unlikely to occur.
- Mon Feb 25, 2019 2:34 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Adding Pt(s) to cell diagram
- Replies: 3
- Views: 382
Re: Adding Pt(s) to cell diagram
When the half-reaction for either reduction or oxidation doesn't contain a solid (reactants and products are both in aqueous form), you would have to use either Pt (s) or C (graphite) as the electrode. Usually, we use Pt (s).
- Thu Feb 21, 2019 11:15 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Anode and Cathode
- Replies: 4
- Views: 495
Re: Anode and Cathode
the anode is where oxidation takes place (the reaction that loses electrons; or electrons show up on the products side). the cathode is where reduction takes place (the reaction that gains electrons; or electrons show up on the reactants side). a good way to remember this is that anode and oxidation...
- Wed Feb 20, 2019 5:38 pm
- Forum: Galvanic/Voltaic Cells, Calculating Standard Cell Potentials, Cell Diagrams
- Topic: Electromotive force
- Replies: 2
- Views: 303
Re: Electromotive force
electromotive force is the difference in cell potential (Ecell) that gives rise to an electric current.
- Mon Feb 18, 2019 1:19 pm
- Forum: Gibbs Free Energy Concepts and Calculations
- Topic: Gibbs Free Energy Problems
- Replies: 3
- Views: 357
Re: Gibbs Free Energy Problems
we won't be expected to have standard enthalpies/entropies of formation memorized for any compound, unless enough information is given for use to solve otherwise. most likely it'll be given to us in the question if we're asked to solve for free energy.
- Wed Feb 13, 2019 8:57 am
- Forum: Entropy Changes Due to Changes in Volume and Temperature
- Topic: C
- Replies: 3
- Views: 348
Re: C
this value can either be Cv or Cp (equations for heat capacity of monoatomic ideal gases are on our equations sheet) depending on which one is constant in the reaction, volume or pressure.
- Wed Feb 13, 2019 8:54 am
- Forum: Entropy Changes Due to Changes in Volume and Temperature
- Topic: Midterm Prep Question
- Replies: 3
- Views: 414
Re: Midterm Prep Question
1. calculate the entropy from the ΔV, by using the equation ΔS=nRlnV2/V1
2. calculate the entropy from the ΔT, by using the equation ΔS=nCvlnT2/T1
3. since entropy is a state function, you can add these values together to get your total entropy of the change in volume and temperature.
2. calculate the entropy from the ΔT, by using the equation ΔS=nCvlnT2/T1
3. since entropy is a state function, you can add these values together to get your total entropy of the change in volume and temperature.
- Mon Feb 11, 2019 9:52 am
- Forum: Concepts & Calculations Using Second Law of Thermodynamics
- Topic: ideal gases and reactions
- Replies: 1
- Views: 240
Re: ideal gases and reactions
There are certain elements of a system that are true when the observed substance is an ideal gas. Cv and Cp do have specific equations, depending on whether that gas is monoatomic, linear, or nonlinear (equations are on equation sheet). There are other factors that are true, such as ΔU=0 for isother...
- Fri Feb 08, 2019 5:14 pm
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Question 8.67 b
- Replies: 1
- Views: 198
Re: Question 8.67 b
The values of enthalpy you should be using to calculate the total enthalpy of the reaction (ΔHrxn) are the bond enthalpies (ΔHb) and they will be given to you in a table. As for determining which bonds are broken/formed, I personally benefit from drawing out the Lewis Structures and from there, visu...
- Wed Feb 06, 2019 10:01 am
- Forum: Reaction Enthalpies (e.g., Using Hess’s Law, Bond Enthalpies, Standard Enthalpies of Formation)
- Topic: Units for Reaction Enthalpies
- Replies: 1
- Views: 250
Re: Units for Reaction Enthalpies
the enthalpy for a reaction is the heat released/abosrbed per mole in the reaction; therefore use kJ/mol
- Mon Feb 04, 2019 11:34 am
- Forum: Thermodynamic Definitions (isochoric/isometric, isothermal, isobaric)
- Topic: Combustion of Glucose
- Replies: 2
- Views: 353
Re: Combustion of Glucose
since the reaction is happening out in the open (open system), we can assume that the only pressure acting upon it is atmospheric pressure, which is constant (1 atm).
