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CBSE CHEMISTRY PRACTICALS CLASS-XII

  

QUALITATIVE ANALYSIS:

SYSTEMATIC ANALYSIS OF BASIC RADICALS

Analysis of basic radicals: 

Analysis of basic radicals involves following steps:

Step - I: 

Preliminary Examination of the Salt for Identification of Cation:

State: Crystalline or amorphous

Color: Green or blue or pink or colorless

Odor: Pungent or vinegar or odorless 

Solubility: Insoluble, sparingly or highly soluble

1. Color Test: 

Characteristic colors of some metal ions:

Light green - Fe2+

Yellow Brown - Fe3+

Blue -Cu2+ 

Bright green- Ni2+ 

Blue, Red, Violet, Pink -Co2+ 

Light pink – Mn+2

2. Flame Test:

Inference from the flame test:

Cu2+ - blue

Sr2+ -Crimson red

Ba2+ - Apple green

Ca2+- Brick red

Step-II: 

3. Wet Tests for Identification of Cations:

Preparation of Original Solution

It is prepared by dissolving slat/mixture in suitable solvent. To prepare transparent and clear original solution, following solvents are used strictly in the order given below:   

(i).Cold water, (ii) Hot water, (iii) Dilute H Cl, (iv) conc. H Cl 

Group Analysis 

(I) Analysis of Zero group cation (NH4 + ion) 

(a) Take 0.1 g of salt in a test tube and add 1-2 mL of Na OH solution to it and heat. If there is a smell of ammonia, this indicates the presence of ammonium ions. 

Bring a glass rod dipped in hydrochloric acid near the mouth of the test tube. White fumes are observed. (b) Pass the gas through Nessler’s reagent.

Brown precipitate is obtained. Chemistry of Confirmatory Tests for NH4+ ion 

Ammonia gas evolved by the action of sodium hydroxide on ammonium salts reacts with hydrochloric acid to give ammonium chloride, which is visible as dense white fume. 

(NH4)2 SO4 + 2NaOH Na2SO4+ 2NH3 + 2H2O 

NH3+ H Cl→NH4Cl.

On passing the gas through Nessler’s reagent, a brown coloration or a precipitate of basic mercury (II) amido-iodine is formed.

2K2HgI4 + NH3 + 3KOH Hg O. Hg (NH2) I + 7KI + 2H2O 

Basic mercury (II) amido-iodine (Brown precipitate) for the analysis of cations belonging to group’s I-VI, the cations are precipitated from the original solution by using the group reagents.

According to the scheme shown in the flow chart given below:

Group reagents for precipitation

Group reagent: Cation Group reagent

Group zero NH4 +  None

Group-I Pb2+ Dilute H Cl 

Group-II Pb2, Cu2, As3+ H2S gas in presence of dil. H Cl 

Group-III Al3+, Fe3+  NH4OH in presence of NH4Cl 

Group-IV Co2+, Ni2+,Mn2+, Zn2+  H2S in presence of NH4OH 

Group-V Ba2+, Sr2+, Ca2+ (NH4)2CO3in presence of NH4OH 

Group-VI Mg2+ None 

                Original Solution + Dil. H Cl→ White Precipitate   Group I

If no precipitateis formed Pass H2S gas(Pb2+) as chloride Precipitate,  Group II (Pb2+, Cu2+, As3+) as sulphides. 

If no precipitate, take original solution+ Heat (O.S.) with conc. HNO3, cool and add solid 

NH4Cl + NH4OH solution in excess Precipitate, 

Group III (Fe3+, Al3+) as hydroxides.

If no precipitate Pass H2S 

Group IV (Co2+, Ni2+, Mn2+, Zn2+) as sulphides Precipitate, If no precipitate, take original solution Add NH4OH and solid (NH4)2 CO3 Precipitate, 

Group V (Ba2+, Sr2+Ca2+) as carbonates.

