Final Copy of Basic Practical Chemistry
Final Copy of Basic Practical Chemistry
DEDICATION:
I dedicate this book to my parents Mr.P’Ochure Michael Ocaya & Mrs.Ocaya
Christian Akumu the late (RIP) for continued love, moral, financial, & spiritual
assistance rendered to me since childhood and throughout my life to-date.
There are those special people in this world who give & give without taking who
offer without asking for much in return, I dedicate this book to the best of them.
ACKNOWLEGEMENTS:
I am grateful to my parents for whatever they have rendered to me.
Work of this nation is by no means a single person’s effort. It has been a result of
many kind and helpful people who have willingly assisted me whenever
approached.
I am also grateful to my great teachers, Mr. Otto Stephen, Mr.Obala Peter RIP,
Okello Charles Waliky & Mr.Kilama Stephen of Sir Samuel Baker School, who
labored to take me thought the impenetrable maze of science to make me
appreciate it to the point of producing work of this nature.
I am also particularly grateful to senior Chemist Mr. Otto Stephen for the tireless
efforts, advice & guidance he accorded to me during the writing of this book so as
to reach this standard.
Am grateful to him for keeping everything going while I am off in my academic
pursuance and university.
More so I am grateful for his sharp editorial eye.
support and advise they rendered to me when I was carrying out research on the
subject.
To my former students of Lira Integrated Senior Secondary School, Especially
Adopo Julius was my greatest motivators.
PREFACE:
Revision questions and Answers are provided topic by topic meanwhile UNEB
sample questions are also provided.
These questions are intended to form the basics of interactions between teachers
and students or student discussion groups.
To emphasize this, the simplified language and approach used in this book aims
at making chemistry as a subject easy to understand, straight forward, attractive
& friendly to students.
This book has been developed in line with the most recent developments of
Uganda national curriculum center teaching syllabus and UNEB syllabus.
It is therefore of great advantage to all secondary schools most especially those
which may not be able to provide a wide range of text books for use by their
teachers, students & the discussion groups.
The trial questions are intended to enhance group discussion for students,
reference questions are for exams & seminars.
We hope that the student who follows the layout of this book will in the end have
got enough experience in enabling a wide range of questions in exams.
The students will be fully prepared to both mock and UNEB examinations.
We have a vision as most students will turn as scientists to meet the ever
increased demand for science graduate in various technical discipline of
medicine, agriculture & forestry.
And finally, I dedicate this book to my special wife Ms Baseke Bridget (Tutor)
Felix Rubangakene Geofrey.
C. This involves examining the appearance, smell and texture of the given
unknown sample. The appearance of the sample gives a rough idea as to
what it could be, particularly whether hydrated or not, transitional or non-
transitional elements.
i. Bases and carbonates are mainly Powderly and anhydrous.
ii. Nitrates, Sulphates and chlorides are mainly crystalline.
iii. Most crystalline substances are hydrated.
iv. Coloured solids in pure state may give a clue (hint) about the
identity of the cation present in the solid.
Cations/anions Colour of the solid or Aqueous
solution/Deductions/Conlusions
Cu 2+ Blue or Green
Fe , Cr , Ni
2+ 3+ 2+ Green
Fe 3+ Yellow/Brown
Co 2+ Pink or Red
Mn 2+ Pink
Cr2O7 2- Orange
CrO4 2- Yellow
Zn ,Pb ,Ca ,Al ,Mg ,NH4 & Ba
2+ 2+ 2+ 3+ 2+ + 2+ White
In general coloured solids suggest the presence of transition metal cations. Non-
coloured (white) solid suggests that the sample provided contains non-transition
metal cations. Examples: Zn2+,Pb2+,Ca2+,Al3+,Mg2+,NH4+,Sn2+,Sn4+ or Ba2+
SOLUBILITY OF COMPOUNDS.
Note: Water and dilute acids are usually used as solvents to dissolve compounds.
a) Completely dissolves in water, -Soluble salt or a mixture of soluble
forming a solution. transition or non-transition salts,
depending on the colour of solution.
b) Partially dissolves in water -A mixture of soluble and insoluble
forming a suspension. salts,I.e The residue is an insoluble
salt while a filtrate is a soluble salt.
2. ACTION OF HEAT ON SOLIDS:
Heating a compound may results in to decomposition, formation of a sublimate,
colourless liquid condensing on cooler parts of the boiling tube or evolution of
gases; which must be tested for and formation of a residue.
A spatula end-ful of the unknown sample is heated gently and then very strongly
in a dry boiling tube until no further change.
Golden tips:
The purpose of heating a solid is to decompose it in to recognizable products.
During heating the following must be noted.
Bromine Bromide,Br-
Iodine vapour Iodide,I-
Propanone (Acetone vapour) Ethanoate,CH3COO-
Carbon dioxide Carbonate, hydrogen
carbonate,Oxalate or Ethanoate
Nitrogen dioxide Nitrate,NO3-
Sulphur dioxide Sulphite,Sulphate or Thiosulphate
ions
Notes:
a) If an ammonium salt is heated, it may sublime, leading to the identification
of ammonium ions.
b) Most sulphates are stable to heat except iron (III) sulphate and copper (II)
sulphate. Which decomposes on heating to their respective oxides
according the equation below?
Equations:
Heat
CuSO4(s) CuO(s) + SO3(g)
2FeSO4(s) Fe2O3(s) + SO3(g) + SO2(g)
c) Many hydrated chlorides undergo self-hydrolysis on heating producing
hydrogen chloride and on stronger heating; forms chlorine e.g. hydrated
copper (II) chloride.
d) Acetates/ethanoates decompose on heating to give acetone (propanone
vapour) which has a sweet smell, carbon dioxide gas and a metallic oxide.
Equations:
(CH3COO)2Ni(s) NiO(s) + CH3COCH3(g) + CO2(g)
(CH3COO)2Pb(s) PbO(s) + CH3COCH3(g) + CO2(g)
MgC2O4(s) MgO(s) + CO2(g) + CO(g)
Certain solids leave coloured residues on heating which may or may not
change colour on cooling.
Residue (Oxide) Colour of residue
Lead (II) oxide, PbO Reddish-brown (Orange) when hot
and yellow when cold
Zinc oxide, ZnO Yellow when hot and white when
cold
Copper (II) oxide, CuO Black both when cold and hot
Iron (III) oxide,Fe2O3 Dark-brown when hot and reddish-
brown when cold
Notes:
Zinc oxide may be confused with lead (II) oxide. To avoid this
confusion; subject the residue to prolonged heating: zinc (II) oxide
Gas turns litmus red i.e. acidic vapour -An acidic gas is evolved.
is evolved examples.
Brown fumes -NO2 gas from Nitrate ion.