- Sat Feb 02, 2019 2:34 pm
- Forum: Thermodynamic Systems (Open, Closed, Isolated)
- Topic: Reversible rxn
- Replies: 5
- Views: 483
Re: Reversible rxn
A reversible process is one that is infinitely slow because it is at equilibrium (any slight change to the reaction can cause a shift, which is why it's called reversible). If the system is doing work on the surroundings, more work is done if the process goes by slowly (because then, less heat is lo...
- Wed Jan 30, 2019 1:30 pm
- Forum: Phase Changes & Related Calculations
- Topic: Water phase change graph
- Replies: 6
- Views: 1496
Re: Water phase change graph
The X axis represents temperature, while the Y axis represents heat. The slated lines represent the water at a set phase, increasing in temperature. As heat is supplied, the slope increases and the temperature of water rises, but the phase does not change. The straight lines represent water going th...
- Mon Jan 28, 2019 6:43 pm
- Forum: Thermodynamic Systems (Open, Closed, Isolated)
- Topic: reversible expansion
- Replies: 3
- Views: 330
Re: reversible expansion
usually, the final and initial volumes will be included in the question.
- Fri Jan 25, 2019 5:26 pm
- Forum: Phase Changes & Related Calculations
- Topic: 6th edition 8.11
- Replies: 2
- Views: 235
Re: 6th edition 8.11
(a) for this part of the problem, we use w=-(Pex)*(deltaV). from the question, we know that the change in volume is 1.20 L. w=-(1.00 atm)*(1.20 L) = -1.20 L atm. Then, convert to Joules. -1.20 L atm x (101.325 J/L atm) = -121.59 J. (b) since the expansion is reversible and isothermic, we use the equ...
- Wed Jan 23, 2019 12:49 pm
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: autoprotolysis
- Replies: 5
- Views: 678
autoprotolysis
will we be expected to derive 14 = pOH + pH from 10^-14=[H3O+][OH-] on the test?
- Mon Jan 21, 2019 4:05 pm
- Forum: Calculating pH or pOH for Strong & Weak Acids & Bases
- Topic: 6th edition 12.81
- Replies: 1
- Views: 218
Re: 6th edition 12.81
If Ka1>>Ka2 (which means if the number is at least 10^3 times bigger), only use the first deprotonation.
- Fri Jan 18, 2019 1:35 pm
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: Adding concentration vs amount
- Replies: 1
- Views: 227
Re: Adding concentration vs amount
Molarity is the measure of the amount of moles / liters of a substance in a reaction. Questions asking about the effect of adding or removing certain substances are usually looking for us to answer which reaction proceeds (the forward reaction which yields products, or the reverse reaction which yie...
- Wed Jan 16, 2019 11:10 am
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: Le Chatelier's Principle and Temperature Changes
- Replies: 3
- Views: 233
Re: Le Chatelier's Principle and Temperature Changes
An easier way to remember this is that if the reaction is endothermic and the temperature is increased, products are formed. If the reaction is exothermic and the temperature is increased, reactants are formed.
- Mon Jan 14, 2019 9:07 am
- Forum: Applying Le Chatelier's Principle to Changes in Chemical & Physical Conditions
- Topic: Types of Chemical Reactions
- Replies: 3
- Views: 256
Re: Types of Chemical Reactions
All chemical reactions require energy to break bonds OR release energy when new bonds are form. It's highly unlikely that these energies will equal one another within the same reaction and "cancel out", therefore each reaction is classified as either endothermic or exothermic. I don't thin...
- Thu Jan 10, 2019 5:00 pm
- Forum: Ideal Gases
- Topic: HW # 5G.5 7th edition
- Replies: 2
- Views: 213
Re: HW # 5G.5 7th edition
If you're having trouble solving part c, the way I did it was by multiplying the initial pressure of X2 (.1 bar)*(1-.545), to find the pressure of X2 molecules at equilibrium (.1 bar)*(100% X2 molecules - 54.5% decomposed X2 molecules). You'll get 0.0455 bar, which is the pressure of X2. To find the...
