OAT Natural Sciences flashcards
OAT Natural Sciences · Build recall with a focused review session.
31 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Cell theory
- All living organisms are composed of one or more cells, the cell is the basic unit of structure and function, and all cells arise from pre-existing cells through division.
- Prokaryote vs eukaryote
- Prokaryotes lack a membrane-bound nucleus and organelles, having circular DNA and 70S ribosomes; eukaryotes have a nucleus, linear chromosomes, membrane-bound organelles, and 80S ribosomes.
- Osmosis direction
- Water diffuses across a semipermeable membrane from the region of lower solute concentration to the region of higher solute concentration, equalizing water potential until equilibrium is reached.
- Km meaning
- Km is the substrate concentration at which an enzyme reaches half its maximum velocity; a low Km indicates high substrate affinity, while a high Km indicates low affinity.
- Competitive inhibition effect
- A competitive inhibitor binds the active site, raising apparent Km because more substrate is needed, but Vmax stays unchanged since high substrate outcompetes the inhibitor.
- Semiconservative replication
- Each new DNA double helix contains one original parental strand and one newly synthesized strand; DNA polymerase adds nucleotides to the 3' end, so synthesis proceeds 5' to 3'.
- Dihybrid cross ratio
- Crossing two heterozygotes for two independently assorting genes produces a 9:3:3:1 phenotypic ratio in the offspring, reflecting independent assortment of alleles during meiosis.
- Glycolysis net yield
- Glycolysis converts one glucose into two pyruvate in the cytoplasm, with a net gain of two ATP and two NADH; it requires no oxygen and occurs in all cells.
- Mitochondrial function
- Mitochondria generate ATP through the Krebs cycle in the matrix and oxidative phosphorylation on the inner membrane, and they contain their own circular DNA and ribosomes.
- Ideal gas law
- PV = nRT relates pressure, volume, moles, and temperature; R is 0.0821 L·atm/(mol·K), and at STP one mole of ideal gas occupies 22.4 liters.
- Molarity definition
- Molarity equals moles of solute divided by liters of solution; it changes with temperature because solution volume expands, whereas molality based on solvent mass does not.
- pH formula
- pH equals the negative log of hydrogen ion concentration; at 25 °C, pH plus pOH equals 14, and each unit change represents a tenfold change in hydrogen ion concentration.
- Henderson-Hasselbalch equation
- pH = pKa + log([conjugate base]/[weak acid]) predicts buffer pH; a buffer resists pH change best when the acid and base concentrations are equal and pH equals pKa.
- Le Chatelier pressure effect
- Increasing pressure on a gaseous equilibrium shifts the reaction toward the side with fewer moles of gas; adding an inert gas at constant volume has no effect.
- Equilibrium constant meaning
- K expresses the ratio of product to reactant activities at equilibrium; K greater than one favors products, K less than one favors reactants, and pure solids and liquids are omitted.
- Gibbs free energy equation
- ΔG = ΔH - TΔS determines spontaneity; a negative ΔG means the process is spontaneous, and ΔG equals zero at equilibrium where ΔG° = -RT ln K.
- Periodic atomic radius trend
- Atomic radius decreases left to right across a period as nuclear charge pulls electrons closer, and increases down a group as additional electron shells are added.
- Colligative properties
- Boiling point elevation and freezing point depression depend on the number of dissolved particles, not identity; formulas are ΔTb = iKb·m and ΔTf = iKf·m.
- Strong versus weak acid
- A strong acid dissociates completely in water, giving a large Ka and low pH; a weak acid partially dissociates and requires an equilibrium expression with its Ka value.
- Oxidation number rules
- Fluorine is always -1, oxygen is usually -2, hydrogen is +1 with nonmetals, and the sum of oxidation numbers equals the ion charge or zero for neutral molecules.
- Limiting reactant
- The limiting reactant is consumed first and determines maximum product yield; compare moles of each reactant divided by its stoichiometric coefficient to identify it.
- Hybridization geometry
- Four electron groups give sp3 hybridization and tetrahedral 109.5° geometry; three groups give sp2 and trigonal planar 120°; two groups give sp and linear 180°.
- Functional group priority
- For IUPAC naming, carboxylic acid outranks ester, amide, aldehyde, ketone, alcohol, amine, alkene, alkyne, and alkane; the highest-priority group determines the suffix.
- SN1 mechanism
- SN1 is a two-step substitution with a carbocation intermediate, favored by tertiary substrates and polar protic solvents; stereochemistry is racemized and rate depends only on substrate.
- SN2 mechanism
- SN2 is a one-step concerted substitution with backside attack, favored by primary substrates and polar aprotic solvents; it gives inversion of configuration and rate depends on both reactants.
- E2 elimination requirements
- E2 is a concerted elimination requiring a strong base and anti-periplanar hydrogen and leaving group; it follows Zaitsev's rule to give the more substituted alkene.
- Markovnikov's rule
- In addition of HX to an alkene, hydrogen adds to the carbon with more hydrogens, placing the halogen on the more substituted carbon; peroxides reverse this regiochemistry for HBr.
- Alcohol oxidation products
- Primary alcohols oxidize to aldehydes then carboxylic acids, secondary alcohols oxidize to ketones, and tertiary alcohols resist oxidation because the carbon lacks a hydrogen.
- Hückel aromaticity rule
- An aromatic ring must be cyclic, planar, fully conjugated, and contain 4n+2 pi electrons; benzene with six pi electrons satisfies this and is aromatic.
- Chirality and R/S
- A carbon with four different substituents is chiral; R/S assignment ranks substituents by atomic number using Cahn-Ingold-Prelog rules and views the lowest priority group away.
- Esterification reaction
- A carboxylic acid reacts with an alcohol in the presence of acid catalyst to form an ester and water; the reaction is reversible and equilibrium favors products with excess alcohol.