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Editorial 1547
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February 2008 Latest General Knowledge 1551
Year—10 Issue—120 Inspiring Young Talent—Topper BHU (Med.)
Rank-22, 2007—Lokesh Kumar Garg 1555
Science Tips 1557
Physics
Sound-III 1560
Nuclear Physics-III 1566
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Chemistry
Chemistry of Alkali Metals 1583
Chemical Thermodynamics 1589
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without the prior written permission from Solved Paper :
the publishers. CBSE Medical Entrance (Mains) Examination, 2007 1643
[‘Competition Science Vision’ arranged an exclusive interview with Sri Lokesh Kumar Garg who
has the credit of being selected in BHU (Med.) and in nearly half a dozen other institutes. For his
brilliant success, he deserves all praise and our heartiest congratulations. This important interview is
presented here in its original form.]
CSV—Congratulations on your CSV—From when did you start Lokesh—I put more weightage
brilliant success. the preparation for it ? on Physics as it is the subject in which
Lokesh—Thank you, sir. Lokesh—I had started my pre- you can make difference with other
paration two months after the board candidates specially in medical
CSV—Before knowing your result
exam of 12th class. entrance exams.
what did you think about those who
CSV—Did you make complete
achieve top positions ?
study of all the topics or of some
Lokesh—My opinion about selective topics ?
toppers has always been that they are Lokesh—Complete study of all
sincere, hard-working, determined and the topics is always better. But I
keep the faith in God and themselves. focussed more on topics having more
weightage in exams. Furthermore,
CSV—Achieving top position has
paper of CBSE-PMT mains require
come as a surprise to you or were selective intensive study.
you confident of achieving it ? CSV—How did you give final
Lokesh—I was hopeful about my touches to your preparation ?
success but I was never sure to be Lokesh—At the completion of
selected in so many exams simul- syllabus, I gave many mock tests and
taneously. revised formulae for Chemistry and
……Competition Science Vision Physics. For Biology, I read important
CSV—What do you think is the is a standard magazine and a topics many times from NCERT book.
secret of your success ? ‘must read’ for medical aspirants. CSV—Did you prepare notes ?
Lokesh—Blessings of God and Its each issue is prepared accord- Lokesh—Yes, I prepared short
family, hardwork, never have die atti- ing to the latest pattern of exams. notes by writing all concepts and
tude and better understanding about —Lokesh formulae of topic at the end of
pattern of exams. chapter.
CSV—What planning did you
CSV—In how many attempts did make for preparation ? Please tell
you get this success ? Bio-Data
something in detail.
Name—Lokesh Kumar Garg
Lokesh—It was my first attempt Lokesh—Initially I tried to under-
stand the basic concepts of the Father’s Name—Sri P.L. Garg
in BHU-PMT and AFMC and second
subject and completed topics one by Mother’s Name—Smt. Uma Garg
attempt in IIT-JEE, AIEEE, CBSE-
PMT and MP-PMT. one with patience. I didn’t get nervous Educational Qualifications—
and bettered my position gradually. H.S./Std. X—89·6% (J.N.V. Hatta,
CSV—What were the shortcom- CSV—How much time did you Madhya Pradesh), 2004.
ings in your preparation in the earlier devote daily and regularly for Physics,
attempts ? How did you make up for Inter/Std. XII—75·6% (J.N.V. Hatta,
Chemistry, Zoology and Botany ? Madhya Pradesh), 2006.
them this time ? Lokesh—I never stick to the strict Special Achievements—
Lokesh—In earlier attempts, I time division according to subjects.
● BHU-PMT (Mains)—AIR 22
was not prepared for facing com- One should read according to the
petitive exams. This attempt was quite ● Selected in AFMC (written,
necessity of topic and practice rotation
interview, physical)
to the point. of subjects to avoid boredom. Apart
● MP-PMT—Rank 73
CSV—From where did you get from PCB, I also gave some time for
Mathematics. ● CBSE-PMT—AIR 2352
the inspiration of choosing a medical
career ? ● IIT-JEE—AIR 3396
CSV—Out of the above four
subjects, to which subject did you give ● AIEEE—AIR 7100
Lokesh—From my father and my
friends. more weightage and why ? ● State Rank—354
[ v2 v2
➠ 2h Note : h = 2g ‚ Rmax = g = 2h ] Distance Work
➠ F × v = Force × Time = Time = Power
8. What is International Ampere ?
➠ The International Ampere is that unvary-
ing current which will deposit 0·0011183 Chemistry
grams of silver per second from a solu-
tion of silver nitrate of a specified nature
21. The property of O 2 molecules which is almost
in cell of given specifications.
