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Termokimia (pertemuan 6)

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    Copyright 2011 Pearson Education, Inc.

    Chapter 6Thermochemistry

    Chemistry: A Molecular Approach, 2nd Ed.

    Nivaldo Tro

    Roy ennedy

    !assachusetts "ay Co##unity College

    $ellesley %ills, !&

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    Che#ical %and $ar#ers

    ' !ost hand (ar#ers (or) *y using the heatreleased +ro# the slo( oidation o+ iron

    - e/s 32/g 4 2 e23/s

    ' The a#ount your hand te#perature risesdepends on several +actors

    the si5e o+ the hand (ar#er

    the si5e o+ your glove, etc.

    #ainly, the a#ount o+ heat released *y the

    reaction

    2Tro6 Che#istry6 & !olecular &pproach, 27e

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    !ani+estations o+ Energy

    Tro6 Che#istry6 & !olecular &pproach, 27e

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    8yste# and 8urroundings

    ' $e de+ine the systemas the #aterial or process(ithin (hich (e are studying the energy changes(ithin

    ' $e de+ine the surroundingsas everything else(ith (hich the syste# can echange energy (ith

    ' $hat (e study is the echange o+ energy*et(een the syste# and the surroundings

    8urroundings

    8yste#

    8urroundings

    8yste#

    -Tro6 Che#istry6 & !olecular &pproach, 27e

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    9nits o+ Energy

    ' joule/: is the a#ount o+ energy needed to#ove a 1;)g #ass a distance o+ 1 #eter1 J = 1 Nm = 1 kgm2/s2

    ' calorie(calis the a#ount o+ energy needed to

    raise the te#perature o+ one gra# o+ (ater 1- :

    1 )ilo(att;hour /)$h = .@0 10@:

    ATro6 Che#istry6 & !olecular &pproach, 27e

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    The irst Ba( o+ Ther#odyna#ics

    Ba( o+ Conservation o+ Energy

    ' Thermodynamicsis the study o+ energy and its interconversions

    ' The irst Ba( o+ Ther#odyna#ics is the Ba( o+ Conservation o+Energy

    ' This #eans that the total a#ount o+ energy in the universe isconstant

    ' ou can there+ore never design a syste# that (ill continue toproduce energy (ithout so#e source o+ energy

    @Tro6 Che#istry6 & !olecular &pproach, 27e

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    Energy lo( and

    Conservation o+ Energy

    ' Conservation o+ energy reDuires that the su# o+ theenergy changes in the syste# and the surroundings

    #ust *e 5ero

    Energyuniverse

    = 0 = Energysyste#

    Energysurroundings

    Is the sy#*ol that is

    used to #ean change +inal a#ount initial a#ount

    FTro6 Che#istry6 & !olecular &pproach, 27e

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    Internal Energy

    ' The internal energyis the su# o+ the )inetic andpotential energies o+ all o+ the particles that co#pose

