The Ace Tutorial Paper1 Sol
The Ace Tutorial Paper1 Sol
com
om
A A B B B B B D B AD AC ACD
Q 56 57 58 59 60 61 62 63 64 65 66
c
A ABD C D B C C B D A C D
g.
Q 67 68 69
ng
A B C B
Consider f (x) = ex – x
h h
(B). CD = h, tan θ = , tan2θ =
ye
(1) y
x L− x
C
.m
a=1
w
w
h
x
w
θ 2θ O
A x L–x B f ' (x) = ex – 1
://
D
L f ' (x) > 0 for x > 0 and f ' (x) < 0 for x < 0
Now, x tan θ = (L – x) tan 2θ ∴ f (x) is increasing ( ↑ ) for x > 0
tp
I I
tan2θ
2θ
tan2θ 2 θ
x= L ; x = tan θ tan2θ L
tan θ + tan2θ θ + 2θ
θ 2θ x
x=0
2L y = ex always lies above y = x i.e. ex – x ≥ 1 for a > 1
limx= Hence never cuts = a = (0, 1] ⇒ B
θ→0 3
(2) (B). For 0 < a ≤ 1 the line always cuts y = ax . (3) (A). SS' = 2ae, where a and e are length of semi-major axis
and eccentricity respectively.
y
(9 − 3) 2 + (12 −4) 2 = 2ae ∴ ae = 5
∴ Centre is mid point of SS'
∴ Center ≡ (6, 8)
y=ax, a ? (0, 1] Let the equation of auxiliary circle be (x – 6)2 + (y – 8)2 = a 2
We know that the foot of the perpendicular from the focus
on any tangent lies on the auxiliary circle
x
O ∴ (1, – 4) lies on auxiliary circle.
i.e. (1 – 6)2 + (– 4 – 8)2 = a2 ⇒ a = 13
For a > 1, say a = e Q ae = 5 ⇒ e = 5/13
1
Powered by http://www.myengg.com
Powered by http://www.myengg.com
om
4 2
δ 2 − m 2c 2
lH = ......... (1) n(n − 1) n(n − 1)
δ 1+ =n ; = (n − 1) ⇒ n = 8 ( a s n ≠ 1)
c
8 8
g.
lx+my = δ 8− r 3r
1 1 4−
B Tr +1 = 8 Cr x .x − r/4 = 8 Cr .
ng
2 . .x 4
( x2, y2 ) r r
A 2 2
Number of terms with integer power of x occur when r = 0,
ye
(x1,y1)
4, 8 ⇒ 3 terms. Hence B and C are correct.
δ2 − c 2l 2 (10) (CD). Given : (f '(x))2 + (g (x))2 = 1
mK =
.m
2δ 2 − c2 ( l2 + m 2 ) c2
(1) + (2) ⇒ lH + mK = = 2δ − 0
δ δ
w
sin4x
Now, substituting g (x) = − in eq. (1)
2f ′(x)
| z | [ | z |2007 −1] = 0
| z | = 0 or | z | = 1, if | z | = 0 ⇒ z = 0 ⇒ (a, b) = (0, 0) sin4x
f ′ (x) − = cos2x − sin2x
if | z | = 1 ; z 2009 = zz = | z |2 = 1 2f ′ (x)
⇒ 2009 values of z ⇒ Total number of ordered pairs = 2010 Put f ' (x) = t
(7) (BD). As a > 2 hence a2 > 2a > a > 2 2t 2 – 2 (cos 2x – sin 2x) t – sin 4x = 0
Now (x – a)(x – 2a)(x – a2 ) < 0 ⇒ the solution set is as 2(cos2x − sin2x) ± 4 (1 − sin4x) + 8sin4x
shown ⇒ t=
4
∴ 4t = 2 (cos 2x – sin 2x) ± 4(1 − sin4x) + 8sin4x
0 a 2a a2
⇒ 2t = (cos 2x – sin 2x) ± 1 + sin4x
Between (0, a) there are (a – 1) positive integers
Between (2a, a2 ) there are (a 2 – 2a – 1) positive integers taking (+) ve sign, 2t = cos 2x – sin 2x + cos 2x + sin 2x
∴ a2 – 2a – 1 + a – 1 = 18 ⇒ a2 – a – 20 = 0 ⇒ t = cos 2x
(a – 5)(a + 4) = 0 taking (–) ve sign, t = – sin 2x
∴ a = 5 and a = –4 but a > 2∴ a = 5 ⇒ (B) and (D) Hence f ' (x) = cos 2x or f ' (x) = – sin 2x
Powered by http://www.myengg.com
Powered by http://www.myengg.com
1 cos2x 1 1 1 4 4 16 4
Integrating, f(x) = sin2x + C1 or f(x) = + C2 P ( A / B1 ) = . = , P ( A / B2 ) = . = =
2 2 6 6 36 6 6 36 9
f (0) = 0 ⇒ C1 = 0 and C2 = –1/2
1 1
1 cos2x − 1 .
