Allen Atomic Structure Solutions
Allen Atomic Structure Solutions
Allen Atomic Structure Solutions
rA
3. = 10 5 19. (A) Energy of ground state ( )
rN +
3
He = –13.6 × 4 eV = –54.4 × 4 eV
VA
VA rA
= (10 5 ) 3 = 10 15 10 –15 (B) P.E. of Ist orbit of H-atom (
VN rN V
N
P.E.)=2T.E.= –2 × 13.6eV = –27.2eV
4. R = R 0 A 1/3 = 1.33 × 10 –13 × (64) 1/3 cm
(C) Energy of II excited state(II
)
= 5.32 × 10 –1 3 × (64) 1/3 cm
1 fm = 10 –15 m 5 fm Z2 (2)2
= –13.6 × = –13.6 ×
C 3 10 8 n2 (3)2
10. = = = 0.75 m
400 10 6 4
14. d = 20 nm = –13.6 × = –6.04 eV
9
20 (D) I.E.= –E 1 = 21.8 × 10
–19
× 4J = 8.7 × 10
–18
J
r = = 10 nm =100 A°
2 1
n2 20. E 5 = –13.6 × = – 0.54 eV
(5)2
r = 0.529 × A° For H atom Z = 1
Z 22. Li+2 & He+ both have same no. of electron so spec-
100 = 0.529 × n 2 n = 14 trum pattern will be similar. Li+2 He+
2
15. E n = – 13.6 ×
Z
n2
1 h 1
E 1 (H) = – 13.6 × = –13.6 eV 23. =
1 2mqV V
4 1 V2 200 2
E 2 (He + ) = – 13.6 × = –13.6 eV
4 2 V1 50 1
32
E 3 (Li 2+ ) = – 13.6 × = –13.6 eV 24. x.p =
32 4
–5 –1
put value p = 1.0 × 10 kg ms
42
E 4 (Be 3+ ) = – 13.6 × 2 = –13.6 eV
4 26. Orbital angular momentum (
)
Ans B h
= ( 1) .
for = 0
16. E = –78.4 kcal/mol 2
2 2 6 2 6 5 2
Z2 28. 25
Mn = 1s , 2s 2p , 3s 3p 3d , 4s
E n = –313.6 × kcal/mol +4 2 2 6 2 6
Mn = 1s , 2s 2p , 3s 3p 3d , 4s
3 0
n2
2+ 2 2 6 2 6 10
1 29. 30
Zn = 1s , 2s 2p , 3s 3p 3d
for H atom Z = 1 –78.4 = 313.6 ×
n2 (unpaired (
–
) de = 0)
313.6 2+ 2 2 6 2 6 6 –
n2 = n = 2 26
Fe = 1s 2s 2p 3s 3p 3d (unpaired de = 4)
78.4
Z Ni
3+ 2 2 6 2 6
= 1s 2s 2p 3s 3p 3d (unpaired de = 3)
7 –
17. V n = 2.188 × 10 6 × m/sec. 28
n
V3 (Li 2 ) Z 3 / n 3 3/3 + 2 2 6
Cu = 1s 2s 2p 3s 3p 3d (unpaired de = 1)
2 6 9 –
= V (Li 2+ ) = V 29
V1 (H ) Z1 / n1 1 /1
Let state (
7
18. ) (1) = n1 30. d =
state ( ) (2) = n2 1 1 1 3
Total spin ( ) = + + + =
r 1 – r 2 = 624 r 0 2 2 2 2
– 2
31. K = 2e = 1s
n12 0.529 n 22 0.529 1 –
L = 8e = 2s 2p
2 4
0.529 × – = 624 ×
Z Z Z –
M= 11e = 3s 3p 3d
2 6 3
2 2 – 2
n – n = 624
1 2
N= 2e = 4s
–
n 1 = 25 for d e = 3, = 2
– 2 2 6 2 6
n2 = 1 33. Cl = 1s 2s 2p 3s 3p
25 1 –
For last e n = 3, l = 1, m = ±1
6 Z Z 1 37. Change in angular momentum = (n 2 – n 1) h
35. (A) v = 2.18 × 10 × v or v
n n n
v v Z/n Z2 (
)
(B) f = or f = 2 f 3
2 r r n /Z n
n 3
mV 2
(n2 – n1) is an integer value ((n2 – n1)
2
(C) r n / Z [T 2 ]
Z
F =
r
)
2 2 2
v (Z / n )
2 Z3
F F 4 so ans (B,C)
r n /Z n
So ans (A,B,D)
(
, 2nd
h2 – h
2
hc 0
2m e 0 2mK.E
5 0 h
2) 2e
[ 0 – ] 2mc
4. 2 2 6 2 6 10 4s 2 4p 6 5s 1
37 Rb = 1s 2s 2p 3s 3p 3d 1
