Search found 56 matches
- Sat Dec 07, 2019 4:22 pm
- Forum: Identifying Acidic & Basic Salts
- Topic: Titration
- Replies: 1
- Views: 162
Re: Titration
You will need to know about the neutralization with a strong acid and a strong base. You will probably have to determine whether the solution will be acidic or basic given the amount of acid and base and the volume of solution.
- Sat Dec 07, 2019 4:20 pm
- Forum: Identifying Acidic & Basic Salts
- Topic: Acidic Rain
- Replies: 3
- Views: 393
Re: Acidic Rain
Acid rain forms from the reaction between CO2, SO2 and NO2 with H2O in the atmosphere. These reactions form the acids H2CO3, H2SO4, and HNO3, which release H+ ions in solution to create acidity. The main way to reduce acid rain is to reduce the emission of CO2, SO2 and NO2 into the atmosphere.
- Sat Dec 07, 2019 4:16 pm
- Forum: Naming
- Topic: transition metal suffix
- Replies: 2
- Views: 278
Re: transition metal suffix
When the complex is negative, you would name the metal with the ending -ate. If it is positive or neutral, the metal name will remain unchanged.
- Sat Dec 07, 2019 4:14 pm
- Forum: Significant Figures
- Topic: Logarithm sigfigs with O
- Replies: 2
- Views: 380
Re: Logarithm sigfigs with O
This counts as one sigfig. Only 0s after a number after the decimal will be significant, like 0.200 will have three sigfigs.
- Sun Dec 01, 2019 8:49 pm
- Forum: Amphoteric Compounds
- Topic: Amphoteric Compound
- Replies: 2
- Views: 247
Re: Amphoteric Compound
If a compound is considered amphoteric, it is able to act as an acid or a base. For bronsted pairs, you could react the compound with water to see if it is able to act as both. For lewis pairs, you could probably see how the compound reacts with a known acid and a known base.
- Sun Dec 01, 2019 8:45 pm
- Forum: Naming
- Topic: Oxidation number
- Replies: 4
- Views: 332
Re: Oxidation number
You look at the charges of the ligands and the overall charge of the compound. If the compound happens to be bound to something else, you would use those charges to determine the charge of the compound.
- Sun Dec 01, 2019 8:43 pm
- Forum: Calculating pH or pOH for Strong & Weak Acids & Bases
- Topic: Super Acids
- Replies: 1
- Views: 144
Re: Super Acids
A super acid is an acid that has a H+ concentration greater than 1.0 mol. L-1, which is equivalent to a pH of 0.
- Sun Dec 01, 2019 8:41 pm
- Forum: Calculating pH or pOH for Strong & Weak Acids & Bases
- Topic: pKa
- Replies: 3
- Views: 260
Re: pKa
pKa is the -log[Ka]. Similarly to pH, it is a simplified way of writing concentration using the -log equation as an operator. We don't need to know how to calculate pKa for this class.
- Sun Dec 01, 2019 8:39 pm
- Forum: Bronsted Acids & Bases
- Topic: Explanation for J. 17.
- Replies: 1
- Views: 203
Re: Explanation for J. 17.
You would need to react each of the given salts with water to determine the acid and base. For part a, for example: NaC6H5O + H2O --> NaOH + C6H5OH. I'm not sure if this question asks you to label the acid/base as strong/weak, but if it does, you should be able to figure out at least one from each p...
- Sun Dec 01, 2019 8:31 pm
- Forum: Calculating pH or pOH for Strong & Weak Acids & Bases
- Topic: Sig Figs for pH
- Replies: 1
- Views: 173
Re: Sig Figs for pH
Yes, exactly. The sig figs from any other numbers in the question should be used to dictate the number of sig figs after the decimal place in your pH answer.
- Sun Dec 01, 2019 8:29 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: Hydrogen Bonds
- Replies: 2
- Views: 225
Re: Hydrogen Bonds
Because the requirements for a H-bond to form are that there is an H bonded to a N, O or F, and that there is another N, O or F nearby that is charged or has a lone pair. Since the lone pair is negatively charged (electron), it can attract the partial positive charge of the hydrogen.
