Energy
description
Transcript of Energy
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Energy
Chem Honors Chapter 10
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7 Forms of Energy
• Sound- from vibration of sound waves• Chemical- fuel, gas, wood, battery• Radiant (light)- electromagnetic energy• Electrical energy- electrons moving among
atoms- as in the conductive wire of an electrical cord
• Atomic- nuclear (from nucleus of an atom)• Mechanical- walk, run• Thermal- heat
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What is energy?
• Energy is the ability to do work or produce heat• Two types:–Potential energy–Kinetic energy
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• Potential energy- energy due to position or composition• Ex: –water behind a dam–Attractive and repulsive forces
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• Kinetic energy – is energy due to the motion of the object and depends on the mass of the object and depends on the mass (m) and velocity (v)
• KE = ½ mv2
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Law of Conservation of Energy
• States that energy can be converted from one form to another but can never be created or destroyed
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Energy form going in- electricalEnergy form going out- heat and light
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Chemical energy stored in bonds of gasoline molecules
converted to mechanical and heat energy through combustion
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Electrical energy converted to mechanical energy
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Hoover Dam- hydropower plant converts mechanical energy (flowing water) to
electromagnetic, which is transported to homes, and then converted back into mechanical energy
in a blender
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• Work- force acting over a distance
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State Function
• Property of a system that does not depend on the pathway to its present state.
– Ex: Displacement is a state function: I send 2 students to the cafeteria…the cafeteria is a specific distance from here….even though the 2 students take different routes to get to the cafeteria, they bith end up the same distance away from this room.
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• Energy is a state function :
• Work and heat are not state functions:
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Temperature and Heat
• What is the difference between warm water and cold water?
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• Thermal energy: random motions of components of an object
• Temperature: measures the random motions of the components of a substance (thermal energy)
• Heat: flow of energy due to a temperature difference
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System and Surroundings
• System- part of the universe that we are focusing our attention on
• Surroundings- everything else in the universe
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• Exothermic process – a process that results in the evolution of heat- energy flows out of the system• Endothermic process- a process
that absorbs energy from the surroundings- energy flows into the system
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Exothermic or endothermic?
• 1. Your hand gets cold when you touch ice• 2. ice melts when you touch it• 3. Ice cream melts• 4. Propane is burning in a propane torch.• 5. Water drops on your skin evaporate after
swimming• 6. Two chemicals mixing in a beaker give off
heat
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• Exothermic• Endothermic• Endothermic• Exothermic• Endthermic• exothermic
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• Energy from an exothermic reaction comes from the difference in potential energy between the products and reactants• Which has lower energy, the
reactants or products?
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Burning match• -Total energy is conserved• -exothermic so energy
flows from system to surroundings• - So the energy gained by
the surroundings must be equal to the energy lost by the system
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Burning match cont.• The potential energy lost from the
burned match came from the stored energy in the bonds of the reactants
• In any exothermic reaction some of the potential energy stored in the chemical bonds is converted to thermal energy- which is random kinetic energy- as heat
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Thermodynamics
• Thermodynamics- study of energy• Law of Conservation of energy is also known
as • THE FIRST LAW OF THERMODYNAMICS!!–The energy of the universe is constant.
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1st Law- A Quantitative application
• We can use the first law to analyze energy changes in chemical systems
• Internal energy (E) of a system is the sum of all of the PE (potential energy) and KE (kinetic energy) of a system
E = PE + KE
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Inte
rnal
E
nerg
y, E
H2 (g) , O2 (g)
H2O (l)
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• The internal energy of a system can be changed by a flow of work or heat or both so mathematically we have
ΔE = q + wΔ = change inq = heat added or liberated by
the systemw = work done on the system
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Thermodynamic quantities have
–Number – indicates the magnitude of the change–Sign (+ or -) – indicates the
direction of the flow from the SYSTEM’s point of view
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q and w• When heat is added to a system, or work
is done on a system, the internal energy increases so–When heat is transferred from the
surroundings to the system q is positive–When work is done on a system by the
surroundings w is positive
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q and w• Work and heat created by the system
transferred to the surroundings lowers the internal energy of the system –When work is done by the system on the
surroundings, w is negative–When heat flows from the system to the
surroundings, q is negative
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• In an exothermic process, what is the sign of q?• In an endothermic process, what is
the sign of q?
