ch 5 thermochemistry Flashcards

1
Q

thermodynamics

A

study of energy and its transformations. Thermochemistry: relationships between chemical reactions and energy changes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

energy definition

A

capacity to do work or to transfer heat

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

kinetic energy3

A

energy of motion. Ek=1/2mv2. m=mass, v=velocity. Kinetic energy increases as speed increases. Atoms/molecules have mass and are in motion=have kinetic energy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

potential energy2

A

energy by virtue of position relative to other objects. Arises when there is a force (push or pull) acting on an object. Ep=mgh. m=mass, g=gravitational constant=9.8m/s2. h=height

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

electrostatic potential energy4

A

arises from interaction between charged particles. Eel is proportional to the electrical charges on the two interacting objects and inversely proportional to the distance between themEel=(kQ1Q2)/d. k=constant of proportionality, =8.99*109J–m/C2. (C =coulomb, unit of electrical charge. J=joule). When Q1 and Q2 have the same sign, they repel one another, and Eel is positive. When they have opposite signs, they attract and Eel is negative.Lower energy of system=more stable.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

SI unit for energy3

A

Joule, J. 1J=1kg–m2/s2. Energy associated with chemical reactions is kilojoules.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

non SI unit for energy4

A

calorie (cal)=amount of energy to raise temperature of 1g of water from 14.5ºC to 15.5ºC. 1 cal=4.184J. 1Cal=1000cal=1 kcal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

closed system

A

can exchange energy but not matter with its surroundings, does not lose or gain mass

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

work2

A

energy used to cause an object with mass to move. w=F*d

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

heat

A

energy used to cause the temperature of an object to increase. Transferred from hot object to cold objects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

first law of thermodynamics

A

energy is conserved. Any energy lost by the system must be gained by the surroundings, and vice versa.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

internal energy defs

A

sum of all kinetic and potential energies of components of system. Represented as E. When E is positive=system gained energy from surroundings. When E is negative=system lost energy to surroundings. Initial state=reactants, final state=products.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

internal energy formulas2

A

E=Eproducts-Ereactants

E=q+w.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

endothermic3

A

system absorbs heat. (melting of ice). Feels cold because heat transferred from our hands (surroundings) to system. E>0

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

exothermic3

A

system loses heat. (combustion). Feels hot as temp of system drops and enters surroundings.
E<0

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

state function

A

property of a system that is determined by the specifying the system’s condition/state. Value of state function depends only on present state of system, not on path system took to reach that state

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

pressure-volume work3

A

work involved in the expansion or compression of gases. When pressure is constant, w=-PV. P=pressure, V=change in volume (Vfinal-Vinitial). When volume expands, V is positive and w is negative, meaning energy leaves system as work and vice versa for when a gas is compressed.

18
Q

enthalpy5

A

thermodynamic function that accounts for heat flow in processes occurring at constant pressure when no forms of work are performed other that P-V work. Denoted by symbol H.
H=E+PV.
H=E+PV=(qP+w)-w=qp. qp emphasizes changes at constant pressure.
Change in enthalpy =heat gained/lost at constant pressure
H>0(meaning when qP>0), heat is gained=endothermic

19
Q

enthalpy of reaction/heat of reaction

A

Hrxn=Hproducts-Hreactants

20
Q

thermochemical equations

A

balanced equations that show the associated enthalpy change where the coefficients represent the number of moles of reactants/products producing the associated enthalpy change.

