MCQ 21cyb101j Unit 1
MCQ 21cyb101j Unit 1
UNIT -1
1. A coordination complex’s core atom/ion is also known as ________
a) Bronsted-Lowry acid
b) Lewis base
c) Lewis acid
d) Bronsted-Lowry base
2. Two or more compounds that have the same chemical formula, but different arrangement of
atoms are called _______
a) isotopes
b) isotones
c) isomers
d) allotropes
3. Which type of isomerism exhibits compounds with same chemical formula and bonds but
different spatial arrangement?
a) Optical isomerism
b) Linkage isomerism
c) Structural isomerism
d) Solvate isomerism
a) [Ag(NH3)2][Ag(CN)2]
b) [Cr(NH3)6][Co(CN)6]
c) [Zn(NH3)4][PtCl4]
d) [Cu(NH3)4][FeCl4]
Answer: [Ag(NH3)2][Ag(CN)2]
5. Identify the coordination isomer of [Fe(CO)4][Zn(CN)4].
a) Tetracyanidozinc(II) tetracarbonylferrate(II)
b) Tetracarbonylzinc(II) tetracyanidoferrate(II)
c) Tetracyanidoiron(II) tetracarbonylzincate(II)
d) Tetracarbonyliron(II) tetracyanidozincate(II)
6. A coordination complex [MX2L2], has a CN=4 and two unidentate ligands X and L. When the
two L ligands are arranged opposite to each other in its geometry, it is called _______ isomer.
a) cis
b) trans
c) fac
d) mer
7. Which of the following do not show geometrical isomerism? (Assume all ligands are
unidentate)
c) Octahedral [MX2L4]
d) Octahedral [MX3L3]
a. Geometrical isomerism
b. Coordination isomerism
c. Linkage isomerism
d. Ionization isomerism
a. Thiosulphato
b. Oxalato
c. Glycinato
d. Ethane-1,2-diamine
13.The s-orbital does not show preference to any direction because _____________
A. It is the smallest orbital
B. It is present in every atom
C. It is spherically symmetric
D. It is the first orbital
14.The shape of a p orbital is?
A. Sphere
B. Dumbbell
C. Pear-shaped lobe
D. Cuboid
21. The crystal field splitting energy for octahedral and tetrahedral complexes is related as
a) ∆t ≈ 4/9 ∆o
b) ∆t ≈ 1/2 ∆o
c) ∆o≈ 2 ∆t
d) ∆o ≈ 4/9 ∆t
22. Among the ligands NH3, en, CN-and CO the correct order of their increasing field
strength, is
(a) CO< NH3 <en< CN–
(b) NH3<en< CN–< CO
(c) CN–< NH3< CO<en
(d) en< CN–<NH3< CO
23. Which of the following octahedral complexes of Co (at. no.27) will be magnitude of Δoct be
the highest?
(a) [Co(CN)6] 3-
(b) [Co(C2O4)3] 3-
(c) [Co(H2O)6] 3+
(d) [Co(NH3)6] 3+
24. The magnetic moment of [Co(NH3)6]CI3 is
(a) 1.73
(b) 2.83
(c) 6.6
(d) Zero
27. What is the coordination number and oxidation state for the cobalt atom in the compound
[Co(NH3)5Cl]Cl2?
a) 4; +2
b) 5 ; +2
c) 6 ; +2
d) 6 ;+3
29. How many unpaired electrons are there in a strong field complex [Co(NH3)6]3+?
a) Zero
b) One
c) Two
d) three
36. Which metal ion have d3 electronic configuration in the following complexes?
A. [Cr(NH3)6]3+
B. [Co(OH2)6]2+
C. [Fe(CN)6]3-
D. [Ni(OH2)6]2+
43. Which of the following elements has completely filled two shells?
A. Ni
B. Ne
C. Na
D. No
47. Which one has the highest value of first ionisation energy _______.
A. Hydrogen
B. Helium
C. Lithium
D. Sodium
48. The correct statement about the atomic of the alkaline earth metals is _______.
A. it is smaller than corresponding alkali metals in the same periods
B. it is larger than corresponding alkali metals in the same periods
C. It is same as the corresponding alkali metals in the same periods
D. None of the above
49. The general electronic configuration of outermost orbital in the elements of Group 13 is
_______.
A. ns2 np2
B. ns2
C. ns2 np1
D. ns2 np3
50. The correct statement about the variation of electronegativity in a group of the periodic table
A. It increases
B. It decreases
C. It remains constant
D. All of the above
51.The correct reason for the increase in the electronegativity across a period in periodic table
A. attraction between the valence electrons and the nucleus increases
B. attraction between the valence electrons and the nucleus decreases
C. increase in the atomic weight
D. decrease in the atomic weight
52. Which of the following outer electronic configurations is characteristic of alkali metals
A. ns1
B. ns2
C. ns2np6
D. ns2np2
61. [Co(NH3)5NO2]Cl2 and [Co(NH3)5 (ONO)]Cl2 are related to each other as?
a) Geometrical isomers
b) Optical isomers
c) Linkage isomers
d) Coordination isomers