If no precipitate, take original solution to test Group VI, Mg2+ 

Analysis of Group-I cations:

Take a small amount of original solution (if prepared in hot conc. H Cl) in a test tube and add cold water to it and cool the test tube under tap water. If a white precipitate appears, this indicates the presence of Pb2+ ions in group –I

Confirmatory tests:

Experiment:

Dissolve the precipitate in hot water and divide the hot solution into three parts. 1. Add potassium iodide solution to the first part. 

Observation:

A yellow precipitate is obtained.

2. To the second part add potassium chromate solution. 

Observation:

A yellow precipitate is obtained which is soluble in Na OH and insoluble in ammonium acetate solution.

3. To the third part of the hot solution add few drops of alcohol and dilute sulphuric acid.

Observation:

A white precipitate is obtained which is soluble in ammonium acetate solution.

Chemistry of the Confirmatory Tests of Pb2+ ions Lead is precipitated as lead chloride in the first group. The precipitate is soluble in hot water. On adding potassium iodide (KI) solution, a yellow precipitate of lead iodide is obtained which

Confirms the presence of Pb2+ ions. PbCl2+ 2KI PbI2 + 2KCl (Hot solution) Yellow precipitate.

This yellow precipitate (Pb I2) is soluble in boiling water and reappears on cooling as shining crystals. 

2. On addition of potassium chromate (K2CrO4) solution a yellow precipitate of lead chromate is obtained. This confirms the presence of Pb2+ ions. 

PbCl2 + K2CrO4 PbCrO4 + 2KCl (Hot solution) Lead chromate (Yellow precipitate) 

The yellow precipitate (Pb CrO4 ) is soluble in hot Na OH solution. 

PbCrO4 + 4NaOH→ Na2 [Pb(OH)4 ] + Na2CrO4Sodium tetra hydroxoplumbate (II).

Analysis of Group–II cations:

If group-I is absent, add excess of water to the same test tube. Warm the solution and pass H2S gas for 1-2 minutes.

Shake the test tube. If a precipitate appears, this indicates the presence of group-II cations.

If the color of the precipitate is black, it indicates the presence of Cu+2

Confirmatory tests for Group-II 

Boil the precipitate of Group II A with dilute nitric acid and add a few drops of alcohol and dil. H2SO4.

If no precipitate is formed, add excess of ammonium hydroxide solution. A blue solution is obtained, acidify it with acetic acid and add potassium Ferro cyanide solution. A chocolate brown precipitate is formed.

2Cu2++ SO4-2+2NH3 +  2H 2O →Cu (OH)2 . CuSO4 + 2NH+4 

Cu (OH)2 .CuSO4+ 8NH3 →2 [Cu(NH3)4 ]SO4 + 2OH–+  SO-24 Tetra ammine copper (II) sulphate (Deep blue) 

(b) The blue solution on acidification with acetic acid and then adding potassium Ferro cyanide

[K4 Fe (CN)6 ] solution gives a chocolate coloration due to the formation of copper Ferro cyanide i.e.

Cu2+ [Fe (CN)6]. [Cu (NH3)4]SO4 + 4CH3COOH →CuSO4 + 4CH3COONH4 

2CuSO4+ K4 [Fe (CN)6 ] →Cu2+ [Fe(CN)6 ] + 2K2SO4 Potassium Copper hex cyanoferrate (II) hex cyanoferrate (II) (Chocolate brown precipitate)

Analysis of Group–III cations

If group-II is absent, take original solution and add 2-3 drops of conc. HNO3 to oxidize Fe2+ ions to Fe3+ ions. Heat the solution for a few minutes. After cooling add a small amount of solid ammonium chloride (NH4Cl) and an excess of ammonium hydroxide (NH4OH) solution till it smells of ammonia. Shake the test tube. If a brown or white precipitate is formed, this indicates the presence of group-III cations.

Confirmatory tests of group-III cations

A gelatinous white precipitate indicates the presence of aluminum ion (A13+). 

Dissolve the white precipitate in dilute H Cl and divide into two parts.

(a) To the first part add sodium hydroxide solution and warm. A white gelatinous precipitate soluble in excess of sodium hydroxide solution. 

(b) To the second part first add blue litmus solution and then ammonium hydroxide solution drop by drop along the sides of the test tube. A blue floating mass in the colorless solution is obtained.