- Wed Jan 09, 2019 9:24 am
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: K
- Replies: 4
- Views: 326
K
When asked to write out the equilibrium constant for an equation, is Kp or Kc preferred?
- Wed Jan 09, 2019 9:20 am
- Forum: Equilibrium Constants & Calculating Concentrations
- Topic: Q and K
- Replies: 1
- Views: 147
Re: Q and K
Q is the reactant quotient, which is a number that changes throughout the course of the reaction, depending on how much product vs. reactant is formed. K is the equilibrium constant, which is an unchanging number that is specific to each equilibrium reaction. Q and K are calculated in the same way (...
- Fri Dec 07, 2018 1:59 pm
- Forum: Amphoteric Compounds
- Topic: Coordination compounds
- Replies: 1
- Views: 175
Re: Coordination compounds
On the test, I would write aqua as (OH2), as how it's listed on the table in the textbook.
- Fri Dec 07, 2018 1:56 pm
- Forum: Lewis Acids & Bases
- Topic: Weak Acids/Bases?
- Replies: 5
- Views: 737
Re: Weak Acids/Bases?
I'm not too sure about bases, but acid strength is determined by bond length and stability of the anion in the compound. The longer/weaker the bond between the atoms, and the more stable the anion, the stronger the acid. For example, HI is a stronger acid than HF because I is a larger atom than F, m...
- Fri Dec 07, 2018 1:50 pm
- Forum: Lewis Acids & Bases
- Topic: Bronsted vs Lewis
- Replies: 4
- Views: 402
Re: Bronsted vs Lewis
The definitions of Bronsted and Lewis acids/bases are different, therefore some compounds like AlCl3 can be one and not the other. Bronsted acid: proton donor Bronsted base: proton acceptor Lewis acid: electron acceptor Lewis base: electron donor Al cannot donate protons, but accepts electrons from ...
- Mon Dec 03, 2018 4:24 pm
- Forum: Naming
- Topic: Ligand Names
- Replies: 2
- Views: 293
Ligand Names
Do we need to memorize the ligand names listed in ONLY table 9C.1 for the final?
- Sun Dec 02, 2018 10:32 am
- Forum: Naming
- Topic: naming coordination compounds for the final
- Replies: 3
- Views: 411
naming coordination compounds for the final
On the syllabus it says we should " be familiar with the rules for naming coordination compounds". What exactly does this entail? Should we know how to name complicated compounds, or will we just be asked to state the general rules for naming?
- Fri Nov 30, 2018 1:47 pm
- Forum: Bronsted Acids & Bases
- Topic: Bronsted Acid
- Replies: 2
- Views: 223
Re: Bronsted Acid
the definition of a Bronsted Acid is "a solution that has an excess of H+ ions", which means that Bronsted Acids are basically proton donors. The strength of the acid is determined by it's dissociation, but just the sole fact that it dissociates to some extent isn't enough to label the com...
- Wed Nov 28, 2018 8:47 am
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Bond Angles
- Replies: 5
- Views: 623
Re: Bond Angles
Unfortunately there's no chart, you have to have all the bond angles memorized.
- Fri Nov 23, 2018 3:36 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Lone Pairs on the Central Atom
- Replies: 5
- Views: 543
Re: Lone Pairs on the Central Atom
Lone pairs do affect the shape of the VSEPR model. Since lone pairs count as a region of electron density, they contribute to the formation of the structure, therefore to the overall molecular shape as well (lone pair electrons repel the atoms further away and change the shape and bond angles). Howe...
- Wed Nov 21, 2018 11:17 am
- Forum: Lewis Structures
- Topic: Complete Lewis Structures
- Replies: 4
- Views: 478
Complete Lewis Structures
How can we tell when we're supposed to draw regular Lewis structures vs. the separated Lewis structures with charges? For questions 2B.9 and 2B.11 in the textbook (7th edition), the question is the same ("Draw the complete Lewis structure for each of the following compounds") yet the answe...
- Mon Nov 19, 2018 1:24 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: AXE formulas
- Replies: 1
- Views: 325
AXE formulas
For test 3 will we need to know the VSPER formulas / molecular shapes for compounds with more than 2 electron pairs on the central atom?
