1.1 General Chemistry Flashcards
SOLID (shape & volume)
Definite *non-compressible
SOLID (Molecular motion)
Vibration *2 stones
LIQUID (shape)
Indefinite *assumes container shape
LIQUID (volume)
Definite
LIQUID (molecular motion)
Gliding *ex. water falls
GAS (shape & volume)
Indefinite *compressible
GAS (molecular motion)
constant random
Plasma/Ionized Gas
4th state; most abundant state of matter
• Has p+ and e- (thus, greatly affected by magnetic field)
• Ex. ionized Ne light, Aurora, Stars, Sun
IFA Strength most ↑ or strongest:
S > L > G > P
Enthalpy (heat/ reaction energy):
P > G > L > S
Melting
*aka: Fusion, Liquefaction, Thawing
Solid to Liquid
Freezing
Liquid to Solid
Evaporation
Liquid to Gass
Condensation
Gas to Liquid
Sublimation
*moth/naphthalene balls
Solid to Gas
Deposition
*dry ice/cardice
Gas to Solid
Recombination
*aka: Deionization
Plasma to Gas
Ionization
Gas to Plasma
Pure substance
- Element
* Compound
Element
simplest form of substance
Compound
2 or more chemical united (separated via
chemical means)
Mixture
- Homogeneous
* Heterogeneous
Mixture
2 or more substance wherein individual substance identifies are retained (separated via physical means. Alcohol +
Water via distillation)
Homogeneous
1 phase; solution *clear colored
Heterogeneous
2 phases; suspension, colloid *ex. milk
Extrinsic Property “Dependent”
Length, mass/weight, volume, pressure, entropy, enthalpy, electrical resistance
Intrinsic Property “Independent”
Density/ SpGr (water = 1g/ml or cc), viscosity (resistance to flow), velocity (m/sec), temperature, color
Law of Conservation of Mass/ Matter
- Antoine Lavoiser
- Mass/ Matter is always constant (neither created nor destroyed)
Law of Definite/Constant Proportions
- Joseph Proust (Proust’s law)
• Chemical compounds always contain the exact proportion of element in fixed ratio (by mass)
• Ex. H2O →2H + O, C6H12O6 = CH2O
Law of Multiple Proportion
- John Dalton • When 2 elements form more than 1 compounds, it can be expressed in a fixed whole number (by mass) • Ex. CO → 28g/mole, CO2 → 44g/mole C = 12g/mole O = 16g/mole
Law of combining weights
• Proportions by weight when chemical reaction takes place can be expressed in small integral unit
• Ex. MgO → 40g/mole (100%)
Mg = 24g/mole (60%); O = 16g/mole (40%)
Democritus
- atomos
- “indivisible”
John Dalton
- Billiard ball
- Matter is made up of atoms
Postulates
- Elements are composed of indivisible, indestructible atoms
- Atoms alike for a given element (isotopes)
- Atoms of different elements differ in size, mass & other properties (isobars)
- Compound are formed form 2 or more atoms at different elements
- Atoms combined in simple numerical ratios to form compounds
J.J. Thompson
- Plum Pudding/Raisin bread
- e- in (+) framework
Ernest Rutherford
- discoverer of proton (Nuclear - Gold foil/a-scattering experiment)
- atom is mostly empty; (+) particles in nucleus
Neil Bohr
- Planetary
- mostly used
Erwin Schrodinger
- Quantum/Mechanical/e- cloud
- Modern atomic Model; estimates the probability of finding an e- in certain position (i.e. at e-cloud/ orbital)
Proton
- (+) ion
• Atomic number (basis of electronic configuration)
• Ernest Rutherford
Electrons
- (-) ion
• negligible weight 1,836x lighter that p+ - J.J. Thompson
- R.A. Millikan
J.J. Thompson
• Cathode ray tube: e- m/2 ratio
R.A. Millikan
Oil drop experiment: measure accurate charge and mass of e-
Neutrons
- no charge
• Atomic mass (Nucleon) = p+ + n0
• James Chadwick
Eugene Gold Stein
discovered anode rays
Electrochemistry
– particle separation based on e-
• Ex: Capillary electrophoresis - separation of compounds based on electrophoretic mobility
ANODE (charge)
(+) electrode
ANODE (undergoes:)
Oxidation
CATHODE (charge:)
(-) electrode
CATHODE (undergoes:)
Reduction
RED CAT ELECT IN
• REDuction happens in CAThode where ELECTrons get IN
VILEORA
• Valence Increase, Loses e-, undergoes Oxidation, Reducing agent
VDGEROA
• Valence Decrease, Gains e-, undergoes Reduction, Oxidizing agent (KMnO4-, Na2Cr2O7)
Isotopes
- same p+/atomic number/ element
* differ in atomic mass
Non-isotopes
19F, 127I, 31P, etc.
