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Which is a stronger reducing agent, Cr2+ or Fe2+ and why?

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प्रश्न

Which is a stronger reducing agent, Cr2+ or Fe2+ and why?

लघु उत्तरीय
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उत्तर

Cr2+ is a stronger reducing agent than Fe2+. In the formation of Cr2+ to Cr3+, the change is d4 to d3, but in the formation of Fe2+ to Fe3+, the change is d6 to d5. In a medium like water, d3 is more stable than d5.

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अध्याय 4: The d-block and f-block Elements - Intext Question [पृष्ठ १०१]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
अध्याय 4 The d-block and f-block Elements
Intext Question | Q 4.7 | पृष्ठ १०१

संबंधित प्रश्न

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Read the passage given below and answer the following question:

The transition metals when exposed to oxygen at low and intermediate temperatures form thin, protective oxide films of up to some thousands of Angstroms in thickness. Transition metal oxides lie between the extremes of ionic and covalent binary compounds formed by elements from the left or right side of the periodic table. They range from metallic to semiconducting and deviate by both large and small degrees from stoichiometry. Since electron bonding levels are involved, the cations exist in various valence states and hence give rise to a large number of oxides. The crystal structures are often classified by considering a cubic or hexagonal close-packed lattice of one set of ions with the other set of ions filling the octahedral or tetrahedral interstices. The actual oxide structures, however, generally show departures from such regular arrays due in part to distortions caused by packing of ions of different size and to ligand field effects. These distortions depend not only on the number of d-electrons but also on the valence and the position of the transition metal in a period or group.

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Assertion: Crystal structure of oxides of transition metals often show defects.

Reason: Ligand field effect cause distortions in crystal structures.


Read the passage given below and answer the following question:

The transition metals when exposed to oxygen at low and intermediate temperatures form thin, protective oxide films of up to some thousands of Angstroms in thickness. Transition metal oxides lie between the extremes of ionic and covalent binary compounds formed by elements from the left or right side of the periodic table. They range from metallic to semiconducting and deviate by both large and small degrees from stoichiometry. Since electron bonding levels are involved, the cations exist in various valence states and hence give rise to a large number of oxides. The crystal structures are often classified by considering a cubic or hexagonal close-packed lattice of one set of ions with the other set of ions filling the octahedral or tetrahedral interstices. The actual oxide structures, however, generally show departures from such regular arrays due in part to distortions caused by packing of ions of different size and to ligand field effects. These distortions depend not only on the number of d-electrons but also on the valence and the position of the transition metal in a period or group.

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