identical to that of Xe atom is
9. Two balls are thrown with same initial velocity at
➠ Ionization energy
angles 25° and 45° with the horizontal. Which ball will
22. The relation between standard free energy change
come to the ground earlier ?
and equilibrium constant is as
➠ The ball thrown at 25°°
➠ ∆G°° = – 2·303 RT log Kc
[Note : Time of flight is proportional to
23. The gas which diffuses fastest through glass and
sin θ when v and g are constant]
plastic materials is
10. What is a low frequency choke ?
➠ Helium
➠ It is an iron core inductor and is appli-
cable for frequency 50 Hz. It is used in 24. The function of a system which takes both enthalpy
the filter circuit of the rectifier. and entropy into account is called
11. The net charge of an electric dipole is ➠ Free energy
➠ Zero 25. The sorption of hydrogen by metals is termed as
12. Calculate the diameter of the K orbit of He. ➠ Occlusion
n2 1 ° 26. First organic compound (Carbamide) was prepared
➠ r = 0·529 × Z = 0·529 × 2 ⇒ 2r = 0·529 A
by heating a mixture of two inorganic salts
13. The S. I. unit of electric dipole moment p is ➠ Potassium cyanate + Ammonium sulphate
➠ Cm (coulomb-metre) 27. The balance which is used for magnetic measure-
[Note : It is not mC which represents milli ments of compounds is known as
coulomb] ➠ Gouy balance
Important
I II
Let the wave moving in positive x-direction be represented by
2π t
y1 = a sin λ (vt –x)
(iii) The amplitude of the stationary wave is given by Characteristics of Stationary Waves
2πx
A = 2a cos (i) Some points of the medium are always stationary
λ i.e., their amplitude is zero. These are called nodes.
(iv) The points where the amplitude of the resultant
(ii) In between the nodes there are points with
wave is maximum are called the antinodes. For anti-
maximum displacements. These are called antinodes.
nodes
λ 3λ (iii) The distance between two consecutive nodes or
x = 0, , λ, , …… nearest antinodes is λ/2· The distance between a node
2 2
and the nearest antinode is λ/4·
and A = ± 2a.
(v) The points where the amplitude of the resultant (iv) Excluding nodes every point of the medium exe-
wave is minimum are called the nodes. For nodes cutes simple harmonic motion about its mean position.
(vi) The distance between two consecutive nodes or (vi) All the points occurring between two nodes
antinodes is λ/2. vibrate in the same phase. They reach their respective
positions of maximum displacement simultaneously and
(vii) Stationary waves can be produced by the super-
also pass through their mean position at the same time.
position of both the longitudinal and transverse waves.
(viii) Longitudinal stationary waves are formed in (vii) Like progressive waves the stationary wave do
flutes and air columns. not proceed forward.
(ix) Transverse stationary waves are formed in sono- (viii) The variations of pressure and density are maxi-
meter, sitar, gitar and strings. mum at nodes but are minimum at antinodes.
1 Reflected wave
Heavy spring Light spring
Fixed end
2
(a) (c) N N N N N
O16 56
8.0 C12
Fe to be about 200 MeV per fission (or about 0·9 MeV per nuc-
4 F18
He N14 U238 leon).
7.0
5. The energy obtained by fission of 1 gm of uranium is
6.0
about 5 × 10 23 MeV. So much energy is obtained from explo-
Li7
5.0 sion of 20 tones of T.N.T. From this energy about 2 × 10 4
4.0 kWh electrical energy can be produced.
3.0 6. 92U238 is fissionable only by fast neutrons (1·2 MeV
2.0 energy) whereas 92U235 is fissionable by slow neutrons
H2 (1 eV) or thermal neutrons (0·025 eV) as well as fast neutrons.
