Summary of Key Chemistry Formulae: d- and f-Block Elements
1. Stoichiometry and Chemical Reactions
1.1 Oxidation States and Stoichiometry
Formulae:
- Oxidation State Calculation: Oxidation state=(Number of bonds to more electronegative atoms)−(Number of bonds to less electronegative atoms)
Explanation: Oxidation states in d- and f-block elements can vary widely due to the involvement of d-orbitals. For example, transition metals such as manganese can exhibit oxidation states ranging from +2 to +7.
Common Mistake: Students often confuse oxidation states with charges on the ion. Remember, oxidation states refer to the hypothetical charge an atom would have if all bonds were ionic.
Example: Manganese in potassium permanganate (KMnO4) has an oxidation state of +7.
1.2 Balancing Redox Reactions
Formulae:
- Nernst Equation for Redox Potential: E=E∘−n0.0591log([reduced form][oxidized form])
Explanation: The Nernst equation helps in calculating the cell potential under non-standard conditions. It is crucial for understanding the redox behavior of transition metals.
Example Application: Calculate the cell potential for a reaction where E∘=1.10,V, the concentration of the oxidized form is 1 M, and the reduced form is 0.1 M.
2. Thermodynamics
2.1 Enthalpy of Atomisation
Formulae:
- Enthalpy of Atomisation: ΔHatomisation=∑ΔHbond dissociation
Explanation: Enthalpy of atomisation is crucial for understanding the strength of metallic bonds in transition metals. Higher enthalpy indicates stronger metallic bonds.
Example: Calculate the enthalpy of atomisation for iron, knowing its bond dissociation enthalpy is high due to its strong metallic bonding.
Common Mistake: Forgetting to consider all bond dissociations when calculating enthalpy of atomisation can lead to incorrect results.
2.2 Standard Electrode Potentials
Formulae:
- Standard Electrode Potential: E∘=−nFΔG∘
Explanation: This formula relates the Gibbs free energy change to the standard electrode potential, which is key in understanding the feasibility of redox reactions.
Example Application: Calculate the standard electrode potential for the reduction of Fe3+ to Fe2+.
NEET Tip: Focus on the trends in electrode potentials across the d-block elements, as they are often tested in NEET.
3. Physical Chemistry
3.1 Magnetic Properties
Formulae:
- Magnetic Moment: μ=n(n+2),BM Where n is the number of unpaired electrons.
Explanation: Magnetic properties of transition elements are due to unpaired electrons in d-orbitals. The magnetic moment provides insight into the number of unpaired electrons, which is useful in determining the electronic configuration of ions.
Example: Calculate the magnetic moment for a Fe3+ ion with 5 unpaired electrons.
Common Mistake: Ignoring the orbital contribution to the magnetic moment, especially for elements in the lower rows of the d-block.
Quick Recap:
- Transition metals exhibit a variety of oxidation states due to the involvement of d-orbitals.
- The Nernst equation is essential for calculating cell potentials in redox reactions.
- Enthalpy of atomisation reflects the strength of metallic bonds, which are stronger in transition metals.
- Standard electrode potentials are linked to Gibbs free energy changes and help predict redox reaction feasibility.
- Magnetic properties are determined by the number of unpaired electrons and are calculated using the magnetic moment formula.
Practice Questions:
- Calculate the oxidation state of manganese in MnO4−.
- Balance the redox reaction: Cr2O72−+Fe2+→Cr3++Fe3+.
- Calculate the enthalpy of atomisation for nickel given bond dissociation energies.
- Determine the magnetic moment for a Co2+ ion.
- Use the Nernst equation to find the potential for a cell with [Cu2+]=0.01M and [Cu]=1M.
This summary provides a comprehensive guide to key formulae and concepts in the chapter "d- and f-Block Elements" from your NCERT textbook, focusing on stoichiometry, thermodynamics, and physical chemistry relevant for NEET preparation.