Term
1st Law of Thermodynamics
(Law of Conservation of Energy) |
|
Definition
- Energy is Conserved
- Energy is not created or destroyed, it is transferred from one form to another |
|
|
Term
Formula to measure change in internal energy of system, ΔE |
|
Definition
|
|
Term
Identify energy of System & Energy of the surroundings: |
|
Definition
|
|
Term
Total Internal energy (E) |
|
Definition
The total internal energy of an isolated system is constant |
|
|
Term
|
Definition
Work = Force x Distance
w = F x d
= -P x A x d
= -PΔV |
|
|
Term
Any energy that flows from the system to the surroundings has a _____ sign because the system has lost it
- Efinal is smaller than Einitial |
|
Definition
|
|
Term
Any energy that flows to the system from the surroundings has a _____ sign because system has gainted it
- Efinal is larger than Einitial |
|
Definition
|
|
Term
|
Definition
A fuction or property whose value depends only on the present state, or condition, of the system, not on the path used to arrive at that state.
- pressure, volume and temperature ARE state functions
- work and heat ≠ state functions |
|
|
Term
When the system returns to its original condition, it's overall change in any state fuction is ____ |
|
Definition
|
|
Term
|
Definition
ΔV = Area x Distance
ΔV = A x d |
|
|
Term
|
Definition
Total kinetic energy (KE) of molecular motions
- heat = q |
|
|
Term
Total energy change of a system, ΔE (formula) |
|
Definition
|
|
Term
Amount of heat transferred (formula) |
|
Definition
|
|
Term
Simpler to ignore work, so...
What would allow us to ignore work? |
|
Definition
1. Work must = 0
2. ΔV = 0,
- (a reaction might be carried out in a closed container with a constant volume)
This means no PV work is done and the energy chance is due ENTIRELY to heat transfer |
|
|
Term
|
Definition
The heat change that occurs @ constant pressure (qp) is called enthalpy (H)
enthalpy = H
constant pressure = qp |
|
|
Term
Enthalpy change (heat of reaction) formula |
|
Definition
Enthalpy (H) of a system is the name given to the quantity E + PV, so...
qp = ΔE + PΔV = ΔH |
|
|
Term
Using Calorimetry to measure ΔE/ΔH |
|
Definition
|
|
Term
|
Definition
q = qh2o
qh2o = (mass of water) x SpHt of H2O x (ΔT)
*Specific heat of H2O: 4.18J/g*c
*ΔT = Tfinal - Tinitial |
|
|
Term
CH4(g) + 2O2(g) ---> CO2(g) + 2H2O(l)
Using folowing information, calculate ΔH°:
CH4(g) + O2 ---> CH2O(g) + H2O(g) ΔH° = -275.6 kJ
CH2O(g) + O2 ---> CO2(g) + H2O(g) ΔH° = -526.7 kJ
H2O(l) ---> H2O(g) ΔH° = 44.0 kJ |
|
Definition
CH4(g) + O2 ---> CH2O(g) + H2O(g) ΔH° = -275.6 kJ
CH2O(g) + O2 ---> CO2(g) + H2O(g) ΔH° = -526.7 kJ
2[H2O(g) ---> H2O(l)] 2[ΔH° = -44.0 kJ] = -88.0 kJ
CH4(g) + 2O2(g) ----> CO2(g) + 2H2O(l) ΔH° = -890.3 kJ
|
|
|
Term
Bond Dissociation Energies (BDE) |
|
Definition
ΔHrxn = Σ(Bond brokens) - Σ(Bonds formed) |
|
|
Term
Standard Heat of Formation (ΔH°f) |
|
Definition
ΔH°rxn = ΔH°f(Products) - ΔH°f(Reactants) |
|
|
Term
Calculate ΔH° in kilojoules for the synthesis of lime (CaO) from limestone (CaCO3), an important step in manufacture of cement.
CaCO3(s) ---> CaO(s) + CO2(g)
ΔH°f [CaCO3 (s)] = -1207.6 kJ/mol
ΔH°f [CaO (s)] = -634.9 kJ/mol
ΔH°f [CO2 (g)] = -393.5 kJ/mol |
|
Definition
ΔH° = [H°f (CaO) + ΔH°f (CO2)] - [ΔH°f (CaCO3)]
= (1 mol)(-634.9 kJ/moll) + (1 mol)(-393.5 kJ/mol) - (1 mol)(-1207.6 kJ/mol)
= 179.2 kJ
So, the reaction is endothermic by 179.2 kJ
|
|
|
Term
Find approximate ΔH° in kilojoules for industrial synthesis of chloroform by reacion of methane with Cl2
CH4(g) + 3Cl2(g) ---> CHCl3(g) + 3HCl(g)
Bond dissociation energies for equation:
C - H D = 410 kJ/mol
C - Cl D = 330 kJ/mol
C - CL D= 243 kJ/mol
H - Cl D = 432 kJ/mol |
|
Definition
ΔH° = [3 DCl-Cl + 4 DC-H] - [DC-H + 3 DH-Cl + 3 DC-Cl]
= [ (3mol)(243 kJ/mol) + (4 mol)(410 kJ/mol)] - [(1 mol)(410 kJ/mol) + (3 mol)(432 kJ/mol) + (3 mol)(330 kJ/mol)]
= - 327 kJ
So, the reaction is exothermic by approximately 330 kJ |
|
|
Term
|
Definition
A process, once started, proceeds on its own without a continuous external influence |
|
|
Term
|
Definition
A process, which takes place only in the presence of a continuous external influence |
|
|
Term
|
Definition
1 atm = 760 mm Hg = 101,325 Pa |
|
|
Term
Boyle's Law
(The relationship between Gas, Volume, and Pressure) |
|
Definition
The volume of an ideal gas varies inversely with pressure (V↑ P↓)
*if pressure halved, volume doubles and vice versa
V = k(1/P) + 0 OR PV = k |
|
|
Term
Charles's Law
(The relationship between Gas, Volume and Temperature) |
|
Definition
The volume of an ideal gas varies directly with absolute temperature
Ex: If gas tempt is doubled, volume is doubled, gas temp halved, volume halved
V/T = k at constant n and P |
|
|