n m s h 0 2
5 0 0 +1/2 e
2mc [ 0 ]
5. Aufbau's principle : electron fills in orbital increasing
order of energy level. 1 3 . m n = mass of neutron ; m p = mass of proton
mn
2m p
2
70 2 atomic mass (m n + m p ) [m n ~ m p ]
6. 30 Zn
= n = A – Z = 70 – 30 = 40
7. n > ,m= – to + (8 + 6) = 14 m p
n s atomic mass (4 + 12) = 16 m p
3 2 ½
The value of cm is wrong 16 – 14
% increase = 100 = 14.28 %
= 2, m = –2, –1, 0, +1, +2 14
1 1 1 1 1 1 n 22 n 12
15. RH 2 2 21. RH 2 – 2 RH 2 2
n
1 n 2 n1 n 2
n1 n 2
for shortest wave length n 2 = , n 1 = 2 2 2
(n n )
22 1 2
1 1 1 4 1 (n 2 n 1 )
RH z 2 = 4R R x
4 H H 1 st line of lymen series n 2 = 2, n 1 = 1
for longest wave length of parchan series n2 = 4, 2 nd line of lymen series n 2 = 3, n 1 = 1
n1 = 3 3 rd line of lymen series n 2 = 4, n 1 = 1
22. The anode ray/canal ray independent to the
1 1 1 1 7
RH z 2 R H x2 electrode material.
9 16 9 16
9 16 1 16
x 23. Energy order decide from (n + ) rule ;(n + ) is
9 7 RH 7
minimum energy is minimum ; if (n + ) value is
16. (IE ) Li2 (IE ) H z 2 equal, lower the value of 'n' lower the energy.
((n + )
; (n
= 21.8 × 10 –19 × 9 J/atom
+ )
; (n
h
= + )
, 'n'
2ME
6.62 10 –34
) e3 > e2 > e4 > e1
=
2 9.1 10 –31 2.18 10 –9 9 r2 r
24. r1 r1 ; r3 = r1 × n2
=1.17 A° n 2
4
17. Fe 2+ = 1s 2 2s 2 2p 6 3s 2 3p 6 3d 6 r 3 = r/4 × 9 r 3 = 2.25 R
–34
h 6.62 10 3600
25. =
unpaired electron (n) = 4 mv 0.2 5
= 2.38 × 10 –30 metre
Magnatic moment (
)
26. Acc to paulis an orbital accomdate maximum two
= n(n 2) BM = 4(6) 24 electron, hence paulis exclusion principle voilates.
orbital angular momentum (
) = (
)
( 1) = 2 (3) 6
27. For d yz , xy and xz are nodal palne
h 1 node = (n – –1) = 6–2–1 3
18.
2 ME ME 29. x y + 4
2 H2
1 1
e ; p y 8 O 18 + 1 H 1
M e 16 E Mp 4 E
y = 9 y 19
1 x = 11 x 23
hence e p Hence x = Na
4M p 4 E ;
Na present in 3 rd period
19. Cu + = 1s 2 2s 2 2p 6 3s 2 3p 6 3d 10 No of neutron = 23 – 11 12
all the electron are paried ; hence it is 4.6
mole of Na = 0.2
paramagnatic 23
(
) Mole of neutron 0.2 × 12 2.4
20. Li (g) Li + + e – n = 520 hc 1240 1240
Li + (g) Li +2 + e n = a KJ/mol. 30. E = ev E = 40 eV
nm 31
Li 2+ (g) Li 2+ + e n = b KJ/mol.
40 = 12.8 + K.E.
b = (IE 2 ) Li = (IE ) Li2 = (IE) n × z 2 = 1313 × 9
K.E. = 10 –12.8 = 27.2 eV
b = (IE 2 ) Li = 11817 KJ/mol K.E. = 27.2 × 1.6 × 10 –19
520 + a + 11817 = 19800 1
27.2 × 1.6 × 10 –19 = × 9.1 × 10 –31 × v 2
2
(IE 2 ) Li = a = 7463 KJ/mol v = 2.18 × 2 × 10 6 m/s
1 v z/n 45. () it is a solution of schrodinger wave equation.