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Measuring Energy Changes
• Common units of energy change–Calorie – amount of energy (heat)
required to raise the temperature of one gram of water one degree Celsius–Joule – in terms of a calorie • 1 calorie = 4.184 J
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Measuring Energy Changes cont.
• Express 60.1 cal of energy as Joules
• 60.1 cal x 4.184 J = 251 J• 1 cal
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Measuring Energy Changes Cont.
• The energy (heat) required to change the temperature of a substance depends on– The amount of substance being heated (grams)– The temperature change– Identity of the substance
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Measuring Energy changes cont
• Identity of the substance- definition of a calorie is based on water, what about other substances?
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Measuring Energy Changes cont.
• Specific heat – the amount of energy required to change the temperature of one gram of any substance by one degree Celsius
– Water 4.184 J/g °C– Iron (s) 0.45 J/g °C– Silver (s) 0.24 J/g °C
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Measuring Energy Changes cont.
• q = mcΔTq = energy in the form of heatm = mass c = specific heatΔT = change in temperature in °C
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Measuring Energy Changes cont.
• Determine the amount of energy (heat) in Joules required to raise the temperature of 7.40 g of water from 29°C to 46°C
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Measuring Energy Changes cont.
• Ex: What quantity of energy (in Joules) is required to heat a piece of iron weighing 1.3 g from 25°C to 46°C ?
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Calorimetry
• A calorimeter is used to determine the heat associated with a chemical reaction
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Calorimeter Constant
• All parts of a calorimeter heat up or cool down as heat is released or absorbed in the chemical process
• Heat capacity of the calorimeter, C, also known as the calorimeter constant– Defined as the sum of the products of the specific
heat and the mass of all components of the calorimeter
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Calorimeter Constant cont.
• Formula for the heat energy produced in the calorimeter is
q = Ccalorimeter ΔT
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Calorimeter Constant Ex
• A calorimeter has a heat capacity of 1265 J/°C• A reaction causes the temperature of the
calorimeter to change from 22.34 C to 25.12 C. How many joules of heat were released in this process?
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• 3517 J
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Calorimetry
• Can determine the temperature change of the reaction, and use the heat capacity of the calorimeter to determine the ΔH of the reaction
• What is H?
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Enthalpy (H)
• For most chemical reactions chemists are interested in the heat generated at constant pressure, which is denoted as qp = H
• H is the heat content of a compound • ΔH= which is the difference in heat between
the reactants and products• so ΔH= Hproducts - Hreactants
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Thermochemistry
• Because chemical reactions occur at constant pressure, ΔH = qp for chemical reaction
• ΔH is a state function- independent of the path
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Energy Diagram
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Energy Diagram with Catalyst
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Energy Diagram
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Hess’s Law
• The enthalpy of a reaction is the sum of the enthalpies of the combined reactions- known as Hess’s Law
• Hess’s Law states that, whatever mathematical operations are performed on a chemical reaction, the same mathematical operations are applied also to the heat of reaction :
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Hess’s Law
• Enthalpies of reaction have been measured and tabulated- which allows us to calculate ΔH of a reaction without making calorimetric measurements for all reactions
• Because enthalpy is a state function, the change in enthalpy is NOT dependent on the path…..doesn’t matter if the reaction takes place in one step, or multiple steps, change in enthalpy is the same
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Hess’s Law continued
• Standard heat of reaction, ΔH°rxn ( ° indicates standard conditions of 25°C and 1 atm) is the heat produced when the specified number of moles in the balanced equation reacts
• Ex:• C3H8(g) + 5O2(g) 3CO2(g) + 4H2O(g)
• ΔH° of rxn = -2044 kJ when 1 mol of propane reacts with 5 mol of oxygen
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Hess’s Law cont.
