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Answer Keys:
General Ability:
1 A 2 C 3 20 4 D 5 150 6 D 7 B
8 C 9 A 10 A
Chemical Engineering:
1 C 2 0.08 3 C 4 0 5 A 6 1 7 D
8 C 9 600 10 A 11 A 12 D 13 C 14 B
15 A 16 6 17 B 18 B 19 1 20 C 21 A
22 A 23 B 24 A 25 C 26 D 27 0.0855 28 D
29 D 30 10.51 31 0.4252 32 B 33 30.397 34 0.027 35 49.64

36 169.6 37 6.28 38 28.28 39 500 40 C 41 127.88 42 B
43 0.016 44 A 45 0.02 46 0.9536 47 A 48 0.5 49 1.18
50 D 51 14971.62 52 D 53 A 54 5 55 B
Explanations:-
General Ability:
3. Let Rajeev’s age 10 years ago be ‘x’ year
His mother’s age 1 decade ago = 4x
( 4x + 10 ) + 10 = 2 ( x + 10 + 10 )
2x = 20
∴ x = 10
∴ current age of rajeev = ( x + 10 ) = 20 years.
4. Let the ten’s digit be ‘x’ and unit digit of number is y.
Then, x + y = 10 (i )
(10x + y ) − (10y + x ) =18
9x − 9y = 18
x−y=2 ( ii )
Adding ( i ) & ( ii )
we get x = 6; y = 4.
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1
CHTest ID: 178274 TarGATE’17 www.gateforum.com
5. 3-Digit number divisible by 6 are 102, 108, 114,….,996
This is an A.P in which a=102, d=6 and l=996
Let the number of terms be n. Then tn = 996.
a + (n-1) d=996
102 + (n-1)6=996
6 (n-1) = 894
Therefore, n=150
Number of terms=150
6. Indefatigable, Untiring is also synonyms.
7. The authenticity of the given statement cannot be deduced. So, I does not follow. Since, the
advertisement talks of quick returns, it implies that people want their money to grow, as an
advertisement always imbibes comments and features that attract the attention of the people
immediately. So, II follows.
8. This is an inference question, so only one choice will logically and inevitably follow from the
stimulus. (A) is actually contradicted by the stimulus, which states directly that a lack of
consensus does not always mean that the applicant is unworthy. (B) goes too far; the stimulus
only says that the process does not always work well; this is no basis for inferring definitively
that it should be completely abandoned.
Choice (C) does follow from the stimulus. First, we know that not all candidates whose essays
fail to generate consensus are unworthy of admission, and furthermore we are told that some
such candidates, who may in fact be worthy of admission, are still denied entry merely
because the committee failed in its task.
(D) is outside the scope; there is nothing here about applicants who gain admission by
dishonest means.
9. Required percentage increase
1.15 × 0.14 + 0.86 − 1

=  × 100
 1 
= 2.1%
1
10. Part of the tank filled by pipe A in 1 minute =
80
1
Part of the tank filled by pipe B in 1 minute =
70
1
Part of the tank filled by pipe C in 1 minute =
60
Here we have to find the proportion of the solution R.
2
Pipe C discharges chemical solution R.

1 1
Part of the tank filled by pipe C in 3 minutes = 3× =
60 20
1 1 1 73
Part of the tank filled by pipe A,B,C together in 1 minute = + + =
80 70 60 1680
73 219
Part of the tank filled by pipe A,B,C together in 3 minute = 3× =
1680 1680
1
 
Required proportion =   =
20 1×1680 1680
=
 219  20×219 4380
 
 1680 
CHEMICAL ENGINEERING:
1. λ3 + 2λ 2 + 2λ + 1 = 0 gives λ = -1, − 1 + i 3 , − 1 − i 3
2 2 2 2
⇒ λ = 1 (By the properties of eigen values of orthogonal matrix)
∴ P is an orthogonal matrix
2. P(E1 ) = 60%;P(E 2 ) = 40%. Let A be the event denote that the student has an IQ of more
than 125, then
( E ) =10%; P ( A E ) = 5%
P A
1 2
Required probability is P(A) = P(E1 ).P A ( E ) + P(E ).P ( A E ) = 0.08

