4.4 how far - entropy

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summarised notes on entropy

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    Enthalpy changes

    The enthalpy changefor a process

    is the heat energy exchanged withthe surroundings at constant

    pressure.

    Enthalpy changes are frequently

    measured under standard conditions,

    !e! 298Kand100kPa. "f an enthalpychange s measured under standard

    condtons, the sym#ol s used n

    superscrpt, !H!

    Enthalpy change s g$en the sym#ol !H!

    %he unts are k&mol'1!

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    Enthalpy changes

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    Exa"ples of enthalpy changes

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    #ond enthalpies

    *hen a chemcal reacton takes place, #onds are #roken n

    the reactants and #onds are formed n the products! Breakng

    #ondss an endother"icprocess! +akng #onds s an

    exother"icprocess!

    %he "ean $ond enthalpys the a$erage mean-

    $ond dissociation enthalpyfor a partcular #ond n

    a range of dfferent compounds!

    .recsely, t s the a$erage enthalpy change for

    #reakng 1 mole of a partcular #ond n a range of

    dfferent compounds n the gas phase!

    %he enthalpy change for a reacton can #e calculated #y

    workng out the enthalpy changes for #onds made and #onds#roken durng the reacton usng mean #ond enthalpes!

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    %alculations using $ond enthalpies

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    &hat is a #orn'(a$er cycle)

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    %onstructing a #orn'(a$er cycle

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    #orn'(a$er cycle for *g%l2

    *g+s,- %l2+g,

    *g+g,- %l2+g,

    Ha

    +*g, -1/0

    *g+g,- 2%l+g,

    2

    Ha+%l,

    2 +-121,

    *g-+g,- 2%l+g,- e'

    Hi+1st,+*g, -3

    Hi+2nd,+*g, -14/0

    *g2-+g,- 2%l+g,- 2e'

    *g2-+g,- 2%l'

    +g,

    2

    Hea+%l,

    2 +'34,

    *g%l2+s,

    Hl+*g%l2, '249

    Hf+*g%l2,

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    %an you construct a #orn'(a$er cycle)

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    #orn'(a$er cycle 5uestions

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    6attice for"ation enthalpies

    *hen an onc lattce s formed, the oppostely charged ons

    are attracted to each other! %he stronger the attracton, the

    hgher the lattce formaton enthalpy!

    %wo factors ncrease the attracton and therefore the lattce

    formaton enthalpy

    hgh charge

    small se!

    7'2''

    6i-7a-K-

    increasing lattice for"ation enthalpy

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    Polari:ation and lattice enthalpy

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    ill in the "issing words; lattice enthalpy

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    Enthalpies of solution and hydration

    The standard enthalpy of solution

    +Hsol, is the enthalpy changewhen one "ole of an ionic

    co"pound is dissol

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    %alculating enthalpies of solution

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    Enthalpy of solution calculations

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    actors affecting enthalpy of hydration

    %he se of the enthalpy of hydraton depends on

    ncreas

    ng

    s3e

    %he charge on the on! %he larger the charge on the on,

    the larger the enthalpy of hydraton!

    %he se of the on! %he smaller the on, the larger theenthalpy of hydraton!

    L

    5a

    6

    '(1

    '40)

    '322

    7'

    8l'

    Br'

    '(0)

    '3)4

    '33(

    =on Hhyd+k>"ol'1, =on Hhyd+k>"ol

    '1,

    =on Hhyd+k>"ol'1, =on Hhyd+k>"ol

    '1,

    7e2 7e3'1(0 '4430

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    &hat is a spontaneous reaction)

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    Entropy

    Entropy is a "easure of disorder? and is gi

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    Entropy change for reactions

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    Predicting entropy changes

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    %alculating entropy changes

    9tandard entropy changes for any chemcal reacton or

    physcal change can #e calculated usng the followng smple

    e:presson

    ;emem#er the followng ponts

    entropes of elements are not ero lke Hf$alues, so they

    should #e ncluded n calculatons!

    the unts of entropy, S, are &6'1mol'1

    S Sproducts' S

    reactants

    % l l i h

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    %alculating entropy changes

    E t h l l ti

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    Entropy change calculations

    E t h i th di

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    Entropy changes in the surroundings

    E t h i th di

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    Entropy changes in the surroundings

    @i$$ f

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    @i$$s free energy

    *hether a reacton s spontaneous depends on

    %he change n a quantty called the @i$$s free energy

    pro$des a measure of whether a reacton s spontaneous!

    %he

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    (ow to calculate !G

    % l l ti !G

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    %alculating !G

    i$ilit f ti

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    easi$ility of reactions

    E$en f Gs post$e at room temperature, there may #e a

    hgher temperature at whch a reacton #ecomes feas#le!

    "f Ss post$e, there may #e a pont at whch TSs #g

    enough to outwegh the enthalpy factor!

    G H' TS

    post$e

    negat$epost$e

    negat$e

    post$e

    post$enegat$e

    negat$e

    makes TS> H

    makes Gmore negat$eno effect Galways post$e

    unlkely to make TS > H

    yes, a#o$e a

    certan temp!

    alwaysne$er

    usually

    H S Bs te"p. increasesC easi$le)

    inding the te"perature

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    inding the te"perature

    8onsder the reducton of alumnum o:de wth car#on

    "f G? 0, then T? H@ S

    %he temperature at whch ths reacton #ecomes feas#le

    can #e calculated! %hs wll #e when G? 0!

    =s #othH

    andS

    are post$e,G

    wll #ecome negat$e fTS > H!

    H -13 k>"ol'1

    Bl2+s,- %+s, 2Bl+s,- %+g,

    S -/81>K'1"ol'1

    T 2299K

    T? 133) @ (1@1000-

    &hen is a reaction feasi$le)

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    &hen is a reaction feasi$le)

    Dolu$ility

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    Dolu$ility

    "n the same way that reactons are only feas#le f GA 0, a

    su#stance wll #e solu#le n water at a specfc temperature

    f GsolA 0!

    Gsol Hsol' TSsol

    post$e

    negat$e

    post$e

    negat$e

    post$e

    post$e

    negat$e

    negat$e

    Hsol Ssol G feasi$ilityfeas#le f Ts large enough to make

    Gnegat$e

    always feas#le

    ne$er feas#le

    usually feas#le Ts unlkely to #e

    large enough to make Gpost$e-

    Ther"odyna"ics

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    Ther"odyna"ics "ol'1

    %+s,- 2+g, %2+g,

    8onsder the reacton n$ol$ng the com#uston of car#on

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    @lossary

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    @lossary

    &hatFs the keyword)

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    &hat s the keyword)

    *ultiple choice 5ui:

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    *ultipleGchoice 5ui: