Symbol/picture cards Flashcards
What is Charle’s law of gases concerning volume and temperature?
The volume (V) of a gas is directly proportional to the absolute temperature (expressed in Kelvins) when P and N are kept constant.
V1/V2 = T1/T2
What is Boyle’s law of gases concerning pressure and volume?
The volume (V) of a fixed weight of gas, held at constant temperature (T) varies inversely with the pressure (P)
V = (constant)(1/P)
What is the combined gas law?
What is Dalton’s law? Give the formula for Dalton’s law and for the mole fraction (Xi)
What does the sum of all mole fractions equal?
Dalton’s Law states that the total pressure observed for a mixture of gases is equal to the sum of the pressures that each individual component would exert were it alone in the container
PT = P1 + P2 + … + Pi
Where PT is the total pressure and Pi is the partial pressure of any component. The ideal gas law applies to any component of a mixture!
The mole fraction of any one gas: (Xi) = ni/n(total)
where ni is moles of one gas, and ntotal is moles of all gas
The sum of all mole fractions must equal 1
The partial pressure (Pi) of a component of a gas mixture is equal to: (formula)
Pi = XiPT
Where Xi = mole fraction = ni/ntotal
Give the formula for the kinetic energy of particles in a gas
KE = ½mv2
Describe a phase diagram
- At any point on the three curves the phases are in equilibrium
- The diagram is split into three areas (solid, liquid, vapour)
- The boiling point is at the transition liquid-vapour at 760 mmHg
- The diagram extends only to the critical point (C) where liquid and vapour are indistinguishable
- AE represents metastable equilibrium (supercooled water and its vapor)
- Line AD shows that increase pressure linearly decreaes melting point (unique property of water, line slants to right for almost all other substances)
- The triple point is the pressure/temperature where solid, liquid and vapour are in equilibrium. Ice and water have the same fixed vapour pressure at this temperature.
What is Raoult’s law (vapour-pressure lowering)?
The vapour pressure of the components of an ideal solution behave as followed:
pi = Xi(pi)pure
Where: pi= vapour pressure of component in equilibrium
(pi)pure= vapour pressure of pure component at the same T
Ximole fraction of component in the liquid
Raoult’s law states that the vapour pressure of any component of a mixture is lowered by the presence of other component. Experimentally it can be observed that when dissolving a solute which cannot evaporate (nonvolatile), the pressure of the resulting solution is lower than that of the pure solvent. The extent depends on the mole fraction of solvent in solution:
P = Po X
wgere P = vapour pressure of solution
Po= vapour pressure of pure solvent (at T)
When arranged this way, Raoult’s law states that the lowering of the vapour pressure of the solvent is proportional to the mole fractio nof solvent and is independent of the chemical nature of the solute
How does the addition of a solute to a solvent effect the solutions boiling point and freezing point?
Give the formulas that can predict the change in boiling point temperature (ΔTB) and freezing temperature (ΔTF)
Boiling point is increased
Freezing point is decreased
ΔT<strong>B</strong> = KB‘XB = KBm
ΔT<strong>F</strong> = KF‘XB = KFm
Where: KB/F’ = boiling/freezing point elevation/depression constant for solvent
KB/F = mole fraction of solute
m = molality (moles solute per kg solvent)
For molecules with strong dissociative properties (eg. NaCL), which gives strong negative and positive ions) the righ thand side is multiplied by a factor ‘n’ equal to number of ionic species generated per mole of solute (eg. NaCl = 2, MgCl2 = 3) because this is an colligative property (depends on # of particles)
Define the equilibrium constant for the solubility product (Ksp) of a substance
Ksp= [X+][X-]
eg. Ag2S: Ksp= [Ag+]2[S2-]
low Ksp indicates low solubility
List 8 strong acids and 8 weak acids
Give the formula for the acid/base equilibrium constant (Ka) and examples of ionization of: HCl, HF and HCN
How is the equilibrium constant for bases calculated?
Describe water dissociation and the ion product constant for water
Water can ionize itself
2H2O ⇋ H3O+ + OH-
At STP, Kw = [H+][OH-] = 10-14 M
In a neutral solution: [H+] = [OH-] = 10-7 M
Kw increases with temperature
What does the pH scale represent? What is it defined as? (formula)
Why is the pH of a neutral solution of pure water 7?
The concentration of hydrogen ions in solution.
pH = -log10[H+]
[H+] = -log10(10-7) = 7
What is the formula for pKwand what is this at pH = 7?
pKw = pH + pOH
At 25°C, pH + pOH = 14
To determine pH values, it is important to remember certain logarithmic properties. Define the following:
- logaa =
- logaMk=
- loga(MN) =
- loga(M/N) =
- 10log10M =
logaa = 1
logaMk = (k)(logaM)
loga(MN) = logaM + logaN
loga(M/N) = logaM - logaN
10log10M = M
How can the pH of weak acids and bases be calculated?
What is the salt of a weak acid?
The salt of a weak acid is a Bronsted base, which will accept protons.
eg. Na+OAc- + H2O ⇋ HOAc + Na+OH-
The HOAc here is undissociated and therefore does not contribute to the pH. This ionization isknown as hydrolysis of teh salt ion. Because it hydrolyzes, sodium acetate is a weak base (the conjugate base of acetic acid). The ionization constant is equal to the basicity constant of the salt. The weaker the conjugate acid, the stronger the conjugate base, that is, the more strongly the salt will combine with a proton.
What is the hydrolysis constant of a salt and how is it calculated?
Describe the relationship between salts and the dissociation constants of acids and bases (as well as the water dissociation constant)
eg. Na+OAc- + H2O ⇋ HOAc + Na+OH-
KH = Kb = [HOAc][OH-]/[OAc-]
KH is the hydrolysis constant of a salt
The product of Ka of any weak acid and Kb of its conjugate base is always equal to Kw
(Ka)(Kb) = Kw
Describe a titration curve between a strong acid and a strong base. Where is the equivalence point?
Describe the titration curve of a weak acid versus a strong base. Where is the equivalence point?
What is Hess’s law and how is it applied to determining net change in enthalpy for multi component reactions?
Application of the fact that H is a state function. By knowing the changes of enthalpy for a system in one reaction, the change in enthalpy in other reactions (or the net reaction) can be determined.
ΔHOVERALL = ΔH1 + ΔH2
- Start by writing the overall reaction that you want to obtain through a series of reaction additions. (keep reactants on left and products on left)
- Number reactions
- Circle or underline first reactant, find reaction in list that involves this reactant (as reactant or product), and rewrite so that reactant is on left (may need to switch H sign). Multiply by stoichiometric coefficient
- Continue until all reaction component H’s are summed
Give the two calorimetric formulas for measuring the amount of heat (Q) released or absorbed during a chemical reaction
Q = mC(T2-T1)
Q = nc(T2-T1)
m: mass of sample
n: number of moles of sample
C: Specigic heat capacity in J/kg/K
c: heat capacity in J/mol/K