Main isotopes
+1: 1H, 12C, 14N, 32S, 35Cl ; +2: 16O, 79Br
Isobars
- same atomic mass
* differ in elements
Isomers
- same molecular formula
* differ in structure
Molecule
– aggregate of 2 or more atoms in definite arrangement held together by chemical bonds
Ions
– with net (+) or (-) charge
Empirical formula
– simplest whole number ratio (might be same with MF). Ex: CH2O vs. C6H12O6
Intermolecular FA/ Van der Waals/ Electrostatic
- Between molecule; weak and short-lived
* Created by “molecule’s polarizability”; exerted when 2 uncharged atoms (n0) approach very closely
H-bonding
- Strongest IFA
- H + S, O, N, X (electronegative atoms)
Keesom orientation (D-D)
- > (next to H-bonding)
- Water-water
Debye Induction (D-ID)
- > (3rd)
- Water-benzene
London Dispersion (ID-ID)
- Weakest IFA
- Aromatics (Benzene-Benzene)
Dipole (D)
- Polar
Induced Dipole (ID)
- Nonpolar
Intramolecular FA
- Within molecule
Covalent
- sharing of e-
- Nonmetal + Nonmetal (Glycosidic & Peptide bond)
Ionic
- Transfer of e-
- Metal + Nonmetal (NaCl)
Glycosidic
- ether bond S─O─S
Peptide bond
– amide bond AA─peptide─AA bond
Covalent Bonding (Lone pair)
Pair of valence electrons that are not shared with another atom in covalent bond
Valence shell electron pair repulsion (VSEPR) theory
Predicts the geometry of the molecule as well as any bonded and unbonded electron pair
Linear (180˚)
- CO2
- Alkynes (Sp)
Tetrahedral/bent (109.5˚)
- CCl4 , H2O Alkanes (Sp3)
* 2 bonded pair, 2 unbonded pair
Trigonal bipyramid
- PF5
Octahedral
- SF5
Valence bond theory
States that bonds are formed by sharing of electron from overlapping atomic orbitals (covalent)
s = spherical
(sigma bond – stronger bond formed; headways overlap)
p = dumbbell
(pi bond – weaker; sideways overlap)
Molecular orbital theory
• States that bonds are formed from interaction of atomic orbitals from molecular orbitals
Bonding
- lower energy (stable)
Antibonding
- higher energy (unstable)
Synthesis/ Combination/ Direct Union
A + B → AB
Decomposition/ Analysis
AB → A + B
- e.g. Complete & Incomplete combustion
Single Displacement
AB + X → AX + B
Double Displacement/ Metathesis/ Exchange
AB + CD → AC + BD
- e.g. Neutralization, Precipitation
Metals
Li > K > Ba > Ca > Na > Mg > Al > Mn > Zn > Cr > Fe > Cd > Co > Ni > Sn > Pb > H2 > Cu > Ag > Hg > Pt > Au
Nonmetals (bases on electronegativity)
F > Cl > Br > I
Covalent compounds
- CO: Carbon monoxide