Greenish-yellow gas turns litmus red -Chloride gas from chloride ion.
and bleaches it
Colourless gas on strong heating -SO2 gas from a sulphate, Sulphite OR
decolorizes acidified KMnO4 S2O32-ions.
Misty gas turns moist/damp blue -SO3 gas from sulphate ion.
litmus paper red.
NOTE: SO42- is not easily decomposed to produce sulphur dioxide gas.
Gas turns wet litmus paper slightly CO2 gas from carbonate, hydrogen
red and lime water milky. carbonate and oxalic acid ions
4. ADDITION OF CONCENTRATED SULPHURIC ACID TO A SOLID SAMPLE:
This reagent is meant to identify a chloride, Cl- ion, ethanoate, CH3COO- or
Nitrate, NO3- ion.
In case of a chloride, Cl- ion, white misty fumes that form dense white
fumes with ammonia solution are given off. The fume of hydrogen chloride.
Equation:
NaCl(s) + H2SO4(l) NaHSO4(s) + HCl(g)
Chlorine gas may be produced by adding concentrated sulphuric acid to a
chloride in the presence of an oxidizing agent such as manganese (IV)
oxide. In the case of hydrogen chloride gas is produced from concentrated
sulphuric acid and a chloride.
But this gas is oxidized to chlorine by the oxidizing agent used.
In case of ethanoate, a CH3COO- ion, a colourless gas with vinegar smells
and turns blue litmus paper red is given off. The gas is ethanoic acid/acetic
acid vapour.
Equation:
CH3COO-(s) + H+(aq) CH3COOH(g)
In the case of nitrate, nitric acid vapour is produced when concentrated
sulphuric acid is added to a solid nitrate, while heating.
5. IDENTIFYING GASES:
Gases may be produced when a solid is heated or when an acid is added to
a solid. Whenever a gas is produced marks are allocated according to:
The colour of the gas.
The odour (smell) of the gas.
The confirmatory test of the gas.
The effect of that gas on litmus paper.
These four scoring points will be under the observation. In deduction the
following will be awarded marks.
The name of the gas.
The anion producing the gas.
6. SOLUBILITY IN WATER:
This is used to separate two salts whereby one is soluble in water and the other
is insoluble; a spatula end full of the given sample is shaken with about 5cm3 of
water to produce either a solution or a suspension, which is then filtered to
generate a filtrate and residue; solid substance that remains on the filter paper.
a) ADDITION OF WATER TO A SOLID SAMPLE WITHOUT FILTERING:
When water is added to unknown solid and later dissolved completely,
then the compound is most likely to be ionic.
Expected observation:
State the colour of the resultant solution.
If the solution is colourless, deduce non-transitional metal ions such
as Pb2+, Ca2+, Mg2+, Al3+, Ba2+, etc.
If the solution is coloured, deduce the corresponding transitional
metal cations i.e.Green solution implies the presence of Cr3+, Fe2+,
Ni2+ & Cu2+.
b) ADDITION OF WATER TO A SOLID SAMPLE,FOLLOWED BY FILTRATION:
When asked to add water to a solid sample and then filter, it means that
the sample is partially soluble or it contains both soluble and insoluble
components.
Expected observation:
After filtering, state the colour of both filtrate and residue. Then deduce
the cations according to the colour of filtrate or residue.
Examples summarized on the table:
Cations/anions Colour of the filtrate or residue
Cu2+ Blue or Green
Fe2+, Cr3+, Ni2+ Green
Fe3+ Yellow/Brown
Co 2+ Pink or Red
Mn 2+ Pink
Cr2O7 2- Orange
CrO4 2- Yellow
Zn ,Pb ,Ca ,Al ,Mg ,NH4 & Ba
2+ 2+ 2+ 3+ 2+ + 2+ White/Colourless
Observation Conclusion
Then the test which comes out to be positive is written under the Test
column with an appropriate observations and deductions.
Note:
When writing a test of own choice the following should be adhered to:
Order of addition of reagents. If order is altered, then the test may
not give the expected observation.
Example:
During identification of manganese (II) ions using concentrated
nitric acid and solid sodium bismuthate, the acid is added first
followed by solid sodium bismuthate.
The physical state of reagent(s) i.e. it may be a solution, solid or
liquid e.g. during identification of zinc,Zn2+ ion
Ammonium chloride is used a solid, while disodium hydrogen
phosphate and ammonia are used as solutions.
Correct spellings of chemical names of the reagents and other
technical terms. Any wrong spelling makes the whole reagent
wrong.
The spelling following chemical names and technical terms normally
disturb candidates.
Correct spelling Wrong spelling
Sooty Shooty
Amine Ammine
Dissolve Dessolve
Tertiary Tertially
Milky Milk
Anhydrous Unhydrous
Aromatic Aromantic
Aliphatic Alimphatic
Electrophilic Electrophilic
Carboxylic Carboxylic
Effervescence Effavscence
Crystallisation Crytalization
Dimethylglyoxime Dimethylglycoxime
Sodium bismuthate Sodium bimuthate
Ammoniacal silver nitrate Ammonical silver nitrate
2,4-dinitrophenylhydrazine 2-4-dinitrophenyhydrazine
Potassium hexacyanoferrate (II) Potassium hexaciynoferrate (II)
or (III) or (III)
Disodium hydrogen phosphate Disodium hydrogen phosphate
acidified
potassium
dichromate (VI)
solution from
orange to green.
Equations:
Ba2+(aq) + SO32-(aq) BaSO3(s)
Pb2+(aq) + SO32-(aq) PbSO3(s)
To the solution, add acidified potassium The purple colour
manganate (VII) solution. of potassium
manganate (VII)
solution turns to
colourless
Equation:
2MnO4-(aq) + 5SO32-(aq) + 6H+(aq) 2Mn2+(aq) + 3H2O(l) + 5SO42-(aq)
To the solution, add iodine solution. Brown solution of
iodine solution
turns to
colourless.
Equation:
I2(aq) + H2O(l) + SO32-(aq) SO42-(aq) + 2H+(aq) + 2I-(aq)
CO32- ions To the solution, add dilute mineral acid Effervescence of a
(i.e. hydrochloric, nitric & sulphuric acid) colourless gas
in either solid or solution state. that turns moist
blue litmus paper
red and lime
water milky.
To the solution, add barium White precipitate
nitrate/chloride solution or silver nitrate that dissolves in
solution or lead (II) nitrate/ethanoate the acid with
solution followed by dilute nitric acid. effervescence of a
colourless gas
that turns lime
water milky.
To the solution, add magnesium sulphate White precipitate
solution. is formed.
HCO3- ions To the solution, add magnesium sulphate No precipitate is
solution. formed but on
boiling, a white
precipitate is
formed.
Boil a solution containing hydrogen White precipitate
carbonate. is formed and a
colourless gas
that turns lime
water milky is
given off.