- Sun Dec 01, 2019 8:27 pm
- Forum: Bronsted Acids & Bases
- Topic: Water as an acid and base
- Replies: 7
- Views: 610
Re: Water as an acid and base
Water acts as a bronsted acid because it can donate a proton: H2O --> H+ + OH-. It acts as a base because it can also accept a proton:
H2O + H+ --> H3O+.
H2O + H+ --> H3O+.
- Sun Dec 01, 2019 8:19 pm
- Forum: Conjugate Acids & Bases
- Topic: Ligands
- Replies: 12
- Views: 681
Re: Ligands
We also probably need to know how to name coordination compounds and to understand the concept of chelating ligands.
- Fri Nov 29, 2019 6:56 pm
- Forum: Amphoteric Compounds
- Topic: Question 6A.11
- Replies: 5
- Views: 461
Re: Question 6A.11
The main characteristic is that they have the potential to donate two protons (H+) since there are two H atoms per molecule. For example, with H2SO4, the first equation would be: H2SO4 + H2O --> HSO4- + H3O+ , and the second equation would be: HSO4- + H2O --> SO4 2- + H3O+
- Fri Nov 29, 2019 6:44 pm
- Forum: Naming
- Topic: Any Givens During the Final?
- Replies: 4
- Views: 522
Re: Any Givens During the Final?
I am pretty sure the only givens are those we have seen on the midterm and tests. You may be able to ask about abbreviations as long as they are not on the periodic table/have been explained in class. It would be best to memorize ion charges, but worst case you can calculate the formal charges of po...
- Fri Nov 29, 2019 6:41 pm
- Forum: Acidity & Basicity Constants and The Conjugate Seesaw
- Topic: triple equal sign
- Replies: 2
- Views: 591
Re: triple equal sign
It could be a typo, but it might be signifying that p is 'equivalent' to -log, rather than 'equal' to -log. The difference would be that the use of p (like in pKA) is the same as the use of -log with [KA], yet saying p = -log would be inaccurate since -log is acting as an operator.
- Fri Nov 29, 2019 4:33 pm
- Forum: Shape, Structure, Coordination Number, Ligands
- Topic: polydentate and shape
- Replies: 3
- Views: 255
Re: polydentate and shape
It is also important to notice whether there are single or double bonds around the atoms with lone pairs, since only single bonds can rotate to form multiple ligands. For example, NH2-CH2-CH2-NH2 has single bonds attaching the Ns, so it can form a shape like \__/, which can be bidentate.
- Fri Nov 29, 2019 4:29 pm
- Forum: Conjugate Acids & Bases
- Topic: 6A.3: Differentiating between acids and bases
- Replies: 2
- Views: 250
Re: 6A.3: Differentiating between acids and bases
In this case, the question tells you that this molecule is an acid, and this will usually happen if they are asking about an amphoteric molecule. However, you can determine whether it is an acid or base depending on the molecule. With -COOH molecules, they will usually either be neutral charge or ne...
- Fri Nov 29, 2019 4:21 pm
- Forum: Calculating pH or pOH for Strong & Weak Acids & Bases
- Topic: pOH scale
- Replies: 2
- Views: 230
Re: pOH scale
I'm not completely sure either, but it might just be traditional as you said, because pH and pOH are just opposite scales.
- Fri Nov 29, 2019 4:14 pm
- Forum: Shape, Structure, Coordination Number, Ligands
- Topic: Metal Oxidation Number
- Replies: 3
- Views: 264
Re: Metal Oxidation Number
Not really, but if you can remember the common oxidation states for the main transition metals, it can help you narrow down the options. Along with this, if you can recognize which ligands are neutral and memorize the charges of other common ligands, it will be easier to figure out the metal's oxida...
- Fri Nov 29, 2019 4:12 pm
- Forum: Bronsted Acids & Bases
- Topic: Bronsted vs. Lewis
- Replies: 5
- Views: 356
Re: Bronsted vs. Lewis
Bronsted acids are proton donors and the bases are proton acceptors, while Lewis acids are lone pair acceptors and the bases are lone pair donors.
- Fri Nov 29, 2019 4:10 pm
- Forum: Bronsted Acids & Bases
- Topic: Strong Acid vs. Weak Acid; Strong Base vs. Weak Base
- Replies: 1
- Views: 552
Re: Strong Acid vs. Weak Acid; Strong Base vs. Weak Base
The main difference between strong acids and weak acids is that strong acids dissociate completely in solution while weak acids do not (the same concept applies for bases). Therefore, strong acids/bases will have higher H+/OH- concentrations in solution (respectively). Because of this, strong acids ...
