The correct option with order of melting points of the pairs (Mn, Fe), (Tc, Ru) and (Re, Os) is :
A.Fe < Mn$\mathrm{Fe} < \mathrm{Mn}$ , Ru < Tc$\mathrm{Ru} < \mathrm{Tc}$ and Re < Os$\mathrm{Re} < \mathrm{Os}$
B.Mn < Fe, Tc < Ru$\mathrm{Mn} < \mathrm{Fe}, \mathrm{Tc} < \mathrm{Ru}$ and Re < Os$\mathrm{Re} < \mathrm{Os}$
C.Mn < Fe, Tc < Ru$\mathrm{Mn} < \mathrm{Fe}, \mathrm{Tc} < \mathrm{Ru}$ and Os < Re$\mathrm{Os} < \mathrm{Re}$
D.Fe < Mn$\mathrm{Fe} < \mathrm{Mn}$ , Ru < Tc$\mathrm{Ru} < \mathrm{Tc}$ and Os < Re$\mathrm{Os} < \mathrm{Re}$
Solution & Explanation
Formulas Used
Melting point trends in 3d$3d$, 4d$4d$, and 5d$5d$ series transition metals depend on the extent of metallic bonding and d$d$-electron participation.
Core Logic
According to NCERT transition element periodic trends:
3d$3d$ Series (Mn$\mathrm{Mn}$ vs Fe$\mathrm{Fe}$): Manganese (Mn$\mathrm{Mn}$, 3d⁵ 4s²$3d^5 4s^2$) has an abnormally low melting point compared to Iron (Fe$\mathrm{Fe}$, 3d⁶ 4s²$3d^6 4s^2$) because its stable, half-filled d⁵$d^5$ configuration holds d$d$-electrons more tightly, reducing their participation in metallic bonding arrow Mn < Fe$\rightarrow \mathbf{\mathrm{Mn} < \mathrm{Fe}}$.
4d$4d$ Series (Tc$\mathrm{Tc}$ vs Ru$\mathrm{Ru}$): Technetium (Tc$\mathrm{Tc}$, 4d⁵ 5s²$4d^5 5s^2$) similarly shows a dip in melting point compared to Ruthenium (Ru$\mathrm{Ru}$, 4d⁷ 5s¹$4d^7 5s^1$) due to the stable 4d⁵$4d^5$ configuration arrow Tc < Ru$\rightarrow \mathbf{\mathrm{Tc} < \mathrm{Ru}}$.
5d$5d$ Series (Re$\mathrm{Re}$ vs Os$\mathrm{Os}$): Rhenium (Re$\mathrm{Re}$, 5d⁵ 6s²$5d^5 6s^2$) has optimal interatomic interaction and a higher melting point than Osmium (Os$\mathrm{Os}$, 5d⁶ 6s²$5d^6 6s^2$) arrow Os < Re$\rightarrow \mathbf{\mathrm{Os} < \mathrm{Re}}$.
Combining these trends yields: Mn < Fe$\mathrm{Mn} < \mathrm{Fe}$, Tc < Ru$\mathrm{Tc} < \mathrm{Ru}$, and Os < Re$\mathrm{Os} < \mathrm{Re}$
Pattern Recognition
Stable half-filled d⁵$d^5$ configurations in 3d$3d$ (Mn$\mathrm{Mn}$) and 4d$4d$ (Tc$\mathrm{Tc}$) restrict d$d$-electron delocalization, creating characteristic dips in melting point curves compared to adjacent metals.
Correct Option:(C)
More The d-and f-Block Elements Previous-Year Questions — Page 7
Q75jee_main_2024_27_jan_morningQualitative Analysis of Lead
Yellow compound of lead chromate gets dissolved on treatment with hot NaOH$\text{NaOH}$ solution. The product of lead formed is a :
A. Tetraanionic complex with coordination number six
B. Neutral complex with coordination number four
C. Dianionic complex with coordination number six
D. Dianionic complex with coordination number four
The reaction yields sodium tetrahydroxoplumbate(II), [Pb(OH)₄]²⁻$[\text{Pb(OH)}_4]^{2-}$. The charge of the complex species is -2$-2$ (dianionic), and it binds 4 hydroxo coordination ligands, matching a coordination number of four.
