Topic Page No.Periodic Table & Periodicity Modern Periodic law and present form of the periodic table, s, p, d and f block elements, periodic trends in properties of elements atomic and
Trang 1Topic Page No.
Periodic Table & Periodicity
Modern Periodic law and present form of the periodic table, s, p, d and f block elements, periodic trends in properties of elements atomic and ionic radii, ionization enthalpy, electron gain enthalpy, valence, oxidation states and chemical reactivity.
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PERIODIC TABLE & PERIODICITY
DOBEREINER TRIAD RULE [1817]
He made groups of three elements having similar chemical properties called TRIAD
NEWLAND OCTAVE RULE [1865]
He arranged the elements in the increasing order of their atomic mass and observe that properties of every
8th element was similar to the 1st one like in the case of musical vowels notation
8
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NeDhaPaMaGaRe
1
Sa
LOTHER MEYER ’ S CURVE [1869]
He plotted a curve between atomic wt and atomic volume of different elements
The following observation can be made from the curve
-(a) Most electropositive elements i.e alkali metals (Li, Na, K, Rb, Cs etc.) occupy the peak positions on thecurve
(b) Less electropositive i.e alkaline earth metal (Be, Mg, Ca, Sr, Ba) occupy the descending position of thecurve
(c) Metalloids (B, Se, As, Te, At etc.) and transition metals occupy bottom part of the curve
MENDELEEV ’ S PERIODIC TABLE [1869]
Mendeleev ’ s Periodic ’ s Law
According to him the physical and chemical properties of the elements are the periodic functions of their
atomic masses
This table was divided into nine vertical columns called groups and seven horizontal rows called periods.The groups were numbered as I, II, III, IV, V, VI, VII, VIII and Zero group
MODERN PERIODIC TABLE (MODIFIED MENDELEEV PERIODIC TABLE)
(i) It was proposed by Moseley.
(ii) Modern periodic table is based on atomic number
(iii) Moseley did an experiment in which he bombarded high speed electron on different metal surfaces and
obtained X-rays
He found out that Z where = frequency of X-rays
(iv) Modern Periodic Law - The physical & chemical propeties of elements are a periodic function of the atomic
nubmer
LONG FORM/PRESENT FORM OF MODERN PERIODIC TABLE
It consist of 7 horizontal periods and 18 vertical columns (groups)
IA, IIIA, IIIB, IVB, VB, VIB, VIIB,
10 9 8
1 2 3 4 5 6 7 11 12 13 14 15 16 17 18
Trang 4S – Block Elements
1
IA
18 VIII A 1
IV A 15
V A 16
VI A 17 VII A
2 He 4.002 3
6 C 12.011
7 N 14.006
8 O 15.999
9 F 18.998
10 Ne 20.179 11
IV B 5
V B 6
VI B 7 VII B 8 VIII 9 VIII 10 VIII 11
I B 12
II B
13 Al 26.981
14 Si 28.085
15 P 30.973
16 S 32.006
17 Cl 35.452
18 Ar 39.948 19
22 Ti 47.88
23 V 50.9415
24 Cr 51.996
25 Mn 54.938
26 Fe 55.84
27 Co 55.933
28 Ni 58.693
29 Cu 63.546
30 Zn 65.39
31 Ga 69.723
32 Ge 72.61
33 As 74.921
34 Se 78.96
35 Br 79.904
36 Kr 83.80 37
40 Zr 91.224
41 Nb 92.906
42 Mo 95.94
43 Tc 98
44 Ru 101.07
45 Rh 102.905
46 Pd 106.42
47 Ag 107.868
48 Cd 112.411
49 In 114.82
50 Sn 118.710
51 Sb 121.757
52 Te 127.60
53 I 126.904
54 Xe 132.29 55
138.905
72 Hf 178.49
73 Ta 180.947
74 W 183.85
75 Re 186.207
76 Os 190.2
77 Ir 192.22
78 Pt 195.08
79 Au 196.666
80 Hg 200.59
81 Tl 204.383
82 Pb 207.2
83 Bi 207.980
84 Po 209
85 At 210
86 Rn 222 87
227
104
Rf 261.11
105 Ha 262.114
106 Sg 263.118
107 Bh 262.12
108 Hs 265
109 Mt 266
110 Uun 269
114 Uuq
58 Ce 140.115
59 Pr 140.907
60 Nd 144.24
61 Pm 145