- Fri Nov 29, 2019 4:05 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: Test 2: Number of Hydrogen Bonding Sites Question
- Replies: 3
- Views: 378
Re: Test 2: Number of Hydrogen Bonding Sites Question
I don't remember the exact number, but this question confused me too. It's supposed to be the total number of potential H-bonding sites on the molecule, and this can be for H-bond sites with ANY molecule, not only more of the same molecule. So, it will be the number of Hydrogens bonded to N,O, and F...
- Fri Nov 29, 2019 3:49 pm
- Forum: Bronsted Acids & Bases
- Topic: Difference between Bronsted and Lewis
- Replies: 2
- Views: 173
Re: Difference between Bronsted and Lewis
A bronsted acid is a proton donor, and the base is a proton acceptor. A Lewis acid is a lone pair acceptor while the base is a lone pair donor. The "opposite" part is just that the "donor" and "acceptor" titles for acids and bases are the opposite for the two categories.
- Wed Nov 27, 2019 11:58 am
- Forum: Amphoteric Compounds
- Topic: Question 6A.11
- Replies: 5
- Views: 461
Re: Question 6A.11
H2CO3 and H2SO4 are considered diprotic, meaning they usually lose two protons as anions. So, when they lose only one, they are able to lose one more and act as an acid, even with a negative charge.
- Wed Nov 13, 2019 9:56 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Polar vs. Nonpolar
- Replies: 12
- Views: 832
Re: Polar vs. Nonpolar
Also, often molecules with different electron domain and VSEPR geometries will be polar, since a lone pair will be in place of the ED and will prevent the dipoles from cancelling. An example of this is PF3.
- Wed Nov 13, 2019 9:49 pm
- Forum: Administrative Questions and Class Announcements
- Topic: Test #2
- Replies: 22
- Views: 2960
Re: Test #2
I'm pretty sure the test doesn't have anything from the midterm. It will most likely focus on polarity, IMFs, VSEPR, and then else everything we cover until the test.
- Wed Nov 13, 2019 9:45 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: Energy
- Replies: 2
- Views: 252
Re: Energy
I think you are right, but also the main reason that the Hydrogen bonds are stronger is due to electronegativity (EN). Since Hydrogen bonds are formed between H (with the lowest EN) and N,O, or F (with the three highest ENs), the EN difference is the greatest and therefore the dipole is strongest. T...
- Wed Nov 13, 2019 9:36 pm
- Forum: Properties of Light
- Topic: Midterm Solution Q2B
- Replies: 2
- Views: 366
Re: Midterm Solution Q2B
Also, once the light passes the threshold energy, it can eject electrons. Since the energy of the light is directly correlated to its frequency, increasing the frequency will only cause the energy of the emitted electron to increase. Therefore, the graph you draw should show a horizontal line (at an...
- Wed Nov 13, 2019 9:26 pm
- Forum: Determining Molecular Shape (VSEPR)
- Topic: Lone Pairs
- Replies: 5
- Views: 322
Re: Lone Pairs
Since lone pairs take up more space, the bond angles adjacent to the lone pairs will increase and the opposing angles will decrease.
- Fri Nov 01, 2019 4:01 pm
- Forum: Ionic & Covalent Bonds
- Topic: Distorted e- with Ionic Bonds
- Replies: 5
- Views: 265
Re: Distorted e- with Ionic Bonds
Not exactly. In a covalent bond, the electrons are shared when the orbitals from each atom overlap. So when the anion distortion occurs, the cation's positive charge attracts the anion's electrons towards it and the orbitals overlap, which is why it is similar to a covalent bond.
- Fri Nov 01, 2019 3:58 pm
- Forum: Trends in The Periodic Table
- Topic: s-block vs. p-block effective nuclear charge
- Replies: 1
- Views: 136
Re: s-block vs. p-block effective nuclear charge
The p-block atoms with more protons will have a higher nuclear charge than those in the s-block because each electron is affected by all of the protons in the atom. This means that if an atom has 8 protons and 8 electrons, for example, each electron will individually experience the nuclear pull from...