NO3-ion To the solution, add freshly prepared iron Brown ring layer
(II) sulphate solution followed by is formed at the
concentrated sulphuric acid which is interface of the
carefully poured down the sides of the test two separate
tube. liquids.
Equation:
KNO3(aq) + H2SO4(aq) KHSO4(aq) + HNO3(aq)
6FeSO4(aq) + 3H2SO4(l) + 2HNO3(aq) 3Fe2(SO4)3(aq) + 4H2O(l) + 2NO(g)
FeSO4(aq) + NO(aq) + 5H2O(l) [Fe(NO)(H2O)5]SO4(aq) or [Fe(H2O)5(NO)]SO4(aq)
Or:
3Fe2+(aq) + NO(aq) + 4H+(aq) 3Fe3+(aq) + 2H2O(l) + NO(aq)
[Fe(H2O)6]2+(aq) + NO(aq) [Fe(H2O)5(NO)]2+(aq) + H2O(l)
Pentaaqua nitroso iron (II) sulphate
Cl- ion To the solution, add silver nitrate solution White precipitate
followed by dilute nitric acid. insoluble in the
acid is formed
Note:
White precipitate of silver chloride dissolves in ammonia
solution to a colourless solution due formation of a soluble
complex, diamine silver Ag(NH3)2+ions.
Add manganese (IV) oxide solid followed Pale green is
by concentrated sulpuric acid and warm. evolved, bleaches
damp litmus
paper.
CrO42- ion To the solution, add lead (II) nitrate or Yellow precipitate
acetate solution. is formed.
Equation:
Pb2+(aq) + CrO42-(aq) PbCrO4(s)
To the solution, add silver nitrate solution. Red precipitate is
formed.
Equation:
2Ag+(aq) + CrO42-(aq) Ag2CrO4(s)
To the solution, add 2-3 drops of An intense blue
hydrogen peroxide solution followed by colouration is
dilute sulpuric acid. formed.
To the solution, add barium nitrate or Yellow precipitate
chloride solution. is formed.
Equation:
Ba2+(aq) + CrO42-(aq) BaCrO4(s)
Cr2O72- ion To the solution, add a few drops of dilute Orange solution
sodium hydroxide solution. turns to yellow
solution.
Equation:
Cr2O72-(aq) + 2OH-(aq) 2CrO42-(aq) + H2O(l)
PO43- ion To the solution, add barium White precipitate
nitrate/chloride solution followed by which dissolves in
dilute hydrochloric or nitric acid. the acid without
effervescence.
Br-/I- ion To the solution, add silver nitrate solution Pale-yellow
followed by ammonia solution drop wise precipitate
until in excess. insoluble in
ammonia
solution.
Br- ion To the solution, add lead (II) White crystalline
nitrate/ethanoate solution. precipitate is
formed which
slightly dissolves
on warming.
To the solution, add carbon tetrachloride Reddish-brown
or chloroform followed by chlorine water colour appears in
and shake the mixture. the organic layer.
then strongly until there which turns copper (II) Water of crystallization
is no further change. sulphate blue, White from a hydrated non
sublimate on the cooler transition salt.
parts of the boiling tube.
Colourless gas turns wet
litmus paper slightly red Acidic gas, CO2 gas from
and lime water milky, CO32-/HCO3-ions.
CO32- is confirmed
Colourless gas also turns present.
wet red litmus paper Ammonia gas from NH4+
blue and forms misty salt.
fumes with rod dipped in
conconcentrated acid. Residue is probably an
Residue is white. oxide of Mn2+, Mg2+ ion.
(b). To about one P partially dissolves in Filtrate probably
spatula end full of P, add water to form a contains:
5cm3 of water and filter. colourless filtrate and a Zn2+,Al3+,Or Pb2+
Keep filtrate and white residue. Residue probably
residue. contains:
Divide in to 4 parts. CO32- of Pb2+,Al3+, or
Zn2+ ions
(i). To the first portion, No precipitate is formed.
add dilute sodium Solution remains Ammonia gas from NH4+
hydroxide solution drop colourless. salt hence NH4+ ion
wise until in excess and On heating,colourless confirmed.
heat. gas given off turns wet
litmus paper blue and
forms misty fumes with
a rod dipped in
concentrated
hydrochloric acid.
(ii). To the second No precipitate formed, NH4+ ion present
portion, add dilute solution remains
ammonia solution drop colourless
wise until in excess.
(iii). To the third White precipitate is SO42-ion.
portion, add dilute acid formed. Confirmed present.
followed by 2-3 drops of
barium nitrate solution.
(c). Wash the residue Effervescence occurs and Acidic gas, CO2 gas from
and dissolve it in dilute a colourless gas evolved, CO32- ion.
nitric acid. Divide the turns wet litmus paper
resultant solution in to 3 slightly red and lime
parts. water milky. A soluble nitrate of Mn2+
Residue dissolves in or Co2+ salt
dilute nitric acid to form
a pale pink solution.
(i). To the first part, add Dirty white precipitate, Mn2+ion
dilute sodium hydroxide insoluble in excess. Suspected present.
solution drop wise until Precipitate rapidly turns
in excess. brown.
(ii). To the second part, Dirty white Precipitate, Mn2+ion
add dilute ammonia insoluble in excess. Suspected present.
solution drop wise until Precipitate turns brown
in excess. on standing.
(iii). To the third part,
carry out a test of your
choice to confirm the
cation in the residue.
Tests:
To the last part, A purple colouration was Mn2+ is oxidized to
concentrated nitric acid observed. MnO4- ion.
was added followed by Hence Mn2+ ion
solid sodium confirmed present.
bismuthate.
Identify the:
i. Cations present in compound P.
NH4+ ion is confirmed in b (i).
Mn2+ ion is confirmed in c (iii).
ii. Anions present in compound P.
SO42-ion is confirmed in b (iii).
CO32- ion is confirmed in (a).
Experiment 2, X is a mixture of BaCl2 & PbCO3:
You are provided with substance X which contains two cations and two anions.
You are required to carry out the following tests on X to identify the cations and
anions in X. Record your observations and conclusion in the table below.
Tests Observations Deductions
hexacyanoferrate (II)
solution.
Or:
Add 2 drops of White precipitate in a
potassium iodide brown solution.
solution.
Identify the:
i. Cations present in compound Y.
Ni2+ ion is confirmed in d (iv).
Cu2+ ion is confirmed in e (iii).
ii. Anions present in compound Y.
CH3COO- ion is confirmed in d (i).
CO32-ion is confirmed in e.
Experiment 4, Z is a mixture of BaCl2 & ZnCO3:
You are provided with substance Z which contains two cations and two anions.
You are required to carry out the following tests on Z to identify the cations and
anions in Z. Record your observations and conclusion in the table below.
