Chapter 10 Energy and Energy changes Flashcards

1
Q

thermochemistry

A

the study of energy and energy transfer in chemical processes

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2
Q

energy

A

the capacity to do work

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3
Q

work

A

a force acting through a distance

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4
Q

pontential energy

A

stored energy, gravitational potential energy, chemical bonds.

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5
Q

kinetic energy

A

energy of motion

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6
Q

system

A

the portion of universe of interest

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7
Q

surrounding

A

the rest of the universe not part of the system

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8
Q

temperature

A

a measure of the average kinetic energy

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9
Q

thermal energy

A

the internal energy present in a system due to its molecular motion

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10
Q

heat

A

the transfer of thermal energy due to differences in temperature

heat moves from a region of higher temperature to a region of lower temperature

the process of heat flow is defined with repeat to the system

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11
Q

endothermic

A

heat is absorbed by the system

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12
Q

exothermic

A

heat is released by the system

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13
Q

Si Units

A

Joule, J

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14
Q

Calorie

A

the energy required to raise exactly 1 g H2O by 1ºC

1cal=1000cal
1cal=1kcal
1cal=4.184 j

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15
Q

types of system

A

characterized by transfer between system and surrounding

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16
Q

state function

A

a value or variable that only depends on the state of the system not how it achieved that state

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17
Q

internal energy, E

A

the sum of all the kinetic and potential energy within a system

E is a state function

E is based on parameters such as temperature, pressure, concentration, phase, etc.

18
Q

Change internal energy, ∆E

A

its is difficult to measure E so ∆E is measured

19
Q

first law of thermodynamics

A

in chemical processes, energy is neither created nor destroyed. the total energy of the universe is constant in all processes, the change in energy of the universe is zero.

20
Q

1 last applied

A

if energy cannot be crated nor destroyed…t=the energy lost by a system must be the same amount gained by the surrounding. The energy gained by a system must be the same amount lost by the surroundings

∆Esystem=-∆Esurrounding
∆Esystem+∆Esurrounding=0

21
Q

changes in internal energy

A

the change in internal energy occurs via two forms:

1.heat(q) 2.work(w)

∆E=q+w

22
Q

heat

A

+q=system gains/absorbs thermal energy

-q= system loses/releases thermal energy

23
Q

work

A

+w=work is done on the system
-w=work is done by the system

pressure-volume

24
Q

P-V work

A

work as a result of a volume change agains an external pressure

w=-P∆V
P:exnternal Pressure, atm
∆V: change in volume
∆V: Vfinal-Vintial

for expansions Vf>Vi work is done by the system w<0
for contraction Vf0

25
Q

constants volume work

A

if the reaction is carried in a sealed container the volume is fixed

∆V=0 w=-P∆V=0J

therefore, the total change in internal energy at constant volume is:

∆E=q+w. ∆E=q+0 ∆E=qw

26
Q

enthalpy

A

often reactions are carried out under constant pressure; not constant volume

∆E=q+w ∆E=qp+(-P∆V)

rearranging, qp=∆E+P∆V, this is defined as enthalpy H: qp=∆H

27
Q

enthalpy H

A

for a system, enthalpy is the sum of the internal energy plus the pressure times volume

∆H>0 endothermic: heat flows into the system
∆H<0 exothermic:heat flows out of the system

28
Q

Stoichiometry of ∆H

A

when ∆H is given for a reaction, it is related to the moles shown in the balanced reaction.

29
Q

Calorimetry

A

the study of heat change in chemical reactions. when a system absorbs heat, there is a change in temperature

experimental it is observed: the change in temperature depends on the amount of heat absorbed

qα∆T

30
Q

heat capacity, c

A

the constant of proportionality that relates the temperature change to the heat absorbed

31
Q

heat capacity (of a system)

A

the quantity of heat required to change temperature of a system by 1ºC

q=C•∆T

the heat capacity depend on the amount of matter present in the system and is report for the system

32
Q

specific heat capacity, Cs

A

the amount of energy required to raise the temperature of 1 gram of substance by 1ºC

q=m•Cs•∆T

33
Q

molar heat capacity, Cm

A

the amount go energy required to raise the temperature of 1 mole of substance by 1ºC

Cm=J/mol ºC

34
Q

constant pressure calorimetry

A

often reaction are conducted at constant pressure, not constant volume

∆Hrxn=qrxn/nreactant

35
Q

thermochemical equation

A

chemical equation that shoes the enthalpy change in addition to the balanced species

36
Q

Manipulating ∆H

A
  1. if a reaction is multiplied by n, the ∆His also multiplied by n
  2. if a reaction is reversed, the sign on ∆H is changed
  3. if a chemical equation can be expressed as the sum of a series of steps, then the ∆Hrxn for the overall reaction is the sum of the individual ∆Hs
37
Q

Standard states for enthalpy

A

a. for a gas the pure gat as a pressure of exactly 1 atm
b. for liquid or solid the pure substance in its most stables from at a pressure of 1 atm and temperature of interest
c. for substance in solution the substance in solution at a concentration of exactly 1 M

38
Q

Standard enthalpy change, ∆H

A

the change in enthalpy for a process when all reactants and products are in their standard states

39
Q

standard enthalpy of formation,∆Hfº

A

for a pure compound the change in enthalpy when 1 mole of the compound is formed from its constituent elements in their standard states

40
Q

standard enthalpy of reaction, ∆Hºrxn

A

the ∆Hfº provides the energy of each substance, therefore for a reaction the ∆Hrxn is given by:

∆Hºrxn= ∑nproduct∆Hfºproduct-∑nreactant∆Hfºreactant
n=number of moles

41
Q

bond enthalpies, ∆HBE

A

the energy required to break 1 mole of the bond for the gas phase species. Also known as bond dissociation energy