- Fri Nov 01, 2019 3:09 pm
- Forum: Ionic & Covalent Bonds
- Topic: Distorted e- with Ionic Bonds
- Replies: 5
- Views: 265
Re: Distorted e- with Ionic Bonds
I think it is because the anion distortion is caused by the cation (which transfers its electrons) attracting the anion's electrons towards itself. This may cause the electrons to be almost shared between the atoms, like in a covalent bond.
- Fri Nov 01, 2019 3:04 pm
- Forum: Resonance Structures
- Topic: Resonance
- Replies: 4
- Views: 189
Re: Resonance
Also, many molecules with resonance structures have charges, so they are likely to form ionic bonds. For example, a lot of polyatomic ions have resonance.
- Fri Nov 01, 2019 2:58 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: Homework 2D #5
- Replies: 1
- Views: 151
Re: Homework 2D #5
This is because in Bi+3, it would lose the three electrons in the 6p block first, while in Tl+3, it would lose its one electron in the 6p block and then the other two electrons from the 6s block since it only has one electron in the 6p block.
- Fri Nov 01, 2019 2:54 pm
- Forum: Ionic & Covalent Bonds
- Topic: Homework 2D #15
- Replies: 5
- Views: 302
Re: Homework 2D #15
I think that the molecule with the strongest bonds would be the one where the C and X atoms have the greatest difference in electronegativity.
- Thu Oct 24, 2019 8:29 pm
- Forum: Lewis Structures
- Topic: Bond strength
- Replies: 7
- Views: 340
Re: Bond strength
To add on to this, covalent bonds are stronger than ionic bonds in biological systems, since molecules will often be dissolved in water. Otherwise, ionic bonds are usually stronger.
- Thu Oct 24, 2019 8:25 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: Electron Configuration Exceptions
- Replies: 3
- Views: 121
Re: Electron Configuration Exceptions
I think those are the main exceptions, and also this same rule will apply to elements in the same position in the 4d section.
- Thu Oct 24, 2019 8:21 pm
- Forum: Lewis Structures
- Topic: Homework 2A c)
- Replies: 1
- Views: 102
Re: Homework 2A c)
This is because the 3d and 4s blocks are at very similar levels in terms of electron shells. Metals in the d block will very often form oxidation states with charges greater than 2+, although they will lose electrons from the 4s orbital first.
- Thu Oct 24, 2019 8:12 pm
- Forum: Electron Configurations for Multi-Electron Atoms
- Topic: 1E 13)
- Replies: 1
- Views: 111
Re: 1E 13)
I think this applies only to the 3d and 4d rows, since they do not include the f block.
- Thu Oct 24, 2019 8:10 pm
- Forum: Trends in The Periodic Table
- Topic: Relationship between Electronegativity and Ionization Energy?
- Replies: 6
- Views: 966
Re: Relationship between Electronegativity and Ionization Energy?
Atoms with low ionization energy will usually have higher electronegativity. Therefore, the atom will be less likely to lose its own electrons and more likely to attract electrons from another atom. Electron affinity, in my experience, is usually given. If not, you can calculate it using other values.
- Wed Oct 16, 2019 10:30 pm
- Forum: Wave Functions and s-, p-, d-, f- Orbitals
- Topic: Untrue PSI From Lecture
- Replies: 2
- Views: 127
Re: Untrue PSI From Lecture
This is because the first 1 is referring to the number of electron shells, which correlates to the first row of the periodic table. The second 1 is referring to a p-orbital. This could not exist since none of the elements with only 1 electron shell can contain a p-orbital.
- Wed Oct 16, 2019 10:26 pm
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: How would you explain this?
- Replies: 3
- Views: 322
Re: How would you explain this?
Yes, since each excited electron will emit a very specific wavelength of light based on the electron level jump, which correlates to a line on the spectrum.
- Wed Oct 16, 2019 10:21 pm
- Forum: DeBroglie Equation
- Topic: Question on applications of the equation
- Replies: 2
- Views: 189
Re: Question on applications of the equation
The equation most likely would not be applied to photons, since they do not have a mass or momentum.