- Wed Nov 14, 2018 1:05 pm
- Forum: Administrative Questions and Class Announcements
- Topic: Octet Rule
- Replies: 6
- Views: 794
Re: Octet Rule
When drawing lewis structures, the first rule to fulfill is the octet rule. Formal charges come after, as a way to guide you to the correct structure by adding and rearranging double/triple bonds to lower the formal charges of each atom. However, the octet rule comes first. Each atom must have an oc...
- Wed Nov 14, 2018 12:56 pm
- Forum: Resonance Structures
- Topic: Formal Charge
- Replies: 13
- Views: 1443
Re: Formal Charge
Ideally, a nonzero formal charge should be located on the outer atoms rather than the central atom. If there's no way of avoiding a formal charge on the central atom, it should be the smallest nonzero formal charge out of all the atoms in the compound.
- Fri Nov 09, 2018 2:20 pm
- Forum: Dipole Moments
- Topic: Dipole induced-dipole
- Replies: 2
- Views: 251
Re: Dipole induced-dipole
A dipole - induced dipole is when 2 compounds, one of each kind (such as HCl which has a dipole moment and N2 which does not), are attracted to one another. N2 has a lone pair of electrons on each N atom, which is slightly negative, but not strong enough to have a dipole moment. When the slightly ne...
- Fri Nov 09, 2018 2:14 pm
- Forum: Lewis Structures
- Topic: Atoms with 8+ valence e-
- Replies: 6
- Views: 1028
Re: Atoms with 8+ valence e-
Elements in the 3rd period and below can have more than an octet because they can access their d orbital electrons, while other elements without d orbital electrons (in period 2, such as C,N,O) cannot, therefore restricting them to only having 8 electrons.
- Wed Nov 07, 2018 2:24 pm
- Forum: Polarisability of Anions, The Polarizing Power of Cations
- Topic: Dispersion/ Induced dipole-Induced dipole
- Replies: 2
- Views: 275
Re: Dispersion/ Induced dipole-Induced dipole
In induced dipole-induced dipole bonds, molecules from 2 compounds that do not have a dipole moment (like N-N) are attracted to each other due to slight charges acquired through the electron clouds of each molecule. The electrons surrounding an atom "fluctuate", and create a (+) or (-) cha...
- Tue Nov 06, 2018 10:36 am
- Forum: Bond Lengths & Energies
- Topic: Resonance Structures
- Replies: 4
- Views: 406
Re: Resonance Structures
Bond lengths are averaged in resonance hybrids; whether it's a single bond or double bond, the average between them is the number used for bond length in the molecule as a whole.
- Sat Nov 03, 2018 8:54 pm
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: Post-Module Q#42
- Replies: 1
- Views: 361
Re: Post-Module Q#42
I use the equation deltaE = -hR((1/nfinal^2) - (1/ninitial^2)) In this situation, since light is emitted, deltaE is negative as well, and deltaE can be rewritten as hv (h x nu). -hv = hR((1/nfinal^2) - (1/ninitial^2) The two negatives cancel out, and the two Planck's constants cancel out, so you're ...
- Wed Oct 31, 2018 11:58 pm
- Forum: Formal Charge and Oxidation Numbers
- Topic: Formal CHarge
- Replies: 5
- Views: 506
Re: Formal CHarge
The formal charge only pertains to each individual atom in a molecule. The molecule as a whole will always remain one indicated charge. For example, SO4^(-2) will always have the charge of -2, although depending on the structure of the molecule, the formal charges for the individual S and O atoms ma...
- Mon Oct 29, 2018 6:15 pm
- Forum: Formal Charge and Oxidation Numbers
- Topic: Finding Formal Charge
- Replies: 3
- Views: 256
Re: Finding Formal Charge
We also find the formal charge of each atom to determine the most stable Lewis Structure of the ion. The closer an atom's formal charge is to equaling 0, the more stable the structure is.
- Thu Oct 25, 2018 1:11 pm
- Forum: Administrative Questions and Class Announcements
- Topic: Midterm
- Replies: 7
- Views: 773
Midterm
Will our midterm only be covering the Review of Chemical and Physical Properties, The Quantum World, and Chemical Bonds?
