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ACID-BASE THEORY:-
ARRHENIUS THEORY:-
Acid is a substance which gives hydrogen ion (H+) in an aqueous
medium.
Base is substance which gives hydroxy ions (OH–) in an aqueous
medium.
These theory are only applicable for aqueous titration.
LOWRYAND BRONSTED’S THEORY:-
Acid is a substance which donate a proton (hydrogen ion).
base is a substance which accept a proton.
LEWIS’S THEORY:-
Acid is a substance which accept electron pair.
Base is a substance which donate electron pair.
ACID BASE TITRATION
USANOVICH THEORY:-
Acid is a chemical species that reactswith a base thereby
donating cations oraccepting anions orelectrons.
Base is achemical species thatreactswith an acid thereby
donating anions orelectronsoraccepting cations.
LUX-FLOOD CONCEPT:-
Acid is a substancewhich acceptoxide-ion.
Base is thesubstancewhich donateoxide ions.
LAW OF MASS ACTION
The rateof achemical reaction is proportional to theactive massesof the
reacting substance.
A + B C + D
According to law of massaction
Vf = k1[A][B]
Vb = k2[C][D]
Vf = Velocity of forward reaction
Vb = Velocity of backward reaction
[A], [B], [C], [D] is equal to molarconcentration of A, B, C & D
K1 & K2 areconstant
Atequilibirium state, velocity of forward reaction is equal tovelocity of
backward reaction
Vf = Vb
k1[A][B] = k2[C][D]
k1 and k2 areconstant hence,
where k is theequilibirium constant of the reaction.
where, a,b,c……..and p,q,rare the no.of moleculesof reacting species.
DISSOCIATION CONSTANT
The [H2O] usuallyconsidered to beconstant
Kw=[H+][OH]
Where kw is ion productof water.
Dissociation concept of acid and base:-
A strong acid dissociate ( or ionizes) completely in aqueoussolution to
form hydronium ions (H3O+)
HCl + H2O H30 + Cl-
A weak acid does notdissociate ( or ionizes) completely in aqueous
solution to form hydronium ions (H3O+)
CH3COOH + H20 CH3COOH + H3O+
A strong basedissociatecompletely in aqueous solution to form
hydronium ions (OH-)
NaOH Na+ + OH-
A weak basedoes notdissociatecompletely in aqueous solution to form
hydronium ions (OH-)
NH4OH NH4+ + OH-
EXAMPLES OF WEAK/ STRONG ACID:-
TYPE EXAMPLES
Strong Acids hydrochloric acid (HCl), sulfuric acid (H2SO4), nitric acid
(HNO3)
Weak Acids acetic acid (CH3COOH), hydrofluoric acid (HF), oxalic acid
(COOH)2
Strong Bases sodium hydroxide (NaOH), potassium hydroxide (KOH),
lithium hydroxide (LiOH)
Weak Bases Liquid ammonia(NH3)
ACID BASE TITRATION
An Acid-base titration is a quantitativeanalysis of acid and bases bywhich
known concentration of an acid or base i.e. titrant neutralizes the
unknown concentrationof an acid or base i.e. titrand.
it is based on neutralization reaction between acid and bases that form
water by combination of H3O+ ions, therefore known as water forming
reaction.
HA(Acid) + H2O H3O+
H3O+ + OH H2O
Theestimationof an alkaline solution by using a standard acidic solution
is known as Acidimetry.
Theestimationof an acidicsolution by using a standard alkalinesolution
is known as Alkalimetry.
The titration progress can be monitored byvisual indicators, PH electrodes
or both.
TYPE OF TITRATION & NEUTRALIZATION CURVE:-
The mechanism of neutralizationcan be understood bystudying the
change in the hydrogen ion concentration during the course of
appropriate titration.
1)Theequivalence pointof an acid-base reaction (the pointatwhich the
amounts of acid and of base are just sufficient to cause complete
neutralization).
2)The pH of thesolutionatequivalence point is dependent on the
strengthof theacid and strengthof the base used in the titration.