1
2
2
−∂f
− ( ye xy − 4y )
= ∂x =
dy y
3. Let f (x, y) = exy − 4xy = 4 then =−
dx ∂f xe xy − 4x x
∂y
4. By Gauss-divergence theorem;
∂F1 ∂F2 ∂F3

∫∫ F.ds = ∫∫ ∫ (∇.F) dv; where ∇.F = ∂x + ∂y + ∂z
s v
= 2xz3 + 2xz3 + 4xz3
= 8xz3 .
3
6 4 2
= ∫ ∫ ∫
z =−6 y =−4 x =−2
8xz 3dx dy dz
6 4
z ( x ) dydz = 0
8 3 2 2
= ∫ ∫
z =−6 y =−4 2
−2
5. Clearly z = 2 is a pole of order-2
e− z
[ Resf (z ) ] = z→lt 2
d
( )
2
z− 2 = 1t − e − z
z=2 dz (z − 2 ) z → 2
= − e −2
6. F = C− P + 2 − R −S
C = Number of components in the system
P = Number of phases in the system
R = Number of independent equations
S = Special Conditions
Given water (Component1 − liquid) and ethanol(Component 2 − Vapor)
C = 2(water & H 2 O)
P = 1(Vapor + Liquid)
R = 0 X az = y az
S =1
F = 2 − 2 + 2 − 0 −1
F =1
1200K
9. η1 = η2
T2 300 Q1
or 1 − =1−
1200 T2
Or T2 = 1200 × 300 = 600K

Q2
HE T2 K
Q2
HE 2
Q3
300K
4
dU
10. r =µ
dy
U
=µ
t
Force = τ × Area
dF = τ × dA
µrω
= × 2πr dr
t
τ = dF × r
µrω
⇒ × 2πr dr × r
t
2πµr 3ω dr
⇒
t
2πµr 3ω dr
dτ =
t
2 2 πµr ω
3
⇒r=∫ dr
0 t
 2πµω  R 3
=  ∫ r dr
 t  0
R
 2πµω   r 
4
=  
 t   4 0
2πµω ( R 4 )  d
= ∴ R = 
4t  2
2πµω  d 4 
=  
4t  16 
πµω d 4
τ=
32t
11. µ α T
να T 2
µ
ν=
ρ
PM
ρ=
RT
1
⇒ ρα
T
ν 20O C = 16 × 10−5 m 2 / s
ν 70O C = ?
2
ν1  T1 
= 
ν 2  T2 
5
2
T 
ν 2 = ν1 ×  2 
 T1 
 70 + 273  343
1.6 × 10−5 ×  −5
 = 1.6 × 10 ×
 20 + 273  293
≈ 2.2 × 10−5 m 2 / s
12. Frictional loss head of equivalent pipe = Frictional loss headpipe1 + Frictional loss head pipe
2 + Frictional loss head pipe 3
4fLV 2 2fLV 2
hf = = D/2
2D D D 2D
Q Q
Where, V = ⇒
A πD 2 L L L
4
 
