Chemistry, HSSC-Punjab Second Year. This chapter is split into 40 topics and has
1,045 practice questions. The topics covered are listed below, followed by
10 free sample questions from the chapter.
Topics in this chapter
Permanganate and iron(II) titrations25 questions
Atomic and ionic radii of 3d elements (Figure 18.1)30 questions
Ligand exchange reactions of copper(II)28 questions
Variable oxidation states: the reason24 questions
Cisplatin and the polarity of geometrical isomers23 questions
Feasibility of redox reactions from E values28 questions
Stability constant and its expression22 questions
Anomalous configurations of chromium and copper22 questions
Physical properties of the 3d transition metals22 questions
Energy, frequency and wavelength in d-d transitions25 questions
Finding the oxidation state of the metal in a complex28 questions
Types and names of ligands27 questions
d orbitals and crystal field splitting25 questions
Mixed practice on 3d elements and complexes (1)20 questions
Exercise and Quick Check style questions28 questions
Geometrical (cis-trans) isomerism in complexes26 questions
Metal complexes: central ion, ligand and dative bond25 questions
Chelate effect and ligand displacement22 questions
Monodentate, bidentate and polydentate ligands26 questions
Mixed practice on 3d elements and complexes (2)20 questions
Transition metals as catalysts23 questions
Unpaired electrons and magnetic behaviour30 questions
Common oxidation states of 3d elements (Table 18.2)30 questions
Calculating oxidation states of transition metals30 questions
Ligand exchange reactions of cobalt(II)27 questions
Other redox reactions of transition metal ions20 questions
Configurations of M2+ and M3+ ions30 questions
Electronic configurations of 3d transition atoms30 questions
Definition and position of transition elements24 questions
Colour of complexes and d-d transitions30 questions
Effect of ligands on splitting and colour25 questions
Melting and boiling points of 3d elements (Figure 18.1)30 questions
Permanganate and ethanedioate reaction28 questions
Copper(II) and iodide: iodine liberated and thiosulphate titration24 questions
Coordination number, sphere and charge of ligands28 questions
Optical isomerism in complexes25 questions
Calculations with stability constants25 questions
Geometries of transition metal complexes30 questions
Predicting the formula and charge of complex ions30 questions
Naming coordination complexes30 questions
Sample questions: Transition Metals
10 sample questions with the correct answer and an explanation. Try to answer each one before reading the explanation.
Q1. In the general structure [M(L)x] of a complex ion, the overall charge is shown
A. only as a name and never written in the formula
B. as a coefficient written before the brackets
C. as a subscript inside the square brackets
D. as a superscript outside the square brackets(correct answer)
Answer: D.The book writes the charge of the complex ion as a superscript after the closing bracket, with x the number of ligands.
Q2. A smaller ΔE in tetrahedral complexes explains why they often absorb
A. lower energy light, e.g. in the red(correct answer)
B. no light
C. gamma rays
D. higher energy light, e.g. in the ultraviolet
Answer: A.Smaller splitting means lower-energy photons are absorbed, giving blue/green colours as in [CoCl₄]²⁻ (standard knowledge).
Q3. In the book's MnO₄⁻/Fe²⁺ example, the overall E°cell is correctly found by
A. multiplying the two E° values
B. subtracting E°(Fe³⁺/Fe²⁺) from E°(MnO₄⁻/Mn²⁺)(correct answer)
C. adding the E° values of the two couples directly
D. dividing the larger E° by the smaller
Answer: B.E°cell = 1.52 - 0.77 = +0.75 V. (The book adds the reversed sign E° = +0.77 to obtain 2.29 V because it prints E°(Fe³⁺/Fe²⁺) as −0.77; the standard value is +0.77 V.)