    the syste#

    ' The change in the internal energy o+ a syste# only

    depends on the a#ount o+ energy in the syste# atthe *eginning and end

    a state !unctionis a #athe#atical +unction (hose result

    only depends on the initial and +inal conditions, not on the

    process usedE = E+inal Einitial

    Ereaction= EproductsG Ereactants

    >Tro6 Che#istry6 & !olecular &pproach, 27e

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    Energy Hiagra#s

    ' Energy diagra#s are a

    JgraphicalK (ay o+ sho(ingthe direction o+ energy +lo(during a process

    InternalEne

    rgy

    initial

    +inalenergy added

    E =

    InternalEnergy

    initial

    +inal

    energy re#oved

    E = L

    ' I+ the +inal condition has a

    larger a#ount o+ internal energy than the initialcondition, the change in the

    internal energy (ill *e

    ' I+ the +inal condition has as#aller a#ount o+ internal

    energy than the initialcondition, the change in the

    internal energy (ill *e L

    Tro6 Che#istry6 & !olecular &pproach, 27e

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    Energy lo(

    ' $hen energy +lo(s out o+ asyste#, it #ust all +lo( intothe surroundings

    ' $hen energy +lo(s out o+ asyste#, Esyste#is L

    ' $hen energy +lo(s into thesurroundings, Esurroundingsis

    ' There+ore6

    LEsyste#= Esurroundings

    8urroundings

    E

    8yste#

    E L

    10Tro6 Che#istry6 & !olecular &pproach, 27e

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    Energy lo(

    ' $hen energy +lo(s into asyste#, it #ust all co#e+ro# the surroundings

    ' $hen energy +lo(s into asyste#, Esyste#is

    ' $hen energy +lo(s outo+ the surroundings,

    Esurroundingsis L

    ' There+ore6

    Esyste#= L Esurroundings

    8urroundings

    E L

    8yste#

    E

    11Tro6 Che#istry6 & !olecular &pproach, 27e

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    energy

    released

    Ern= L

    energy

    a*sor*ed

    Ern=

    Energy lo( in a Che#ical Reaction' The total a#ount o+ internal energy in 1#ol

    o+ C/s and 1 #ole o+ 32/g is greater thanthe internal energy in 1 #ole o+ C32/g

    at the sa#e te#perature and pressure

    ' In the reaction C/s 32/g 4 C32/g, there(ill *e a net release o+ energy into the

    surroundings GEreaction= Esurroundings

    ' In the reaction C32/g 4 C/s 32/g, there(ill *e an a*sorption o+ energy +ro# the

    surroundings into the reaction

    Ereaction= G Esurroundings

    Inte

    rnalEnergy

    C32/g

    C/s, 32/g

    8urroundings

    8yste#

    C 324 C32

    8yste#

    C32 4C 32

    12Tro6 Che#istry6 & !olecular &pproach, 27e

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    Energy Echange' Energy is echanged *et(een the syste# and

    surroundings through heatand (or)q= heat /ther#al energyw= (or) energyqand ware N3T state +unctions, their value depends

    on the processE= q+ w

    1Tro6 Che#istry6 & !olecular &pproach, 27e

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    Energy Echange

    ' Energy is echanged *et(een the syste# andsurroundings through either heat echange or

    (or) *eing done

    1-Tro6 Che#istry6 & !olecular &pproach, 27e

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    %eat, $or), and Internal Energy' In the previous *illiard *all ea#ple, the Eo+ the (hite *all is the sa#e

    +or *oth cases, *ut qand ware not

    ' 3n the rougher ta*le, the heat loss, q, is greater qis a #ore negative nu#*er

    ' "ut on the rougher ta*le, less )inetic energy is trans+erred to the purple*all, so the (or) done *y the (hite *all, w, is lesswis a less negative nu#*er

    ' The Eis a state +unction and depends only on the velocity o+ the (hite*all *e+ore and a+ter the collision in *oth cases it started (ith A.0 ): o+ )inetic energy and ended (ith 0 ): *ecause it

    stopped

    q wis the sa#e +or *oth ta*les, even though the values o+ qand ware di++erent

    1ATro6 Che#istry6 & !olecular &pproach, 27e

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    Ea#ple @.16 I+ the *urning o+ the +uel in a potato cannon

    per+or#s >AA : o+ (or) on the potato and

    produces 1-22 : o+ heat, (hat is E+or the *urning o+ the +uelM

    the unit is correct, the sign #a)e sense as the +uel

    should lose energy during the reaction

    qpotato= >AA :, wpotato= 1-22 :

    E+uel,:

    Check"

    #olution"

    Concept $lan"

    %elationships"

    &i'en"

    ind"

    qsyste#= Gqsurroundings, wsyste#= Gwsurroundings, E = q + w

    1@Tro6 Che#istry6 & !olecular &pproach, 27e

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    Practice Reacting A0 #B o+ %2/g (ith A0 #B o+ C2%-/g

    produces A0 #B o+ C2%@/g at 1.A at#. I+ the reaction

    produces .1 102: o+ heat and the decrease in volu#e

    reDuires the surroundings do F.@ : o+ (or) on the gases, (hat

    is the change in internal energy o+ the gasesM

    1FTro6 Che#istry6 & !olecular &pproach, 27e

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    I+ the reaction produces .1 102: o+ heat and the decrease in

    volu#e reDuires the surroundings do F.@ : o+ (or) on the

    gases, (hat is the change in internal energy o+ the gasesM

    the units are correct, the sign is reasona*le as the a#ount o+ heat lost in the

    reaction is #uch larger than the a#ount o+ (or) energy gained

    qreaction= G10 :, (surroundings= GF.@ :