Forstrong acid-strong base titration, pH = 7 at
equivalence point
Forweak acid-strong base titration, pH > 7 atequivalence
point
Forstrong acid-weak base titration, pH < 7 atequivalence
point
The neutralizationcurvecan becategorized into four
classes, which enlist below:-
1) Titrationof a strong acid with strong base
2) Titrationof a weak acid with a strong base
3) Titrationof a strong acid with aweak base
4) Titrationof aweak basewithaweak acid
1) TITRATION OF A STRONG ACID WITH STRONG BASE:-
Supposeanalyte is hydrochloricacid HCl (strong acid) and the titrant is
sodium hydroxide NaOH (strong base).
If westart plotting the pH of theTitrationcurveof a strong acid witha strong
base.
Point1:-
At point 1, No NaOH added yet, so the pH of theanalyte is low (becauseof it
predominantlycontains H3O+ fromdissociationof HCl).
HCl + H2O H30 + Cl-
As NaOH is added dropwise, H3O+ slowlystartsgetting consumed by OH-
produced bydissociationof NaOH.
Analyte is still acidicdue topredominanceof H3O+ ions.
Point2:-
This is the pH recorded ata time point just beforecomplete neutralization
takes place.
Equivalent point
Point 3:-
This is theequivalence pointwhere, moles of NaOH is equal to moles of HCl
in theanalyte.
At this point, H3O+ ionsarecompletely neutralized by OH- ions.
Thesolutiononly has salt (NaCl) and waterand thereforethe pH is neutral
i.e. pH 7.
HCl + NaOH
Equivalentpoint
NaCl + H O
2
Point4:-
Addition of NaOH continues, pH starts becoming basic because HCl has
been completely neutralized and nowexcessof OH- ions are present in the
solution (fromdissociationof NaOH).
Afterthis NaOH reactwith indicatorand producecolorthat is end point.
NaOH Na+ + OH-
2) TITRATION OF A WEAK ACID WITH A STRONG BASE:-
Let’sassumeouranalyte is aceticacid CH3COOH (weak acid) and the titrant
is sodium hydroxide NaOH (strong base).
If we start plotting the pH of the analyte against the volume of NaOH that
weareadding from the burette, wewill geta titrationcurveas shown below.
Point1:-
No NaOH added yet, so the pH of theanalyte is low (it predominantly
contains H3O+ fromdissociationof CH3COOH).
CH3COOH + H2O CH3COOH- + H3O+
As NaOH is added dropwise, H3O+ slowlystartsgettingconsumed by OH-
produced bydissociationof NaOH).
Butanalyte is still acidicdue topredominanceof H3O+ ions.
Point2:-
This is the pH recorded ata time point just beforecomplete neutralization
takes place.
Equivalentpoint
Point 3:-
This is theequivalence point. At this point, molesof NaOH added is equal to
moles of CH3COOH in the analyte. The H3O+ are completely neutralized by
OH-ions.
Thesolutioncontainsonly CH3COONasaltand H2O.
CH3COOH + NaOH Equivalentpoint CH3COONa + H2O+
In thecaseof aweak acid versusa strong base, the pH is not neutral at the
equivalence point.
Thesolution is basic (pH~9) at theequivalence point. Let’s reason thisout.
Point4:-
Addition of NaOH continues, pH starts becoming basic because
CH3COOH has been completely neutralized and now excess of OH- ions
are present in thesolution (fromdissociationof NaOH).
Afterthis NaOH reactwith indicatorand producecolorthat is end point.
3) TITRATION OF A STRONG ACID WITH A WEAK BASE:-
Supposeouranalyte is hydrochloricacid HCl (strong acid) and the titrant is
ammonia NH3 (weak base).
If westart plotting the pH of theanalyte against thevolumeof NH3 are
adding from the burette, wewill geta titrationcurveas shown below.
Point1:-
No NH3, added yet, so the pH of theanalyte is low (it predominantlycontains
H3O+ fromdissociationof HCl).
HCl + H2O H30 + Cl-
As NH3 is added dropwise, H3O+ slowlystartsgetting consumed by NH3.
Analyte is still acidicdue topredominanceof H3O+ ions.
NH3 + H3O NH4+ + H2O
Point2:-
This is the pH recorded ata time point just beforecomplete neutralization
takes place.
Point3:-
This is theequivalence point. At this point, molesof NH3 added is equal to
the molesof HCl in theanalyte.
The H3O+ ionsarecompletely neutralized by NH3.
In thecaseof aweak baseversusa strong acid, the pH is not neutral at the
equivalence point.