Tests Observations Deductions
(a).Heat strongly one Colourless Water of crystallization
spatula end-ful of Z in a liquid/condensate that is given off.
dry test tube. turns anhydrous copper
(II) sulphate blue. ∴hydrated salt is present
Colourless gas that turns
moist blue litmus paper
red & lime water milky. Carbon dioxide gas is
given off.
White powder turns to ∴CO32-, C2O4 & HCO3- are
yellow residue-hot & suspected present.
white-cooling Non-transitional metal
ions, Zn2+, Ba2+, Ca2+&
Al3+ ions are suspected
present.
ZnO is formed.
(b).To one spatula end- Effervescence, Misty Hydrogen chloride gas is
ful of Z in a test-tube, fumes with a chocking given off.
add 2-3 drops of smell, turned moist blue
concentrated sulphuric litmus paper red and ∴Cl- ion is suspected
acid. forms dense white fumes present.
with ammonia solution.
c. (i).To the 1st part of White precipitate Al3+, Pb2+, Zn2+, Sn2+ &
acidic solution, add soluble in excess to give Sn4+ ions are suspected
dilute sodium hydroxide a colourless solution. present.
solution drop-wise until Colourless gas which
in excess. turns moist red litmus Ammonia gas is given
paper blue & forms off.
white fumes with ∴NH4+ ion is confirmed
concentrated present.
hydrochloric acid.
c. (ii).To the 2nd part of White precipitate Al3+, Pb2+, Sn2+ & Sn4+
the acidified solution, insoluble in excess. ions are suspected
add dilute ammonia present.
solution drop-wise until
in excess.
c. (iii).To the 3rd part of No observable change Pb2+ ion is absent.
the acidic solution, add occurs.
2-3 drops of potassium Or Rej:Al3+ ion present
iodide solution. No yellow precipitate.
c. (iv).To the 4th part of Blue precipitate soluble Al3+ ion confirmed
the acidified solution, forming a blue solution. present.
add 2-3 drops of litmus Or
solution followed by Blue lake.
ammonia solution drop-
wise until in excess.
c.(v).To the 5th part of White precipitate. SO42- & Cl- ions are
the acidified solution, suspected present.
add 2-3 drops of lead (II)
ethanoate solution. CO32- & SO32- are rejected
b’se the solution was
acidic.
c. (vi).Use the 6th part of
the acidified solution to
carry out a test of your
own choice to confirm
one of the anion in V.
Test:
To the 6th part of the
acidified solution, add 3 White precipitate. SO42- ion is confirmed
drops of barium nitrate present.
solution/barium
chloride solution.
Note:
No need of adding the
acid b’se the solution
was acidic.
(d).Wash the residue Residue dissolves to give Cu2+ ion is suspected
with distilled water & a blue solution. present.
dissolve it in dilute
hydrochloric acid. Divide Accept: Green solution. Ni2+, Cu2+, Fe2+ & Cr3+
the solution in to three ions are suspected
parts. present.
d. (i).To the 1 part of
st Blue precipitate Cu2+ ion is suspected
the acidic solution, add insoluble in excess. present.
dilute sodium hydroxide
solution drop-wise until
in excess.
d. (ii). To the 1st part of Blue precipitate soluble Cu2+ ion is suspected
the acidic solution, add in excess forming a present.
dilute ammonium deep-blue solution.
hydroxide solution drop-
wise until in excess.
d. (iii). To the 1st part of Brown precipitate. Cu2+ ion is confirmed
the acidic solution, add present.
2-3 drops of potassium Accept; Maroon
hexacyanoferrate (II) precipitate.
solution.
Identify the:
i. Cations present in compound V.
Al3+ ion is confirmed in c (iv).
Cu2+ ion is confirmed in d (iii).
NH4+ ion is confirmed in c (i).
ii. Anions present in compound V.
SO42- ion is confirmed in c (vi).
Experiment 7, U is a mixture of NiCO3 & FeSO4.7H2O:
You are provided with substance U which contains three cations and two anions.
You are required to carry out the following tests on U to identify the cations and
anions in U. Record your observations and conclusion in the table below.
Tests Observations Deductions
Test:
To the 3rd part of the Red precipitate. Ni2+ ion is confirmed
solution, add aqueous present.
ammonia solution until
the solution is alkaline,
then add 2 drops of
dimethylglyoxime
solution.
Identify the:
i. Cations present in compound U.
Ni2+ ion confirmed in c (iii).
Fe2+ ion is confirmed in b (iii).
ii. Anions present in compound U.
SO42- ion is confirmed in b (v).
CO32- ion is confirmed in c.
Experiment 8, T is a mixture of (CH3COO)2Ni & Al2SO4:
You are provided with substance T which contains two cations and two anions.
You are required to carry out the following tests on T to identify the cations and
anions in T. Record your observations and conclusion in the table below.
Tests Observations Deductions
(a).Heat two spatula Colourless Water is given off.
end-fuls of T strongly in condensate/liquid that ∴ Hydrated salt is
a dry test tube. turns anhydrous copper present.
(II) sulphate blue.
Colourless gas that turns Sulphur dioxide gas is
moist blue litmus paper given off.
red & acidified ∴SO32-, & SO42- ions are
potassium dichromate suspected present.
(VI) solution from
orange to green.
Colourless gas with Propanone is given off.
sweet smell & forms ∴CH3COO- ion is
yellow ppt with Brady’s suspected present.
reagent.
Carbon dioxide gas is
Colourless gas that turns given off.
lime water milky. ∴CO32-, C2O42- & HCO3-
ions are suspected
present.
(a).Heat two spatula Colourless gas that turns Carbon dioxide gas is
end-fuls of R strongly in moist blue red & lime given off.
a dry test tube. water milky. ∴CO32- , C2O4 & HCO3-
ions are suspected
present.
Yellow residue-hot & ZnO is formed.
white –cold.
(b).To three spatula end- Dissolves with Carbon dioxide gas is
ful of R, add dilute nitric bubbles/effervescence given off.
drop-wise until no of colourless of a
further change & warm. colourless gas that turns ∴CO32- ion is confirmed
moist blue litmus red & present.
lime water milky.
drops of hydrogen
peroxide, boil the
mixture & divide it in to
two parts.
b.(i).To the 1st part of Yellow precipitate. PbCrO4 is formed.
the solution, add 2-3
drops of lead (II) ∴Cr3+ ion is suspected
ethanoate solution. present.
Allow it to cool.
b.(ii).To the 2nd part of Blue colour in butan-1-ol Cr3+ ion is confirmed
the solution, add about layer. present.
1cm3 of butan-1-ol
followed by dilute
sulphuric acid.
(iii).To the 3rd part of the White precipitate. Cl-, SO32-, SO42- & CO32-
filtrate, add 3-4 drops of ions are suspected
lead (II) ethanoate present.
solution.
(iv).Use the 4th part of
the filtrate to carry out a
test of your own choice
to confirm one of anions
in I.