2fL  Q 
=  
D  πD2 
 
 4 
32fLQ2
hf = 2 5
πD
32fLQ2 32fLQ2 32fLQ2 32fL × 4L × Q 2
= 2 2 + +
π 2 D5 πD π2 ( 2D )
2 5
2D
π  
2
LEqu L  1
5
= 1 + 32 + 8 
D D5
 1
⇒ L Equ = L 33 
 8
 dT   dT 
13. K W   = KG  
 dy  w  dy  g
K w = Thermal conductivity of water
K G = Thermal conductivity of gas
 dT 
⇒ 0.6 1 × 104  = 1.2  
 dy  g
0.6  dT 
⇒ 1 × 104  =  
1.2  dy  g
⇒ 0.5 1 × 104 
⇒ 0.5 × 104
6
15. D A = Gilli land equation
1 1
0.0043T3/2 +
methnol mair
DA =
V 1/3
ethnol + Vair
1/3
T = 298 O K
methnol = C2 H5OH ⇒ 46
mair = 29
C2 H5OH
V = (2 ×14.8) + 6(3.7) + 1(7.4)
Vethnol = 59.2
Vair = 29.9
1 1
0.0043T3/2+
DA = 46 29
( 59.2) + ( 29.9)
1/3 1/3
DA = 0.749
16. α = 2.4
x F = 0.4
x D = 0.9
x W = 0.1
According to Fenske Equation,
 x (1- x W ) 
n +1 = log  D 
 x W (1- x D ) 
 0.9 (1- 0.1) 
 
 0.1(1- 0.9 ) 
n +1 = log
log 2.4
n = 4.98 ⇒ 5Stages
17. Initial concentration a 0

a0  a0 
Concentration after 1st half life =
2  2 
 a0 
nd a 0  2 
Concentration after 2 half life =
4 2
 a0 
a 0  4 
Concentration after 3rd half life =
8 2
7
n
 a0   1 
Concentration after nth half life  2n  =  2  a 0
   
19. A → 3B
x = 10%
x = 100%
V − Vx = 0
⇒ E = x =1
Vx = 0
Initial Final
1 mole of feed
⇒ 0.5 mole of A 1.5 mole of B
⇒ 0.5 mole of inerts 0.5 mole of inerts
↓ ↓
1 mole 2 mole
Vx =1 − Vx =0
⇒E=
Vx =0
2 −1
⇒ =1
1
20. For upper bound,

w = 0, φ = tan −1 ( − wt ) = tan −1 ( 0 ) = 0for lower bound,
π π
w = ∞, φ − tan −1 ( −∞ ) = −  0, − 
2 2
21. 1st order system
8
1
G(S)=
TS + 1
1
AR =
TS + 1
⇒ S = − jω
1 T ( − jω ) − 1
⇒ ×
T ( − jω ) + 1 T ( − jω ) − 1
T ( − jω ) − 1
AR =
(T ω 2 2
+ 1)
 −b 
φ = tan −1  
 a 
φ = tan ( ωT )
−1
1
AR =
T ω2 + 1 2
log AR = − log ( T 2 ω2 + 1)
1
2
For everychangein frequency theamplitude will be change.
Logarithm of AR versus logarithm of w represents one of the graph in bode diagram.
2−λ −2 3
26. The characteristic equation is 10 −4 − λ 5 =0
5 −4 6−λ
⇒ λ 3 − 4λ 2 + 5λ − 2 = 0
⇒ M 3 − 4M 2 + 5M − 2I = 0 (Using Cayley-Hamilton theorem)
Multiplying by A −1 we get
1
M 2 − 4M + 5I − 2M −1 = 0 ⇒ M −1 = (M 2 − 4M + 5I)
2
27. Let x denote the length of the call made by the person in the booth.
1
Given λ = .
10
We know that cumulative distribution function
a
F(a) = P(X ≤ a) = ∫ λe−λx dx
0
9
=1 − e−λa , a ≥ 0.
Required probability
= P(20) ≤ X ≤ 30)
= F(30) − f(20)
= (1 − e −3 ) − (1 − e −2 )
= e −2 − e −3 .
= 0.1353 − 0.0498
= 0.0855
28. f 1 (x) = 0 , where x ∈ (−1,1) (using Roller’s Theorem)

⇒ 3x 2 − 2x − 1 = 0
⇒ x = −1 , 1 here x = 1 is not possible
3
 −1   −1   −1 
3 2
32
∴ x = −1 ⇒ y =   −   −   + 1 =
3  3   3   3  27
 −1 32 
∴ The required point is  , 
 3 27 
29. f (x, y, z) = xyz