- SiO2: Silicon dioxide
- N2O: Dinitrogen monoxide
- CCl4: Carbon tetrachloride
Ionic compounds
Ex: Pb(NO3)4
• Classical: Plumbic nitrate
• Stock: Lead(IV) nitrate
Monovalent
\+1 = Group 1 (H, Li, Na, K ׀ Ag) \+2 = Group 2 (Be, Mg, Ca, Sr, Ba ׀ Zn, Cd) -2 = Group 6A (Oxide, Sulfide) -1 = Group 7A (Fluoride, Chloride, Bromide, Iodide)
+1 = Group 1
(H, Li, Na, K ׀ Ag)
+2 = Group 2
(Be, Mg, Ca, Sr, Ba ׀ Zn, Cd)
-2 = Group 6A
(Oxide, Sulfide)
-1 = Group 7A
(Fluoride, Chloride, Bromide, Iodide)
Multivalent (with variable charges)
+1, +2 = Hg, Cu
+1, +3 = Au
+2, +3 = Fe, Co, Ni
+3, +5 = Bi, Sb
+1, +2
= Hg, Cu
+1, +3
= Au
+2, +3
= Fe, Co, Ni
+3, +5
= Bi, Sb
ClO-
- Hypochlorite
- Hypochlorous acid (HClO)
ClO2-
- Chlorite
- Chlorous acid (HClO2)
ClO3-
- Chlorate
- Chloric acid (HClO3)
ClO4-
- Perchlorate
- Perchloric acid (HClO4)
NO2-
- Nitrite
- Nitrous acid (HNO2)
NO3-
- Nitrate
- Nitric acid (HNO3)
SO3^2-
- Sulfite
- Sulfite Sulfurous acid (H2SO3)
SO4^2-
- Sulfate
- Sulfuric acid (H2SO4)
PO4^3-
- Phosphate
- Phosphoric acid (H3PO4)
HCO3-
Bicarbonate (Hydrogen carbonate)
HSO3-
Bisulfite
HSO4-
Bisulfate
HPO4^-2
Biphosphate
H2PO4^-1
Dihydrogen phosphate
Aufbau Principle
- Atoms may be built by progressive filling of energy of main energy sub level (i.e., levels of lower energy levels are occupied first)
- s=2, p=6, d=10, f=14
Principal Quantum Number (n = 1 to 7)
- main energy level; size of orbital (electron cloud), distance of e- from nucleus
- Ex. O2 = 1s2. 2s2. 2p4 (n=2)
Azimuthal/ Angular Momentum (ℓ = 0 to 3)
- Angular momentum & shape of orbital; subshell
* Ex. O2 = ℓ = 1
ℓ = 0 ─ s :
sharp (spherical shape)
ℓ = 1 ─ p :
principle (dumbbell shape)
ℓ = 2 ─ d :
diffuse (clover leaf)
ℓ = 3 ─ f :
fundamental
Magnetic Quantum Number (mℓ = -ℓ, 0, +ℓ)
- Orientation of orbital in space
* Ex. O2 = mℓ = -1, 0, +1
Magnetic Spin (ms = + ½ , - ½ )
• Magnetic moment/ Rotation Spin ↑ = Incomplete; clockwise + ½ ↑↓ = Complete; counterclockwise = - ½ • Ex. Oxygen = ms= + ½
Diagmagnetism
– no unpaired e-
Paramagnetism
– at least 1 unpaired e-
• No 2 e- will have same set of quantum number (“exclusive”
Pauli’s exclusion theory
• Impossible to predict/ accurately determine the particle’s velocity (position & momentum)
Heisenberg’s uncertainty theory
- Orbitals are filled up singly before pairing up
* Most stable arrangement of e- in subshells is the one with greatest no. of parallel spins.