∴ f (x) = sin2x or f(x) = P(B1 / A) = 2 36 =
1
2 2 1424 3 1 1 1 16 17
If f ' (x) = cos 2x then g (x) = – sin 2x E1 . + .
2 36 2 36
If f ' (x) = – sin 2x then g (x) = cos 2x
1 1 16
i.e. f(x) = sin2x and g (x) = – sin 2x ⇒ (C) .
16
E1
2 P(B2 / A ) = 2 36 = E
1424 3 1 16 1 1 17
cos2x − 1 E2 . + . E2
f(x) = and g (x) = cos 2x ⇒ (D) 2 36 2 36
2
(11) (A). y = | ln x | not differentiable at x = 1 E : third ball drawn is red
P (E) = P (E ∩ E1 ) + P (E ∩ E2 )
π 3π
,
y = | cos | x | | is not differentiable at x = 1 5 16 2 5 32 37
2 2 = . + . = + =
x ∈ (0, 2π) 17 6 17 6 102 102 102
om
y = cos–1 (sgn x) = cos–1 (1) = 0 differentiable
(18) (A). f (0) = 2,
1 1
(12) (C). Let ∫ f (t)dt = k , so f (x) = kx + 1, now ∫ (kt + 1) dt = k x x
c
0 0 f(x) = (ex + e− x )cosx − 2x − x ∫ f ′ (t)dt − ∫ t{ {
f ′ (t)dt
g.
0 0 I II
k
⇒ + 1 = k, so k = 2
ng
2 f(x) = (ex + e− x )cosx − 2x
∴ f (x) = 2x + 1,
ye
x
∫
3 x
− xf(x) −xf(0) − t.f(t) 0 − f (t)dt
Also ∫ f(x)dx = 12 ⇒ Option (C) is correct
.m
0
0
(B). Let x1 , x2 , x3 ∈ R be the roots of f (x) = 0
f(x) = (ex + e− x )cosx − 2x − x f ( x ) + 2x
(13)
w
∴ f (x) = (x – x1 ) (x – x2 ) (x – x3 )
f (i) = (i – x1 ) (i – x2 ) (i – x3 )
w
x
| f (i) | = | x1 – i | | x2 – i | | x3 – i | = 1 + x f ( x ) − ∫ f (t)dt
w
0
∴ x12 + 1 x22 + 1 x32 + 1 = 1
://
........... (1)
⇒/ all roots are zero. 0
ht
Powered by http://www.myengg.com
Powered by http://www.myengg.com
om
8 4(4 − k) So, B > A > C = D
+ +2= 0 (28) (A). At resonance XL = XC and Z = Zmin = R
h2 h2
4 + 2 (4 – k) + h 2 = 0 1
c
XL = ωL and = XC
x2 = 2 (y – 12) ωC
∴ latus rectum = 2
g. If ‘f’ is decreased then ω will decrease and hence XC will
ng
(23) (A). increase therefore at f < fr, circuit behaves as capacitative.
If the slopes are complementary then m1 m2 = 1 VL and VC always differ in phase by 180° at any frequency
(29) (A).
ye
2
∴ m3 = – 1 2 1
h = +
.m
F FL Fm
2
using m3 = – in (1) we get
////////////// ///
h
////////////////
w
8 4
w
− 2
+ (4 − k) +2=0
h h2
w
///
⇒ – 4 + 2 (4 – k) + h 2 = 0 ⇒ h 2 + 4 – 2k = 0
://
∴ x2 = 2 (y – 2)
x2 = 2Y R
Fm = ∞ Fm =
tp
where Y = y – 2 2
⇒ a = 1/2
ht
R R
y= –a F1 = F2 =
2 ( n − 1) 2n
∴ 2y – 3 = 0
(24) (C).
F1 n
4S Ratio = =
P1 − P0 = ......... (1) F2 n − 1
2R
P2 (30) (BCD). Intensity increases no. of photon coming on plates
4S therefore it wouldn’t change stopping potential, work func-
P2 − P1 = ......... (2)
R P1 tion and maximum K.E.
Add (1) and (2) (31) (ABC). When return to same point displacement is zero
P0 therefore average velocity is also zero.