1.0
7. Each of the three neutrons carries an energy of about 2
0.0
0 20 40 60 80 100 120 140 160 180 200 220 240 MeV. The fast neutrons will escape and will not cause the
Mass number (A) fission of U235 nuclei. In order to utilise them to cause fission
Important Conclusions of three other nuclei of U235, these neutrons have to be
slowed down.
1. The nuclei having mass number around 60 (for 8. On an average 2·5 neutrons are emitted per fission.
example Fe with A = 56) have maximum binding energy
9. Energy is released in the form of kinetic energy of
per nucleon (≈ 8·7 MeV). These nuclei are most stable. fission fragments. Some of the energy is also released in the
2. For heavier nuclei, the binding energy per nucleon form of γ-rays, heat energy, sound energy and light energy.
gradually decreases. For uranium A = 238 it is about 7·6 10. The pressure and temperature are very high in the
MeV. fission process.
3. For nuclei having mass number below 56 also, the 11. The elements formed lie nearly in the middle of the
periodic table.
binding energy decreases and below A = 20, it decreases
12. Fission fragments are radioactive and they decay to
very rapidly. For example, for heavy hydrogen (A = 2) it is
stable products by emitting α-, β- and γ-rays.
only 1 MeV. It shows that nuclei of A < 20 are relatively
less stable.
Chain reaction in nuclear fission—In the nuclear
4. The special positions of He4, C12 and O16 on the fission of each uranium nucleus 2 or 3 fresh neutrons are
curve indicate that these nuclei are more stable than their liberated which under favourable conditions fission other
neighbouring nuclei. uranium nuclei. This establishes a chain of nuclear fission
which continues until the whole uranium is consumed. In
5. The binding energy per nucleon of very light and
the chain reaction, the number of nuclei undergoing
very heavy nuclei is generally less than that of the nuclei
fission increases very fast producing tremendous amount
in the middle. Thus if a very heavy nucleus (e.g., of energy.
uranium) is broken into comparatively lighter nuclei, Difficulties in chain reaction—(i) The major part of
then the binding energy per nucleon will increase. natural uranium is the isotope U238 the isotope U235 is
Hence a large quantity of energy will be liberated in this very little (only 0·7%). U 238 can be fissioned only by fast-
process. This phenomenon is called ‘nuclear fission’. neutrons (energy more than 1 MeV). The neutrons of
6. Similarly, if two or more very light nuclei (e.g., energy less than this are absorbed by U 238 . U235 can be
nuclei of 1H2) are combined into a relatively heavier fissioned with slow as well as fast neutrons. Though the
nucleus (e.g., 2He 4), then also the binding-energy per low-energy neutrons can fission U235, but the probability
of their absorption by U238 is much more. Thus the fresh
nucleon will increase. In this process also energy is
neutrons released in the fission of ordinary uranium are
liberated. The phenomenon is called ‘nuclear fusion’. not able to continue the chain reaction.
Nuclear fission—It is the process in which a heavy (ii) The second difficulty in the maintenance of chain
unstable nucleus breaks into two nuclei of nearly same reaction is that the fast neutrons liberated by the fission of
mass with the liberation of energy. Nuclear fission was U235 nucleus travel a distance of about 10 cm in the subs-
discovered by two German scientists Otto-Hahn and tance before they are slowed down and fission other
Strassman. nuclei. If the uranium block to be fissioned is of small size,
235
the most of the neutrons will escape before fissioning any
92 U + 0n1 → (92U236) → 56Ba141 + 36Kr92 + 3(0n1) nucleus, and the chain reaction will stop. Therefore to
It is not necessary that the fission products are Ba continue the chain-reaction, the size of the fissionable
and Kr. Other nuclei may also be produced. substance should be bigger than a certain critical size.
1. Apsara—This is 1MW reactor situated in Mumbai. An 4. The chain reaction is The chain reaction is main-
alloy of uranium and aluminium is used as fuel in it. This is maintained by fast neu- tained by slow neutrons.
also known as swimming pool type reactor. trons.
2. Cirus—It is a 40MW reactor, made in collaboration with 5. Number of neutrons pro- The number of neutrons pro-
Canada and is used to produce radioactive isotopes. duced per fission is more. duced per fission is less.