Hund’s rule
P₁𝑽₁ = 𝑷₂𝑽₂ 𝑜𝑟 𝑷 ∝
1/𝑣
• Temperature (in K)
Boyle’s/Mariotte
𝑻₁𝑽₁ = 𝑻₂𝑽₂
𝑜𝑟 𝑽 ∝ �
• Pressure (in atm)
Charles
𝑷₁𝑻₁ = 𝑷₂𝑻₂
𝑜𝑟 𝑷 ∝ 𝑻
• Volume (in L)
Gay-Lussac’s
𝑷₁𝑽₁ 𝑻₁ = 𝑷₂𝑽₂ 𝑻₂
Combined
𝑷𝑽 = 𝒏𝑹𝑻
Ideal
• Equal volumes of different gases have same no. of moles at
STP
𝑽₁𝒏₁ = 𝑽₂𝒏₂
𝑜𝑟 𝑽 ∝ 𝒏 𝑜𝑟 𝑽/𝒏 = k
Avogadro’s
• Total pressure in a mixture (non-interacting gases) is equal to the sum of the partial pressures of each gas. 𝑃𝑡 = 𝑃1 + 𝑃2 + 𝑃3
Dalton’s Law of Partial Pressures
• Rate of effusion (diffusion) and speed gas are inversely proportional to the square root of their density providing the temperature and pressure are same for 2 gases
Graham’s
Rate at which 2 gases mix
Diffusion
Rate at which gas escapes through a pinhole vaccume
Effusion
• Diffusion rate (flux) of liquid or gas is directly proportional to the concentration gradient (ftom high concentration to low
concentration)
Fick’s 1st Law
𝑷𝒓𝒆𝒔𝒔𝒖𝒓𝒆 ∝ 𝑺𝒐𝒍𝒖𝒃𝒊𝒍𝒊𝒕𝒚
• Decrease temperature, Increase Pressure (i.e., sealed container), more CO2 is dissolved in water.
Henry’s Law of Gas Solubility
Solute + Solvent
Solution
• Study of energy conversion/transformation in the universe
Thermodynamics
Allows exchange of energy and matter
Open System
Allows exchange of energy but not matter
Closed System
Does not allow exchange of both energy and matte
Isolated System “Adiabatic Walls”
- Independent (depends only on initial & final states of system)
- Ex. Enthalpy (H), Internal energy (U), Gibb’s Free Energy (G), Entropy (S)
State Function
- Dependent
* Work and Heat
Non-state Function
• If two systems are in thermal equilibrium respectively with a third system, they must be in thermal equilibrium with each
other
Zeroth Law
• Energy is neither created nor destroyed but can be transformed from one form to another
1ST LAW: Law of conservation of Energy
∆H is independent of reaction/steps that occurred (only the initial and final steps is the basis)
Hess’ Law
∆H = (+) → heat is absorbed;
COLD (endothermic)
∆H = (-) → heat is released;
HOT (exothermic)
- No way but UP
* For an isolated system, Total entropy can never decrease over time
2ND LAW: Law of Entropy
Measure of system’s thermal energy per unit temperature; degree of disorderliness or randomness
Entropy (∆S)
- If an object reaches absolute zero temperature (0 K = -273.15 = -459.67 °)
- Entropy of perfect, solid, crystalline substance is zero at absolute 0 temperature
3RD LAW
- Thermodynamic state function that combines enthalpy and entropy
- ∆G = ∆H ‒ T∆S
Gibb’s free energy (∆G)
• Study of reaction rates and reaction mechanism
Chemical Kinetics
- Change in concentration of a reactant or product concentration with time
- aA + bB → cC + dD
Reaction Rate (M/s)
• Expresses relationship of the rate of reaction to the rate constant (K) and concentration of reactants raised to some
power
• aA + bB → cC + dD
Rate Law
• rate of chemical reaction is proportional to the number of collisions per time
Collision Theory
• (Formation of Intermediate Complex) - rate depends on Ea required to form intermediate state (where new bonds are
formed and old bonds are broken)
Transition Theory
= ↑ reactivity ↑ reaction rate (faster)
Nature of Reactants
= ↑ concentration ↑ reaction rate
Concentration of Reactants (except Zero order)
= ↑ reaction rate
Catalyst
= ↑ SA ↓ particle size ↑ reaction rate ↓ reaction time
Surface Area
= ↑ Temp ↑ KE ↑ mobility of molecules ↑ collision ↑ reaction rate; Arrhenius Equation (T, Ea, RR)
Temperature