Chemical and Physical Foundations Section Flashcards
Chromatography
the separation of a mixture by passing it in solution or suspension or as a vapor (as in gas chromatography) through a medium in which the components move at different rates.
- The solute concentration will affect the size of the spots on the paper chromatogram, not the average migration rate.
- Thickness of the paper affects the amount that each component can be fully separated, not the relative migration rates of components.
- stationary phase will be an immobilized surface, not a solution.
- migration rate may depend on hydrogen bonding
amino acids
a group of organic molecules (organic is primarily made of carbon molecules) that consist of a basic amino group (NH2-), an acidic carboxyl group (-COOH) and an organic R group (side chain that Is unique to each amino acid). Each amino acid contains a central (alpha) carbon.
non polar amino acids
They are hydrophobic, in water, they will bury their side chains on the inside. (polarity is based on the side chain)
Nonpolar= alanine, valine, leucine, glycine, isoleucine, methionine, tryptophan, phenylalanine, proline
polar, uncharged amino acids
serine, cysteine, asparagine, glutamine, threonine, tyrosine.
must have at least one atom (N, S, O) with electron pairs available for hydrogen bonding to water and other molecules.
acidic amino acids
Aspartic and glutamic acid
Each has a carboxylic acid on it side chain which gives it electron donating properties. At a physiological pH, these amino acids will ionize, giving them a charge of -1. The ionic forms are aspartate and glutamate.
basic amino acids
arginine, histidine, and lysine. Each side chain is basic- meaning it can accept a proton
in dehydration reaction
-OH is lost from the carboxyl group and an H is lost from the amino group. This will take a molecule of H2O and leave an amide linking two amino acids.
Carbocation intermediate
SN1, E1, and alkene addition reactions will have a carbocation intermediate.
carbocation intermediate from Alkene addition
adding strong acid to an alkene gets us a carbocation
strong acid
any acid that ionizes completely in a solution. That means, a great number of hydrogen ions or protons will dissociate. Strong acids are able to conduct electricity.
HClO3, HBr, HCl, HI, HNO3, HCLO4, H2SO4
Good nucleophile
A good base is usually a good nucleophile. So, strong bases — substances with negatively charged O, N, and C atoms — are strong nucleophiles. Examples are: RO⁻, OH⁻, RLi, RC≡C:⁻, and NH₂⁻. Some strong bases are poor nucleophiles because of steric hindrance.
SN1 reaction
The SN1 reaction is a substitution reaction in organic chemistry. “SN” stands for “nucleophilic substitution”, and the “1” says that the rate-determining step is unimolecular. Thus, the rate equation is often shown as having first-order dependence on electrophile and zero-order dependence on nucleophile
The SN1 reaction mechanism involves an intermediate carbocation that is formed by loss of the leaving group. A nucleophile can react with the planar carbocation from either side, leading to the inversion or retention of the configuration at the site of the substitution.
Electrophile
In chemistry, an electrophile is a chemical species that forms bonds with nucleophiles by accepting an electron pair. Because electrophiles accept electrons, they are Lewis acids.
Good Electrophiles
Good electrophiles typically contain weak polar or polarizable bonds. This means that electrons can favor one side of a bond over the other, creating dipoles.
carbon-centric
Organic chemistry is carbon-centric. Carbon is the key atom in these reactions and carbon atoms do some very predictable things- like many four bonds.
Cis and Trans Isomers
cis isomer has two groups on the same side. Trans isomer has two groups on opposite sides.
Non polar molecule identification
Non polar molecules will be made up of one element. For example, N2, O2, Cl2, and noble gases are non polar. Containing only carbon and hydrogen is non polar. Does the molecule have symmetry?
CO2 is non polar, for example. I-Br is also non polar because the electronegativity difference between the atoms is not great along the bond.
Polar molecule identification
If hydrogen is directly attached to N, O, F, it is polar. Ex, water, CH3OH (presence of alcohol), CH3COOH, if molecule lacks symmetry and the bond is polar then it will be a polar molecule.
stereospecific
A reaction in which the stereochemistry of the reactants controls the outcome of the reaction. In general, one stereoisomer of certain reactant produces one stereoisomer of a certain product, whereas a different stereoisomer of the same reactant produces a different stereoisomer of the same product. You wouldn’t end up with a mixture of cis and trans alkenes in the product.
aldehyde
Carbon atom shares a double bond with oxygen, a single bond with H, and a single bond with R. Derived from alcohols.
H-C-R
=O (the equal sign should be vertical). That is the carbonyl group.
Carboxyl group
Same as Aldehyde except for there is an O where the H would’ve been. A carboxyl group can react with an amine to form a peptide bond.
amine group
Contain basic nitrogen atom with a lone pair. These form peptide bonds. The conjugate base of an amine is also called an amide (like the bond that is made when a peptide is formed).
amine group
Contain basic nitrogen atom with a lone pair. These form peptide bonds. The conjugate base of an amine is also called an amide (like the bond that is made when a peptide is formed).
alkyl
contains only carbon and hydrogen atoms in a chain. Ex: CH3.
backside attack SN2
results in an inversion of configuration where the product’s configuration is opposite of the substrate’s. Inversion at the carbon that bears the leaving group.
steric hindrance
At a secondary carbon, there is more crowding from the adjacent carbon chains, which makes nucleophilic substitution slower.