31. Frequency = 2 46. 2r = n [acc to de-broglie theory]
T r n /z
47. m y = 0.25 m x , v y = 0.75 v x
1 z2 n3 1 / 4 1
Frequency = 3 T 2 = h h h
T n z 8 / 1 32 = x = , y =
mv mxvx myvy
32. Radial node (
) = (n – – 1)
h
Angular node ( ) = y = y = 5.33 A
0.25M x 0.75 v x
4s, 5p x , 6 dxy having 3 radial node. 48. Orbital angular momentum (
) =
angular node in all 's' orbital in zero.
(
's'
) ( 1)
33. s-orbital is spherical hence it is non-directional. s p d f
(s-
) = 0 1 2 3
34. B.E. = I.E. m 1
(I.E.) any atom = (I.E.) H × z 2 48. m = (2 +1) =
2
122.4
= z2 50. Mn 4+ = 1s 2 2s 2 2p 6 3s 2 3p 6 3d 3
13.6
z2 = 9 z = 3
E 2 – E 1 = 122.4 – 30.6 = 91.8 eV 51. Acc to (n + ) rule, after np, (n +) s always filled.
h 52. Ni 2+ = 1s 2 2s 2 2p 6 3s 2 3p 6 3d 8
35. x = 2p x .2p =
4
h h n = 2
2 (p) 2 = (v) 2 = 8 m 2
4 magnatic moment (
) = n(n 2)
1 h 1
v = v =
2m 2 2m 2(4) = 58 = 2.83
n3 T1 n 13
45° 53. T = = 1/8
36. z2 T2 n 23
54. E – E 1 = hv 1 , E 1 hv 1
37. n =5 l = 0, 1, 2, 3, 4, s, p, d, f, g
E2 – E 1 = hv 2
38. From (n + ) rule, same as Q.23
E – E 2 = hv 3 , E 2 hv 3
39. The value of = 0 to (n – 1)
–hv 3 + hv 1 = hv 2
Number of electron for given value of = 2 (2+1)
(n 1) v 2 v1 – v 3
hence 2(2 1)
0 v 3 v1 – v 2
h hc
40. = v =
mv 55. EC – EB = ...(i)
1
h h hc
2 = EB – EA = ...(ii)
m m
2
41. Acc to schrodinger model e– behave as wave only. hc
(
e– EC – EA = ...(iii)
3
) add equation (1) and (2)
42. The maximum porbability of finding an electron is 1 1
decribe the orbital, which is denote by 2 . E C – E A =hc
1 2
(
put in equation (3)
2
1 1 hc
) hc =
1 2 3
h
43. m = e =
mv 1
2
h h ve mn = 1 3 1 2
= = 3 1 2 1 2
mcvc mnvn vn mc
hc 58. n 2 = 4 , n 1 =3 ;
56. E =
n 2 = 5 n 1 =4 ;
hc n 2 = 6 n 1 =5 ;
E = (for H atom) n ( n – 1)(n 4)
1
59. n 2 = 5, n1 = 1
hc
E × z 2 = (for He + atom) total number of stectrum line are
2
hc hc 1 (5 – 1) 4
4 2
1 2 4 4 4 + 3 + 2 + 1
57. First Excitation potential (
) lymer Balmer Pascher brackett
= E2 – E1 – 4 + 16 12 eV 3 line in visible reigon.