62 Sm 150.36
63 Eu 151.965
64 Gd 157.25
65 Tb 158.925
66 Dy 162.50
67 Ho 164.930
68 Er 167.26
69 Tm 168.934
70 Yb 173.04
71 Lu 174.967 90
Th 232.038
91 Pa 231
92 U 238.028
93 Np 237
94 Pu 244
95 Am 243
96 Cm 247
97 Bk 247
98 Cf 251
99 Es 252
100 Fm 257
101 Md 258
102 No 259
103 Lr 260
Classification of the Elements :
s-block elements : When shells upto (n – 1) are completely filled and the last electron enters the s-orbital of the
outermost (nth) shell, the elements of this class are called s-block elements
p-block elements : When shells upto (n – 1) are completely filled and differentiating electron enters the
p-orbital of the nth orbit, elements of this class are called p-block elements
d-Block elements : When outermost (nth) and penultimate shells (n – 1)th shells are incompletely filled anddifferentiating electron enters the (n – 1) d orbitals (i.e., d-orbital of penultimate shell) then elements of this classare called d-block elements
(1) Ist transition series i.e 3d series contains 10 elements and starts from 21Sc –30Zn Filling of electronstakes place in 3d sub-shell
(2) IInd transition series i.e 4d series contains 10 elements and starts from 39Y – 48Cd Filling of electronstakes place in 4d sub-shell
(3) IIIrd transition series i.e 5d series contains 10 elements and starts from 57La, 72Hf – 80Hg Filling ofelectrons takes place in 5d sub-shell
(4) IVth transition series i.e 6d series contains 10 elements and starts from 89Ac, 104Rf –112Uub Filling ofelectrons takes place in 6d sub-shell (incomplete series)
f-Block elements : When n, (n – 1) and (n – 2) shells are incompletely filled and last electron enters into orbital of antepenultimate i.e., (n – 2)th shell, elements of this class are called f-block elements Generalelectronic configuration is (n – 2) f1-14 (n – 1) d0-1 ns2
f-The elements of f-blocks have been classified into two series
1. st inner transition or 4 f-series, contains 14 elements 58Ce to 71Lu Filling of electrons takes place in
4f subshell
2. IInd inner transition or 5 f-series, contains 14 elements 90Th to 103Lr Filling of electrons takes place
in 5f subshell
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PERIODIC PROPERTIES :
VALENCY : It is defined as the combining capacity of the elements The word valency is derived from an
Italian word “Valentia” which menas combining capacity
(b) In period - Density first increases till maximum and then decreases (s-block to d-block increases,
d-block to p-block decreases)
(c) In group - From top to bottom in a group density increases regularly
e.g In VIIA gp - F and Cl are gases (Low density)
Br is liquid (density 3.19 gm/cm– 3)
I is solid (density 4.94 gm/cm– 3)
number of shells containing electrons Due to the presence of these intervening electrons, the valenceelectrons are unable to experience the attractive pull of the actual number of protons in the nucleus Theseintervening electrons act as shield between the valence electrons and protons in the nucleus Thus, thepresence of intervening (shielding) electrons reduces the electrostatic attraction between the protons in thenucleus and the valence electrons because intervening electrons repel the valence electrons The concept ofeffective nuclear charge helps in understanding the effects of shielding on periodic properties
The effective nuclear charge (Zeff) is the charge actually felt by the valence electron Zeff is given by