Test:
To the 4th part of the
filtrate, add 3 drops of White precipitate Cl- ion is confirmed
silver nitrate solution insoluble in the acid. present.
followed by dilute nitric
acid.
(c).Wash the residue Effervescence of Carbon dioxide gas is
with distilled water & colourless gas that turns given off.
dissolve it in 2M moist blue litmus paper ∴CO32- ion is confirmed
sulphuric acid & divide red & lime water milky. present.
the solution in to three Green solution is formed. Ni2+, Cr3+, Fe2+ & Cu2+
parts. ions are present.
c.(i).To the 1st part of the Green precipitate Ni2+ & Fe2+ ions are
solution, add dilute insoluble in excess. suspected present.
sodium hydroxide
divide the solution in to moist blue litmus paper ∴CO32- ion is confirmed
four portions. red & lime water milky. present.
c.(i).To the 1 part of the
st
solution, add dilute White precipitate Mg2+, Ba2+ & Ca2+ ions
sodium hydroxide insoluble in excess. are suspected present.
solution drop wise until
in excess.
c.(ii).To the 2nd part of
the solution, add dilute White precipitate Mg2+& Ba2+ ions are
ammonia solution drop insoluble in excess. suspected present.
wise until in excess.
c.(iii).To the 3rd part of No observable change Ba2+ ion is absent.
the solution, add 2-3 occurs.
drops of potassium Or
chromate (VI) solution. No yellow precipitate.
c.(iv).To the 4 part of
th
filter. Keep both the White residue. Ca2+, Ba2+, Mg2+, Zn2+ &
filtrate & residue. Divide Pb2+ ions are suspected
the filtrate in to 6 parts. present.
b.(i).To the 1st part of
the filtrate, add dilute Brown precipitate Fe3+ion is suspected
sodium hydroxide insoluble in excess. present.
solution drop wise until
in excess.
b.(ii).To the 2nd part of
the filtrate, add dilute Brown precipitate Fe3+ion is suspected
ammonia solution drop insoluble in excess. present.
wise until in excess.
b.(iii).To the 3rd part of
the filtrate, add 2-3 Dark-blue precipitate is Fe3+ion is confirmed
drops of potassium formed. present.
hexacyanoferrrate (II)
solution.
b.(iv).To the 4th part of
the filtrate, add Brown vapour with I2 & Br2 vapour are
potassium dichromate pungent smell. evolved.
(VII) solution followed
by a few drops of Orange colour of the ∴I2- & Br2- ions are
concentrated sulphuric solution turns green. suspected present.
acid & warm.
b.(v).To the 5th part of
the filtrated, add silver Yellow precipitate I2- & Br2- ions are
nitrate solution followed insoluble in the acid. suspected present.
by dilute nitric acid.
b.(vi).To the 6th part of
the filtrate, add 1cm3 of Reddish-brown Br2- ion is confirmed
carbon tetrachloride colourless appears in the present.
followed by chlorine CCl4 layer.
water.
(c).Wash the residue
with distilled water &
then dry it between the
filter paper. Heat a little White solid remains. BaO, CaO & MgO are
of the residue strongly in formed.
a dry test tube strongly.
d.(i).To the 1st part of White precipitate Pb2+, Zn2+, Sn2+, Al3+ &
the acidic solution, add soluble in excess to form Sn4+ ions are suspected
sodium hydroxide a colourless solution. present.
solution drop wise until
in excess.
d.(ii).To the 2nd part of White precipitate Pb2+, Sn2+, Al3+ & Sn4+
the acidic solution, add insoluble in excess. ions are suspected
aqueous ammonia present.
solution drop wise until
in excess.
d.(iii).To the 3rd part of White precipitate. Pb2+ion is suspected
the acidic solution, add present.
dilute sulphuric acid.
d.(iv).Use the 4th part of
the acidic solution to
carry out a test of your
own choice to confirm
one of the cations
present in W.
Test:
To the 4th part of the Yellow precipitate Pb2+ion is confirmed
acidic solution, add 3 present.
drops of potassium
iodide solution.
Or
Add potassium chromate Yellow precipitate
(VI) solution followed by soluble forming a yellow
sodium hydroxide solution.
solution until in excess.
(e).To two spatula end- Colourless filtrate. Non-transitional metals
fuls of W, add about ions, I.e.:
5cm3 of distilled water, & Al3+, Pb2+, Zn2+, Mg2+,
shake & filter. Ca2+& Ba2+ ions are
Divide the filtrate in to White residue. suspected present in
five parts. both the filtrate &
residue.
e.(i).To the 1 part of the White precipitate
st Mn2+ ion is suspected
filtrate, add sodium insoluble in excess, turns present.
brown.
(i).To the 1st part of the No observable change Pb2+, Ag2+ & Hg2+ ions
solution, add dilute occurs. are suspected present.
hydrochloric acid.
(ii).To the 2nd part of the No observable change
solution, add iron (III) occurs.
chloride solution.
(iii).To the 3rd part of the White precipitate. SO42- , SO32- & CO32- ions
solution, add barium are suspected present.
nitrate solution.
(iv).To the 4th part of the Dirty green gelatinous Fe2+ ion is suspected
solution, add dilute precipitate persisted in present.
sodium hydroxide excess.
solution drop wise until
in excess & filter. Keep White precipitate Al3+, Zn2+ & Sn2+ ions
both the filtrate & dissolves in excess. are suspected present.
residue.
(c).Acidify the filtrate
with dilute hydrochloric
acid & divide it in to
three portions.
(i).To the 1st portion of No observable change Al(OH)4- & Zn(OH)42-
the acidified filtrate, add occurs. are formed.
dilute sodium hydroxide
solution drop wise until
in excess.
(ii).To the 2nd portion of No observable change Al(OH)4- is formed
the acidified filtrate, add occurs. ∴Al3+ ion is confirmed
dilute ammonia solution present.
drop wise until in excess.
(iii).To the 3rd portion of No observable change Pb2+ ion is suspected
the acidified filtrate, add occurs. absent.
2-3 drops of potassium
iodide solution
(d).Wash the residue &
dissolves it in dilute
hydrochloric acid. Divide
the resultant solution in
to two parts.
(i).To the 1st part of the Dirty green gelatinous Fe2+ ion is suspected
resultant solution, add precipitate insoluble in present.
dilute sodium hydroxide excess.
solution until in excess.
(ii).To the 2nd part of the Dirty green gelatinous Fe2+ ion is confirmed
resultant solution, add precipitate insoluble in present.
dilute ammonia solution excess.
drop wise until in excess.
Identify the:
i. Cations present in compound Z.
Al3+ ion is confirmed in c (ii).
Fe2+ ion is confirmed in d (ii).
ii. Anions present in compound Z.
S042- ion is confirmed in b (iii).