hc 0.53 10 3 100 h
Energy of photon used for this purpose = = m.x.x =
40 9.1 99.99 4
6.625 10 34 3.0 10 8
= = 7.83 × 10 –19 J 5.27 10 34
253.7 10 –9 x = = 1.447 × 10–3 × 100
1
Energy left after dissociat ion of bond = 9.1 10 31 40 0.04
100
(7.83 – 7.15) × 10 –19
ATOMIC STRUCTURE EXERCISE # 4[B]
1. Given that 1 = 486.1 × 10 –9 m 4. Since we obtain 6 emission lines, it means electron
= 486.1 × 10 –7 cm comes from 4th orbit energy emitted is equal to,
2 = 410.2 × 10 –9 m = 410.2 × 10 –7 cm less than and more than 2.7 eV. So it can be like
this :
1 1
and v v 2 v 1 (
6
4th
2 1
1 1 1 1
2.7
eV
= RH = 2 2 R H 2 2
)
2 n2 2 n1
E 4 – E 2 = 2.7 eV, E4– E3 < 2.7 eV,
1 1
v = RH 2 2 ........(i) E 4 – E 1 > 2.7 eV
n1 n 2 (a) n = 2,
For line I of Balmer series
(E 4 – E 2 ) atom = (E 4 – E 2 ) H × Z 2
1 1 1 1 1 2.7 = 2.55 × Z 2 = 1.029
R H 2 2 = 109678 2 2 (b) IP = 13.6 Z 2 =13.6 × (1.029) 2 = 14.4 eV
1 2 n1 2 n1
(c) Maximum energy emitted=E4–E1 = (E4 – E1)H × Z2
1 1 1 = 12.75 × (1.029) 2
or 7 = 109678 2 2 n 2 = 13.5eV
456.1 10 1
Minimum energy emitted=E4 – E3 =(E 4 – E 3) H × Z2
n1 = 4
= .66 × (1.029) 2 = 0.7eV
For line II of Balmer series ;
5. n 2E = 27.2eV(17 + 10.2)
E – E 2 17eV
1 1 1 1 1 n 3E=10.2eV(4.25+5.95.2) 3
R H 2 2 = 109678 2 2
1 2 n2 2 n2 17 eV = 1.89 × Z 2 Z = 3
E 2 = –3.4 × 9 = –30.6 eV
1 1 1 E n – E 2 = 27.2 eV
or 7 = 109678 2 2 n 2 E n = 27.2 + E 2 = –3.4 eV
410.2 10 2
n2 = 6 13.6 3 2
E n = – 3.4 = – n 2 = 36 n = 6
Thus given electronic transition occurs from 6th to n2
6. = 975 Å
4 th shell. Also by eq. (i)
(
6th 4th
) c 6.626 10 –34 3 10 8
E= = =2.03×10 –18 J=12.75eV
975 1010
1 1 1
v= 109678 2 2 So electron will excite to 4th energy level and when
4 6
comeback number of emission line will be 6.
= 2.63 × 10 –4 cm minimum energy emit ted = E 4 – E 3 = 0.66 eV
1 (
4th
2. E ext = 2.18 × 10 –19 1 × 6.023 × 10 23 =
6
)
9
116.71 kJ/mol H hc 1.9878 10 –25
= = = 1.882 × 10 –6 m =
D.E. = 116.71 × 2.67 = 311.62 kJ/mol H 2 E .66 1.6 10 –19
18820 Å
PV 1 7. (a) kE = qV = 2 × 1.6 –19 × 2 × 10 6 = 6.4 × 10 –13 J
n = = 0.04
RT 0.082 300 (b) At distance d = 5 × 10 –14 m let K.E. is x J and
T.E. = 0.04 × 311.62 + 0.08 × 116.71 = 21.8kJ
k q1 q2 9 10 9 2 1.6 10 –19 47 1.6 10 –19
1240 PE = =
3. E(ev) = d 5 10 14
(nm)
1240 PE = 4.33 × 10 –13 J
Energy of 1st photon = = 11.428 eV By energy conservation :
108.5
1240 6.4 × 10 –13 = x + 4.33 × 10 –13
Energy of 2st photon = =40.79 eV x = 2.06 × 10 –13 J, kE = PE
30.4
En = 52.217– 54.4 = – 2.182 eV (E1 = –54.4 eV) 9 10 2 47 (1.6 10 –19 )2
9
6.4 × 10 –13 =
13.6 4 d
–2.182 = n= 5 d = 3.384 × 10 –14 m
n2
1.9878 10 –25
ke 2 du ke 2 = = 0.3039 × 10 –7 m = 303.9
8. pE = 3 , since F =
= 4 6.54 10 18
3r dr r Å
ke 2 ke 2 ke 2 150
T.E = 3
3 = + ...(3) (b) = A° = 2 A° = 1.414 A°
2r 3r 6r 3 V
nh nh h h
Form bohr's postulate mvr = V = (c) since p = dp 2 d
2 2 mr
z = 6
2
(b) (kE) 1 = – E 1 =13.6 × 36 = 489.6 eV 6
(c) Energy required = –E 1 = 489.6 eV
nh
1240 13. mvr = 3.1652 × 10 –34 = n
= = 2.53 nm 2
489.6
10. E 1 = IP
6.626 10 34
= –4 R = –4 × 2.18 × 10 –18 J
2 3.14
= –8.72 × 10 –18 J
n = 3
E1
E2 = = –2.18 × 10 –18 J
4
1 1 8R
c R – 2=
E = E 2 – E 1 = 6.54 × 10 –18 J = 1 3 9