Directional derivative of f(x, y, z) at (4,2,2) in the direction of line through P(4,2,2) and Q
→
PQ
(6,2,6)= (∇f ).(4,2,2) →
PQ
yz ∧ xz ∧ xy ∧ 1∧ ∧ ∧
∇f (4,2,2) = i+ j+ k ∇f (4,2,2) = i + j+ k
2 xyz 2 xyz 2 xyz 2
→ ∧ ∧ ∧
PQ = < 2, −4, 4 > = 2 i − 4 j+ 4 k.
∧
→ ∧ ∧
PQ 2i − 4 j+ 4k 1 ∧ 2 ∧ 2 ∧
∴ = = i − j+ k
PQ 22 + 42 + 42 3 3 3
∴ DD of f at (4, 2,2) in the direction of line

→
PQ
= (∇ f ) .
(4,2,2)
PQ
1∧ ∧ ∧  1∧ 2∧ 2 ∧
=  i + j + k  . i − j + k 
2  3 3 3 
1
=
6
10
30. On the basis on solubility of NaCl

If 140gms of NaCl Saturated solution at 100°C (140 – 94gms of crystals is
is dissolved Weighs (140g + 100g) formed after cooling to 30°C
32g of NaCl is Saturated solution at 100°C y g of crystals is formed after
dissolved in solution weighs m gram cooling to 30°C
32
m= (140 + 100 ) = 54.85g
140
32
m= (140 − 100 ) = 10.51gm
140
31. Heat of reaction = Heat of formation of products- Heat of formation of reactants

∴∆H° = −392.51 − ( −110.52 − 241.83)
= −40.16 Kj / kg
Standard free energy change of the reaction
∆G ° = −394.40 − ( −137.27 − 228.6 )
= −28.53 KJ / Kg
Equilibrium constant & standard state (K) is related ∆G ° as
∆G ° = −ℓnk ... (1)
RT
∆G ° per Kmol of CO 2 = −28.53 × nw = −28.53 × 44 = −1255.32 KJ / km
Similarly ∆H ° Kmol of CO 2 = −40.16 × 44 = −1767.04 KJ / kmol
from egn (1)
−1255.32
= ℓnk
8.314 × 298
at 25°C, K = 1.66
Heat of reaction ( ∆H ° ) is assumed to remain const with T
 1 1
ℓnK / K1 = ∆H° / R  −  ....... ( 2 )
 T2 T1 
From (2) K at any T can be found from known
Values of K1 & T1. If T1 is 298OC & K1 = 1.66
ℓnk 1767.04  1 1 
=  − 
1.66 8.314  273 + 800 298 
∴ K = 0.4252 ( at 800°C )
32. Given m = 0.5Kg
11
P1 =1bar = 1 ×102 KN
m2
P2 = 8 bar = 8 × 102 KN 2
m
T = 10 CO
V1 = 0.09m3
V2 = 0.02m3
T1 =10 + 273 = 283K
Cp
= r and C p − C v = R
Cv
Cp − C v R
⇒ =
Cv Cv
P1V1
PV = mRT ⇒ R =
mT1
1×102 0.09
= − − − − > (1)
0.5 × 283
PV γ − Const
⇒ P1V1γ = P2 V2γ
γ
P1  V2 
= 
P2  V1 
γ
 V  P 
⇒ 1  = 2 
 2V2   P1 
γ
V  P 
⇒  1  = ln  2 
 V2   P1 
V  P 
γ ln  1  = ln  2 
 V2   P1 
P 
ln  2 
P
⇒ γ=  1 
V 
ln  1 
 V2 
0.0675
Cv = = 0.1662
1.382 − 1
CP = γ C v
= 1.382 × 0.1662
= 0.2297
V2 = 0.3m3
33. Given
Barmometer pressure =760mmHg
= 101.325KPa
ICP–Intensive Classroom Program eGATE-Live Internet Based Classes DLP TarGATE-All