Thesolution is in fact acidic (pH~5.5) at theequivalence point.
At theequivalence point, thesolutiononly has ammonium ions NH4 and
chloride ions Cl-. Whereammonium ion NH4 is theconjugateacid of the
weak base NH3. So NH4 is a relatively strong acid (weak base NH3 has a
strong conjugate acid), and thus NH4 will react with H2O to produce
hydronium ions making the solutionacidic.
NH4+ + H2O NH3 + H3O+
Makessolutionacidicatequivalentpoint
Point 4:-
After the equivalence point, NH3 addition continues and is
in excess, so the pH increases. NH3 isaweak baseso the pH
isabove 7.
After this NaOH react with indicatorand producecolor that
isend point.
4) TITRATION OF A WEAK BASE WITH A WEAK ACID:-
Supposeouranalyte is NH3 (weak base) and the titrant is aceticacid
CH3COOH (weak acid).
If westart plotting the pH of theanalyteagainst thevolumeof aceticacid
thatweareadding from the burette, wewill geta titrationcurveas shown
below.
There isn’tany steep bit in this plot.
There is just becauseof a ‘pointof inflexion’ at theequivalence point.
Lack of anysteepchange in pH throughoutthe titrationrenders.
Titration of a weak baseversus a weak acid is difficult, and not much
informationcan beextracted fromsuch acurve.
The chief feature of the curve is that change of PH near equivalent point
and during whole titration is verygradual hence theend pointcannot be
detected byordinary indicatorso mixed indicatoris often used.
Even itcan bedone by using non aqueousacid base titration.
CHOICE OF INDICATOR IN TITRATION
S.NO TYPE OF TITRATION PH INDICATOR
1 Strong acid verses strong base 2-10 Any indicators can be used like
Phenolphthaleine
Methyl orange
Methyl Red
2 Strong acid verses weak base 2-6 Methyl orange
Methyl Red
3 Weak acid verses strong base 8-10 Phenolphthaleine
Thymol Phthaleine
4 Weak acid verses Weak base - Mixed indicators are used like neutral
red methylene blue for dilute
ammonia or ethanoic acid.
S.No INDIACATOR
NAME
PH COLOR OBSERVATION
ACID BASE
1 Thymol blue 1.2-2.8 Red Yellow
2 Quinaldine Red 1.4-3.2 Colourless Red
3 Methyl orange 2.9-4.6 Red Orange
4 Methyl Red 4.2-6.3 Red Yellow
5 Bromo Thymol
blue
6-7.6 Yellow Blue
6 Phenol Red 6.8-8.6 Yellow Red
7 Phenolphthaleine 8.3-10 Colourless Pink
8 Thymol Phthaleine 9.5-10.5 Colourless Blue
MIXED INDICATOR:-
Mixtureof twoor more indicatorsare used togivea sharpend pointovera
narrowand selected rangeof PH.
MIXTURE OF
INDICATOR
COMPOSITION PH COLOR CHANGE
Bromocresol Green :
Methyl Green
1 Part of 0.1% aqueous solution of
sodium salt : 1 Part of 0.2% Water.
4.3 Orange blue green
Bromocresol Green :
Chlorophenol Red
1 Part of 0.1% aqueous solution of
sodium salt : 1 Part of 0.1% aqueous
solution of sodium salt.
6.1 Pale green blue violet
Bromomethyl blue :
Neutral Red
1 Part of 0.1% solution in ethanol : 1
Part of 0.1% solution in ethanol.
7.2 Rose Pink green
Bromomethyl blue :
Phenol Red
1 Part of 0.1% aqueous solution of
sodium salt : 1 Part of 0.1% aqueous
solution of sodium salt.
7.5 Yellow violet
Thymol blue : Cresol
Red
3 Part of 0.1% aqueous solution of
sodium salt : 1 Part of 0.1% aqueous
solution of sodium salt.
8.3 Yellow violet
UNIVERSAL INDICATOR:-
A universal indicator is made of a solution of several compound likewater, propane 1-
ol, Phenolphthaleine, sodium salt, Thymol blue etc. that exihibit several color
changesovera wide range of PH values to indicate the acidityor basicityof solutions.
PH
RANGE
DESCRIPTION COLOUR
< 3 Strong acid Red
3–6 Weak acid Orange or yellow
7 Neutral Green
8–11 Weak alkali Blue
> 11 Strong alkali Violet or Indigo
Thank you……

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acidbasetitration-210409125353.pptx

  • 1.