21
Q

enthalpy diagram

A

another way of representing enthalpy change through a diagram. If reaction is exothermic, reactants are written higher than products with an arrow drawing down to indicate loss of heat

22
Q

facts about enthalpy change5

A

The enthalpy change of a reaction is equal in magnitude but opposite in sign to H for the reverse reaction.
When H is large and negative, it is spontaneous/thermodynamically favored
When H is large and positive, it is spontaneous in the reverse direction
Gases have greater internal energy than liquids, so if liquids were changed to gas on the reactant side, H would decrease but if liquid changed to gas on product side, H would increase

23
Q

calorimetry

A

measurement of heat flow. Calorimeter: device used to measure heat flow

24
Q

heat capacity2

A

represented as C, the temperature change experienced by an object when it absorbs a certain amount of heat. Amount of heat required to raise its temperature by 1 K (or 1ºC). Greater heat capacity, the greater the heat required to produce a given increase in temp

25
Q

molar heat capacity

A

Cmolar, heat capacity of one mole of a substance.

26
Q

specific heat3

A

heat capacity of 1g of a substance. Represented as s.
s=q/(mT).
q=s
m*T

27
Q

coffee cup calorimeters4

A

since they are not sealed, the reaction occurs under constant pressure of the atmosphere.
Heat gained/lost by the reaction (system) must be gained/lost by the solution(surroundings). qsoln= -qrxn. qsoln=ssolnmsolnT=
-qrxn.
A temp increase(T>0) in the solution means the reaction is exothermic (qrxn<0)

28
Q

bomb calorimeters5

A

combustion reactions.
Substance to be studied is placed in a small cup within a sealed vessel called a bomb which can withstand high pressures.
Bomb is sealed and pressurized with oxygen and placed in insulated container (calorimeter) when a measured quantity of water.
Combustion reaction occurs, causing water temp to rise. qrxn=-Ccal*T. (Ccal is total heat capacity of calorimeter)
Because reactions in bomb calorimeters are carried out out under constant volume conditions, heat transferred corresponds to change in internal energy, E, rather than change in enthalpy, H

29
Q

hess law

A

if a reaction is carried out in a series of steps, Hfor the overall reaction will equal the sum of the enthalpy changes for the individual steps.
H is the same whether the reaction takes place in one step or in a series of steps

30
Q

enthalpy of formation/heat of formation

A

Hf, enthalpy change associated with formation of a compound from its elements. Subscript f indicates the substances has been formed from its component elements.

31
Q

standard state

A

state of a substance at its pure form at atmospheric pressure, 1 atm, and 25ºC/298 K. Standard enthalpy change of a reaction is the enthalpy change when all reactants and products are in their standard states. Denoted as Hºwhere superscript º indicates standard-state conditions

32
Q

standard enthalpy of formation

A

Hºf, is change in enthalpy for the reaction that forms one mole of the compound from its elements, with all substances in their standard states. They are reported in kJ/mol. Each reactant is an element in its standard state and product is one mole of the compound.
The standard enthalpy of formation of the most stable form of any element is zero because there is no formation reaction needed when the element is already in its standard state.

33
Q

standard enthalpy of reaction formula

A

Hºrxn= { nHºf(products)-
{ mHºf(reactants). = { sum of, n and m=stoichiometric coefficients of the chemical equation. First term represents formation reactions of products written in forward direction (elements reaction to form products), second term represents reverse of formation reactions of reactants (reactants decompose to form elements)

34
Q

fuel value

A

energy released when one g of a material is combusted. Reported as positive numbers
Greater percentage of C and H in a fuel=higher its fuel value

35
Q

fossil fuels

A

coal, petroleum, natural gas which have formed over millions of years from decomposition of plants and animals and are being depleted faster than being formed, nonrenewable

36
Q

natural gas

A

gaseous hydrocarbons

37
Q

petroleum

A

liquid composed of hundreds of compounds, mostly hydrocarbons

38
Q

coal

A

solid, contains hydrocarbons of high molecular weight
Coal gasification: coal is pulverized and treated with superheated steam a produces mixture of gaseous hydrocarbons (syngas)

39
Q

nuclear energy

A

energy released in either splitting or fusion of nuclei of atoms, nonrenewable. Produce radioactive waste products

40
Q

renewable energy

A

solar, wind, geothermal, hydroelectric, biomass energy