water chemistry 2012
TRANSCRIPT
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WaterChemistry
Dr.AtifHassanKhirelsied
DepartmentofBiochemistry
InternationalUniversityofAfrica,Khartoum,Sudan
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Biomoleculesassumespecificshapesinwater.
Biomoleculesundergochemicalreactionsinan
a ueous environment.
a er sa eyreac an nmanyreac ons,usua y n
theformofH+andOH ions.
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Waterisoxidizedinphotosynthesistoproduce
molecularoxygen,
O2.
Ex enditure of ener under aerobic conditions
leadsto
the
reduction
of
O2 backtowater.
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Thestructureofwaterapproximatesatetrahedron
withits
two
hydrogen
atoms
and
the
two
lone
pairs
ofelectronsofitsoxygenatomoccupyingthe
verticesofthetetrahedron.
Thehi helectrone ativit ofox enrelativeto
hydrogenresultsintheestablishmentofa
ermanentdi ole in
water
molecules.
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The
3dimensional
structure
of
awater
molecule,
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Thepolar natureofwaterresultsinelectrostatic
interaction(hydrogenbond) betweenneighboringwatermolecules.
Hydrogenbond
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H dro enbonds
Waterisstronglyhydrogenbonded
Each
water
molecule
participates
in
four
hydrogen
bondswithitsneighbors.
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H dro enbonds
Hydrogenbondscommonlyformbetweenwatermolecules
andthepolarfunctionalgroupsofbiomolecules,or
betweenthepolarfunctionalgroupsthemselves.
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Thestronglyhydrogenbondedcharacterofwateris
responsiblefor
many
of
its
characteristic
properties,
mostnotably:
(a)Ahighheatoffusion,whichallowswatertoact
asaheatsink suchthat reaterheatlossis
necessaryforthefreezingofwatercomparedto
othersubstances
of
similar
molecular
mass.
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moreheatmustbeinputtovaporizewatercompared
c
n
a y
o
sso vemos
po ar
compoun s.
(d)Anopenstructuremakesicelessdensethanliquidwater,therebymakingicefloat,insulatingthewaterbeneathit,andinhibitingtotalfreezingoflarge
bodiesofwater.
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Avarietyofweakelectrostaticinteractionsarecritical
tothe
structure
and
reactivity
of
biological
molecules.
These interactions include in order of increasin
strength,
,
dipoledipoleinteractions,
,
ionicinteractions
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Waterisanexcellentsolventofpolarandionicsu s ances ue o sproper yo surroun ngpo ar
moleculesandionswithorientedshellsofwater
therebyattenuatingtheelectrostaticforcesbetween
thesemoleculesandions.
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Thetendencyofwatertominimizeitscontactwith
nonpolar
(hydrophobic)
molecules
is
called
the
hydrophobiceffect. This
effect
is
largely
driven
by
the
increase
in
entropy
causedb thenecessit forwatertoorderitself
aroundnonpolarmolecules.
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Thehydrophobiceffectcausesthenonpolarmolecules
to
aggregate,
thereby
reducing
the
surface
areathatwatermustorderitselfabout.
Consequently,nonpolar substances
are
poorly
solubleina ueoussolution.
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Manybiologicalmoleculeshavebothpolar(or
charged)and
non
polar
functional
groups
and
are
thereforesimultaneouslyhydrophilicand
hydrophobic.
Thesemoleculesaresaidtobeam hi hilic or
amphipathic.
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Osmosisisthemovementofsolventacrossasem permea e mem rane romareg ono ower
concentrationofsolutetoare ionofhi her
concentrationofsolute.
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Diffusion istherandommovementofmoleculesin
so u on or n egasp ase .
Itisresponsibleforthemovementofsolutesfroma
regionofhighconcentrationtoaregionoflow
concentration.
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Waterisaneutral,polarmoleculethathasaslight
tendencyto
ionize
into
H
+
andOH
.
The roton is never free and binds to a water
moleculeto
form
H3O+
(hydroniumion).
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Theionizationofwaterisdescribedasanequilibrium
betweenthe
unionized
water
(reactant)
and
its
ionizedspecies(products)
Inwhich
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Theconcentrationofwaterisessentiallyconstant
(55.5M),
the
concentration
of
H2O
is
incorporated
intothevalueofK,whichisreferredtoasKw,theionizationconstantofwater.
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ThevaluesofbothH+ andKareinconvenientlysmall;
hence,their
values
are
more
conveniently
expressed
asnegativelogarithms,sothat
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BrnstedLowrydefinition,anacidisasubstancethat
can
donate
aproton,
and
abase
is
asubstance
thatcanacceptaproton.
Thestrength
of
aweak
acid
is
proportional
to
its
dissociationconstant whichisex ressedas
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T epHo aso utiono awea aci is etermine y
the
relative
concentrations
of
the
acid
and
its
conjugate ase.
Theequilibrium
expression
for
the
dissociation
of
a
weakacidcanberearran edto
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H n r nH l l h i n
Whentheconcentrationofaweakacidise ualto
theconcentrationofitsconjugatebase,pH=pK.
Hence,the
stron er
the
acid,
the
lower
its
K.
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SolutionsofaweakacidatpHsnearitspK resistlargechangesinpHasOH orH+ isadded.
Added rotons react with the weak acids con u ate
baseto
reform
the
weak
acid;
whereas
added
OH
combineswiththeacidtoformitscon u atebase
andwater.
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Asolution
of
aweak
acid
and
its
conjugate
base
(in
theformofasalt)isreferredtoasabuffer. Buffers
are
effective
within
1pH
unit
of
the
pK ofthe
.