He India Test Series
12
= 101.325 KN
m2
V2 = 0.3m3
V1 = 0m3
The displacement work
Wd = ∫
cylinder
Pdv ∫
balloon
Pdv
(∵work done by the cylinder is zero)

Wd = ∫
balloon
Pdv = p ∫ Pdv = P(V2 − V1 )
V1
=101.325(0.3 − 0)
= 30.3975kJ
Hence the displacement work is +ve, t
∴ Work done by the system.
34. Cd, Coefficient of discharge = 0.64

Cv, coefficient of velocity = 0.98
Area of jet at vena contracta AC
Cc, coefficient of contraction =
Area of orifice A
As we know
Cd 0.64
Cd = C v C c ⇒ C c = = = 0.653
C v 0.98
Ac
A = 0.042m 2 Cc = 0.653 =
0.042
A c = 0.027 m 2
Q v ρ.g.h tot
35. Indicated power =
(1000 ) η
(
ρ =1.2 ρH2 o )
η= 0.65 × 0.96 × 0.95 = 0.5928
2.5
×1200 × 9.81× 60
I.P = 60 = 49.64KW
1000 × 0.5928
P  1 1 
36. Bond’s law = 0.3162Wi  − 
M  DP DP 
 b a 
Dp a = 2 × 2.54cm = 50.8mm, Dp b = 1 / 6 × 2.cm = 3.1* 5mm
P  1 1 
= 0.3162 × 12.74 ×  − 
M  3.175 50.8 
P = 169.6KW
13
P  1 1 
37. = 0.362  − 
M  D DF 
 P
P
= const
M
P P
⇒ 1 = 2
m1 m 2
P1
⇒ P2 = × m2 =
m1
88
⇒ × 11
44
P2 = 6.28Kmol
5
38. mh = 5Kg min = Kg Sec = 0.0833Kg Sec
60
20
m c = 20 Kg min = Kg Sec = 0.333Kg Sec
60
Cph = 4.6 KJ Kg.K = 4.6 ×103 J Kg.K
Cpc = 4.18 KJ Kg.K = 4.18 ×103 J Kg.K
Capacity rate of hot liquid = C h = m h Cph = ( 0.0833) ( 4.6 ×103 )
= 383.18 W K
Capacity rate of cold liquid = Cc = m c C pc = ( 0.0333) ( 4.18 ×103 )
=1391.94 W K
Ch = Cc
Cmin imum = C h = 383.18 W K
NTU =
UA
=
(1000 )(10.84 )
Cmin imum 383.18
NTU = 28.28
Th1 − Th 2
39. E=
Th1 − Tc1 t h1
t h2
t h2
t c1
14
Minimum possible heat transfer

E=
Maximum possible heat transfer
TC2 − TC1
E=
Th1 − Tc1
TC − 200
0.5 = 2
600 − 200
⇒ 0.5 ( 400 ) = TC2 − 200
TC2 = 400°C
40. U=?
A = 40m 2
H S = 2800 KJ / Kg O K
h S = 2250 KJ / Kg O K
mS = 4000 KJ / Kg O K
Q = ms h S
Q = 4000(2800 − 2250)
Q = 4000(550)
Q = 2250KN
2200 × 103 = U(40)(140 − 100)
2200 × 103
=U
(40)(40)
U = 1375 W / m 2 O K
41. Heat balance gives m h cph ( 340 − 210 ) = m c c pc ( 90 − 30 ) 340°C

m h.Cph
= 0.4615
m c c pc
T °c
Suppose T be lowest temperature upto which oil
must be cooled and it must be equal to the
highest temperature of water
m h c ph ( 340 − T ) = mc c pc ( T − 30 ) 30°C
m h.Cph T − 30
= = 0.4615
mc c pc 340 − T
T = 127.88°C
42. For gaseous system, the diffusion flux

