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Aldehydes Ketones and Carboxylic Acids question

2021 · 18 Mar · Shift 2 · Q14
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Aldehydes Ketones and Carboxylic Acids question

2021 · 18 Mar · Shift 2 · Q14

JEE MainChemistryAldehydes Ketones and Carboxylic AcidsNumerical+4 / −1
In Tollen's test for aldehyde, the overall number of electron(s) transferred to the Tollen's reagent formula [Ag(NH3)2]+[Ag(NH_3)_2]^+[Ag(NH3​)2​]+ per aldehyde group to form silver mirror is ‾\underline{\hspace{2cm}}​. (Round off to the Nearest Integer).
Numerical answer
View written solutionFree

Correct answer: 2

  1. Identify the oxidation and reduction in Tollen’s test

    • An aldehyde group, −CHO-CHO−CHO, is oxidized to a carboxylate/carboxylic acid.
    • Tollen’s reagent, [Ag(NH3)2]+[Ag(NH_3)_2]^+[Ag(NH3​)2​]+, is reduced to metallic silver, AgAgAg.
  2. Write the oxidation half-reaction for aldehyde

    In basic medium, the aldehyde is oxidized as: RCHO+3OH−→RCOO−+2H2O+2e−RCHO + 3OH^- \rightarrow RCOO^- + 2H_2O + 2e^-RCHO+3OH−→RCOO−+2H2​O+2e−

    This shows that one aldehyde group loses 2 electrons.

  3. Write the reduction half-reaction for Tollen’s reagent

    Each silver ion in Tollen’s reagent gains one electron: [Ag(NH3)2]++e−→Ag+2NH3[Ag(NH_3)_2]^+ + e^- \rightarrow Ag + 2NH_3[Ag(NH3​)2​]++e−→Ag+2NH3​

    So, one mole of [Ag(NH3)2]+[Ag(NH_3)_2]^+[Ag(NH3​)2​]+ accepts 1 electron.

  4. Compare electrons transferred

    Since one aldehyde group produces 2e−2e^-2e−, it can reduce two silver complexes: RCHO+2[Ag(NH3)2]++3OH−→RCOO−+2Ag+4NH3+2H2ORCHO + 2[Ag(NH_3)_2]^+ + 3OH^- \rightarrow RCOO^- + 2Ag + 4NH_3 + 2H_2ORCHO+2[Ag(NH3​)2​]++3OH−→RCOO−+2Ag+4NH3​+2H2​O

  5. Conclusion

    Therefore, the overall number of electrons transferred to Tollen’s reagent per aldehyde group is: 2\boxed{2}2​

    Rounded to the nearest integer, it remains 222.

  6. Comparison with stored correct answer

    Stored correct answer = 222

    Our derived answer = 222

    Hence, they agree.

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