  • 2. ACID-BASE THEORY:- ARRHENIUS THEORY:- Acid is a substance which gives hydrogen ion (H+) in an aqueous medium. Base is substance which gives hydroxy ions (OH–) in an aqueous medium. These theory are only applicable for aqueous titration. LOWRYAND BRONSTED’S THEORY:- Acid is a substance which donate a proton (hydrogen ion). base is a substance which accept a proton. LEWIS’S THEORY:- Acid is a substance which accept electron pair. Base is a substance which donate electron pair. ACID BASE TITRATION
  • 3. USANOVICH THEORY:- Acid is a chemical species that reactswith a base thereby donating cations oraccepting anions orelectrons. Base is achemical species thatreactswith an acid thereby donating anions orelectronsoraccepting cations. LUX-FLOOD CONCEPT:- Acid is a substancewhich acceptoxide-ion. Base is thesubstancewhich donateoxide ions.
  • 4. LAW OF MASS ACTION The rateof achemical reaction is proportional to theactive massesof the reacting substance. A + B C + D According to law of massaction Vf = k1[A][B] Vb = k2[C][D] Vf = Velocity of forward reaction Vb = Velocity of backward reaction [A], [B], [C], [D] is equal to molarconcentration of A, B, C & D K1 & K2 areconstant Atequilibirium state, velocity of forward reaction is equal tovelocity of backward reaction Vf = Vb
  • 5. k1[A][B] = k2[C][D] k1 and k2 areconstant hence, where k is theequilibirium constant of the reaction. where, a,b,c……..and p,q,rare the no.of moleculesof reacting species.
  • 6. DISSOCIATION CONSTANT The [H2O] usuallyconsidered to beconstant Kw=[H+][OH] Where kw is ion productof water.
  • 7. Dissociation concept of acid and base:- A strong acid dissociate ( or ionizes) completely in aqueoussolution to form hydronium ions (H3O+) HCl + H2O H30 + Cl- A weak acid does notdissociate ( or ionizes) completely in aqueous solution to form hydronium ions (H3O+) CH3COOH + H20 CH3COOH + H3O+ A strong basedissociatecompletely in aqueous solution to form hydronium ions (OH-) NaOH Na+ + OH- A weak basedoes notdissociatecompletely in aqueous solution to form hydronium ions (OH-) NH4OH NH4+ + OH-
  • 8. EXAMPLES OF WEAK/ STRONG ACID:- TYPE EXAMPLES Strong Acids hydrochloric acid (HCl), sulfuric acid (H2SO4), nitric acid (HNO3) Weak Acids acetic acid (CH3COOH), hydrofluoric acid (HF), oxalic acid (COOH)2 Strong Bases sodium hydroxide (NaOH), potassium hydroxide (KOH), lithium hydroxide (LiOH) Weak Bases Liquid ammonia(NH3)
  • 9. ACID BASE TITRATION An Acid-base titration is a quantitativeanalysis of acid and bases bywhich known concentration of an acid or base i.e. titrant neutralizes the unknown concentrationof an acid or base i.e. titrand. it is based on neutralization reaction between acid and bases that form water by combination of H3O+ ions, therefore known as water forming reaction. HA(Acid) + H2O H3O+ H3O+ + OH H2O Theestimationof an alkaline solution by using a standard acidic solution is known as Acidimetry. Theestimationof an acidicsolution by using a standard alkalinesolution is known as Alkalimetry. The titration progress can be monitored byvisual indicators, PH electrodes or both.
  • 10. TYPE OF TITRATION & NEUTRALIZATION CURVE:- The mechanism of neutralizationcan be understood bystudying the change in the hydrogen ion concentration during the course of appropriate titration. 1)Theequivalence pointof an acid-base reaction (the pointatwhich the amounts of acid and of base are just sufficient to cause complete neutralization). 2)The pH of thesolutionatequivalence point is dependent on the strengthof theacid and strengthof the base used in the titration. Forstrong acid-strong base titration, pH = 7 at equivalence point Forweak acid-strong base titration, pH > 7 atequivalence point Forstrong acid-weak base titration, pH < 7 atequivalence point
  • 11. The neutralizationcurvecan becategorized into four classes, which enlist below:- 1) Titrationof a strong acid with strong base 2) Titrationof a weak acid with a strong base 3) Titrationof a strong acid with aweak base 4) Titrationof aweak basewithaweak acid
  • 12. 1) TITRATION OF A STRONG ACID WITH STRONG BASE:- Supposeanalyte is hydrochloricacid HCl (strong acid) and the titrant is sodium hydroxide NaOH (strong base). If westart plotting the pH of theTitrationcurveof a strong acid witha strong base.