Experiment 18, U is a mixture of CuCO3 & Fe(SO4)3:
You are provided with substance U which contains two cations and two anions.
You are required to carry out the following tests on U to identify the cations and
anions in U. Record your observations and conclusion in the table below.
Tests Observations Deductions
(a).Heat a spatula end- U is agreen solid. Cu2+, Fe2+, Ni2+ & Cr3+
ful of strongly in a dry ions are suspected
test tube. present.
(b).Place two spatula Green-blue filtrate. Cu2+, Fe2+& Ni2+ ions are
end-fuls of U in a test suspected present.
tube, add about 5cm3 of Brown residue. Fe(OH)3 & MnO2 are
distilled water, shake & formed.
filter. Keep both the Effervescence of Carbon dioxide gas is
filtrate & residue. Divide colourless gas that given off.
the filtrate in to five turned lime water milky. ∴CO32- ion is present.
portions.
(i).To the 1st portion of Blue precipitate Cu2+ ion is suspected
the filtrate, add dilute insoluble in excess. present.
sodium hydroxide
solution drop wise in
excess.
(ii).To the 2nd portion of Blue precipitate soluble Cu(NH3)42+ is formed
the filtrate, add dilute to form a deep-blue Cu2+ ion is suspected
ammonia solution drop solution. present.
wise until in excess.
(iii).To the 3rd portion of Dark-brown precipitate. Cu2+ ion is confirmed
the filtrate, add few present.
drops of potassium
hexacyanoferrate (II)
solution.
(iv).To the 4th portion of White precipitate CO32-,SO32- & SO42- ions
the filtrate, add 2 drops insoluble on warming. are suspected present.
of lead (II) nitrate
solution & warm.
(v).Use the 5th portion of
the filtrate to carry out a
test of your own choice
to confirm one of the
anions in U.
Test:
To the 5th portion of the White precipitate SO42- ion is confirmed
filtrate, add dilute nitric insoluble in dilute nitric present.
acid followed by barium acid.
nitrate solution.
Or
Dilute HCl/BaCl2
(c).Wash the residue Brown residue remains. Fe(OH)3 ,Fe2O3 & MnO2
with distilled water. are formed.
Heat a small portion of
the residue strongly in a
dry test tube.
(d).Transfer the rest of Brown residue dissolves Fe3+ ion is suspected
the residue to a test tube to give green-yellow present.
& dissolve in in dilute solution.
hydrochloric acid. Divide
the solution in to three
portions.
(i).To the 1st part of the Brown precipitate Fe3+ ion is suspected
solution, add dilute insoluble in excess. present.
sodium hydroxide
solution drop wise until
in excess.
(ii).To the 2nd part of the Brown precipitate Fe3+ ion is suspected
solution, add dilute insoluble in excess. present.
ammonia solution drop
wise until in excess.
(iii).To the 3rd part of the Blood-red solution. Fe3+ ion is confirmed
solution, add 2-3 drops present.
of potassium thiocyanate
solution
Identify the:
i. Cations present in compound U.
Cu2+ ion is confirmed in a (iii).
Fe3+ ion is confirmed in d (iii).
ii. Anions present in compound U.
CO32- ion is confirmed in a.
S042- ion is confirmed in b (v).
ORGANIC PRACTICALS ANALYSIS:
Organic chemistry is a branch of chemistry concerned with the compounds of
carbon: Originally confined to compounds produced by living organisms but now
extended to include man made substances based on carbon, such plastics.
Organic compounds consist of molecules held together by weak Vander waals
forces or hydrogen bonds. As a result organic compounds are often liquids at
room temperature. If they are solids, they easily melt or sublime on heating.
OH O
The presence of the -OH group means that hydrogen bonding occurs
between the molecules of alcohols/hydrogen bonding has two
consequences.
All alcohols with relatively short carbon chains (up to and including
propanol) mix with water forming a neutral solution.
The shorter chain alcohols are normally colourless liquids at room
temperature with a pleasant spirit smell.
They have boiling points (and melting points) being much higher than
those of alkanes of comparable relative molecular mass.
Common Tests Observations
Addition of sodium metal Colourless gas which explodes
with a pop sound when lit is given
off.(Hydrogen gas)
Add of anhydrous zinc (II) chloride (i). Tertiary alcohol-An
followed concentrated hydrochloric immediate cloudy solution is
acid (Lucas reagent) formed at room temperature.
(ii). Secondary alcohol-A cloudy
solution is formed after standing
for five minutes at room
temperature.
(iii). Primary alcohol-No cloudy
solution is formed at room
temperature.
Lucas’s test for primary, secondary and tertiary alcohols is summarized
in the equations below:
Anhy. ZnCl2
R3COH + Conc.HCl 25°C R3C Cl + H2O
3°C Alcohol Anhy. ZnCl2 Immediate cloudy solution
R2CHOH + Conc.HCl 25°C R2CHCl + H2O
2°Alcohol Anhy. ZnCl2 Cloudy solution on standing about 5Mins
RCH2OH + Conc.HCl RCH2Cl + H2O
1° Alcohol 25°C No observable change occurs.
Oxidation of Alcohols: Acidified potassium dichromate
Addition of acidified potassium solution changes from orange to
dichromate, and heat. green
Explanation:
(i).Primary alcohol-Oxidized to
aldehydes and further to
carboxylic acids.
(ii).Secondary alcohol-Oxidized to
ketones and resistant to further
oxidation.
Note: Tertiary alcohol: No observable colour change. Solution remains
orange (3°alcohols are resistant to oxidization)
Dehydration of alcohols: All primary, secondary or tertiary
alcohols gives off a colourless
vapour,if bubbled in:
(i).Addition of concentrated Bromine water, changes it from
sulphuric acid, and heat. brown to colourless.
Acidified potassium
permanganate, from purple to
pink.
(ii).Addition of iodine solution A yellow precipitate of CHI3 is
followed by sodium hydroxide formed.
solution until the colour of iodine is
just discharged. (Iodoform test).
Equation:
OH
CH3C + 3I2 + 4NaOH CHI3 + CH3CO2-Na+ + 3H2O + 3NaI
(Yellow ppt)
Methyl alcohols from a yellow precipitate of CHI3 (Iodoform).
Ethanol (CH3CH2OH) also gives a yellow precipitate.
Tertiary alcohols with structure formula,(CH3)3COH do not gives a
yellow precipitate of CHI3
Addition of dilute sulphuric acid A solution with sweet smell is
followed by few drops of ethanoic formed.
acid and heat.
Pour the resultant solution in a
beaker containing water.
Equation:
H+
RCO2H + CH3CH2OH RCO2CH2CH3 + H2O
Addition of phosphorus Evolution of misty gas hat forms
pentachloride solution. white fumes with ammonia.