1,2 hydride shift
carbocation rearrangement which a hydrogen atom in a carbocation migrates to the carbon atom bearing the formal charge of +1 (carbon 2) from an adjacent carbon (carbon 1)
least to most stable carbocations
primary= least stable, secondary, tertiary- most stable.
A primary carbocation is attached to one other carbon, a secondary to two, and a tertiary to 3 other carbons.
how does a carbocation form
A carbocation is an organic molecule, an intermediate, that forms as a result of the loss of two valence electrons, normally shared electrons, from a carbon atom that already has four bonds.
This is a carbon atom bearing a positive charge where it’s fourth bond should be. It wants to have four bonds but if it has 3, it could be a carbocation. Positively charged species would mean that they are electron-poor.
in gas to liquid chromatography:
the first peak to emerge will be from the least polar, most volatile compound. 2-Methyl-2-butene is nonpolar and the most volatile because it only has London forces for intermolecular attraction. (no dipole will mean no force of attraction).
Larger and heavier molecules typically have stronger dispersion forces than smaller, lighter ones.
Look for the non polar option to be the most volatile, and the first peak- those that interact the fastest.
S v R stereochemistry
When determining from heaviest to lightest and excluding the H, left is S (think of how you would begin drawing it) and right is R (think of r and R)
When determining organic chem products
Count the carbons, look for configuration (look at what atoms were replaced when determining configuration).
which reactant loses the -OH group?
an oxygen atom on ethanol must be radiolabeled. 100% of the alcohol will be retained in the ester. Acetic acid only supplies OH that is lost to form water.
Eye lens is a converging lens.
The negative sign of lens strength is indicative of a diverging lens. When solving these problems, for example, 0.02^-1, but 1/0.02^1, I multiplied each and got 0.5 which is like 50.
If you want to slow the ionization of a compound in a solution…
you could add a strong acid because it will increase the amount of H+ in a solution and therefore decrease the amount of other compound that is ionizing.
diluting a solution would…
increase the amount of ionization occurring. From Le Chatelier’s Principle, adding water to the equilibrium would cause the equilibrium to shift to the right. A shift to the right implies that more acid would be in dissociated form, and thus the percent ionization increases accordingly.
Ohm’s law
according to Ohm’s law, current is equal to voltage divided by resistance. If current increases and resistance is constant, then voltage increases as well.
V=IR
I=V/R
current through a conductor between two points is directly proportional to the voltage across the two points.
Math tip: division of numbers that aren’t whole
The MCAT will give options that look wrong, looks right, and are right- for example. 3/2.1
answer options:
0.7, 2.1, 3.0, 1.4. Think to yourself: how many times does 2.1 go into 3? If you think of it that way, you can easily rule out options.
Intensity of radiation emitted:
The energy of electromagnetic radiation equals to the number of photons, and the intensity of electromagnetic radiation, and is defined as energy emitted per unit time.
Intensity of radiation is not related to propagation speed, wavelength, or polarization state- but to the number of photons emitted per unit of time and their respective frequency.
1 THz (tetrahertz) =
1012 hertz
so 610 THz= 610 (1012) hz
practice math problem
610 THZ) (6.6x10^-34)= ? (4.0 x10^19
- multiply 610 by 1012 to get in Hz= 6.1 x10^12
- multiply the whole numbers first… like 6x6 is 36 (and look for answer with a little more)
- Then, focus on exponentials… -34 + 12 is 19, 20… close to that is 19
MCAT doesn’t give calculators so be creative and think your way around these math problems like you always do.
substituting equations
Ex problem: Substitute Pp = Ps – Pd into equation PMPA = Pd + (Ps – Pd)/3.
- Substitute Pp into the parentheses because they are equal.
- write as PMPA= Pd + Pp/3.
- To match up with correct answer option, I could multiply each part by 3. For example. 3PMPA= 3pD + Pp, then rearrange to Pp= 3PMPA- 3pD. That’s simple algebra- think back to 8th grade! You got this.
When you looked at this one, you talked your way through it. You’re smart… you know what you’re doing. Pull off of old material I’ve learned. If you think you have an idea of the answer, you probably do.
Work (w)=
J/s, so calculated answer will be in joules… change to appropriate unit. For example, if options show kJ, take away 3 decimal places.
disulfide bridges S-S
intermolecular covalent bonding
intramolecular v intermolecular
intramolecular hold atoms together within molecules while intermolecular hold molecules together within a compound.
aliphatic
carbons form open chains, not aromatic rings
Cross-linking region is different from the
cell adhesion region