Equilibria Flashcards

1
Q

dynamic equilibrium

A

when the rates of the forward and back reactions are equal
- no net change in concentrations of reactants or products

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2
Q

equilbrium constant

A

K - quantify the relative concentrations of reactants and products at equilibrium

aA +bB –> cC + dD
k = [C]c [D]d / [A]a [B]b

only effected by temperature

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3
Q

if K is small…

A

then more reactants, equilibrium lies left

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4
Q

if K is large …

A

then more prodcuts, reaction lies right

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5
Q

if K is intermediate…

A

then similar magnitude

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6
Q

reaction quotient

A

gives us an indication of the reaction progress at all points of chemical reaction, even before the equilibrium occurs

same equation as K

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7
Q

if Q=K

A

then reaction is already at equilibrium

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8
Q

if Q<K

A

need to increase Q, so increase product concentration, equilbrium shift to the right in order to get to equilibrium

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9
Q

if Q>K

A

need to decrease Q so increase reactant concentration, equilibrium shift towards the reactants left

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10
Q

changes in temperature and equilbrium

A

a change in temperature will cause the system to shift to counteract the change

increase in temp causes shift to endothermic reaction as increase heat will be absorbed

decrease in temp causes shift to exothermic reaction as heat will be released

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11
Q

change in pressure for equilbrium/conc

A

a change in pressure will cause a shift to counteract change, only taking into occur the gaseous molecules though

increasing pressure shifts equilibrium to side with less moles gas

decreasing pressure shifts eq to side with more moles

this idea is same with concentration

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12
Q

effective oxygen transport

A

ultises le chatiler principle
Hb(aq) + 4O2 (g) –> Hb(O2)4 (aq)

in the lungs, high pressure - system shifts to the least number of molecules so oxygen binds to haemoglobin

in body tissue, low pressure so system shifts to most moles so oxygen is released

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13
Q

haemoglobin

A

a protein that transports oxygen from lungs to body tissue through the blood,

has 4 sub units 2 alpha and 2 beta chain

each sub unit has a heme group with iron ion that binds to one oxygen

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14
Q

oxygen binding and shape of heme group

A

deoxygenated heme is domed/non planar

oxygenated heme is planar

binding of oxygen brings the Fe into the plane,called cooperative binding and distorts the shape to allow for oxygen to bind to the other 3 sites

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15
Q

bohr effect

A

co2 and H+ promotes the release of oxygen as when a low ph
H+, the histidine residue is protonated which leads to the formation of salt bridges to distort the heme iron, favouring the domed conforrmation

co2 role - co2 binds to the amino group to produce a negatively charged group -NHCOO- to favour domed

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16
Q

blood colour

A

the different conformations give the blood different colours

oxygenated haemoglobin absorbs blue/green light so appears red

deoxygenated haem absorbs red so give blue tinge

17
Q

porphyria

A

blood disorder which affects the ability of body to make haemologbin and ability to take up oxygen

leads to blue/purple blood and sensitivity to light

18
Q

gibbs free energy and equilbrium

A

for reactions at equilbrium
- no capacity to do work so gibbs free energy = 0

for forward
- Q is less than K so gibbs free energy G<0 negative so Q=K

for backwards
- Q is higher than K so gibbs is >0 positive

19
Q

vant hoff isotherm

A

delta rG = - RTlnK

used for determining if a reaction is sponanteous and in which direction

when Q<K, the forward reaction is favour, ln(Q/K) < 0 S, delta r G <0, so it is negative so forward reaction is favoured

when Q>K, backward reaction is favoured, ln(Q/K) >0 so delta r G >0, so positive, reverse reaction is favoured.

20
Q

example of van’t Hoff:
reaction between glucose and phosphate to form glucose 6 phosphate, concen at equilbrium 298k, [G] = 0.0080M, [P] = 0.0125M, [6GP] = 2.78X10-5M. Calculate K and delta r G, is it spontaneous ?

A

delta r G = -RTlnK

first K = 2.78x10-5 / 0.008, 0.0125 =0.278

delta r G = -8.314 x 298 x ln 0.278 = 3.17kjmol-1

forward reaction is not spontaneous but backward is as delta rG >0

21
Q

parallel coupling

A

reactions occur at same place and same time

22
Q

sequential coupling

A

one reaction occurs then using outcome of reaction to power the next

aims to exploit le chateliers principle regarding concentration change

23
Q

acid base equilbria

A

proton transfer is rapid so all acid base systems can be considered to be at equilbrium

  • so dont need to worry about Q
24
Q

autoprotolysis of water

A

H2O + H2O –> H3O+ + OH-

ionic product of water at 25 degrees = kw = 1x10-14

25
Q

blood ph range

A

7.4 normal value
cannot deviate more than +- 0.4 units

26
Q

weak acids

A

HA + H2O –> H3O+ + A-
HA = weak acid
A- = conjugate base

only partially dissociates

27
Q

Ka

A

ka = [h3o+] x[a-] /[ha]

the larger ka is the more acidic
pka = -log10ka - the smaller this is the more acidic

28
Q

weak bases

A

B + H2O –> BH+ + OH-
BH = weak base

OH = conjugate acid

29
Q

conjugate acid base pairs in aqueous solution

A

when combining Ka and Kb, get [h3o+][oh-] which is equal to kw

therefore kw = ka x kb

andddddd, pkw = pka + pkb

this implies that a strong acid will have a weak conjugate base and vice versa

30
Q

temperature and ionisation of water

A

at a higher temperature, the ionisation of water increases because the reaction is endothermic so increase temp, equilibrium shifts to right to increase products

this increases h3o+ so at higher temps, the ph is also lower, more acidic as more acid

31
Q

buffers

A

to resist changes in ph
must have an acid component to react with OH

must have basic component to react with h3o+

uses weak acid and its salt to get conjugate base

32
Q

if acid is added to buffer solution

A

increase in h+ conc, cause a shift to the left to decrease
h+ will react with conjugate base to reform acid

equilibrium shifts to the left/backward

33
Q

if base is added to buffer

A

increase in oh- so equilbrium shifts to the right/forward to increase h+ conc

34
Q

henderson hasselbalch equation

A

ph = pka + log ([A-]/[HA])

rearranging Ka equation to make H+ the subject then taking logs of both sides

can use this to calculate the ph of buffers

35
Q

buffer capacity

A

the maximum amount of either strong acid or strong base that can be added before a significant change in pH will occur

36
Q

polprotic acids

A

can have multiple uses as has lots of hydrogens to donate

37
Q

titratation curve strong base and acid

A

starts ph low and ends high

100% ionised so products dominate

ph of 7 = equivialnce point

38
Q

molarity

A

to work out concentration
mol / volume in litres

39
Q

titration of weak acid and strong base

A

not so low ph starting,