3. Zerlina—0 MW reactor. Atom Bomb Hydrogen Bomb
4. Purnima—0 MW reactor.
1. It is based on fission pro- It is based on fusion process.
cess.
Power Reactors
2. In it critical size is impor- There is no limit to size.
1. Tarapur (Maharashtra) 400 MW tant.
2. Rana Pratap Sagar (Rajasthan) 400 MW 3. In this, explosion is possi- In this extremely high tempe-
3. Kalpakkam (Tamil Nadu) 220 MW ble at normal temperature rature and pressure is requi-
4. Narora (U.P.) 200 MW and pressure. red to explode it.
5. Kaiga (Karnataka) 200 MW 4. In this, harmful radiations In this harmful radiations are
6. Kakarapar (Gujarat) 200 MW are produced. not produced.
Example 1. Find the binding energy per nucleon Given the binding energy per nucleon of 1H2 and
for 3Li7 if mass of 3Li7 is 7·01653 amu 2 He 4is 1·125 MeV and 7·2 MeV respectively.
[Given : mp = 1·00759 amu, mn = 1·00898 amu] Solution : B.E. per nucleon of ∆E = 1·125 MeV
Solution : The binding energy per nucleon ∴ E = A × ∆E
∆E
E = = 2 × 1·125 MeV
A
= 2·25 MeV
∆m × 931
=
A
MeV ∴ B.E. of two 1 H2 = 2 × 2·25 MeV
∆m = (3 mp + 4 mn) – Mass of 3Li7 Ed = 4·5 MeV
1H
2 + 1H2 = 2He
4 = 16 × 10–4 kg = 1·6 gm
OBJECTIVE QUESTIONS
1. m, mn and mp are the masses of 2. An element A is converted to C 3. The nucleus with maximum bind-
A
ZX nucleus, neutron and proton through following reactions : ing energy per nucleon out of the
respectively. If the nucleus is A → B + 2He 4 following is—
broken into its constituents, (A) 92U238 (B) 2He 4
then— B → C + 2e– (C) 8O 16 (D) 26Fe 56
(A) m > [(A – Z)mn + Zmp] Then— 4. The following nuclear reaction
(A) A and C are isobars represents
(B) m < [(A – Z)mn + Zmp] 14 1 15
(B) A and C are isotopes 7N + 1H → 8 O + 7·3 MeV
(C) m = [(A – Z)mn + Zmp] (C) A and B are isobars (A) Nuclear fusion
(D) m = [Zmn + (A – Z)mp] (D) A and B are isotopes (B) Nuclear fission
1. (B) The mass of nucleus is less Net final binding energy 19. (C) Ordinary uranium is U238. The
than the sum of the masses of its = 4 × 7 = 28 MeV isotope U235 is only 0·7% in it. In
constituent particles. enriched uranium the isotope
∴Energy released
2. (B) In the first reaction Z becomes U235 is increased from 0·7% to
= 28 – 4·4 = 23·6 MeV
(Z – 2) and A becomes (A – 4). 2·3%.
6. (A) Heavy water (D2O) is the best
In the second reaction (Z – 2) 20. (A) ●●●
moderator.
becomes Z again and (A – 4)
remains unchanged. Thus for A 7. (B) 8. (C) 9. (A) 10. (D) 11. (D)
and C, Z is the same and A 12. (B)
differs i.e., they are isotopes. 13. (C) ∆E = ∆m × c2
3. (D) The nuclei having mass = 1 × (3 × 10 8)2
number ≈ 60 (for example, Fe = 9 × 1016 joule
whose mass no. is 56) have ≈ 1017 joule
maximum binding energy per
14. (A) 15. (D) 16. (B) 17. (C)
nucleon (about 8·7 MeV).