- Thu Oct 25, 2018 1:08 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: Online Modules
- Replies: 4
- Views: 355
Re: Online Modules
no, she didn't specify!
- Wed Oct 24, 2018 2:15 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: Online Modules
- Replies: 4
- Views: 355
Re: Online Modules
I asked a UA and she said that no more online modules will be posted for the rest of the quarter.
- Mon Oct 22, 2018 2:22 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: 7th Edition HW 1E.5
- Replies: 1
- Views: 193
Re: 7th Edition HW 1E.5
(a) false; the effective nuclear charge (Zeffe) IS dependent on the number of electrons in an atom. The effective nuclear charge is the charge experienced by the electrons themselves, so the physical number of electrons affects the value of Zeffe. (b) true; s-orbital electrons are closer to the nucl...
- Wed Oct 17, 2018 11:51 pm
- Forum: Quantum Numbers and The H-Atom
- Topic: Equation sheet
- Replies: 4
- Views: 527
Re: Equation sheet
We'll also have a reference sheet of all the equations / constant values needed for each test stapled to the front (like we just had on test #1), so no need to stress over memorizing!
- Mon Oct 15, 2018 9:22 pm
- Forum: Ideal Gases
- Topic: Reading the textbook
- Replies: 262
- Views: 160154
Re: Reading the textbook
This doesn't have to do with the physical textbook, but does anyone know if we'll be needing the access code for chem 14A at all?
- Mon Oct 15, 2018 12:33 pm
- Forum: Administrative Questions and Class Announcements
- Topic: DOWNLOAD SESSION WORKSHEETS HERE - Sundays 4-6pm (Karen) [ENDORSED]
- Replies: 135
- Views: 39802
Re: DOWNLOAD SESSION WORKSHEETS HERE - Sundays 4-6pm (Karen) [ENDORSED]
Thank you! These are an immense help (especially for studying for the tests)
- Fri Oct 12, 2018 8:23 pm
- Forum: Photoelectric Effect
- Topic: Photoelectric Effect
- Replies: 1
- Views: 147
Photoelectric Effect
What kind of device would be used to detect the electrons removed from photons bouncing off the metal? (from the experiment we went over in lecture)
- Fri Oct 12, 2018 8:19 pm
- Forum: Ideal Gases
- Topic: Reading the textbook
- Replies: 262
- Views: 160154
Re: Reading the textbook
I think viewing the video modules is the best way to review topics you didn't understand in lecture; as far as the textbook goes, it's a great resource for more examples and longer descriptions/definitions of terms and concepts!
- Mon Oct 08, 2018 8:27 pm
- Forum: Administrative Questions and Class Announcements
- Topic: Number of questions on test one [ENDORSED]
- Replies: 39
- Views: 21883
Re: Number of questions on test one [ENDORSED]
The test will only be covering what we learned in high school chemistry, which is the "Review of Chemical and Physical Principles" unit we just learned.
- Fri Oct 05, 2018 9:34 pm
- Forum: SI Units, Unit Conversions
- Topic: How does grading for discussion posts work?
- Replies: 80
- Views: 9680
Re: How does grading for discussion posts work?
Do our 3 posts a week need to fall within the Monday-Friday of said week, or do weekends count as well?
- Wed Oct 03, 2018 1:03 pm
- Forum: SI Units, Unit Conversions
- Topic: SI Units
- Replies: 10
- Views: 784
Re: SI Units
Today in lecture we learned the SI units for: mass (kg), length (m), time (s), volume (m³), density (kg/m³), and the prefixes specific to those units. Since our first test is a only a review of high school chemistry, these should be all we need to know! I hope this helps :)
- Mon Oct 01, 2018 8:56 pm
- Forum: SI Units, Unit Conversions
- Topic: Week 1 Homework Assignment [ENDORSED]
- Replies: 16
- Views: 1317
Re: Week 1 Homework Assignment [ENDORSED]
On the syllabus it says one of the homework problems from each unit will be on the test, so I think it's best to try to do all of them, then choose whichever 7 you're most confident on to turn in for homework credit!