1. Test for Aluminum ions (A13+) (a) When the solution containing aluminum chloride is treated with sodium hydroxide, a white gelatinous precipitate of aluminum hydroxide is formed

Which is soluble in excess of sodium hydroxide solution due to the formation of sodium meta aluminate.

AlCl3+ 3NaOH Al(OH)3 + 3NaCl Al(OH)3 + Na OH NaAlO2+ 2H2O White gelatinous Sodium precipitate meta aluminate

Analysis of group-IV cations:

If group-III is absent, pass H2S gas in the solution of group-III for a few minutes. If a precipitate appears (white, black or flesh colored), this indicates

Confirmatory test for Group-IV cations

Dissolve the precipitate in dilute H Cl by boiling. Divide the solution into two parts.

(a) To the first part add sodium hydroxide solution. A white precipitate soluble in excess of sodium hydroxide solution confirms the presence of Zn2+ ions. 

(b) Neutralize the second part with a m m o n i u m hydroxide solution and add potassium

f e r r o c y aide solution. A bluish white precipitate appears.

Test for Zinc ion (Zn2+) 

Zinc sulphide dissolves in hydrochloric acid to form zinc chloride. Zn S + 2HCl→ ZnCl2 + H2S

On addition of sodium hydroxide solution it gives a white precipitate of zinc hydroxide, which is soluble in excess of Na OH solution on heating. 

This confirms the presence of Zn2+ ions. 

ZnCl2 + 2NaOH→ Zn (OH)2 + 2NaCl 

Zn (OH)2+ 2NaOH→ Na2ZnO2 + 2H2O Sodium zincate 

When potassium Ferro cyanide K4 Fe (CN)6 solution is added to the solution after neutralization by NH4OH solution, a white or a bluish white precipitate of zinc Ferro cyanide appears. 

2 ZnCl2 + K4 [Fe (CN) 6] → Zn2[Fe (CN)6 ] + 4 K Cl Zinc Ferro cyanide.

(VI) Analysis of Group–V cations

If group-IV is absent then take original solution and add a small amount of solid NH4Cl and an excess of NH4OH solution followed by solid ammonium carbonate (NH4 )2CO3 . If a white precipitate appears,

Dissolve the white precipitate by boiling with dilute acetic acid and divide the solution into three parts one each for Ba2+, Sr2+ and Ca2+ions. Preserve a small amount of the precipitate for flame test.

Confirmatory test for Group–V cations:

(a) If both barium and strontium are absent, take the third part of the solution. Add ammonium oxalate solution and shake well. A white precipitate of calcium oxalate is obtained. 

(b) Perform the flame test with the preserved precipitate. A brick red flame, which looks greenish-yellow through blue glass, confirms the presence of Ca2+ ions.

Test for Calcium ion (Ca2+) 

Solution of the fifth group precipitate in acetic acid gives a white precipitate with ammonium oxalate solution.

CaCO3 + 2CH3COOH→ (CH3COO)2 Ca + H2O + CO2

(CH3COO)2 Ca + (NH4)2C2O4→(COO)2Ca + 2CH3COONH4 Ammonium Calcium oxalate oxalate (White precipitate) 

(b) Flame test: Perform the flame test as mentioned above. Calcium imparts brick red color to the flame.

Analysis of Group–VI cations

If group–V is absent then perform the test for Mg2+ ions as given below:

Chemistry of Confirmatory Tests of Group–VI cations Test for Magnesium ion (Mg 2+ )

Test for Magnesium ion (Mg2+)

(a) If group–V is absent the solution may contain magnesium carbonate, which is soluble in water in the presence of ammonium salts because the equilibrium is shifted towards the right hand side. 

NH+ 4 + CO-2 3→ NH3 +  HCO-- 3   

The concentration of carbonate ions required to produce a precipitate is not attained. When disodium hydrogen phosphate solution is added and the inner walls of the test tube are scratched with a glass rod, a white crystalline precipitate of magnesium ammonium phosphate is formed which indicates the presence of Mg2+ ions. 

