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    IDENTIFYING THE Ca++ BASIC RADICAL PRESENT IN GIVEN INORGANIC SALT

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    1. Experiment 19: IDENTIFYING THE Ca++ BASIC RADICAL PRESENT IN GIVEN INORGANIC SALT
    2. OBJECTIVE:
    3. TO IDENTIFY THE BASIC RADICAL PRESENT IN GIVEN INORGANIC SALT
    4. APPARATUS REQUIRED
    5. CHEMICALS REQUIRED
    6. THEORY
    7. PROCEDURE
    8. OBSERVATION
    9. 1. Preliminary test:
    10. Group Separation Table
    11. 2. Confirmatory test for group IV metal ion (Sr++, Ca++, Ba++):
    12. Test of Ca++ ion
    13. Reactions involved:
    14. RESULT
    15. CONCLUSION
    16. PRECAUTION

    Experiment 19: IDENTIFYING THE Ca++ BASIC RADICAL PRESENT IN GIVEN INORGANIC SALT

    OBJECTIVE:

    TO IDENTIFY THE BASIC RADICAL PRESENT IN GIVEN INORGANIC SALT

    APPARATUS REQUIRED

    CHEMICALS REQUIRED

    • Dil. HCl
    • H2S
    • NH4OH
    • NH4Cl
    • (NH4)2CO3
    • (NH4)2CO4
    • K4[Fe(CN)6

    THEORY

    Qualitative inorganic analysis is concerned with the detection and identification of radicals present in inorganic salt or a mixture of salts. Inorganic salts are the outcome of the neutralization of acids with base. Each inorganic salt consists of two parts. The part contributed by acid is called acid radical or anion and the part contributed by base is called basic radical or cation. For example, in sodium chloride, which can be obtained by the neutralization of base NaOH with acid HCl, Na+ is the basic radical and Cl– is the acid radical.

    PROCEDURE

    The original solution was prepared by dissolving the given salt sample in water. The sample was subjected to several tests to detect the basic radical of the salt.

    OBSERVATION

    1. Preliminary test:

    a. State: Solid
    b. Odour: Odourless
    c. Colour: White
    d. Solubility: Soluble in water

    Group Separation Table

    ExperimentObservationInference
    1. 2 ml of the original solution was taken in a clean and dry test tube and a few drops of dil. HCl was added to it.White ppt. was not formedAbsence of Group I metal ions
    2. The solution above was passed to the H2S solution.No any ppt. was formedAbsence of Group II
    metal ions
    3. 2 ml of the original solution was taken in a clean and dry test tube and a double volume of NH4Cl was added
    and shaked. Then NH4OH solution was added.
    No any ppt. was formedAbsence of Group IIIA
    metal ions
    4. The solution above in 3 was warmed and H2S was passed.No any ppt. was formedPresence of Group IIIB
    metal ions
    5. 2 ml of the original solution was taken in a clean and dry test tube and NH4Cl and NH4OH solution were
    added. It was warmed and ammonium carbonate solution was added.
    White ppt. was formedPresence of Group IIIA
    metal ions

    2. Confirmatory test for group IV metal ion (Sr++, Ca++, Ba++):

    ExperimentObservationInference
    1. 2 ml of the original solution was taken in a clean and dry test tube and a few drops of K2CrO4 solution were added to it.No any ppt. was formed.Presence of Ca++

    Test of Ca++ ion

    ExperimentObservationInference
    1. 2 ml of the original solution was taken in a clean and dry test tube and a few drops of (NH4)2CO3 solution were added to it.White ppt. was formed that dissolved in acetic
    acid and dil. HCl with effervescence.
    Presence of Ca++
    2. 2 ml of the original solution was taken in a clean and dry test tube and a few drops of (NH4)2C2O4 solution were added to it.White ppt. was formed
    that didn’t dissolve in
    acetic acid but dissolved in dil. HCl.
    Presence of Ca++
    3. 2 ml of the original solution was taken in a clean and dry test tube and a few drops of K4[Fe(CN)6 solution was added to it.White ppt. was formedPresence of Ca++

    Reactions involved:

    IDENTIFYING THE Ca++ BASIC RADICAL PRESENT IN GIVEN INORGANIC SALT reactions

    RESULT

    Hence, the sample was identified as Ca++ basic radical.

    CONCLUSION

    Hence, we can test the basic radicals of a salt by wet ways testing the original solution with several reagents.

    PRECAUTION

    1. Concentrated solutions should be handled carefully.
    2. The colour of the precipitate should be observed carefully.
    3. Check whether the original solution is clear and transparent.

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