  • 13. Point1:- At point 1, No NaOH added yet, so the pH of theanalyte is low (becauseof it predominantlycontains H3O+ fromdissociationof HCl). HCl + H2O H30 + Cl- As NaOH is added dropwise, H3O+ slowlystartsgetting consumed by OH- produced bydissociationof NaOH. Analyte is still acidicdue topredominanceof H3O+ ions. Point2:- This is the pH recorded ata time point just beforecomplete neutralization takes place.
  • 14. Equivalent point Point 3:- This is theequivalence pointwhere, moles of NaOH is equal to moles of HCl in theanalyte. At this point, H3O+ ionsarecompletely neutralized by OH- ions. Thesolutiononly has salt (NaCl) and waterand thereforethe pH is neutral i.e. pH 7. HCl + NaOH Equivalentpoint NaCl + H O 2 Point4:- Addition of NaOH continues, pH starts becoming basic because HCl has been completely neutralized and nowexcessof OH- ions are present in the solution (fromdissociationof NaOH). Afterthis NaOH reactwith indicatorand producecolorthat is end point. NaOH Na+ + OH-
  • 15. 2) TITRATION OF A WEAK ACID WITH A STRONG BASE:- Let’sassumeouranalyte is aceticacid CH3COOH (weak acid) and the titrant is sodium hydroxide NaOH (strong base). If we start plotting the pH of the analyte against the volume of NaOH that weareadding from the burette, wewill geta titrationcurveas shown below.
  • 16. Point1:- No NaOH added yet, so the pH of theanalyte is low (it predominantly contains H3O+ fromdissociationof CH3COOH). CH3COOH + H2O CH3COOH- + H3O+ As NaOH is added dropwise, H3O+ slowlystartsgettingconsumed by OH- produced bydissociationof NaOH). Butanalyte is still acidicdue topredominanceof H3O+ ions. Point2:- This is the pH recorded ata time point just beforecomplete neutralization takes place.
  • 17. Equivalentpoint Point 3:- This is theequivalence point. At this point, molesof NaOH added is equal to moles of CH3COOH in the analyte. The H3O+ are completely neutralized by OH-ions. Thesolutioncontainsonly CH3COONasaltand H2O. CH3COOH + NaOH Equivalentpoint CH3COONa + H2O+ In thecaseof aweak acid versusa strong base, the pH is not neutral at the equivalence point. Thesolution is basic (pH~9) at theequivalence point. Let’s reason thisout.
  • 18. Point4:- Addition of NaOH continues, pH starts becoming basic because CH3COOH has been completely neutralized and now excess of OH- ions are present in thesolution (fromdissociationof NaOH). Afterthis NaOH reactwith indicatorand producecolorthat is end point.
  • 19. 3) TITRATION OF A STRONG ACID WITH A WEAK BASE:- Supposeouranalyte is hydrochloricacid HCl (strong acid) and the titrant is ammonia NH3 (weak base). If westart plotting the pH of theanalyte against thevolumeof NH3 are adding from the burette, wewill geta titrationcurveas shown below.
  • 20. Point1:- No NH3, added yet, so the pH of theanalyte is low (it predominantlycontains H3O+ fromdissociationof HCl). HCl + H2O H30 + Cl- As NH3 is added dropwise, H3O+ slowlystartsgetting consumed by NH3. Analyte is still acidicdue topredominanceof H3O+ ions. NH3 + H3O NH4+ + H2O Point2:- This is the pH recorded ata time point just beforecomplete neutralization takes place.
