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Which periodic trend is partially responsible for the observation that the maximum oxidation state of the transition-metal elements peaks near groups 7 B and 8 B? (a) The number of valence electrons reaches a maximum at group 8 B. (b) The effective nuclear charge increases on moving left across each period. (c) The radii of the transition-metal elements reach a minimum for group 8B, and as the size of the atoms decreases it becomes easier to remove electrons.

Short Answer

Expert verified
The periodic trend that is partially responsible for the observation that the maximum oxidation state of the transition-metal elements peaks near groups 7B and 8B is option (c): "The radii of the transition-metal elements reach a minimum for group 8B, and as the size of the atoms decreases it becomes easier to remove electrons."

Step by step solution

01

Understanding Oxidation States and Periodic Trends

Oxidation state is the charge attributed to an atom where it is assumed that the electrons have been transferred completely to the more electronegative atom from the less electronegative one. Various factors can affect the oxidation state of elements, such as electronegativity, atomic radius, and effective nuclear charge. Understanding the relationship between these factors and the oxidation state will help us evaluate the given options.
02

Assess Option (a): Number of Valence Electrons

Option (a) states that "The number of valence electrons reaches a maximum at group 8B." While it is true that the number of valence electrons influences the oxidation state, there is no logical correlation between the maximum oxidation state of transition elements and the maximum number of valence electrons in group 8B. So, this option doesn't support the statement.
03

Assess Option (b): Effective Nuclear Charge

Option (b) says that "The effective nuclear charge increases on moving left across each period." This statement is incorrect. The effective nuclear charge increases when moving right across a period. Moving left results in a decrease in effective nuclear charge, so this option contradicts the periodic trend.
04

Assess Option (c): Atomic Radii

Option (c) says that "The radii of the transition-metal elements reach a minimum for group 8B, and as the size of the atoms decreases, it becomes easier to remove electrons." This statement is correct. As we move across a period, the atomic size decreases due to an increase in effective nuclear charge, causing a stronger attraction between the nucleus and the electrons. As a result, it becomes easier to remove electrons, leading to higher oxidation states. This supports the statement and is the best answer among the given options.
05

Final Answer

Based on the analysis of the given options, we can conclude that option (c): "The radii of the transition-metal elements reach a minimum for group 8B, and as the size of the atoms decreases it becomes easier to remove electrons." is the periodic trend that is partially responsible for the observation that the maximum oxidation state of the transition-metal elements peaks near groups 7B and 8B.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Oxidation State
The concept of an oxidation state is integral to understanding how elements interact in chemical reactions. In essence, the oxidation state reflects the degree of oxidation of an atom within a compound. It's denoted by integers, which can be positive, negative, or zero, and represents the hypothetical charge that the atom would have if all bonds to unlike atoms were 100% ionic.

Consider water (H2O) as an example: the oxygen has an oxidation state of -2, while each hydrogen has an oxidation state of +1. This illustrates how electrons are unequally shared, with the more electronegative oxygen atom having a greater share of the electrons.

Oxidation states also play a crucial role in redox reactions, which involve the transfer of electrons between species. An increase in the oxidation state corresponds to oxidation, while a decrease corresponds to reduction. Therefore, recognizing how oxidation states change helps predict the chemical behavior and reaction pathways of elements.
Effective Nuclear Charge
The effective nuclear charge (often symbolized as Zeff) is a concept used to explain how strongly electrons are held in an atom. It's the net positive charge experienced by electrons in the valence shell, after accounting for the shielding effect of other electrons. As a basic rule, the effective nuclear charge increases from left to right across a period in the periodic table. This occurs because as protons are added to the nucleus, the overall positive charge increases, but the added electrons mainly populate the same shell, providing minimal additional shielding.

Understanding Zeff is crucial because it affects atomic radius, ionization energy, and an element's ability to attract electrons in chemical bonds (its electronegativity). Higher effective nuclear charges result in tighter hold on the electrons, higher ionization energies, and generally increase an atom's tendency to assume higher oxidation states, which are often required for the formation of certain compounds.
Atomic Radius
The atomic radius is a measure of the size of an atom. It can be thought of as the distance from the nucleus to the outer boundary of the electron cloud. Atomic radius generally decreases across a period on the periodic table as Zeff increases—and vice versa: it increases down a group as additional electron shells are added, which are further from the nucleus and less tightly bound due to the shielding effect.

The size of atoms has a profound impact on their chemical properties, including their oxidation states. Smaller atoms can achieve higher oxidation states more easily than larger ones. For transition metals, this is partly because the electrons are closer to the nucleus and held more tightly, which stabilizes the higher oxidation states. Additionally, smaller atomic radii facilitate the overlap of orbitals during bond formation, which is essential in polyatomic ions and complex compounds where transition metals often exhibit their maximum oxidation states.

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Most popular questions from this chapter

Indicate the coordination number and the oxidation number of the metal for each of the following complexes: (a) K3[Co(CN)6] (b) Na2[CdBr4] (c) [Pt(en)3](ClO4)4 (d) [Co(en)2(C2O4)]+ (e) NH4[Cr(NH3)2(NCS)4] (f) [Cu(bipy)2I]I

Which type of magnetic material cannot be used to make permanent magnets, a ferromagnetic substance, an anti-ferromagnetic substance, or a ferrimagnetic substance?

Given the colors observed for VO43 (orthovanadate ion), CrO42 (chromate ion), and MnO4 (permanganate ion (see Exercise 23.84), what can you say about how the energy separation between the ligand orbitals and the empty d orbitals changes as a function of the oxidation state of the transition metal at the center of the tetrahedral anion?

The complexes [V(H2O)6]3+ and [VF6]3 are both known. (a) Draw the d -orbital energy-level diagram for V(III) octahedral complexes. ( b) What gives rise to the colors of these complexes? (c) Which of the two complexes would you expect to absorb light of higher energy?

Consider the tetrahedral anions VO43 (orthovanadate ion), CrO42 (chromate ion), and MnO4 (permanganate ion). (a) These anions are isoelectronic. What does this statement mean? (b) Would you expect these anions to exhibit dd transitions? Explain. (c) As mentioned in "A Closer Look" on charge-transfer color, the violet color of MnO 4 is due to a ligand-to-metal charge transfer (LMCT) transition. What is meant by this term? (d) The LMCT transition in MnO4 occurs at a wavelength of 565 nm. The CrO42 ion is yellow. Is the wavelength of the LMCT transition for chromate larger or smaller than that for MnO 4? Explain. (e) The VO 43 ion is colorless. Do you expect the light absorbed by the LMCT to fall in the UV or the IR region of the electromagnetic spectrum? Explain your reasoning.

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