Zeff = Z –, (where Z is the actual nuclear charge (atomic number of the element) and is the shielding(screening) constant) The value of i.e shielding effect can be determined using the Slater’s rules
Atomic radius :
Covalent radius : It is one-half of the distance between the centres of two nuclei (of like atoms) bonded by
a single covalent bond as shown in figure
(a) For homodiatomic molecules dA
Trang 6Vander Waal ’ s radius (Collision radius) : It is one-half of the internuclear distance between two adjacent
atoms in two nearest neighbouring molecules of the substance in solid state as shown in figure
Vander Waal’s radius does not apply to metal and its magnitude depends upon the packing of theatoms when the element is in the solid state
Metallic radius (Crystal radius) : It is one-half of the distance between the nuclei of two adjacent metal
atoms in the metallic crystal lattice as shown in figure
Thus, the covalent, vander Wall’s and metallic radius magnitude wise follows the order,
rcovalent < rcrystal < rvander Walls
IONISATION POTENTIAL OR IONISATION ENERGY OR IONISATION ENTHALPY :
(i) Minimum energy required to remove most loosly held outer most shell e– in ground state from an isolated
gaseous atom is known as Ionisation Potential
(a) For an atom M, successive ionisation energies are as follows
-M + E1 M+ + e– E1 = IP1
M+ + E2 M+2 + e– E2 = IP2
M+2 + E3 M+3 + e– E3 = IP3
IP3 > IP2 > IP1(b) e– can not be removed from solid state of an atom, it has to convert in gaseous form, Energy required forconversion from solid state to gaseous state is called Sublimation energy
(c) IP is always an endothermic process (H = +ve)
In a period : In a period atomic size decreases and zeff increases so removal of electron become difficult
and IE increases
.increasesIE
increaseszeff
,decreasessize
atomic
NeFONCBBeLi
ELECTRON AFFINITY / ELECTRON GAIN ENTHALPY
The amount of energy released or absored when electron is added to the valence shell of an isolated gaseousatom
X + e– X– + E.A
known as Electron affinity
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Mostly energy is released in the process of first E.A
Zero
Ar
NeClS
FOP
NSiAl
CBMg
BeNa
Due to small size of fluorine, electron density around the nucleus increses The incoming electron
suffers more repulsion In case of chlorine electron density decreases due to large size, decreasing order ofelectron affinity of halogen Cl > F > Br > I
S > O > P > N
Si > C > P > N
N & P have low electron affinity due to stable half filled configuration
Difference between EN and EA
– Tendency of an atom in a molecule – Energy released when an electron is added to
to attract the bonded electrons neutral isolated gaseous atom
– Relative value of an atom – Absolute value of an atom
– It regularly changed in a period – It does not changes regularly
or group
– It has no unit – It is measured in eV/atom or KJ mol– 1
or K.cal mole– 1
ELECTRONEGATIVITY (EN)
(i) The tendency of an atom to attract shared electrons towards itself is called electronegativity
(ii) EN and EA both have tendency to attract electrons but electron affinity is for isolated atoms Where as
electronegativity is for bonded atoms
(iii) A polar covalent or ionic bond of A – B may be broken
as (a) A – B AA– : + B+ (EN A > EN B)
or (b) A – B AA+ + :B– (EN A < EN B)
depending on their tendency to attract bonded electron
(iv) There is no unit of electronegativity as EN is tendency of a bonded atom not an energy
H2.1
8 2
Trang 8PART - I : OBJECTIVE QUESTIONS
* Marked Questions are having more than one correct option.