  • 21. Point3:- This is theequivalence point. At this point, molesof NH3 added is equal to the molesof HCl in theanalyte. The H3O+ ionsarecompletely neutralized by NH3. In thecaseof aweak baseversusa strong acid, the pH is not neutral at the equivalence point. Thesolution is in fact acidic (pH~5.5) at theequivalence point. At theequivalence point, thesolutiononly has ammonium ions NH4 and chloride ions Cl-. Whereammonium ion NH4 is theconjugateacid of the weak base NH3. So NH4 is a relatively strong acid (weak base NH3 has a strong conjugate acid), and thus NH4 will react with H2O to produce hydronium ions making the solutionacidic. NH4+ + H2O NH3 + H3O+ Makessolutionacidicatequivalentpoint
  • 22. Point 4:- After the equivalence point, NH3 addition continues and is in excess, so the pH increases. NH3 isaweak baseso the pH isabove 7. After this NaOH react with indicatorand producecolor that isend point.
  • 23. 4) TITRATION OF A WEAK BASE WITH A WEAK ACID:- Supposeouranalyte is NH3 (weak base) and the titrant is aceticacid CH3COOH (weak acid). If westart plotting the pH of theanalyteagainst thevolumeof aceticacid thatweareadding from the burette, wewill geta titrationcurveas shown below.
  • 24. There isn’tany steep bit in this plot. There is just becauseof a ‘pointof inflexion’ at theequivalence point. Lack of anysteepchange in pH throughoutthe titrationrenders. Titration of a weak baseversus a weak acid is difficult, and not much informationcan beextracted fromsuch acurve. The chief feature of the curve is that change of PH near equivalent point and during whole titration is verygradual hence theend pointcannot be detected byordinary indicatorso mixed indicatoris often used. Even itcan bedone by using non aqueousacid base titration.
  • 25. CHOICE OF INDICATOR IN TITRATION S.NO TYPE OF TITRATION PH INDICATOR 1 Strong acid verses strong base 2-10 Any indicators can be used like Phenolphthaleine Methyl orange Methyl Red 2 Strong acid verses weak base 2-6 Methyl orange Methyl Red 3 Weak acid verses strong base 8-10 Phenolphthaleine Thymol Phthaleine 4 Weak acid verses Weak base - Mixed indicators are used like neutral red methylene blue for dilute ammonia or ethanoic acid.
  • 26. S.No INDIACATOR NAME PH COLOR OBSERVATION ACID BASE 1 Thymol blue 1.2-2.8 Red Yellow 2 Quinaldine Red 1.4-3.2 Colourless Red 3 Methyl orange 2.9-4.6 Red Orange 4 Methyl Red 4.2-6.3 Red Yellow 5 Bromo Thymol blue 6-7.6 Yellow Blue 6 Phenol Red 6.8-8.6 Yellow Red 7 Phenolphthaleine 8.3-10 Colourless Pink 8 Thymol Phthaleine 9.5-10.5 Colourless Blue
  • 27. MIXED INDICATOR:- Mixtureof twoor more indicatorsare used togivea sharpend pointovera narrowand selected rangeof PH. MIXTURE OF INDICATOR COMPOSITION PH COLOR CHANGE Bromocresol Green : Methyl Green 1 Part of 0.1% aqueous solution of sodium salt : 1 Part of 0.2% Water. 4.3 Orange blue green Bromocresol Green : Chlorophenol Red 1 Part of 0.1% aqueous solution of sodium salt : 1 Part of 0.1% aqueous solution of sodium salt. 6.1 Pale green blue violet Bromomethyl blue : Neutral Red 1 Part of 0.1% solution in ethanol : 1 Part of 0.1% solution in ethanol. 7.2 Rose Pink green Bromomethyl blue : Phenol Red 1 Part of 0.1% aqueous solution of sodium salt : 1 Part of 0.1% aqueous solution of sodium salt. 7.5 Yellow violet Thymol blue : Cresol Red 3 Part of 0.1% aqueous solution of sodium salt : 1 Part of 0.1% aqueous solution of sodium salt. 8.3 Yellow violet
  • 28. UNIVERSAL INDICATOR:- A universal indicator is made of a solution of several compound likewater, propane 1- ol, Phenolphthaleine, sodium salt, Thymol blue etc. that exihibit several color changesovera wide range of PH values to indicate the acidityor basicityof solutions. PH RANGE DESCRIPTION COLOUR < 3 Strong acid Red 3–6 Weak acid Orange or yellow 7 Neutral Green 8–11 Weak alkali Blue > 11 Strong alkali Violet or Indigo