Practicing Success

Target Exam

CUET

Subject

Chemistry

Chapter

Inorganic: D and F Block Elements

Question:

The elements in which the last electron enter the ante-penultimate energy level, i.e., (n - 2)f-orbital are called f-block elements. These elements have been termed as f-block elements as the last electron enters in one of the f-orbitals. These elements are also known as the inner transition elements. This is because the last electron in them enters into (n - 2)-orbital, i.e., inner to the penultimate energy level and they form a transition series within the transition series. The general electronic configuration is:

\[(n - 2)f^{1-14}(n - 1)d^{0-1}ns^2\]

Classification of f-block elements:

Depending upon whether the last electron enters a 4f-orbital or a 5f-orbital, the f-block elements have been divided into two series as follows: 

(i) Lanthanides:The elements in which the last electron enters one of the 4f-orbitals are called 4f-block elements or first inner transition series. These are also called lanthanides or lanthanons or lanthanoids because they come immediately after lanthanum.

(ii) Actinides: The elements in which the last electron enters one of the 5f-orbitals are called 5f-block elements or second inner transition series. These are also called actinides or actinons or actinoids because they come immediately after actinium.

What is the prominent oxidation state of lanthanoid?

Options:

+3

+2

+4

+2 and + 4

Correct Answer:

+3

Explanation:

The correct answer is option 1. +3.

The lanthanoids (or lanthanides) are a series of elements in the periodic table that range from lanthanum (La) to lutetium (Lu). The most prominent oxidation state for these elements is +3. Here’s a detailed explanation of why this is the case:

The general electron configuration of lanthanoids is [Xe] 4f^n 5d^0-1 6s^2, where \( n \) ranges from 1 to 14 as you move from lanthanum to lutetium.

Stability of the +3 Oxidation State

1. Energy Considerations:

Removing the first two 6s electrons and one 4f or 5d electron to achieve a +3 oxidation state requires less energy compared to removing additional electrons. This is because the 4f orbitals are relatively deep within the electron cloud and well-shielded by the 5s and 5p electrons.

2. Ionic Radius and Effective Nuclear Charge:

In the +3 state, lanthanoid ions have a high charge density, meaning they have a relatively small ionic radius for a given charge. This high charge density stabilizes the +3 oxidation state.  Additionally, as electrons are removed, the effective nuclear charge (the net positive charge experienced by electrons) increases, which further stabilizes the +3 state.

3. Crystal Field Stabilization:

The +3 ions of lanthanoids exhibit significant crystal field stabilization when they form compounds, such as oxides and halides, which further stabilizes the +3 oxidation state.

Examples of +3 Oxidation State

Lanthanum (La): The electron configuration is \([Xe] 5d^1 6s^2\), and in the \(+3\) state, it becomes \([Xe]\), a stable configuration.

Neodymium (Nd): The electron configuration is \([Xe] 4f^4 6s^2\), and in the \(+3\) state, it becomes \([Xe] 4f^3\).

Gadolinium (Gd): The electron configuration is \([Xe] 4f^7 5d^1 6s^2\), and in the \(+3\) state, it becomes \([Xe] 4f^7\), which is half-filled and particularly stable.

Other Oxidation States

While +3 is the most stable and common oxidation state, some lanthanoids can exhibit other oxidation states such as +2 and +4, but these are less common:

+2 Oxidation State: This occurs in a few lanthanoids where the 4f^n configuration can provide additional stability (e.g., Eu^2+ with a half-filled 4f^7 configuration).

+4 Oxidation State: This is less common and occurs in a few cases where additional stabilization is possible (e.g., Ce^4+).

The prominent oxidation state of lanthanoids is +3 due to the relatively low energy required to remove three electrons, the stability provided by the resulting electron configuration, and the favorable ionic size and charge density. The +3 oxidation state leads to stable compounds and is energetically favorable compared to other possible oxidation states.