Chem 2nd Paper Practical
Chem 2nd Paper Practical
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Exp. No: 01
Principle: Anhydrous sodium carbonate is a primary standard substance. So its standard solution can be
prepared directly by weighing the specific mass of Na2CO3 is 106. We know, if 1 mol of any substance
dissolved in 1L or 1000 mL or 1 dm3 solution then the concentration of that solution is 1M.
For preparing,
1000 mL 1M solution, required amount of Na2CO3 = 106 g
100×0.1×106 CMV
100 mL 0.1M “ “ “ = ( )
1000 1000
= 1.06 g Na2CO3
So therefore, for preparing 100 mL 0.1M of primary standard solution required amount of Na2CO3 is 1.06 g.
Theoretically it is difficult to measure the weight. Standard solutions are therefore usually prepared by
measuring more or less mass of a certain quantity and the following equation is used to determine the
strength.
taken weight of 𝑁𝑎2 𝐶𝑂3
Concentration of solution = × specific conc.
Required amount of 𝑁𝑎2 𝐶𝑂3
b) Preparation of solution:
1.06 g of Na2CO3 is poured into a 100 ml volumetric flask using a funnel. Slowly pour water from a wash
bottle into the funnel and fill the flask up to the mark by shaking. Prepared solution is 0.1M Na2CO3
solution.
1.07
= × 0.1
1.06
= 0.101M
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Result: The concentration of the prepared Na2CO3 is 0.101M
Precautions:
1. Na2CO3 must be pure and anhydrous.
2. Weight of Na2CO3 must be taken very carefully.
3. While pouring into the funnel, all the sodium carbonate should be washed with distilled water and taken
up in the flask.
4. If necessary, fill the volumetric flask up to the specified mark with a dropper.
Wash Bottle
Calibration Mark
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Exp. No: 02
Name of the Experiment: Preparation of a primary standard solution of oxalic acid of M/20 (0.05M)
Principle: Oxalic acid is a primary standard substance. So its standard solution can be prepared by
weighing the required mass of oxalic acid with the help of a chemical balance directly. The formula of
oxalic acid is C2H2O4. 2H2O. Since it remains as di-hydrate form and molecular mass of oxalic acids is 126.
Therefore, to prepare M/20 oxalic acid solution. 6.3g of oxalic acid should be dissolved per 1000cm3 of
solution. So (6.3/2)g= 3.15g of oxalic acid crystals should be dissolved in water to prepare 500 cm3 of
oxalic acid solution.
Procedure:
1. The narrow tube of a funnel is entered to the face of the volumetric flask of 500cm3.
2. A weighing bottle with oxalic acid is weighed by a chemical balance and then nearly 3.l5g of oxalic acid
(C2H2O4 .2H2O) is transferred to the volumetric flask with the help of a funnel.
3. Wash the funnel with distilled water. Transfer the washing into the volumetric flask.
4. Add enough distilled water to the volumetric flask carefully up to just below the etched mark on it, with
the help of wash bottle.
5. Add the last few drops of distilled water with a pipette until the lower level of the meniscus just touches
the mark on the measuring flask.
6. Stopper the measuring flask and shake gently to make the solution uniform throughout.
Calculations:
Required amount of oxalic acid for preparing 500cm3 of 0.05M solution= 3.15 g
Taken weight of oxalic acid= 3.l8g
Precautions:
1. Oxalic acid must be anhydrous and pure.
2. Weighing bottle must be dried.
3. The state of the balance must be checked before each weighing. Remove dust from the pans with a soft
brush and find the zero point of the balance.
4. The knob of balance must be turned slowly and carefully.
5. Should not move the balance from its place.
6. The funnel should be washed with distilled water so that all oxalic acid is transferred into the flask.
7. Distilled water must be added to the measuring flask carefully up to the mark on at the shake gently to
make a homogeneous mixture.
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Exp. No: 03
Name of the Experiment: Determination of concentration of sample H2SO4 solution with 0.1 M
Na2CO3 solution.
Principle: Anhydrous Na2CO3 is a primary standard solution. Therefore, by preparing 0.1M standard solution of
anhydrous Na2CO3 and determine the strength of sample H2SO4 solution by neutralization reaction. Methyl
orange is used as an indicator in this case. The neutralization reaction is as follows:
Na2CO3+ H2SO4═ Na2SO4+ CO2+H2O
Required Apparatus: Conical flask, pipette, Burette, stand and clamp, Beaker
Required Chemicals: 0.1M primary standard Na2CO3solution, sample H2SO4 solution, methyl orange indicator.
Procedure:
1. At first fill a burette with the dilute H2SO4 solution and place well on the burette stand with the help of
clamps. Now record the initial burette reading (1st reading).
2. Pipette 10 mL of the standard Na2CO3 into a 250 mL conical flask.
3. Then add 2-3 drops methyl orange indicator into a flask. The color of the solution turns yellow.
4. Titrate the Na2CO3 in the conical flask with H2SO4 from the burette slowly while shaking the flask until the
indicator color change from yellow to red. Record the burette reading (2nd reading) at the end point of the
titration.