Section (A) : Atomic and Ionic Radius
A-1. The correct order of atomic size of C, N, P, S follows the order
A-4. The screening effect of delectrons is
-(A) Equal to the p-electrons (B) Much more than p-electrons
(C) Same as f-electrons (D) Less than p-electrons
A-5. In which of the following compounds manganese shows maximum radius
-(A) MnO2 (B) KMnO4 (C) MnO (D) K3[Mn(CN)6]
A-6. Arrange in the increasing order of atomic radii of the following elements O, C, F, Cl, Br
-(A) F < O < C < Cl < Br (B) F < C < O < Cl < Br
(C) F < Cl < Br < O < C (D) C < O < F < Cl < Br
A-7. The correct order of size would be
-(A) Ni < Pd ~ Pt (B) Pd < Pt < Ni (C) Pt > Ni > Pd (D) Pd > Pt > Ni
A-8. Which group of atoms have nearly same atomic radius
-(A) Na, K, Rb, Cs (B) Li, Be, B, C (C) Fe, Co, Ni (D) F, Cl, Br, I
A-9. In the ions P3 –, S2 – and Cl– the increasing order of size is
-(A) Cl– < S2 – < P3 – (B) P3 – < S2 – < Cl– (C) S2 – < Cl– < P3 – (D) S2 – < P3 – < Cl–
A-10. Atomic radii of Fluorine and Neon in Angstrom units are given by
-(A) 0.72, 1.60 (B) 1.60, 1.60 (C) 0.72, 0.72 (D) None of these
A-11. Which of the following has largest radius
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A-13. Arrange the following in order of increasing atomic radii Na, Si, Al, Ar
-(A) Na < Si < Al < Ar (B) Si < Al < Na < Ar
(C) Ar < Al < Si < Na (D) Na < Al < Si < Ar
A-14. Consider the isoelectronic series :
K+, S2 –, Cl– and Ca2+, the radii of the ions decrease as
-(A) Ca2+ > K+ > Cl– > S2 – (B) Cl– > S2 – > K+ > Ca2+
(C) S2 – > Cl– > K+ > Ca2+ (D) K+ > Ca2+ > S2 – > Cl–
A-15. Which of the following is not isoelectronic
series-(A) Cl–, P3 –, Ar (B) N3 –, Ne, Mg+2 (C) B+3, He, Li+ (D) N3 –, S2 –, Cl–
A-16. In the isoelectronic species the ionic radii (Å) of N3–, Ne and Al+3 are respectively given by
A-19. Element Hg has two oxidation staters Hg+1 & Hg+2, the right order of radii of these ions
(A) Hg+1 > Hg+2 (B) Hg+2 > Hg+1 (C) Hg+1 = Hg+2 (D) None of these
A-20. The correct order of increasing atomic size of element N,F, Si & P
(A) N < F < Si < P (B) F > N < P < Si (C) F < N < P < Si (D) F < N < Si < P
A-21. The correct order of atomic / ionic size
(A) N < Li < B (B) Cl < Mg < Ca (C) Ca+2 < S–2 < Cl¯ (D) Na+ < Mg+2 < Cl¯
Section (B) : Ionization Energy or Potential
B-1. Correct orders of Ist I.P are
-(i) Li < B < Be < C
(ii) O < N < F
(iii) Be < N < Ne
(A) (i), (ii) (B) (ii), (iii) (C) (i), (iii) (D) (i), (ii), (iii)
B-2. The maximum tendency to form unipositive ion is for the elment with the electronic
B-4. A sudden large jump between the values of 2nd and 3rd IP of an element would be associated with
the electronic
configuration-(A) 1s2, 2s2 2p6, 3s1 (B) 1s2, 2s2 2p6, 3s2 3p5
(C) 1s2, 2s2 2p6, 3s2 3p2 (D) 1s2, 2s2 2p6 3s2
B-5. The ionization energy of sodium is 495 kJ mol–1 How much energy is needed to convert atoms persent
in 2.3 mg of sodium into sodium ions
-(A) 4.95 J (B) 49.5 J (C) 495 J (D) 0.495 J
B-6. Ionisation energy increases in the order
-(A) Be < B < C < N (B) B < Be < C < N (C) C < N < Be < B (D) N < C < Be < B
Trang 10B-7. IP1 and IP2 of Mg are 178 and 348 K.cal mol The enthalpy required for the reqction
Mg Mg2+ + 2e– is
-(A) + 170 K.cal (B) + 526 K.cal (C) – 170 K.cal (D) – 526 K.cal
B-8. Highest ionisation potential in a period is shown by
