ACIDS AND BASES

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65 Terms

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Bronsted-Lowry acids

proton donors

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Bronsted lowry acids release H+ ions when mixed in water

which combine with H2O to form hydroxonium ions H3O+

<p>which combine with H<sub>2</sub>O to form hydroxonium ions H<sub>3</sub>O<sup>+</sup></p>
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Bronsted Lowry base

proton acceptors

<p>proton acceptors</p>
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acids and base dissociate in water

  • acids break up into positive charged ions

  • bases break up into negative charged ions

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the strength of the acid/ base depends on

their ability to dissociate

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the stronger the acid/base

the more they dissociate/ ionise in water

<p>the more they dissociate/ ionise in water</p>
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<p>weak acids like carboxylic/citric acids</p>

weak acids like carboxylic/citric acids

only very slightly dissociate in water so only number of H+ form

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weak acid equilibrium

lies heavily on the left

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<p>weak bases like ammonia</p>

weak bases like ammonia

only slightly dissociate in water

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weak base equilibrium

lies heavily on the left

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acids can only get rid of protons

if a base is available to accept them

<p>if a base is available to accept them</p>
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when water is added to acid

water acts as a base

<p>water acts as a base</p>
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<p>water dissociates into hydroxonium ions AND hydroxide ions</p>

water dissociates into hydroxonium ions AND hydroxide ions

so an equilibrium exists in water

<p>so an equilibrium exists in water</p>
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you can write the equilibrium constant expression for the equilibrium of water

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water dissociates in TINY amounts

so thr equilibrium lies HEAVILY on the left

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waters concentration is so much larger that the cocnentration of H+ and OH-

that the concentration of water is considered a constant value

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ionic product of water Kw

multiplying the Kc expression by the concentration of water produces ANOTHER constant

<p>multiplying the Kc expression by the concentration of water produces ANOTHER constant</p>
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Kw value is the same for an aqueous solution at a certain temperature

FOR EXAMPLE: 298K → 1.00×10-14 mol2 dm-6

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the value of Kw changes

as the temperature changes

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in PURE water the ration of H+ to OH- is 1:1

so [H+]=[OH-]

<p>so [H<sup>+</sup>]=[OH<sup>-</sup>]</p>
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<p>pH scale</p>

pH scale

the measure of the hydrogen ion concentration in a solution

<p>the measure of the hydrogen ion concentration in a solution</p>
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<p>you can calculate the concentration of a solution from the pH</p>

you can calculate the concentration of a solution from the pH

[H+]=10-pH

<p>[H<sup>+]</sup>=10<sup>-pH</sup></p>
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monoprotic acids like HCl and HNO3

each molecule of acid releases 1 proton when it dissociates

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each mole of monoprotic acid produces 1 mole of hydrogen ions

meaning the H+ conc is the same as the acid conc

<p>meaning the H+ conc is the same as the acid conc</p>
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<p>diprotic acids like H2SO4</p>

diprotic acids like H2SO4

each molecule of acid will release 2 protons when it dissociates

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diprotic acids produce 2 moles of hydrogen ions for each mole of acid

meaning the H+ conc is twice the conc of the acid

<p>meaning the H+ conc is twice the conc of the acid</p>
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STRONG ACID EXAMPLES THAT DONATE 1 MOLE OF OH- PER MOLE OF BASE

  • sodium hydroxide

  • potassium hydroxide

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<p>[base]=[OH-]</p>

[base]=[OH-]

0.2 mol dm-3 of sodium hydroxide has 0.2 mol dm-3 [OH-]

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if you know [OH- and the Kw value you can calculate the {H+]

  • find the value of Kw and [OH-]

  • rearrange the equation to make [H+] the subject

  • using the [H+] find the pH using: -log10[H+]=pH

<ul><li><p>find the value of Kw and [OH-]</p></li><li><p>rearrange the equation to make [H+] the subject</p></li><li><p>using the [H+] find the pH using: -log<sub>10</sub>[H+]=pH</p></li></ul><p></p>
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weak acids and bases dissociate only slightly in solution

so the [H+] isn’t the same as the [acid conc]- making it trickier to find the pH

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acid dissociation constant

Ka

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for weak aqueous acid, HA, you get the equilibrium