- Wed Oct 16, 2019 10:16 pm
- Forum: Photoelectric Effect
- Topic: relation of photoelectric effect to equations
- Replies: 2
- Views: 130
Re: relation of photoelectric effect to equations
The equation E=hv is not exactly proven by the photoelectric effect, but it shows the positive relationship between energy of the photon and frequency. The photoelectric effect proves (or shows) that photons have particle-like properties, since increasing the intensity of light did not eject electro...
- Wed Oct 16, 2019 10:10 pm
- Forum: Photoelectric Effect
- Topic: When energy is equal to work function
- Replies: 9
- Views: 1018
Re: When energy is equal to work function
If the energy is equal to the work function, the electron would not be ejected from the metal, therefore it would have 0 kinetic energy.
- Sat Oct 12, 2019 10:18 pm
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: Post Module Assessment Number 20
- Replies: 3
- Views: 111
Re: Post Module Assessment Number 20
Yes, it is D, because there is one electron that will be excited by every one photon (1:1 ratio).
- Sat Oct 12, 2019 10:15 pm
- Forum: Properties of Electrons
- Topic: QM description
- Replies: 2
- Views: 132
Re: QM description
This relates to the photons emitted by the electrons after they drop from energy levels. Since they are discrete, they can only emit specific wavelengths, and therefore each atom has a unique emission spectrum.
- Sat Oct 12, 2019 10:12 pm
- Forum: Properties of Electrons
- Topic: Series
- Replies: 2
- Views: 125
Re: Series
I think he mainly focused on Balmer and Lyman, but there are also the Paschen, Brackett, and Pfund series. The Balmer series corresponds to the visible light spectrum, the Lyman series corresponds to UV light, and the last three correspond to infrared light. They are differentiated by wavelength.
- Sat Oct 12, 2019 10:06 pm
- Forum: Properties of Light
- Topic: Question on 1A 11
- Replies: 4
- Views: 240
Re: Question on 1A 11
The grouping is also most likely determined by the wavelengths of the emitted photons, which are grouped based on UV light (Lyman) and visible light (Balmer).
- Sat Oct 12, 2019 9:59 pm
- Forum: Bohr Frequency Condition, H-Atom , Atomic Spectroscopy
- Topic: Lyman, Balmer, Paschen, & Bracket Series?
- Replies: 4
- Views: 800
Re: Lyman, Balmer, Paschen, & Bracket Series?
So the Lyman series (for UV) will correlate to any energy level drop that includes the drop from n=2 to n=1, since that is the largest energy level difference. The Balmer series (for visible light) will correlate to the energy level drop that includes that from n=3 to n=2, since that is the second l...
- Sun Oct 06, 2019 11:42 pm
- Forum: SI Units, Unit Conversions
- Topic: Angstrom(Å)
- Replies: 4
- Views: 227
Re: Angstrom(Å)
Yes, I think that the Angstrom is a more commonly used unit in this situation, so you can use it as if it is an SI unit.
- Sun Oct 06, 2019 11:39 pm
- Forum: Balancing Chemical Reactions
- Topic: H.25
- Replies: 3
- Views: 937
Re: H.25
Since you have the molar masses and the percentage composition, you just convert the percent composition to grams and divide by the molar mass. Then, using the molecular formulas, you can write a chemical reaction and balance it.
- Sun Oct 06, 2019 11:35 pm
- Forum: SI Units, Unit Conversions
- Topic: Si Units
- Replies: 3
- Views: 180
Re: Si Units
When we start learning the Quantum unit, we will be using more of pico- and nano- units. Also, in biology, micro- units are very commonly used.
- Sun Oct 06, 2019 11:31 pm
- Forum: Limiting Reactant Calculations
- Topic: Different Way to Find the Limiting Reactant
- Replies: 3
- Views: 199
Re: Different Way to Find the Limiting Reactant
I actually learned this method in high school too! It is actually similar to one of the methods Lavelle taught, where he told us to solve for the amount of products each molar amount of the reaction would form. This method basically just removes the second step of solving for the products.
- Sun Oct 06, 2019 11:25 pm
- Forum: Limiting Reactant Calculations
- Topic: Reducing reactants
- Replies: 2
- Views: 152
Re: Reducing reactants
Lavelle says that we are doing reduction reactions later in the quarter, so don't worry about it now because you won't find this problem on the test.