D AB P
'A' = P(A 2 - A1 ) - -- > 1
RT(Z2 - Z1 ) PBhm
PB2 - PB1
PBhm =
P
ln B2
PB1
15
PB1 = P - PA1 = 87000N / m 2

PB2 = P - PB2 = 93500N / m 2
93500 -87000
= = 90, 200N / m 2
93500
ln
87000
Substituting all the valuesin equation1
1.87×10-5 ×100000(13, 000 - 6500)
Weget 'A' =
8314× 273× 0.002×90, 200
= 2.97×10-5 Kmol / m 2s
43. PA = 2.64 Kpa

Partial pressure of vapors free gas (PB ) = Total pressure – partial pressure of vapor
= 100 - 2.64 = 97.63
PA 2.64
Ym = = = 0.027mol H 2 O / mol
PB 97.63
Y = 0.6207
Ym = 0.6207× 0.027
= 0.0168Kg H 2 O / mol
44. air - Water

288 O K®291 O K
⇒ 70%moistureis removed
2.06
Initialconcentartion = Þ0.0213
98.66
Finalconcentartion = 0.3×0.0213Þ0.00639
Molar ration = Partial pressure
0.00639 1.07
⇒ =
1-1.00639 1-1.07
⇒ P = 168.61Kpa
45. Basis 1000 m3entering gases

Partial pressureof moisture
Molar humidity of increasing air =
Partial pressureof dry air
3.33
= = 0.03316mol
102.65 - 3.33
3.33 Absolute humidity = molal humidity × 0.6207
= 0.0336× 0.6207 = 0.0208 KJ / Kg dry air
16
46. A → B (first order)

dp
= −0.2atm / kg ….(1)
dw
Given Po=20 atm, W=60 kg
From equation (1), dp=-0.2 dW
⇒ P − Po = −0.2W ⇒ P = Po − 0.2W …(2)
For packed bed reactor
dFA
= −rA = KCA …(3)
dW
Here pressure is changing.
So, concentration will also changes with pressure
P
C A = CA o (1 − x)
Po
Equation (3) becomes
dX P
− FA o = kC Ao (1 − x)
dW Po
dX kp
−ν o CA o = C (1 − x)
dW Po Ao
dx k(Po − 0.2 w)(1 − x)
⇒ −ν o =
dw Po
XA dx k 60  20 − 0.2w 
⇒∫ = ∫   dw
0 1 − x νo 0
 20 
k 1  0.2(602 − 0) 
⇒ ln(1 − X) = ×  20 × 60 − 
ν o 20  2 
Put X = 0.865,
k
= 0.04768
vo
Put ν o = 20 m 3 / sec
k = 20 × 0.047678 = 0.9536
47. Branch A v = 50
Branch B v = 100
v v
  = 
 F A  F B
F v 20 50 1
⇒ A = A = = =
FB v B 70 + 30 100 2
⇒ FB = 2FA
F = FA + FB
F = FA + 2FA
17
F = 3FA
1
FA = F
3
1
FB = 2 × F
3
2
FB = F
3
FA = 2FB
48.
dcr
= ( CA ) ( CB )
1.5 0.3
k1 R ( desired ) dt
A+B
k2 s ( undesired ) dcs
= ( C A ) ( CB )
0.5 1.8
dt
For 90% conversion

CA = CA0 (1 − x A )
⇒10(1 − 0.9) =1
R dcR
φ  =
 A  dcR + dcS
C0.5 0.3
A CB
=
A CB + C A CB
C0.5 0.3 1.5 0.3
C1.0 1
= A
⇒
C A CB1.5
1 + C0.5A
1 1 1
= = = = 0.5
1+1 0.5
1+1 2
49. For a CSTR,

FA0 X FA0 X FA0 X
V= = =
− rA k C A kCA0 (1 − X )
K at these temperature, has been given
∴ V = 1.18 dm 3 .
50. t1 = 30min T1 = 773K

T2 = 15 sec = 0.25 min T2 = 923K
Now
K  r  t  E1 1 
ℓn  2  = ℓn  2  = ℓn  1  =  − 
 K1   r1   t 2  R  T1 T2 
t  E1 1  30  E  1 1 
ℓn  1  =  −  ⇒ ℓn  = −
 t 2  R  T1 T2   0.25  8.314  773 923 

