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🤳 BOM FREE ONLINE ETEA MODEL TEST PROCEDURE

Vanadium
1.      Vanadium was discovered by mistaken by Andres Manuel del Rio in 1801.
2.      Vanadium was rediscovered by Swedish chemist Nils Gabriel Sefstrom.
3.      The word Vanadis means goddess of beauty and love in Scandinian mythology.

Oxidation states of vanadium(23)
4.      V+2 → Violet
5.      V+3 → Green
6.      V+4 → Blue
7.      V+5 → Colorless

As catalyst as contact process
8.      Platinum was used as catalyst for conversion of SO2 to SO3 but as it is susceptible to poisoning by arsenic impurities
9.      Vanadium oxide V2 O5 is used as catalyst for conversion of SO2 to SO3.
10.  V2 O5  is also used as catalyst in oxidation of alcohol and hydrogenation of olefins or alkenes.
11.  Sulfuric acid is manufactured by contact process.

Chromium
12.  Atomic number 24
13.  Corrosion resistant
14.  Discovered by French chemist Louis Nicolas Vauquelin in1797.
15.  Chromium forms a large number of coloured compounds.
16.  21st in nature abundance among the elements in earth crust.
17.  Atomic weight 51.996
18.  Melting point 1907 degree C or 3465 0F.
19.  Boiling point 2672 degree C or 4842 0F.
20.  Specific gravity 7.2.

Chromium minerals
21.  Chromite or chrome iron stone (FeO.Cr2O3).
22.  Chrome ochre (Cr2O3)
23.  Crocite (PbCr2O3)

Oxidation states
oxides
CrO
Cr2O3
CrO3
Oxidation state
+2
+3
+6
Nature
Basic
Amphoteric
Acidic

Ionic
Ionize to some extent
Covalent

Chromous salt
Chromic compound


Oxidation
Stable
Reduction

The chromate – Dichromate equilibrium
24.  K2Cr2O4 or solid potassium chromate, when dissolved in water, it forms a yellow solution.
25.  K2Cr2O7 or solid potassium dichromate,when dissolved in water, it forms a orange solution.
26.  The colours come from the negative ions; CrO4-2 and CrO7-2 .
27.  CrO4-2 + 2H+ are in equilibrium with CrO7-2 + H2O
28.  Addition of acid to the reactant shifts the equilibrium towards right and yield more orange colour.
29.  The addition of a base promotes the conversion of dichromate to chromate.

Reduction of chromate (VI) with zinc and an acid;
30.  Potassium dichromate (VI) can be reduced to chromium (lll) and chromium (ll) ions by using Zinc either dilute sulphuric acid or hydrochloric acid.

Potassium Dichromate as oxidizing agent in organic chemistry
31.  Potassium dichromate (VI) solution acidified with dilute sulphuric acid commonly used as an oxidizing agent in organic chemistry.
32.  Potassium dichromate (VI) oxidizes primary alcohol to formaldehyde.
33.  Potassium dichromate (VI) formaldehyde to formic acid.
34.  Potassium dichromate (VI) oxidizes secondary alcohol to ketones.
35.  Potassium dichromate (VI) does not oxidizes tertiary alcohol.

Potassium Dichromate as oxidizing agent in titration
36.  In redox reaction a standard solution of potassium dichromate K2Cr2O7 is used to determine the unknown concentration of a solution of Fe+2.
37.  Dichromate ion reduces to chromium (III)
→ CrO7-2 + 14H+ +6e → 2Cr+3 + 7H2O
38.  Fe (II) is oxidized to Fe(III).
→ 6Fe+2 →6Fe+3 + 6e-
39.  CrO7-2 + 14H+ +6Fe+2 → 2Cr+3 + 7H2O + 6Fe+3
40.  CrO7-2 → orange
41.  Cr+3  → green
42.  The 1:6 mole ratio with respect to amount of CrO7-2  and Fe+2 is consumed.

Manganese
43.  Hite, silvery metallic element
44.  Used in making alloys
45.  First isolated by Swedish chemist John Gorrlieb Gahn in 1774.
46.  Corrodes in moist air.
47.  Dissolves in acids.
48.  Melting point, 1245 degree C or 2271 0F.
49.  Boiling point, 2061 degree C or 3742 0F.
50.  Specific gravity of7.4.
51.  Atomic weight, 54.968

52.  Manganese does not exist in free state, except in meteors.
53.  Manganese is distributed in all world in the form of ores, such as
·         Pyrolusite → magnet
·         Rhodochrosite
·         Franklinite
·         Psilomelane
·         manganite
54.  The word manganese come from Latin world ‘magnes’ meaning magnet.
55.  Manganese  ranks about 12th in abundance among elements in Earth’s crust.

Oxidation state of manganese
56.  +7 → Mn2O7 and MnO4-
57.  +6 →MnO3, Manganic salt (H2MnO4) and manganates (K2MnO4)
58.  +4 → MnO2
59.  +3  → H2Mn2O4 and Mn2(SO4)3
60.  +2 →[Mn(H2O6]+2,  MnO, MnCO3, MnSO4, MnCl2.
61.  +3 → manganic compound
62.  +2 →manganous compounds

Potassium manganite (VII) as an oxidizing agent in organic chemistry
63.  Alkenes react with potassium manganite (VII) solution in cold.
64.  The colour change depends upon on whether potassium manganite (VII) is used under acidic condition or alkaline condition.
65.  Under acidic condition manganite (VII) is reduced to manganese (II) ions.
66.  Under basic condition the manganite (VII are first reduced to green manganite (VI) ions and then to dark brown solid manganese (IV) oxide or manganese oxide.
67.  7 → 6 (dark green solution)
68.  6→ 4 (dark brown precipitate)

Potassium manganite (VII) as an oxidizing agent in titration
69.  KMnO4 is a strong oxidizing agent with intense dark purple colour.
70.  During reduction the purple permanganate ion changes into colourless Mn+2 ion.
71.  The solution turns from dark purple to faint pink colour at equivalence point.
MnO4- + C2O4-2+ → Mn+2 + CO2
72.  No addition indicator is used in this titration because KMnO4 acts itself as an indicator.
73.  KMnO4 solution is used to find the concentration of Fe(II) ions in a solution. The redox reaction is given below;
KMnO4 + Fe+2 → Mn+2 + Fe+3

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