6S
P2 − P0 =
R Total distance 2 ( u2 /2g) u
Average speed = = =
Totaltime 2(u/g) 2
4
Powered by http://www.myengg.com
Powered by http://www.myengg.com
(32) (ABD). Equivalent circuit (38) (D).V1 + V2 = V0 (remains same st. line)
C
1 1 1
MV12 + MV22 + C1 = MV02
2 2 2
C
C K2 C1 is loss in kinetic energy
C On solving, V02 = V12 + V22 + C 2
( )
2
V12 + V22 = V 02 −C 2 ; V1 + V2 = V02 −C2
2 2
K1
V
1 R = V02 − C2 (< V0 )
When K1 is closed energy stored = CV2
2
Therefore it yields circle of smaller radius.
5C (39) (A). In inelastic collision radius will be less but straight line
When K2 is also closed equivalent capacitance = of momentum conservation will be same.
3
(40) (A). Velocity of object I will always be less than object II,
2 therefore from above two solutions (0.5, 1.5) is correct.
1 1 5 C 2 5CV
Energy stored E = Ceq V2 = V =
om
2 2 3 6 V2
2 (0.5, 1.5)
5CV 2 CV2 2 1
c
Change = − = CV 2 = CV 2
g.
6 2 6 3 A
(1.5, 0.5)
(33) (AC). B
ng
V1
2
ye
.m
(1)
(41) (C). Just after closing, capacitor behaves as short circuit
(2)
and all current flows through it hence ammeter reads zero.
w
(42) (A). After long time capacitor behaves as open circuit and
w
δ1 + δ2 = 0
tp
Powered by http://www.myengg.com
Powered by http://www.myengg.com
l 1 m l2
EQl + mg + mgl = + ml2 ω 2 O
–
2 2 3
O O EtO O
– EtOOC
EtO – EtO EtO
+ EtO
OE t
E O O O EtO O OEt O
OEt OEt
Q
m
O O O
EtOOC EtOOC EtOOC
EtO –
COOEt COOEt
EtO COOEt
O O O OEt
–
(50) (B).
mgQ 3mgl 2ml 2 2 By replacement of 'c' by 'b' in the complex [Ma2 bcde]n± it
− l + = ω
2Q 2 3 becomes [Ma2 b 2 de]n±
om
Geometrical isomers of [Ma2 b 2 de]n±
2ml2 2 3gl
mgl = ω ; v=
3 2 b b a b d
c
a b a b b d a d a b
g.
M M M M M
4ml2 mgl 4ml2 3g a a a e b e a e a b
(B). EQl = α ; = α ; =α
ng
(46) e d a b e
3 2 3 8l cis cis
Total number of Trans
3g
ye
at = Geo. iso. = 6
8
Geometrical : Isomers of [Ma2 bcde]n±
.m
3g a a a
a r = ω2 r = e a e a d a
w
2
M M M
w
EQ c c d c
d e
w
2 2
3g 3g 3g 1 3g b b b
a = + = +1 = 17
8 2
://
2 16 8 a a a
e a d a c a
tp
M M M
(47) (B). d b e b d b
ht
c c e
O O
..
H – O – S – O – H + H – .O. – N O cis
O base
a a a
acid e e b d b
H O M M M
– + d c c d e c
HSO 4 + H – O – N O H2O + NO2 a a
+ a
(48) (B). Trans
O2 – B.O. = 1.5 ; O2 2– B.O. = 1.0 ; F2 B.O. = 1.0 ; Total number of
O2 + B.O. = 2.5 Geometrical isomers = 9
O2 2– and F2 have same bond order and they are different Hence, decrease in number of Geometrical isomers = 3
molecular species, hence bond length is decided by size of
( −1) × 2 × 300
atoms bonded. (51) (D). − 190 = ∆E +
Bond length in O2 2– > Bond length in F2 because size of 1000
O– > size of F. ∆ E = – 189.4 kcal/mol
Powered by http://www.myengg.com
Powered by http://www.myengg.com
om
0.9C
1°H : 2°H : 3°H = 1 : 3.82 : 4.5
10−14
Ka = = 9.1 × 10− 13 H
c
0.011 |
(A) CH 3 − CH − CH − CH 2 − CH3
Due to cationic hydrolysis resultant solution is acidic
(AC). XY (aq) → X+ (aq) + Y– (aq) g. |
CH 2 − CH3
ng
(54)
X+ (aq) + H2 O (l) ƒ XOH (aq) + H+(aq)
At equilibrium : Cl
ye
C (1 – α) – Cα Cα |
→ CH3 − CH − CH − CH2 − CH3 (Major product)
.m
|
Kw 10−14 80 1
[H+] = Cα = ×C ; (10− 5 ) 2 = −5
× × CH 2 − CH3
Kb 4 × 10 M 2
w
1° H = 9 × 1 = 9
2° H = 6 × 3.82 = 22.92 (major) % of 2-chloro-3-ethyl pen-
w
Kh
M = 100 gm/mol; %α = × 100 ⇒ 2.5 × 10− 3 tane
w
C
22.92
3° H = 1 × 4.5 = 4.5 (minor) = = 62.93%
://
+ −
a for XY : 3a = 2 ( r + r ) 36.42
Total ⇒ 36.42 ≈ 63% ∴ X = 63
tp
Powered by http://www.myengg.com
Powered by http://www.myengg.com
om
So we obtain four types of product (given in bracket)
∴Z=4 H2O2/OH
(D) X + Y + Z = 63 + 12 + 4 = 79 NH 3
(J)
c
2–
CrO4
NiCl 2
g.