Mg2++ Na2HPO4 →Mg (NH4) PO4 + NH4OH + 2Na+ + H2O Magnesium ammonium phosphate (White precipitate)

Precautions:

(a) Always use an apron, an eye protector and hand gloves while working in the chemistry laboratory.  

(b) Before using any reagent or a chemical, read the label on the bottle carefully. Never use unlabeled reagent. 

(c) Do not mix chemicals and reagents unnecessarily. Never taste any chemical.

(d) Be careful in smelling chemicals or vapors. Always fan the vapors gently towards your nose 

(e) Never add sodium metal to water or throw it in the sink or dustbin.

(f) Always pour acid into water for dilution. Never add water to acid. 

(g) Be careful while heating the test tube. The test tube should never point towards yourself or towards your neighbors while heating or adding a reagent.

(h) Be careful while dealing with the explosive compounds, inflammable substances, poisonous gases, electric appliances, glass wares, flame and the hot substances. 

(i) Keep your working surroundings clean. Never throw papers and glass in the sink. Always use dustbin for this purpose.

(j) Always wash your hands after the completion of the laboratory work. 

(k) Always use the reagents in minimum quantity. Use of reagents in excess, not only leads to wastage of chemicals but also causes damage to the environment.

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CBSE CHEMISTRY PRACTICALS CLASS-XII-2

Identification of functional groups in organic compounds

  

EXPERIMENT: 1

Tests for the functional groups present in organic compounds:

Aim: To identify the functional groups present in an organic compound:

Apparatus and chemicals required:

Test tube and test tube stand, Droppers, spatula and water bath (use 50 mL glass beaker as water bath), Organic compound. And Bromine reagent, Bayer’s reagent.

Tests for Unsaturation

There are two tests for determining unsaturation in an organic compound.

Procedure:

1. Bromine Test

Dissolve 0.1 g or 5 drops of organic compound in 2 mL of carbon tetrachloride in a test tube and add 2% solution of bromine in carbon tetrachloride or bromine water drop by drop with continuous shaking.

Observation:

The orange-red color of bromine solution remain same no color change is observed 

Inference:

An unsaturated organic compound (unsaturated hydrocarbon) is absent 

May be saturated organic compound may be present, May be alcohol or carboxylic acid is present.

                   

2. Baeyer’s Test (Alkaline KMnO4 Test)

Procedure: Dissolve 25-30 mg of organic compound in 2 mL of water (free of alcohol) and add 1% potassium permanganate solution containing equal volume of 1% sodium carbonate solution. Observation:

Pink color of KMnO4 not disappeared. 

Inference: unsaturated organic compound is absent may be saturated organic compound ethanol may be may be present.

Precautions: 

(a) The tests should be performed at room temperature. (b) Handle bromine solution carefully. Do not inhale the vapors and also avoid its contact with the skin.

Tests for Alcoholic Group:

The alcoholic group can be detected by the following tests:

Procedure:

1. Sodium metal test

Take 3ml of given organic compound in a dry test tube add 1g of CaCl2 to it then filter it. Then add a piece of sodium metal to the filtrate.

Observation:

Alcohols react with active metals like sodium and liberate hydrogen gas that can be observed in the form of effervescence.

 

Inference:

May be Alcohol or phenol or ethanoic acid present.

2. Ester test:

Procedure: Take about 0.1 g compound in a test tube, add 1 mL ethanol or methanol and 2-3 drops of concentrated sulphuric acid. Heat the reaction mixture for 10-15 minutes in a hot water bath at about 50°C. Pour the reaction mixture in a beaker containing aqueous sodium carbonate solution to neutralize excess sulphuric acid and excess carboxylic acid.

Observation: Sweet smell of the substance formed

Inference: the presence of -OH functional group in the compound.

 

3. Ceric ammonium nitrate test:

Procedure:

Take 1 mL solution of organic compound dissolved in a suitable solvent. Add a few drops of ceric ammonium nitrate solution. Alcohols reacts with ceric ammonium nitrate to form a red colored alkoxy cerium (IV) compound.

Observation: Appearance of red color.

 

Inference: Alcohol ethanol (-OH) is confirmed.