NEUTRAL COMPOUNDS: CARBONYL COMPOUNDS:
(Aldehydes and ketones)
Functional Group: Carbonyl group (C═O)
Organic Compounds:
C=O Cr3+(aq) + C OH
Add ammoniacal silver nitrate A silver deposit on the walls of
(Tollen’s reagent). the test tube.
Equation:
R-CHO + Ag(NH3)2+OH- Ag(s) + RCOO- + Other product
Aldehyde Tollen's reagent Silver mirror
Add Fehling’s solution. Brown precipitate is formed.
Equation:
RCHO + Cu2+(aq) + 3OH-(aq) Cu2O(s) + CH3CO2H +H2O
(Blue tartrate complex) Brick red ppt)
Ketones:
Add Iodine solution followed by A yellow precipitate is formed
sodium hydroxide solution until for methyl ketones.
colour of iodine is just discharged. (CH3CO-)
Equation:
CH3COR + 3I2 + 4NaOH CHI3 + CH3COO-Na+ +3H2O + 3NaI
Yellow p.p.t
OH
+ H2O
(aq) + H3O+(aq)
Add neutral iron (III) chloride Purple/violet colouration is
solution observed.
Equation:
OH O-
+ FeCl3(aq)
+ 3HCl(aq)
3 Fe
Addition of bromine water. White precipitate
Equation:
OH OH
Br Br
+ Br2/H2O + 3HBr
Room Temp
Br
White p.p.t
ACIDIC COMPOUNDS: 2.CARBOXYLIC ACIDS.
Functional group : Carboxylate group (-CO2H)
Organic compounds : Carboxylic acids: (i). Aliphatic carboxylic acids.
(ii). Aromatic carboxylic acids.
Physical Properties:
The acids have a characteristic smell as that of vinegar, the shorter
chain acids are normally colourless liquids at room temperature.
They form hydrogen bonds with water molecules, this result in
carboxylic acids dissolving well in water, provided that their carbon
chains are fairly short.
Tests Observations
Addition of universal indicator Turns universal indicator red
or litmus solution (Showing that it’s acidic)
Equation:
H+
RCO2H(l) + H2O(l) RCO2-(aq) + H3O+(aq)
Addition of saturated Na2CO3. Colourless gas turns lime water
milky (CO2 gas) is evolved
Equation:
Na2CO3(aq)
2RCO2H(l) 2RCO2-Na+(aq) + CO2(g) + H2O(l)
Saturated
Add Neutral Iron (III) chloride Brown precipitate is formed.
solution.
Equation:
CO2H CO2-
+ FeCl3(aq)
+ 3HCl(aq)
3 Fe
Add soda lime solution and heat Colourless gas that turns
limewater (CO2 gas)
Equation:
Soda lime
RCO2H(l) RH + CO2(g)
Heat
Clear solution
Add dilute sulphuric acid A solution with a sweet smell is
followed by 1cm3 of ethanol and formed.
heat. Pour the resultant solution
in a beaker containing Water.
Equation:
H+
RCO2H + CH3CH2OH RCO2CH2CH3 + H2O
Addition of sodium metal Colourless gas with ‘pop’ sound
when lighted is evolved.
A colourless solution is formed.
Equation:
RCO2H + Na(s) RCO2-Na+ + H2(g)
BASIC COMPOUNDS: AMINES
Functional group: Amino group (-NH2)
Organic compounds: Amines
Aliphatic primary, secondary or tertiary Amines.
Aromatic primary, secondary or tertiary Amines.
Physical properties:
They have a characteristic fishy smell. Indeed of rotting fish. Smell
produced by decomposition of proteins.
Primary and secondary amines can hydrogen bond to molecules of water
or alcohols, so primary amines with chain length up to C4 are colourless
and very soluble in water. Forming a basic solution.
Phenyl amine is a brown liquid and not very soluble in water due to the
benzene ring.
Tests Observations
Detect the smell (Take care) Aliphatic amines have a fishy smell.
I.e smell of decaying fish.
Equation:
cool. CH3 C R
(f).To 3cm3 of H, add No observable change Ethanol is suspected
1cm of acidified
3 occurs. absent.
potassium dichromate ∴Ketone is suspected
(VI) solution & warm present.
the mixture.
CH3 C R
Experiment 3 (B = Propan-2-ol or Butan-2-ol):
3. You are provided with substance B which is an organic compound. You are
required to determine the nature of B. carry out the following tests and
identify any gases liberated. Record your observations in the table below.
Tests Observations Deductions
(a).Burn a small Colourless liquid that Saturated aliphatic
amount of B on a burns with a yellow compound with low C:
spatula end or in a non-sooty flame. H ratio or low carbon
porcelain dish. content.
(b).Add 6 drops of B Miscible with Polar aliphatic
to about 3cm of3 water/dissolves to compound of low
distilled water, shake form a colourless molecular mass or
& allow to stand. solution that has no neutral compound
Divide the solution in effect on litmus. probably alcohol,
to three parts. ketone, aldehyde or
ester.
b.(i).To the 1 part of No observable change/ Carboxylic acid is
st
OH
CH3CH R
Experiment 4 (C = Propan-2-ol or Ethanol):
4. You are provided with substance C which is an organic compound. You are
required to determine the nature of C. carry out the following tests and
identify any gases liberated. Record your observations in the table below.
Tests Observations Deductions
(a).Burn a small Colourless liquid that Saturated aliphatic
amount of C on a burns with a blue non- compound with C: H
crucible lid or spatula sooty flame. ratio.
end.
(b).To 5 drops of C, Dissolves to form a Polar aliphatic
add about 1cm of3 colourless solution & compound with low
distilled water & solution has no effect molecular mass.
shake. Test the on litmus paper. ∴Neutral compound
mixture with litmus. like alcohol, ketone,
aldehyde or ester.
(c).To 5 drops of C, Purple solution turns Reducing agent
add 2-3 drops of to colourless. probably primary &
acidified potassium secondary alcohols or
manganate (VII) aldehyde are
solution & warm. suspected present.
(d).To 5 drops of C, Pale-yellow precipitate Alcohol of the type:
add 1cm of iodine
3 OH
solution followed by
dilute sodium CH3 C Or ethanol.
hydroxide solution ∴Yellow precipitate is
drop wise until the CHI3.
mixture is pale-yellow.
Warm, then cool under
running tap
(e).To 5 drops of C, No observable change Aldehyde & ketone are
add 2-3 drops of occurs. suspected absent.
Brady’s reagent.
(f).Carry out a test of
your own choice to
confirm the functional
group in C.
Test:
To a few drops of C, Colourless solution Ester is formed.
add 3 drops of with pleasant fruity ∴Alcohol is conformed
ethanoic acid followed (sweet) smell. present.
by 2 drops of
concentrated
sulphuric acid & warm.
Or
Add phosphorus White fumes which
pentachloride solution forms dense white
or add sodium metal. fumes with
Or concentrated ammonia
solution.
