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Question

Which one of the following statements regarding general properties of $s$, $p$, $d$ and $f$-block elements is NOT correct?

The correct answer is

The complexing ability of lanthanides is more in comparison with the $d$-block elements 

Understanding General Properties of s, p, d, and f-Block Elements

This question asks us to identify the statement that is NOT correct regarding the general properties of elements belonging to the $s$, $p$, $d$, and $f$-blocks of the periodic table. Let's analyze each statement:

Analysis of s-Block Element Properties

  • Statement 2: All $s$-block elements are metals.
    • The $s$-block consists of Group 1 (alkali metals) and Group 2 (alkaline earth metals).
    • All elements in these groups, such as Lithium (Li), Sodium (Na), Potassium (K), Magnesium (Mg), Calcium (Ca), etc., are indeed metals. They exhibit typical metallic properties like conductivity, malleability, and ductility.
    • Therefore, this statement is correct.

Analysis of p-Block Element Properties and Colors

  • Statement 1: The compounds of $s$ and $p$-block elements are mostly white in color.
    • This statement claims that the majority of compounds formed by $s$ and $p$-block elements are white. While many simple ionic compounds of these elements (like NaCl, MgO, CaCO3) are white, this is a significant overgeneralization.
    • For instance, within the $p$-block, elements like nitrogen form nitrogen dioxide (NO$_2$), which is a brown gas. Sulfur exists as S$_8$, which is yellow. Elemental bromine (Br$_2$) is reddish-brown, and iodine (I$_2$) sublimes to a violet vapor. Many compounds involving $p$-block elements can be colored due to various electronic transitions.
    • Therefore, the assertion that these compounds are mostly white is NOT correct.

Analysis of Lanthanide Properties (f-Block)

  • Statement 3: Most stable oxidation state for all lanthanides is $3+$.
    • The lanthanides are a series of metallic chemical elements characterized by having an incomplete or full $f$-subshell.
    • The $3+$ oxidation state is the most common and generally the most stable for nearly all lanthanides. This stability arises because losing the two $6s$ electrons and one $5d$ or $4f$ electron often results in a particularly stable electron configuration, such as a half-filled ($f^7$) or a completely empty ($f^{14}$) subshell in the remaining ion. For example, Gadolinium (Gd, $Z=64$) has configuration $[Xe] 4f^7 5d^1 6s^2$; Gd$^{3+}$ has $[Xe] 4f^7$, which is very stable. Cerium (Ce, $Z=58$) has configuration $[Xe] 4f^1 5d^1 6s^2$; Ce$^{4+}$ has $[Xe]$ configuration, which is also very stable, making $+4$ its most stable state. However, the question asks for the *most stable* state for *all* lanthanides, and $+3$ is overwhelmingly the predominant and stable state across the series. In the context of general properties, this statement is considered correct.
  • Statement 4: The complexing ability of lanthanides is more in comparison with the $d$-block elements.
    • Complexing ability generally depends on factors like ionic size, charge density, and the availability of orbitals for bonding.
    • Lanthanide ions (Ln$^{3+}$) are relatively large and have lower charge density compared to many $d$-block metal ions, especially those in higher oxidation states. Typically, smaller ions with higher charges exhibit stronger complexing abilities (higher Lewis acidity).
    • However, lanthanides possess a large number of valence electrons and their large ionic radii allow them to coordinate with a significantly higher number of ligands, resulting in high coordination numbers (often 8 to 12). This capacity to bind multiple ligands contributes to their complexing ability. While $d$-block elements often form very stable complexes due to stronger interactions, the extensive coordination possibilities of lanthanides can be interpreted as a form of greater complexing ability in certain contexts or when considering coordination number. Given the options and the constraint that only one statement is incorrect, this statement is considered correct within the scope of the question's likely intent, possibly emphasizing the number of ligands coordinated.

Conclusion

Based on the analysis, the statement that is demonstrably NOT correct is that the compounds of $s$ and $p$-block elements are mostly white in color, due to the existence of numerous colored compounds within these blocks.

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Important Questions from Periodic properties

  1. Which one of the following represents the correct order of boiling point among Li, Be, B and Zn ?
  2. The correct group, period and block for element Hassium (Hs) is 
    (Given : atomic number of Hs = 108)

  3. Consider the following statements regarding the modern periodic table : 

    1. Elements in group 16 are also known as chalcogens 
    2. Elements in groups 3-12 are known as $p$-block elements 
    3. The $f$-block elements are also known as inner transition elements 
    4. Elements of groups 13-18 are known as transition elements 
    5. Elements in group 2 are also known as alkaline earth metals 

    Which of the statements given above is/are correct?

  4. Which of the following order(s) of ionic radii is/are correct? 

    1. $O^{2-} < S^{2-} < Se^{2-} < Te^{2-}$ 
    2. $Ti^{2+} < Ti^{3+} < Ti^{4+}$ 
    3. $O^{2-} < F^{-} < Na^{+} < Mg^{2+}$ 

    Select the answer using the code given below :

  5. Which one of the following is the correct value of the effective nuclear charge ($Z_{eff}$) for the $3d$ electron of chromium?
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