• Note that the physical states of the reactants and products are indicated (s,l,g, etc)
• H2(g) + ½ O2(g) H2O(g) ΔH = - 241.8 kJ
• H2(g) + ½ O2(g) H2O(l) ΔH = -285.8 kJ
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*Hess’s Law*
• 1. If the coefficients of a chemical reaction are all multiplied by a constant, ΔH° rxn is multiplied by the same constant- once this is done, the reaction is no longer standard, drop the °
• Recall combustion of propane….
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• C3H8(g) + 5O2(g) 3CO2(g) + 4H2O(g)
• ΔH°rxn = -2044 kJ when 1 mol of propane reacts with 5 mol of oxygen
• If we multiply the reaction by 2, 2C3H8(g) + 10 O2(g) 6CO2(g) + 8H2O(g)
ΔHrxn = -4088 kJ • If we multiply the reaction by ½,½ C3H8(g) + 5/2 O2(g) 3/2CO2(g) + 2H2O(g)
ΔHrxn = -4088 kJ
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• 2. If two or more reactions are added together to obtain an overall reaction, the heats of these reactions are also added to give the heat of the overall reaction
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Hess’s Law
• Ex:
N2(g) + O2(g) 2NO2(g) ΔH = 68 kJ
We could also break down the rxn into 2 steps….
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• N2(g) + O2(g) 2NO(g)
ΔH2 = 180 kJ
2NO(g) + O2(g) 2NO2(g)
ΔH3 = -112 kJ
ΔH2 + ΔH3 = 68 kJ
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*Hess’s Law*• 3. ΔH°forward rxn = - ΔH°reverse rxn
• Ex: C3H8(g) + 5O2(g) 3CO2(g) + 4H2O(g)
ΔH°rxn = -2044 kJ
• when 1 mol of propane reacts with 5 mol of oxygen In this ex, burning propane produced a large amount of heat. It would be almost impossible to experimentally calculate the reverse reaction. But the Hess’s Law states hat if we reverse the reaction, we can reverse the sign of ΔH
• So the energy needed to produce the reverse reaction would be + 2044 kJ
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Hess’s Law Example
• Ex: pg 286• Using the enthalpies of combustion for
graphite and diamond, calculate the ΔH°rxn for the conversion of graphite to diamond
• Cgraphite(s) Cdiamond(s)
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Hess’s Law example cont.
• The combustion reactions are:• Cgraphite(s) + O2(g) CO2(g) ΔH° = -394 kJ
• Cdiamond(s) + O2(g) CO2(g) ΔH° = -396 kJ
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Hess’s Law Example continued
• If we reverse the second reaction and add them together the compounds that are on both sides of the reaction cancel out
• Cgraphite(s) + O2(g) CO2(g) ΔH = -394kJ
• + CO2(g) Cdiamond(s) + O2(g) ΔH = -(-396kJ)
Cgraphite(s) Cdiamond(s)
ΔHrxn = +2kJ
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Hess’s Law Another Example
• Given the following data:• 4CuO(s) 2Cu2O(s) + O2(g) ΔH° = 288 kJ
• Cu2O(s) Cu(s) + CuO(s) ΔH° = 11 kJ
• Calculate the ΔHrxn° for the following reaction
• 2Cu(s) + O2(g) 2CuO(s)
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Specific ΔH• ΔH°f = heat energy absorbed or released during
synthesis of one mole of a compound from its elements at standard conditions
• ΔH°sol = heat energy absorbed or released when a substance dissolves in a solvent
• ΔH°comb = heat energy released when a substance reacts with oxygen to form CO2 and H2O
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Second Law of Thermodynamics
• States that the entropy of the universe is always increasing–Entropy (S) is a measure of disorder or
randomness–Spontaneous process- occurs in
nature without outside intervention