Add concentatred Effervescence of Alkene.
sulphuric acid & heat. colourless gas that ∴Alcohol is present.
turns potassium
permanganate (VII)
solution from orange
to colourless.
Comment on the nature of C.
C is saturated aliphatic primary or secondary alcohol.
∴ Primary or secondary alcohol of the type:
OH
CH3 C
Experiment 5 (D = 2-Methylpropan-2-ol):
5. You are provided with substance D which is an organic compound. You are
required to determine the nature of D. carry out the following tests and
identify any gases liberated. Record your observations in the table below.
Tests Observations Deductions
(a).Burn a spatula end- Colourless liquid that Aliphatic compound
ful of D on a porcelain burns with a yellow with low C: H ration.
dish or at the end of non-sooty flame. Or
spatula. Saturated aliphatic
compound of low
carbon content.
(b).Shake 1cm of D
3 Immiscible with water. Neutral compound
with about 3cm of 3 Mixture has no effect probably alcohol,
distilled water & test on litmus. esters re carbonyl
potassium dichromate
(VII) solution and
warm.
(c).Dissolves one No observable change Carbonyl compounds
spatula end-ful of F in occurs. are suspected absent.
2cm of methanol &
3 Or
add 2-3 drops of No orange precipitate.
Brady’s reagent.
(d).To about a spatula Pleasant fruity (sweet) Ester is formed.
end-fuls of F, add smelling liquid. ∴Carboxylic acid is
about 5cm of ethanol
3 suspected present.
followed by 2-3 drops
of concentrated
sulphuric acid. Heat
the mixture & pour it
in to a small beaker of
cold water, allow to
stand.
(e).To a spatula end ful Purple solution turns Unsaturated
of F in a test tube, add to colourless solution. compounds are
3cm3 of distilled water, suspected present.
warm and add 2-3
drops of acidified
potassium
permanganate (VII)
solution.
From your results above, Comment the nature of compound F.
F is unsaturated aromatic carboxylic acid.
Experiment 8 (G = Secondary alcohol):
8. You are provided with substance G which is an organic compound. You are
required to determine the nature of G. carry out the following tests and
identify any gases liberated. Record your observations in the table below.
Tests Observations Deductions
(a).Burn a small Colourless liquid that Aliphatic
amount of G on a burns with a yellow non- saturated/with low
spatula end. sooty flame. C: H ratio or low
carbon content.
/ R CHCH3 .
OH
COOH
warm. Test the turns blue litmus paper carboxylic acid &
solution with litmus red. phenol are suspected
paper & divide it in to present.
three equal portions.
c.(i).To the 1st portion No observable change Carbonyl compounds
of the solution, add 2- occurs. are suspected absent.
3 drops of Brady’s Or
reagent. No orange precipitate.
c.(ii).To the 2 part
nd Violet/purple Phenol is suspected
of the solution, add 2- colouration. present.
3 drops of iron (III)
chloride solution.
c.(iii).To the 3rd Effervescence/bubbles Carboxylic acid is
portion of the of colourless gas. suspected present.
solution, add a
spatula end-ful of
solid sodium
hydrogen carbonate.
(d).To 2cm3 of Sweet fruity smell. Esterification has
ethanol, add a spatula occurred.
end-fuls of H then ∴Carboxylic acid is
add 2-3 drops of confirmed present.
concentrated
sulphuric acid &
warm the mixture.
From your results above, Comment the nature of compound H.
H is aromatic compound with a hydroxyl group attached to the benzene
ring & also contains a carboxyl (-COOH) group.
Or aromatic carboxylic acid with a hydroxyl group attached to.
O
Experiment 10 (J = Benzoquinone ( ):
10.You are provided with substance J which is an organic compound. You are
required to determine the nature of J. carry out the following tests and
identify any gases liberated. Record your observations in the table below.
Tests Observations Deductions
solution is pale-yellow
& warm.
From your results above, Comment the nature of compound J.
J is aromatic ketone without a methyl group attached to the carbon
carrying the functional group.
OH
CHO
Experiment 11 (K = Vaniline ( ):
11.You are provided with substance J which is an organic compound. You are
required to determine the nature of J. carry out the following tests and
identify any gases liberated. Record your observations in the table below.
Tests Observations Deductions
(a).Burn a small White crystals/solid Aromatic compound.
amount of K on a burns with a yellow Or
spatula end. sooty flame. Aliphatic unsaturated
compound.
Or
Aliphatic compound
with low C: H ration.
(b).To a spatula end- Dissolves in sodium Acidic compound
ful of K in a test tube, hydroxide solution to probably phenol &
add 3cm of sodium
3 form a colourless carbonyl compounds
hydroxide solution solution & on adding are suspected present.
followed by dilute dilute sulphuric acid,
sulphuric acid. white precipitate is
formed.
(c).To a spatula end- Insoluble in cold, but High molecular
fuls of K in a test tube, dissolves on warming mass/aromatic
add about 4cm3 of to form a colourless compound probably
water, warm the solution that turns phenol & carboxylic
mixture & test the blue litmus to red. acid are suspected
solution with litmus. present.
Divide the solution in
to five parts.
c.(i).To the 1st part of No observable change carboxylic acid is
the solution, add a half occurs. suspected absent
spatula end-ful of Or
sodium carbonate. No effervescence.
12.You are provided with substance L which is an organic compound. You are
required to determine the nature of L. carry out the following tests and
identify any gases liberated. Record your observations in the table below.
Tests Observations Deductions
(a).Burn a spatula Colourless liquid that Aromatic compound.
end-ful of L on a burns with a yellow Or
porcelain. sooty flame. Aliphatic unsaturated
compound.
Or
Aliphatic with high C:
H ratio.
Or
High carbon content.
(b).Shake 1cm of L3 Miscible Polar aliphatic
with about 2cm of 3 with/soluble/dissolves compound of low
distilled water & test to form a colourless molecular mass.
with litmus paper. solution. Or
Divide the mixture in Solution has no effect no Neutral compound
to four parts. effect on litmus. probably alcohol,
ester or carbonyl
compounds.
b.(i).To the 1 part of No observable change
st Carboxylic acid is
the mixture, add 2-3 occurs. suspected absent.
drops of sodium Or
carbonate solution. No effervescence.
b.(ii).To 2nd part of No observable change Phenol is suspected
the mixture, add 2-3 occurs. absent.
drops of neutral iron Or
(III) chloride solution No violet/purple
colouration.
b.(iii).To the 3rd part No observable change Ketone & aldehyde
of the mixture, add 2- occurs. are suspected absent.
3 drops of Brady’s Or
reagent. No yellow precipitate.
b.(iv).To the 4th part No observable change Reducing agent i.e
of the mixture, add 2- occurs. primary & secondary
3 drops of acidified alcohols are
potassium suspected present.
dichromate (VI)