⇒ E = 189325 J / mol
18
51. T1 = 80O C
T21 = 600O C
r2 = 5r1
K2 E  1 1 
ℓn =  − 
K1 R  T1 T2 
r2 K
=5 2
r1 K1
E  1 1 
ℓn ( 5 ) = −
8.314  873 1073 

⇒ E = 62671.22J
but 1cal = 4.186J
62671.22
⇒E= cal = 14971.62cal
4.186
52. ωc = 2 rad / min
K c = 2.4
K u = 0.6 ( 2.4 ) =1.44 min
2π
Ultimate period = ⇒π
2
Using Ziegler − Nichols controller settings for PID controller

Pu
τI =
2
π
⇒ = 1.57
2
53. Centrifuge = 3500000
n = 10
Salvage value = 500000
i
A = (P − SV)
(1 + i) n
D = A(1 + i)0
D=A
∴ Book value = P − D1
⇒ D1 = A
19
0.08
= ( 3500000 − 500000 ) ×
(1 + 0.08)10 − 1
= 207088.47
Book value = 2500000 − 207088.47
= 3292911lakhs
Va = V (1 − f )
n
54.
1 1
 V n  1.5  8
f =1−  s  =1−   = 0.3548
V  50 
5.9 = V = 50 (1 − 0.3548 )
n
n = 5 Year
55. P - 3, Q - 1, R -4
Option (B) is correct
20

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29 D 30 10.51 31 0.4252 32 B 33 30.397 34 0.027 35 49.64

43 0.016 44 A 45 0.02 46 0.9536 47 A 48 0.5 49 1.18

3. Let Rajeev’s age 10 years ago be ‘x’ year

His mother’s age 1 decade ago = 4x

4. Let the ten’s digit be ‘x’ and unit digit of number is y.

5. 3-Digit number divisible by 6 are 102, 108, 114,….,996

This is an A.P in which a=102, d=6 and l=996

Let the number of terms be n. Then tn = 996.

6. Indefatigable, Untiring is also synonyms.

9. Required percentage increase

1.15 × 0.14 + 0.86 − 1

Pipe C discharges chemical solution R.

Required probability is P(A) = P(E1 ).P A ( E ) + P(E ).P ( A E ) = 0.08

∂F1 ∂F2 ∂F3

= 2xz3 + 2xz3 + 4xz3

5. Clearly z = 2 is a pole of order-2

Or T2 = 1200 × 300 = 600K

15. D A = Gilli land equation

17. Initial concentration a 0

20. For upper bound,

21. 1st order system

Logarithm of AR versus logarithm of w represents one of the graph in bode diagram.

⇒ M 3 − 4M 2 + 5M − 2I = 0 (Using Cayley-Hamilton theorem)

28. f 1 (x) = 0 , where x ∈ (−1,1) (using Roller’s Theorem)

29. f (x, y, z) = xyz

∴ DD of f at (4, 2,2) in the direction of line

30. On the basis on solubility of NaCl

31. Heat of reaction = Heat of formation of products- Heat of formation of reactants

32. Given m = 0.5Kg

ICP–Intensive Classroom Program eGATE-Live Internet Based Classes DLP TarGATE-All

(∵work done by the cylinder is zero)

34. Cd, Coefficient of discharge = 0.64

Minimum possible heat transfer

41. Heat balance gives m h cph ( 340 − 210 ) = m c c pc ( 90 − 30 ) 340°C

42. For gaseous system, the diffusion flux

PB1 = P - PA1 = 87000N / m 2

43. PA = 2.64 Kpa

44. air - Water

45. Basis 1000 m3entering gases

46. A → B (first order)

For 90% conversion

49. For a CSTR,

50. t1 = 30min T1 = 773K

52. ωc = 2 rad / min

Using Ziegler − Nichols controller settings for PID controller

53. Centrifuge = 3500000

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