Chapter Mix
Class 12 Chemistry: d-and f-Block Elements
Class 12 Chemistry: Coordination Compounds
Q78jee_main_2024_27_jan_morningChromyl Chloride Test
NaCl$\text{NaCl}$ reacts with conc. H₂SO₄$H_2SO_4$ and K₂Cr₂O₇$K_2Cr_2O_7$ to give reddish fumes (B), which react with NaOH$\text{NaOH}$ to give yellow solution (C). (B) and (C) respectively are;
The electronic configuration for Neodymium is:
[Atomic Number for Neodymium 60]
A.[Xe] 4f⁴ 6s²$\text{[Xe]} 4f^4 6s^2$
B.[Xe] 5f⁴ 7s²$\text{[Xe]} 5f^4 7s^2$
C.[Xe] 4f⁶ 6s²$\text{[Xe]} 4f^6 6s^2$
D.[Xe] 4f¹ 5d¹ 6s²$\text{[Xe]} 4f^1 5d^1 6s^2$
Solution
Core Logic
The noble gas configuration of Xenon (Z=54$Z=54$) provides the primary core layout. For Neodymium (Z=60$Z=60$), the 6 remaining valence electrons distribute into the inner 4f$4\text{f}$ orbital subshell rather than filling the 5d$5\text{d}$ subshell due to shielding effects. This results in an absolute atomic ground state electronic configuration of [Xe] 4f⁴ 6s²$\text{[Xe]} 4\text{f}^4 6\text{s}^2$.
Pattern Recognition
Lanthanide filling sequences generally bypass 5d$5d$ progression except for specific exceptions (La, Gd, Lu).
Potassium permanganate (KMnO₄$KMnO_4$) is a strong oxidizing agent. When heated to 513K$513\mathrm{K}$, it undergoes thermal decomposition to give potassium manganate (K₂MnO₄$K_2MnO_4$), manganese dioxide (MnO₂$MnO_2$), and oxygen gas (O₂$O_2$).
The products formed along with O₂$O_2$ are K₂MnO₄$K_2MnO_4$ (green) and MnO₂$MnO_2$ (black).
Chapter Mix
Class 12 Chemistry: d and f Block Elements
Q63jee_main_2024_29_jan_morningPotassium Dichromate and Chromyl Chloride Test
In chromyl chloride test for confirmation of Cl^-$Cl^-$ ion, a yellow solution is obtained. Acidification of the solution and addition of amyl alcohol and 10%$10\%$H₂O₂$H_2O_2$ turns organic layer blue indicating formation of chromium pentoxide. The oxidation state of chromium in that is
Acidification of the yellow CrO₄²⁻$CrO_4^{2-}$ solution followed by the addition of H₂O₂$H_2O_2$ and amyl alcohol yields a blue-colored organic layer due to the formation of chromium pentoxide (CrO₅$CrO_5$).
Potassium Dichromate and Chromyl Chloride Test diagram for Q63 - JEE Main 2024 Morning
The structure of chromium pentoxide (CrO₅$CrO_5$) features a distinctive "butterfly" arrangement. It contains one double-bonded oxide oxygen (O²⁻$O^{2-}$) and four peroxide oxygens (O₂²⁻$O_2^{2-}$). Therefore, there are 2 peroxo linkages.
Let the oxidation state of Chromium be x$x$.
x + 1(-2) + 4(-1) = 0$$x + 1(-2) + 4(-1) = 0$$
x - 2 - 4 = 0$x - 2 - 4 = 0$x = +6$x = +6$
Thus, the oxidation state of Cr in CrO₅$CrO_5$ is +6$+6$.
Pattern Recognition
A classic oxidation state trap. Calculating simply via formula CrO₅$CrO_5$ yields x - 10 = 0 x = +10$x - 10 = 0 \implies x = +10$, which is impossible for Chromium (max +6). Whenever calculation exceeds the maximum group valency, peroxide bonds are present.
Chapter Mix
Class 12 Chemistry: d and f Block Elements
Class 11 Chemistry: Redox Reactions
Practice past-year questions one chapter at a time. Pick an exam → subject → chapter and get every PYQ for that topic — pulled together from all past papers — with the chapter's key formulas alongside.