-(A) Alkali metals (B) Noble gases (C) Halogens (D) Representative elements
B-9. In which of the following electronic configuration ionisation energy will be maximum
(A) [Ne] 3s2 3p1 (B) [Ne] 3s2 3p2 (C) [Ne] 3s2 3p3 (D) [Ar] 3d10 4s2 4p3
B-10. The ionization energy will be maximum for the process
(A) Ba Ba++ (B) Be Be++ (C) Cs Cs+ (D) Li Li+
B-11. The correct order of second I.P
(A) Na < Mg > Al < Si (B) Na > Mg < Al > Si (C) Na > Mg > Al < Si (D) Na > Mg > Al > Si
B-12. Amongst the following, the incorrect statement is
(A) IE1 (Al) < IE1 (Mg) (B) IE1 (Na) < IE1(Mg) (C) IE2 (Mg) > IE2 (Na) (D) IE3 (Mg) > IE3 (Al)
Section (C) : Electron affinity or Electron Gain Enthalpy
C-1. In which case the energy released is minimum
-(A) Cl Cl– (B) P P– (C) N N– (D) C C–
C-2. In the formation of a chloride ion, from an isolated gaseous chlorine atom, 3.8 eV energy is released,
which would be equal to
-(A) Electron affinity of Cl– (B) Ionisation potential of Cl
(C) Electronegativity of Cl (D) Ionisation potential of Cl–
C-3. The correct order of electron affinity is
-(A) Be < B < C < N (B) Be < N < B < C (C) N < Be < C < B (D) N < C < B < Be
C-4. Electron addition would be easier in
C-5. In the process Cl(g) + e– HCl–(g), H is
-(A) Positive (B) Negative (C) Zero (D) None
C-6. O(g) + 2e– O2( g) Heg = 744.7 KJ/mole The positive value of Heg is due to
-(A) Energy is released to add to 1 e– to O–1 (B) Energy is required to add to 1 e– to O–1
(C) Energy is needed to add on 1 e– to O (D) None of the above is correct
C-7. Which of the following process energy is liberated
-(A) Cl Cl+ + e– (B) HCl H+ + Cl– (C) Cl + e– Cl– (D) O– + e– O–2
C-8. Second electron affinity of an element is
-(A) Always exothermic (B) Endothermic for few elements
(C) Exothermic for few elements (D) Always endothermic
C-9. The element having very high ionization enthalpy but zero electron gain enthalpy
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C-13. The electron affinity of the members of oxygen family of the periodic table, follows the sequence
C-16. Which of the following statement is not true?
(A) F atom can hold additional electron more tightly than Cl atom
(B) Cl atom can hold additional electron more tightly than F atom
(C) The incoming electron encounters greater repulsion for F atom than for Cl atom
(D) It is easier to remove an electron from F¯ than Cl¯
C-17. Increasing order of Electron affinity for following configuration
D-3. Bond distance C–F in (CF4) & Si–F in (SiF4) are respective 1.33Å & 1.54 Å C–Si bond is 1.87 Å Calculation
the covalent radius of F atom ignoring the electronegativity differences
D-4. Two elements A & B are such that B E of A–A, B–B & A–B are respectively 81 Kcal / mole,
64 Kcal / mole, 76 Kcal / mole & if electronegativity of B is 2.4 then the electronegativity of 'A' may beapproximately
D-5. The lowest electronegativity of the element from the following atomic number is
D-6. Which one is not correct order of electronegativity
(A) F > Cl > Br > I (B) Si > Al > Mg > Na (C) Cl > S > P > Si (D) None of these
D-7. Calculate the bond length of C–X bond if C – C bond length is 1.54 Å and X–X bond length is 1.2 Å and
electronegativities of C and X are 2.0 and 3.0 respectively
D-10. Which one of the following is incorrect ?