5. Determine the volume of H2SO4 solution from the difference between 2nd and 1st burette reading.
6. Repeat the titration process (No 2, 3, 4) 3 times.
7. Record all data in a table as shown in the datasheet.
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Calculation:
Precautions:
1. Great care must be taken while adding H2SO4 acid to the burette.
2. Addition of H2SO4 must be slowly and stir constantly.
3. Addition of H2SO4 should be stopped as soon as the color changes.
4. The reading should be viewed avoiding parallax error.
Burette
Name of the Experiment: Determination of the strength of sample HCl solution with 0.1 M Na2CO3
solution.
Principle: Anhydrous Na2CO3 is a primary standard solution. Therefore, by preparing 0.1M standard solution of
anhydrous Na2CO3 and determine the strength of sample HCl solution by neutralization reaction. Methyl orange
is used as an indicator in this case. The neutralization reaction is as follows:
Required Apparatus: Conical flask, pipette, Burette, stand and clamp, Beaker
Required Chemicals: 0.1M primary standard Na2CO3 solution, sample HCl solution, methyl orange indicator.
Procedure:
1. At first fill a burette with the dilute HCl solution and place well on the burette stand with the help of
clamps.Now record the initial burette reading (1st reading).
2. Pipette 5 mL of the standard Na2CO3 into a 250 mL conical flask.
3. Then add 2-3 drops methyl orange indicator into a flask. The color of the solution turns yellow.
4. Titrate the Na2CO3 in the conical flask with HCl from the burette slowly while shaking the flask until the
indicator color change from yellow to red. Record the burette reading (2nd reading) at the end point of the
titration.
5. Determine the volume of HCl solution from the difference between 2nd and 1st burette reading.
6. Repeat the titration process (No 2, 3, 4) 3 times.
7. Record all data in a table as shown in the datasheet.
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Calculation:
𝑆𝑏 × 𝑉𝑏 × 𝑛𝑎
𝑆𝑎 =
𝑉𝑎 × 𝑛𝑏
0.1 × 5 × 2
= Sb= conc. of Na2CO3 = 0.1 M
10 × 1
Vb = volume of Na2CO3 = 5 mL
= 0.1 M
Va = volume of HCl = 10.0 mL
Result: The strength of HCl solution is 0.1M Sa= conc. of HCl = ?
na= mol no. of acid = 2
Precautions: nb= mol no. of base = 1
Burette
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Experiment No: 05
Name of the Experiment: Determination of concentration of amount of Fe2+ ions by using standard solution of
KMnO4
Principle: In presence of sulfuric acid, in the reaction between KMnO4 and salt Fe2+ion, KMnO4 acts as a strong
oxidizing agent while Fe2+ is the reducing agent. The reaction is as follows
KMnO4 +8 H2SO4 +1OFeSO4 =K2SO4 +MnSO4 + Fe2(SO4)3 + 8H2O
Procedure:
a. Prepare 100 ml 0.02M of KMnO4 standard solution
b. First we take 10ml of FeSO4 solution in a conical flask
c. Then we take 10ml of 1M H2SO4 solution into it by a Pipette
d. We then set up a burette of over the flask using stamp and clamp with KMnO4 in it
e. We record the initial mark of the KMnO4 on burette scale and start pouring it in drops, while stirring the
flask
f. When the end point is obtained, we notice the color change and stop the flow of KMnO4
g. We record the end mark on burette scale ad repeat the entire process three or four time
h. We the average of three closest values and calculated the concentration of FeSO4 following amount of
Fe2+ion
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Data collection: (Titration data)
Burette Reading (ml) Average Volume
Volume of Used KMnO4
Sl of KMnO4
FeSO4 solution solution from burette
No. solution
(ml) First reading Second reading (2nd -1st )ml
(ml)
01 10 0.00 10.1 10.1
02 10 10.1 20.1 10 10.03
03 10 20.1 30.1 10
Calculation:
Reaction:
KMnO4 +8 H2SO4 +1OFeSO4 =K2SO4 +MnSO4 + Fe2(SO4)3 + 8H2O
Precautions:
a. The H2SO4 should be added in distinct drop
b. The acid should not come in contract with body
c. The conical flask should be constantly stirred
d. The last phase of dropping should be slowly
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Exp.No: 06
Name of the Experiment: Detection of functional groups (-COOH, -CHO, >CO, -OH) of organic
compounds.
Physical experiment:
Solubility test:
Litmus test:
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ii) Detection of aldehydic (–CHO) group
Physical test:
Solubility test:
Litmus test:
Tollen’s reagent + organic A shiny silver mirror formed on the test tube Aldehydic group
compound + Immerse it in a (-CHO)
CH 3CHO + 2AgNO3 + 3NH4OH 2Ag +
beaker of hot water for a while Confirmed
CH3COONH4 +2NH4NO3 + 2H2O
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iii) Detection of ketonic (>C=O) group
Physical test:
Solubility test:
Litmus test:
Tollen’s reagent + organic No silver mirror is formed on the test tube ketonic group
compound + Immerse it in a (>C=O)
beaker of hot water for a while confirmed
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iv) Detection of alcoholic (-OH) group
Physical test:
Solubility test:
Litmus test:
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