Experiment-2

Aim:

The phenolic group can be detected by the following tests:

1. Litmus test

Phenol is a weak acid, it gives red colour with litmus paper. The dissociation of phenol in water is represented as follows:

 

2. Ferric chloride test

Take 2 mL of aqueous or alcoholic solution of the organic compound in a test tube, add neutral ferric chloride solution dropwise and note the color change.

Observation: Phenol reacts with ferric ions to form violet colored complex.Appearance of a blue, green, violet or red color

 

Precautions: (a) Always use freshly prepared, neutral and very dilute solution of ferric chloride. (b) Phenol is toxic and corrosive in nature and should be handled with care.

3.Phthalein Dye test

Take 0.1 g of organic compound and 0.1 g of phthalic anhydride in a clean dry test tube and add 1-2 drops of conc. H2SO4. Heat the test tube for about 1 minute in an oil bath. Cool and pour the reaction mixture carefully into a beaker containing 15 mL of dilute sodium hydroxide solution.

Observation: Appearance of pink, blue, green, red etc. colors.

Inference: the presence of phenolic –OH group in the compound is confirmed.

Experiment-3 and 4:

Carbonyl groups in aldehydes and ketones are identified by the following tests:

Aim: To identify the presence of functional group in given organic compound.

Procedure:

1. 2, 4-dinitrophenyl hydrazine test (2,4-DNP test):

Take 2-3 drops of the liquid compound in a test tube or in case of solid compound, dissolve a few crystals of it in 2-3 mL alcohol. Add a few drops of an alcoholic solution of 2,4-dinitrophenylhydrazine

Observation:

Appearance of yellow, orange or orange-red precipitate.

Inference: confirms the presence of carbonyl group.

 

If precipitate does not appear at room temperature, warm the mixture in a water bath for a few minutes and cool.

Test for aldehyde:

2. Sodium bisulphite test

Procedure:

Take a saturated solution of sodium bisulfite in a clean test tube. Add 1ml of the given organic compound. Shake well and leave it for 15-20 minutes.

Observation:

White precipitate is observed.

Inference: The presence of the carbonyl group is confirmed.  

Note: Acetone phenone and benzophenone do not give this test.

1. Schiff’s Test:

Procedure:

Take 3-4 drops of the liquid compound or dissolve a few crystals of organic compound in alcohol and add 2-3 drops of the Schiff’s reagent.

Observation: Appearance of pink color.

Inference: Presence of Aldehyde is confirmed.

 

Note: With benzaldehyde the pink color develops slowly.

2.Tollen’s Test

Procedure:

Take 1 mL of freshly prepared (~ 2 %) silver nitrate solution in a test tube. Add 1-2 drops of sodium hydroxide solution to it and shake, a dark brown precipitate of silver oxide appears. Dissolve the precipitate by adding ammonium hydroxide solution drop-wise.

Heat the reaction mixture of step (ii) in a water bath for about 5 minutes.

Observation: Formation of a layer of silver metal on the inner surface of the test tube.

Inference: the presence of an aldehyde is confirmed.

 

3. Fehling’s Test

Procedure:

Take nearly 1 mL of Fehling’s solution A and 1 mL of Fehling’s solution B in a clean dry test tube. To this add 2-3 drops of the liquid compound or about 2 mL of the solution of the solid compound in water or alcohol. Heat the content of the test tube for about 2 minutes in a water bath.  

Observation:

Formation of brick red precipitate is observed.

Inference: the presence of aliphatic an aldehyde. 

Precautions: Always use freshly prepared reagents to perform the tests. (b) Do not heat the reaction mixture directly on a flame. (c) After performing the test, destroy the silver mirror by adding dilute nitric acid and drain off the solution with excess of water.

Test for Ketones:

1. m-dinitrobenzene Test

Procedure:

Take 2ml of given organic compound add 0.5g of solid m-nitrobenzene and add few drops of Aqueous solution of sodium hydroxide and shake the contents.

Observation: A violet coloration is appeared. After sometime it faded away.

Inference: Ketone functional group confirmed.