(A) An element which has high electronegativity always has high electron gain enthalpy
(B) Electron gain enthalpy is the property of an isolated atom
(C) Electronegativity is the property of a bonded atom
(D) Both electronegativity and electron gain enthalpy are usually directly related to nuclear charge andinversely related to atomic size
Trang 12PART - II : MISCELLANEOUS QUESTIONS
Comprehensions Type
Comprehension # 1
Read the following passage carefully and answer the questions.
The minimum amount of energy required to remove the most loosely bound electron from an isolatedatom in the gaseous state is known as ionisation energy or first ionisation energy or ionisationenthalpy (IE1) of the element The energy required to remove the second electron from the monvalentcation is called second ionisation enthalpy (IE2) Similarly, we have third, fourth ionistion enthalpies.The values of ionisation energy depends on a number of factors such as (i) size of the atom (ii)screening effect (iii) nuclear charge (iv) half filled and fully filled orbitals
In a group, the ionisation energy decreases from top to bottom In a period, the value of ionisationenergy increases from left to right with breaks where atoms have somewhat stable configurations
1. Compared to the second ionisation energy (IE2) of an atom, the third ionisation energy (IE3) is
-(A) The same (B) Greater (C) Smaller (D) Half
2. In a period, the ionisation energy is lowest for the
-(A) Noble gases (B) Halogens
(C) Alkaline earth metals (D) Alkali metals
3. The electronic configurations of some neutral elements are given below
Pauling gave method to calculate univalent ion radii by assuming that
(i) In ionic crystal (let M+X¯ ) cations and anions are is contact of each other and sum of their radii is equal to
interionic distance, i.e
¯) X
— M (
d =
X
M r r
(ii) The radius of an ion having noble gas configuration is inversely proportional to the effective nuclear charge
felt at the periphery of the ion, i.e.r(M) =
) M ( eff
Z C
Here C is constant of proportionality whose value depends on electronic configuration of ion Thus,
¯)
X M (
d
=
) M ( eff
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5. The value of constant C for NaF crystals is [given that interionic distance of NaF = 231 pm] :
(A) 231 (B) 115.5 (C) 614.5 (D) 307.25
6. The value of univalent radii for F¯ as calculated by Pauling method is (given that interionic distance of
NaF = 231 pm) :
(A) 94.5 pm (B) 136.5 pm (C) 111.68 pm (D) 115.5 pm
7. The value of ‘C’ for Na+, Mg2+ and Al3+ will be in the order :
(A) Al3+ > Mg2+ > Na+ (B) Al3+ < Mg2+ < Na+ (C) Al3+ = Mg2+ = Na+ (D) Can’t be compared
Comprehension # 3
The amount of energy required to remove, an electron from the last orbit of an isolated (free) atom ingaseous state is known as ionisation energy or first ionisation energy of the element Similarly the energyrequired for the removal of the electron from the unipositive ion (M+ produced above) is referred to assecond ionization energy and thus the third, fourth etc
The ionisation energy depends on various factors like nuclear charge, size of atom, type of configurations,screening effect and penetration power of the electrons
8. Which of the following statement is correct ?
(A) Ionisation energies of elements decrease along the period
(B) Ionisation energies of the IIA group elements are less than that of the corresponding III A group elements.(C) Ionisation energies of group 15 elements are less than that of the corresponding group 16 elements.(D) Ionisation energy of Ga is greater than Al
9. The dominating factor responsible for the decreasing ionisation energies of the elements on moving down
the group is :