(G)
(55) (A) p, q, r, (B) – p, q, s, (C) – r, (D) – p, q, r Yellow sol. sol.
For 2s : Number of radial node = 1, number of maxima in 2+
ng
[Ni(NH3) 6]
radial probability distribution curve = 2, No. of angular Et2 O H2 O2 /H + Deep blue
node = 0 (K)
ye
node = 0 Blue
(56) (A) r, s; (B) – r ; (C) p, r, s ; (D) p, q
Mn 2+ + NH3 + 2H 2O
→ Mn(OH) 2 ↓ +2NH +4
w
∆
(A) CuS + 2O2
→ CuSO4
w
∆ H2O2
CuS + CuSO4
→ 2Cu + 2SO2 ↑
w
∆ MnO.(OH) 2 ↓ orMnO 2
PbS + 2O2
→ PbSO 4
://
Brownishblack
∆
PbSO4 + PbS → 2Pb + 2SO 2 ↑ (62) (B). Ni2+ in [Ni(NH3 )6 ]2+
tp
Powered by http://www.myengg.com
Powered by http://www.myengg.com
CH3 Br Br
HOCl
excess
OH O OH
OH Cl
CH– COOK CO – CHO C – CHCl2 C – CH
Cl
Intramolecular KOH
Cannizaro
om
(G) (F)
(67) (B).
c
(I) eg
dx2– y2 dz2
g.
0
t2g
ng
dxy dyz dzx
In d 1 , d 2 , d 3 system for octahedral ligand field, electronic distribution of any metal cation does not change, whatever may be
ye
ligands.
(II) eg
.m
dx2– y2 dz2
0
t2g
w
5d6
w
Due to increased Zeff value for 3rd transition series metal cation, ∆0 value gets increased, and P < ∆0 , therefore electronic
distribution for d 6 will not change, whatever may be the ligands.
://
tp
(III) eg
dx2– y2 dz2
0
ht
t2g
dxy dyz dzx
Electronic distribution for d8 system for any octahedral ligand field does not change, hence, hybridization and magnetic
moment do not change.
(IV)
4s 4p 4d 4s 4p 4d
eg eg
dx 2– y 2 dz2 dx 2– y 2 dz2
0 0
t2g t2g
dxy dyz dzx dxy dyz dzx
P> 0 P< 0
d7 d7
Hybridisation : sp3d2 Hybridisation : d2 sp3
µeff : 3.89 B.M. µeff : 1.732 B.M.
Hence for d 7 system hybridisation and µeff value changes according to strong or weak field ligand.
9
Powered by http://www.myengg.com
Powered by http://www.myengg.com
(68) (C).
(III) eg
dx2– y2 dz2
0
(I) eg t2g
dx2– y2 dz2 dxy dyz dzx
0
t2g
d3
dxy dyz dzx
For given P < ∆0
d5 Hybridisation : d 2 sp 3
For given P > ∆0 Inner orbital complex
Hybridisation : sp3 d 2 µeff : 3.89 B.M.
µeff : 5.9 B.M.
Outer orbital complex/high spin complex. (IV) eg
dx2– y2 dz2
0
4d t2g
4s 4p
dxy dyz dzx
(II) d6
For given P > ∆0
om
eg Hybridisation : sp3 d 2
dx2– y 2 dz 2
0 Outer orbital/high spin/spin free complex.
t2g (69) (B).
c
dxy dyz dzx (A) Due to higher oxidation state of Cobalt in
g.
d7
III
[Co(H 2O) 6 ]3+ , P < ∆0 , also H2 O lies towards stronger
ng
For given P < ∆0
Hybridisation : d 2 sp 3 ligand side in spectrochemical series.
(B) Due to high value of Zeff in Ir+3 , which belongs to IIIrd
ye
plex
(D) Due to high value of Zeff of Pd 2+, which belongs to
2nd transition series, [P < ∆0 ]
w
w
w
://
tp
ht
10
Powered by http://www.myengg.com