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प्रश्न
Describe the preparation of potassium permanganate. How does the acidified permanganate solution react with SO2? Write the ionic equation for the reaction.
Indicate the steps in the preparation of KMnO4 from pyrolusite ore.
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उत्तर १
Potassium permanganate can be made by the following methods:
It is produced industrially by the electrolytic oxidation of manganate (VI), followed by the alkaline oxidative fusion of MnO2.
\[\ce{MnO2 ->[Fused with KOH, oxidised with air or KNO3] \underset{manganate ion}{MnO^2-_4}}\]
\[\ce{\underset{manganate}{MnO^2-_4} ->[Electrolytic oxidation in alkaline solution] \underset{permanganate ion}{MnO^-_4}}\]
The chemical reactions of acidic potassium permanganate are as follows:
\[\ce{2MnO^-4 + 2H2O + 5SO2 -> 2Mn^2+ + 4H^+ + 5SO^2-_4}\]
उत्तर २
\[\ce{2MnO2 + 4KOH + O2 ->[\Delta] 2K2MnO4 + 2H2O}\]
\[\ce{3MnO^2-_4 + 4H+ -> 2MnO^-_4 + MnO2 + 2H2O}\]
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संबंधित प्रश्न
When chromite ore FeCr2O4 is fused with NaOH in presence of air, a yellow-coloured compound (A) is obtained, which on acidification with dilute sulphuric acid gives a compound (B). Compound (B) on reaction with KCl forms an orange coloured crystalline compound (C).
(i) Write the formulae of the compounds (A), (B) and C.
(ii) Write one use of compound (C).
Complete the following equations : 2 MnO2 + 4 KOH + O2 →
Complete the following equations : 2 Na2CrO4 + 2 H + →
Complete the following equations : MnO4- + 4H+ + 3e- →
Name the oxometal anions of the first series of the transition metals in which the metal exhibits the oxidation state equal to its group number.
Give an example and suggest a reason for the following feature of the transition metal chemistry:
A transition metal exhibits the highest oxidation state in oxides and fluorides.
Write the formula of an oxo-anion of Manganese (Mn) in which it shows the oxidation state equal to its group number.
Account for the following :
Manganese shows maximum number of oxidation states in 3d series.
Answer the following question.
When MnO2 is fused with KOH in the presence of KNO3 as an oxidizing agent, it gives a dark green compound (A). Compound (A) disproportionates in an acidic solution to give a purple compound (B). An alkaline solution of compound (B) oxidizes KI to compound (C) whereas an acidified solution of compound (B) oxidizes KI to (D). Identify (A), (B), (C), and (D).
On addition of small amount of \[\ce{KMnO4}\] to concentrated \[\ce{H2SO4}\], a green oily compound is obtained which is highly explosive in nature. Identify the compound from the following.
Which of the following reactions are disproportionation reactions?
(a) \[\ce{Cu^{+} -> Cu^{2+} + Cu}\]
(b) \[\ce{3MnO^{-}4 + 4H^{+} -> 2MnO^{-}4 + MnO2 + 2H2O}\]
(c) \[\ce{2KMnO4 -> K2MnO4 + MnO2 + O2}\]
(d) \[\ce{2MnO^{-}4 + 3Mn^{2+} + 2H2O -> 5MnO2 + 4H^{+}}\]
Which of the following is amphoteric oxide?
\[\ce{Mn2O7, CrO3, Cr2O3, CrO, V2O5, V2O4}\]
In the form of dichromate, \[\ce{Cr (VI)}\] is a strong oxidising agent in acidic medium but \[\ce{Mo (VI)}\] in \[\ce{MoO3}\] \[\ce{and W (VI)}\] in \[\ce{WO3}\] are not because:
(i) \[\ce{Cr(VI)}\] is more stable than \[\ce{Mo(VI)}\] and \[\ce{and W(VI)}\].
(ii) \[\ce{Mo(VI)}\] and \[\ce{and W(VI)}\] are more stable than \[\ce{Cr(VI)}\].
(iii) Higher oxidation states of heavier members of group-6 of transition series are more stable.
(iv) Lower oxidation states of heavier members of group-6 of transition series are more stable.
Why \[\ce{HCl}\] should not be used for potassium permanganate titrations?
Complete the reaction mentioning all the products formed:
\[\ce{Cr2O^{2-}7 + 3H2S + 8H^+ ->}\]
Indicate the steps in the preparation of \[\ce{K2Cr2O2}\] from chromite ore.
Indicate the steps in the preparation of \[\ce{K2Cr2O7}\] from chromite ore.
Indicate the steps in the preparation of \[\ce{K2Cr2O7}\] from chromite ore.
Describe the preparation of potassium permanganate. How does the acidified permanganate solution react with oxalic acid? Write the ionic equation for the reaction.