    Egases,:

    Check"

    #olution"

    Concept $lan"

    %elationships"

    &i'en"

    ind"

    qsyste#= Gqsurroundings, wsyste#= Gwsurroundings, E = q + w

    1>Tro6 Che#istry6 & !olecular &pproach, 27e

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    %eat Echange

    ' )eatis the exchangeo+ ther#al energy *et(een thesyste# and surroundings

    ' %eat echange occurs (hen syste# and surroundingshave a di++erence in te#perature

    ' Temperatureis the measureo+ the a#ount o+ ther#alenergy (ithin a sa#ple o+ #atter

    ' %eat +lo(s +ro# #atter (ith high te#perature to #atter(ith lo( te#perature until *oth o*?ects reach the sa#e

    te#perature

    ther#al eDuili*riu#

    1Tro6 Che#istry6 & !olecular &pproach, 27e

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    uantity o+ %eat Energy &*sor*ed6

    %eat Capacity

    ' $hen a syste# a*sor*s heat, its te#peratureincreases

    ' The increase in te#perature is directlyproportional to the a#ount o+ heat a*sor*ed

    ' The proportionality constant is called the heatcapacity* Cunits o+ C are :7

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    actors &++ecting %eat Capacity

    ' The heat capacity o+ an o*?ect depends on itsa#ount o+ #atter

    usually #easured *y its #ass

    200 g o+ (ater reDuires t(ice as #uch heat to raise itste#perature *y 1

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    8peci+ic %eat Capacity

    ' !easure o+ a su*stanceOs intrinsic

    a*ility to a*sor* heat

    ' The speci!ic heat capacityis thea#ount o+ heat energy reDuired to

    raise the te#perature o+ one gra#o+ a su*stance 1

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    uanti+ying %eat Energy

    ' The heat capacity o+ an o*?ect is proportional toits #ass and the speci+ic heat o+ the #aterial

    ' 8o (e can calculate the Duantity o+ heata*sor*ed *y an o*?ect i+ (e )no( the #ass,the speci+ic heat, and the te#perature change

    o+ the o*?ect

    Heat= (mass + (speci!ic heat + (temp, change

    q= (m + (Cs + (T

    2Tro6 Che#istry6 & !olecular &pproach, 27e

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    Ea#ple @.26 %o( #uch heat is a*sor*ed *y a copper

    penny (ith #ass .10 g (hose te#perature rises +ro#

    G>.0

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    Practice Calculate the a#ount o+ heat released

    (hen F.-0 g o+ (ater cools +ro# -< to 2 :7gQC

    2ATro6 Che#istry6 & !olecular &pproach, 27e

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    Practice Calculate the a#ount o+ heat released

    (hen F.-0 g o+ (ater cools +ro# -< to 2 :7gC /Ta*le @.-

    T1= -

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    D = # Cs T

    Cs, &l= 0.0 :7g'QC, Cs, %23= -.1> :7g'QC/Ta*le @.-

    Ea#ple @.6 & 2.A;g cu*e o+ alu#inu# initially at -A.>

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    Practice & hot piece o+ #etal (eighing

    A0.0 g is heated to 100.0

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    Copyright 2011 Pearson Education, Inc.2

    Practice Calculate the speci+ic heat and

    identi+y the #etal +ro# the data

    q= # Cs T q#etal= Gq%23

    the units are correct, the nu#*er indicates the

    #etal is copper

    #etal6 A0.0 g, T1= 100.0

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    Copyright 2011 Pearson Education, Inc.