HA⇄H+ + A-, where only a small amount of HA dissociates

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[HA]»[H+]

[HA at the start]≂[HA at equilibrium]

<p>[HA at the start]≂[HA at equilibrium]</p>
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when dealing with WEAK acids you can assume H+ ions come from the acid

[H+]≂[A-]

<p>[H+]≂[A-]</p>
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finding the pH weak acids

  • write expression for Ka

  • rearrange the equation and substitute values known to find [H+]

  • take the SQUARE ROOT of the number to find [H+]

  • substitute [H+] into -log10 [H+] to find the pH

<ul><li><p>write expression for Ka</p></li><li><p>rearrange the equation and substitute values known to find [H+]</p></li><li><p>take the SQUARE ROOT of the number to find [H+]</p></li><li><p>substitute [H+] into -log10 [H+] to find the pH</p></li></ul><p></p>
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finding the concentration of weak acids

  • substitute the pH value into 10-pH to calculate [H+]

  • write expression for Ka

  • rearrange the equation to give the conc of the acid

  • substitute the value of Ka and [H+] into the equation and solve it

<ul><li><p>substitute the pH value into 10<sup>-pH</sup> to calculate [H+]</p></li><li><p>write expression for Ka</p></li><li><p>rearrange the equation to give the conc of the acid</p></li><li><p>substitute the value of Ka and [H+] into the equation and solve it</p></li></ul><p></p>
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find the Ka of weak acids

if you know the concentration and the pH you can sue them both to find Ka of a weak acid

<p>if you know the concentration and the pH you can sue them both to find Ka of a weak acid</p>
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the value of Ka varies massively between acids

sometimes its easier to find the Ka value from its logarithmic constant pKa

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<p>pKa=-log<sub>10</sub>Ka</p>

pKa=-log10Ka

Ka=10-pKa

<p>Ka=10<sup>-pKa</sup></p>
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questions may ask to calculate the pH of a weak acid and give the concentration of acid and the pKa value

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things to ensure your titration results are as accurate as possible:

  • measure the neutralisation volume as precisely as you possibly can to the nearest 0.05cm3

  • its a good idea to repeat the titration at least 3 times to get a mean titre value

  • don’t use anomalous results, must be within ∓0.1cm3

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a pH curve of the titration can be drawn if you find the pH using a pH probe/meter

the pH of the solution is the equivalence point/ midpoint

<p>the pH of the solution is the equivalence point/ midpoint </p>
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<p>calculating concentration of monoprotic acids</p>

calculating concentration of monoprotic acids

  • write balanced equation for the titration reaction

  • decide what you know already and what you need to know, usually you’re given 2 volumes and a concentration and you’ll need to work out the other concentration

  • for one reagent, you’ll know both the concentrations and volume so you can calculate the number of moles

  • use the molar ratios in the balanced equation to find out how many moles of the other reagent reacted

  • calculate the unknown concentration using conc=(Mol×1000)÷volume

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diprotic acids release 2 protons in a solution like ETHANEDIOIC ACID (HOOC-COOH) the reaction happens in 2 stages because 2 protons are removed from the acid separately,

this means when you titrate ethanedioic acid with a really strong base you get a pH curve with 2 equivelance points

<p>this means when you titrate ethanedioic acid with a really strong base you get a pH curve with 2 equivelance points</p>
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buffer

a solution that resists changes in pH when a small amount of acid/alkali is added

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there are 2 types of buffers

  • acidic buffer

  • basic buffer

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acid buffers pH is less that 7

they contain a mixture of a weak acid with one of its salts

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acid buffers resist pH change when

either a base/acid is added to the solution

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<p>a mixture of ethanoic acid + sodium ethanoate is an example of a buffer solution</p>

a mixture of ethanoic acid + sodium ethanoate is an example of a buffer solution

in the solution there will be loads of undissociated ethanoic acid molecules CH3COOH and ethanoate ions CH3COO- from the salt

altering the concentration of H+/OH- means the equilibrium is able to shift to counteract the change