2. Sodium nitroprusside Test

Procedure:

Take 2ml of given organic compound in a test tube add 1ml of sodium hydroxide solution followed by sodium nitro-presside solution. 

Observation: The anion of the ketone formed by a alkali reacts with nitroprusside ion to form a red colored complex.

Inference: Ketone functional group is confirmed.

 

Experiment: 5

Tests for Carboxylic group

Aim: To identify the functional group present in given organic compound.

The following tests can be used to identify carboxylic acids:

1. Litmus Test:

Take 2ml of given organic compound in dry test tube dip blue litmus paper in solution.

Observation: Blue litmus solution changes to red color.

Inference: May be carboxylic acid present or phenol.

 

2. Sodium Hydrogen Carbonate Test

Procedure: take 2ml of given organic compound in dry test tube and add 0.5g of sodium hydrogen carbonate.

Observation: A colorless gas which can be seen in the form of a brisk effervescence.

Inference: - COOH functional may be present.-OH functional group is absent.

 

3. Ester Test

Procedure: take 2ml of given organic compound into a dry test tube add equal quantity of ethanol and few drops of concentrated sulphuric acid and heat on water bath for 5 minutes.

Observation: a fruity smell will be observed. 

Inference:-COOH Functional group is confirmed. 

 

Experiment-6

Tests for Amines:

Aim :To identify the functional group present in given organic compound.

1. Solubility Test:

Procedure:

Take 1 mL of given organic compound in a test tube and add a few drops of dilute H Cl to it. Shake the contents of the test tube well.

 

Observation: the organic compound dissolves in dilute H Cl.

Inference: it shows the presence of an amine.

2. Litmus Test

Amines are basic in nature and turns red litmus blue.

 

3. Carbylamines Test:

Procedure:

Take 2-3 drops of the compound in a test tube and add 2-3 drops of chloroform followed by addition of an equal volume of 0.5 M alcoholic potassium hydroxide solution. Heat the contents gently.

Observation: An obnoxious smell is evolved.

Inference: the presence of primary amino group in the given organic compound.

 

4. Azo-Dye Test

Procedure:

Dissolve nearly 0.2 g of the compound in 2 mL of dilute hydrochloric acid in a test tube. Cool the content of the test tube in ice. 

(ii) To the ice cooled solution add 2 mL of 2.5% cold aqueous sodium nitrite solution. 

(iii) In another test tube, dissolve 0.2 g of β-naphthol in dilute sodium hydroxide solution. 

(iv) Add diazonium chloride solution prepared in step (ii) into the cold β-naphthol solution slowly with shaking.

Observation: The formation of a scarlet red dye will be observed.

Inference: confirms the presence of aromatic primary amine.

  

Chemistry Projects

List of chemistry projects for class -12

  

Projects for class 12 Chemistry

PROJECTS 

Scientific investigations involving laboratory testing and collecting information from other sources A few suggested Projects. 

Projects from chemistry in day life:

1. Role of Paracetamols and Hydroxyl chloroquine in controlling COVID -19 pandemic conditions.

2. Need of Azithromycin and vaccine in COVID -19 Pandemic situations.

3. Role of disinfectants in controlling and prevention of spread of viral and bacterial diseases.  (Sanitizers and soaps, Dettol’s)

4. Study of the presence of oxalate ions in guava fruit at different stages of ripening. 

5. Study of quantity of casein present in different samples of milk.

6. Preparation of soybean milk and its comparison with the natural milk with respect to curd formation, effect of temperature, etc. 

7. Study of the effect of Potassium Bisulphate as food preservative under various conditions (temperature, concentration, time, etc.) 

8. Study of digestion of starch by salivary amylase and effect of pH and temperature on it. 

9. Comparative study of the rate of fermentation of following materials: wheat flour, gram flour, potato juice, carrot juice, etc. 

10. Extraction of essential oils present in Saunf (aniseed), Ajwain (carum), Illaichi(cardamom). 11. Study of common food adulterants in fat, oil, butter, sugar, turmeric power, chilli powder and pepper. 

Note: Any other investigatory project, which involves about 10 periods of work, can be chosen with the approval of the teacher.

Sample project

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