    Pressure Solu#e $or)' PS (or) is (or) caused *y a volu#e change against

    an eternal pressure' $hen gases epand, S is , *ut the syste# is doing

    (or) on the surroundings, so wgasis L

    ' &s long as the eternal pressure is )ept constant

    Workgas= -+ternal $ressure + Change in .olumegas

    w= $. to convert the units to ?oules use 101. : = 1 at#B

    0Tro6 Che#istry6 & !olecular &pproach, 27e

    Ea#ple @ -6 I+ a *alloon is in+lated +ro# 0 100 B to

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    Ea#ple @.-6 I+ a *alloon is in+lated +ro# 0.100 B to

    1.>A B against an eternal pressure o+ 1.00 at#,

    ho( #uch (or) is doneM

    the unit is correct the sign is reasona*le *ecause (hen a gas

    epands it does (or) on the surroundings and loses energy

    S1 = 0.100 B, S2 = 1.>A B, P = 1.00 at#

    w,:

    Check"

    #olution"

    Conceptual

    $lan"

    %elationships"

    &i'en"

    ind"

    101. : = 1 at#B

    1Tro6 Che#istry6 & !olecular &pproach, 27e

    Practice & certain process results in a gas syste# releasing

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    Practice & certain process results in a gas syste# releasing

    @>. ): o+ energy. Huring the process, 1A.> )cal o+ heat is

    released *y the syste#. I+ the eternal pressure is )ept

    constant at 1.00 at# and the initial volu#e o+ the gas is 10.0 B,

    (hat is the +inal volu#e o+ the gasM/1 cal = -.1> :, 101. : = 1.00 at#'B

    2Tro6 Che#istry6 & !olecular &pproach, 27e

    Practice & certain process results in a gas syste# releasing @> ): o+

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    Practice & certain process results in a gas syste# releasing @>. ): o+

    energy. Huring the process, 1A.> )cal o+ heat is released *y the syste#.

    I+ the eternal pressure is )ept constant at 1.00 at# and the initial volu#e

    o+ the gas is 10.0 B, (hat is the +inal volu#e o+ the gasM

    so *oth E and qare G, and E q,w#ust *e G and (hen w

    is G the syste# is epanding, so S2should *e greater than S1

    and it is

    E= G@>. ):, q= G1A.> )cal, S1 = 10.0 B, P = 1.00 at#

    S2, B

    Check"

    #olution"

    Conceptual

    $lan"

    %elationships"

    &i'en"

    ind"

    E= q w, w= GPS, 1 ): = 1000 :, 1 cal = -.1> :, 101. : = 1 at#B

    q, E w

    S2P, S1

    E= G@.> 10-

    :, q= G@.@0- 10-

    :, S1 = 10.0B, P = 1.00 at#

    S2, B

    Tro6 Che#istry6 & !olecular &pproach, 27e

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    Echanging Energy "et(een

    8yste# and 8urroundings

    ' Echange o+ heat energy

    q = #ass speci+ic heat Te#perature

    ' Echange o+ (or)w= GPressure Solu#e

    -Tro6 Che#istry6 & !olecular &pproach, 27e

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    !easuring E,

    Calori#etry at Constant Solu#e' "ecause E = q + w, (e can deter#ine E*y #easuring qand

    w

    ' In practice, it is easiest to do a process in such a (ay that thereis no change in volu#e, so w= 0

    at constant volu#e, Esyste#= qsyste#' In practice, it is not possi*le to o*serve the te#perature changes

    o+ the individual che#icals involved in a reaction so instead, (e#easure the te#perature change in the surroundings use insulated, controlled surroundings

    qsyste#= Gqsurroundings

    ' The surroundings is called a 0om0 calorimeterand is usually#ade o+ a sealed, insulated container +illed (ith (ater

    qsurroundings= qcalorimeter= qsystem

    ATro6 Che#istry6 & !olecular &pproach, 27e

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    "o#* Calori#eter

    ' 9sed to #easure E

    *ecause it is a constantvolu#e syste#

    ' The heat capacity o+ thecalori#eter is the a#ount

    o+ heat a*sor*ed *y the

    calori#eter +or each

    degree rise in

    te#perature and is called

    the calorimeter constant

    Ccal, ):7QC

    @Tro6 Che#istry6 & !olecular &pproach, 27e

    Ea#ple @ A6 $hen 1 010 g o+ sugar is *urned in a *o#*

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    Ea#ple @.A6 $hen 1.010 g o+ sugar is *urned in a *o#*

    calori#eter, the te#perature rises +ro# 2-.2 .

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    Practice $hen 1.22 g o+ %CF%A32/!! 122.12 is *urned in

    a *o#* calori#eter, the te#perature rises +ro# 20.2F

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    g F A 2calori#eter, the te#perature rises +ro# 20.2F