(A) atomic radius (B) type of electron to be removed
(C) the valence shell electron configuration (D) all of these
10. Which of the following order is not correct ?
(A) E(I) of Be > E(I) of B but E(II) of Be < E(II) of B
(B) E(I) of Be < E(I) of B but E(II) of Be < E(II) of B
(C) E(II) of O > E(II) of N
(D) E(I) of Mg > E(I) of Al
Match the column
11. Match list-I (atomic number of element) with list-II (position of elements in periodic table) and select
the corect anwer using the codes given gelow the lists :
(A) 1s2 (p) Show highest negative oxidation state
(B) 1s2 2s2 2p5 (q) Show highest first ionisation energy
(C) 1s2 2s1 (r) Show highest reducing power in aqueous solution.(D) 1s2 2s2 2p3 (s) Show highest electron affinity
(t) Show highest electronegativity
Trang 1413. Column-I contains some increasing orders of various species and column-II has the properties of the
elements / ions Accordingly match the column-I and column-II
14. In Column-I, there are given electronic configurations of some elements Match these with the correct
metals given in Column-II :
(C) Second ionisation energy (r) Lutetium
(D) Inner transition element (s) Antimony
18. Match the type of elements / characteristic of the elements listed in Column-I with the correct element
listed in Column-II
(A) Highest 1st ionisation energy (p) Technitium
(B) Highest electronegativity (q) Lithium
(D) Strongest reducing agent (s) Fluorine
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19. The Column-I has certain details about the elements of s-, p- and d-block elements Match those with
the group number of the elements listed in Column-II
(A) An element whose fourth shell contains two p-electrons (p) 8th group
(B) An element whose valence shell contains one unpaired p-electron (q) 12th group
(C) An element which receives last electron in (n – 1) d-subshell (r) 14th group
(D) An element with the ground-state electron configuration [Ar]4s23d10 (s) 17th group
Assertion / Reasoning
DIRECTIONS :
Each question has 5 choices (A), (B), (C), (D) and (E) out of which ONLY ONE is correct.
(A) Statement-1 is True, Statement-2 is True; Statement-2 is a correct explanation for Statement-1.(B) Statement-1 is True, Statement-2 is True; Statement-2 is NOT a correct explanation for Statement-1.(C) Statement-1 is True, Statement-2 is False
(D) Statement-1 is False, Statement-2 is True
(E) Statement-1 and Statement-2 both are False
20 Statmemt-1 : F atom has less electron affinity than Cl atom.
Statmemt-2 : Additional electrons are repelled more strongly by 3p electrons in Cl atom than by 2p
electrons in F atom
21 Statmemt-1 : Noble gases have highest ionization enthalpies in their respective periods.
Statmemt-2 : Noble gases have stable closed shell electronic configuration.
22 Statmemt-1 : Electron gain enthalpy of oxygen is less than that of fluorine but greater than that of
nitrogen
Statmemt-2 : Ionization enthalpy is as follows : N > O > F
23 Statmemt-1 : Cs and F combines violently to form CsF.
Statmemt-2 : Cs is most electropositive and F is most electronegative.
24 Statmemt-1 : Nitrogen has higher IE than that of oxygen.
Statmemt-2 : Nitrogen atom has smaller atomic size than that of oxygen.
25 Statement-1 : Electron affinity values of the 3rd period elements on extreme right of the periodic table
except noble gases are generally more than the 2nd period element of the same group
Statement-2 : Due to smaller atomic size of the 2nd period element, its electron density increases
which eases the addition of electron
26 Statement-1 : In a period noble gas has largest atomic radius.
Statement-2 : In case of noble gases vander Waal's radius is defined and there is much inter electronic
repulsions
27 Statement-1 : The 5th period of periodic table contains 18 elements not 32
Statement-2 : n = 5 , = 0, 1, 2, 3 The order in which the energy of available orbitals 4d , 5s and 5pincreases is 5s < 4d < 5p and the total number of orbitals available are 9 and thus 18 electrons can beaccommodated
True / False
28. Among K+, Mg2+ and Al3+ ions, Al3+ is the smallest one
29. The negative value of electron gain enthalpy of Cl > F because there is weak electron-electron
repulsion in the bigger 3-p sub-shell of Cl as compared to compact 2p-subshell of F
30. Formation of S2 – and Ar–, both require the absorption of energy
31. The following set of elements does not represent the correct order of electron affinity values
S > Se > Te > O
32. The size of the isoelectronic species is effected by electron-electron interaction in the outer orbitals