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resisting an acid

  • the large amount of CH3COO- ensure the buffer can cope with the addition of acid

  • more CH3COOH is produced as the equilibrium shifts left to reduce the concentration of H+ so the pH doesn’t change

<ul><li><p>the large amount of CH3COO- ensure the buffer can cope with the addition of acid</p></li><li><p>more CH3COOH is produced as the equilibrium shifts left to reduce the concentration of H+ so the pH doesn’t change</p></li></ul><p></p>
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resisting a base

  • the large amount of CH3COOH ensure the buffer can cope with the addition of a base

  • CH3COOH dissociates to form H+ IONS SHIFTING THE EQUILIBRIUM RIGHT

<ul><li><p>the large amount of CH3COOH ensure the buffer can cope with the addition of a base</p></li><li><p>CH3COOH dissociates to form H+ IONS SHIFTING THE EQUILIBRIUM RIGHT</p></li></ul><p></p>
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basic buffers have a pH greater than 7

they contain a mixture of weak bases with its salt and can resist the addition of acids/base

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a mixture ammonia as a weak base and ammonia chloride as a salt of ammonia is an example of a basic buffer

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Basic buffer resisting an acid

  • the large amount of ammonia ensure the buffer can resist the addition of acid

  • when H+ is added to a solution it can react with OH- to make water

  • this shifts the equilibrium right to replace the OH- used up

  • water reacts with ammonia to produce NH4+ and OH-

<ul><li><p>the large amount of ammonia ensure the buffer can resist the addition of acid</p></li><li><p>when H+ is added to a solution it can react with OH- to make water</p></li><li><p>this shifts the equilibrium right to replace the OH- used up</p></li><li><p>water reacts with ammonia to produce NH4+ and OH-</p></li></ul><p></p>
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basic buffers resisting a base

  • a large amount of ammonium chloride ensure the buffer resist the addition of a base

  • the extra OH- reacts with the NH4+ to form ammonia and water

  • the equilibrium shifts left to remove OH- from the solution

<ul><li><p>a large amount of ammonium chloride ensure the buffer resist the addition of a base</p></li><li><p>the extra OH- reacts with the NH4+ to form ammonia and water</p></li><li><p>the equilibrium shifts left to remove OH- from the solution</p></li></ul><p></p>
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acidic and basic vuffers also resist pH change when diluted by water

water slightly dissociates so the extra H+ and OH- puh the equilibrium the same amount in both directions leaving it unchanged

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alkaline conditions makes hair rougher

  • shampoos have a pH around 5;5 to keep hair smooth and shiny

  • buffers are in shampoo to maintain the pH while washing hair

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biological washing powders contain buffers

they maintain the pH at the right level for enzymes to work best

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its vital blood stays at a pH near 7.4

so our system contain buffers

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<p>if given the Ka and concentration of the weak acid and its salt you can calculate the pH of an acidic buffer</p>

if given the Ka and concentration of the weak acid and its salt you can calculate the pH of an acidic buffer

  • write expression for Ka

  • rearrange the equation to give an expression for [H+]

  • substitute the value of Ka and the concentration of the acid and its salt into the equation

  • solve the equation to find a value for [H+]

  • substitute the [H+] into -log10[H+]

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other ways to make buffers

mixing a weak acid and a small amount of alkali to that some of the acid is neutralised is salt while some is left unneutralised

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this reaction mixture would contain a weak acid and its salt to technically it is still an acidic buffer so you can work out its pH

  • write out neutralisation equation

  • calculate number of moles of acid/base at the start of reaction

  • use the molar ratios in the equation to work out the moles of acid and salt left at the end of the reaction

  • calculate the conc of the acid and salt in the buffer solution by dividing the moles at the end of the reaction by the volume of the solution

  • then calculate the pH using Ka

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