0·3
4. (A) 18. (B) ∆m = × 1 = 0·003 kg
100
5. (A) 1H2 + 1H2 → 2He 4 ∆E = ∆mc2
Net initial binding energy = 0·003 × (3 × 108)2
= 4 × 1·1 = 4·4 MeV = 2·7 × 1014 joule
20. The initial pressure and volume (A) 30° (B) 45° °
(A) 6060 A °
(B) 5940 A
of a gas are P and V respec- (C) 60° (D) 90°
°
(C) 5500 A °
(D) 6500 A
tively. First its volume is expan- 25. A Carnot’s engine works as a
ded to 4V by isothermal process refrigerator between 250 K and 31. Consider the following statements
and then its volume is restored 300 K. If it receives 750 calories in case of specific heat of
to V by adiabatic process. The of heat from the reservoir at lower gases—
final pressure of the gas is— temperature, the amount of heat 1. Specific heat of a gas is zero
(γ = 1·5) rejected at the higher temperature when it undergoes an adia-
is— batic change.
(A) 8P (B) 4P
(A) 900 cal (B) 625 cal 2. Specific heat of a gas is infi-
(C) P (D) 2P
(C) 750 cal (D) 1000 cal nite when it undergoes iso-
21. The specific heat of a gas at 26. A real image of a distant object thermal change.
constant pressure is greater than is formed by a plano-convex lens 3. The difference between prin-
its specific heat at constant on its optical axis. Spherical cipal specific heats is the
volume because— aberration is— same for all gases.
(A) At constant pressure work is (A) Absent
4. The ratio of principal specific
done in expanding the gas (B) Smaller if the curved surface heats is the same for all
against constant external of the lens faces the object gases.
pressure (C) Smaller if the plane surface
Of these correct statements are—
(B) At constant volume work is of the lens faces the object
done when pressure increa- (D) The same whichever side of (A) 1, 2, 3 (B) 2, 3, 4
ses the lens faces the object (C) 1, 2 (D) 1, 2, 3, 4
1. (A) µ =
sin ( )
A+δ
2 6. (D)
→ ^
v RM = 3(– j )
9. (B) 10. (A) 11. (C) 12. (B) 13. (A)
14. (A) 15. (C) 16. (E)
sin A/2 → → 17. (A) In planetary motion angular
= vR – vM
Since δ = A, we get momentum remains constant,
→ ^ ^ i.e.,
sin A ∴ vR = – 3 j + 4 i
3 = mv1r1 = mv2r2
sin A/2 ⇒ vR = 32 + 42
v 1 r1
2 sin A/2 cos A/2 = 5 km hr–1 v2 =
= r2
sin A/2 7. (C) T1 = 727 + 273 = 1000 K
2 × 107 × 2 × 10 10
A 3 T2 = 1727 + 273 = 2000 K =
cos = = cos 30° 3 × 1012
2 2
A/2 = 30°
H2
H1
= ()
T2 4
T1 = 1·33 × 105 m/s
∴
2. (A)
A = 60°
2
= ( )
2000 4
1000
= 16
18. (A)
19. (C) The thin layer of water wets
mv k the plates over an almost
3. (B) Iron l1 = 4 cm, 8. (C) = 2
r r circular area which is concave
k1 = ? 1 k outwards as shown in figure.
K.E. = mv2 = …(i)
2 2r r
Silver l2 = 10 cm,
Force acting on the particle is d
k2 = 1 conservative in nature. Hence
In Ingen Housz experiment du
F = – The excess pressure p inside the
dr
k1 l1 2 or du = – Fdr
liquid film over the outside atmos-
= 2 pheric pressure is given by
k2 l2 r
k1 =
(4)2
× 1 = 0·16
U = – ∫ ∞
Fdr
p = T ( ) 1 2
–
(10)2 r
r d
k
4. (B) Point has two displacements
πr and 2r in two mutually per-
= ∫ ∞
r2
dr
Since r >> d,
1
r
can be neglected
pendicular directions. The resul- k in comparison to 2/d.
⇒ U = –
tant displacement r
2T
Total energy Hence p = –
= (πr)2 + (2r)2 k k d
K.E. + P.E. = – Thus, the excess pressure inside
2r r
= r π2 + 4 k the film is less than the outside
= –
5. (A) 2r atmospheric pressure (as is clear
⇒ v 2′ = v 1′·
v2
v1
29. (C) Maximum current than be
sent through resistances is
NB = m × ()
1 3
2
24. (C) Conditions of the problem are 20 = I 2 × 10 m
=
shown in the figure from which it 8
is clear that ⇒ I = 2A NA
∴ = 1
M2 Clearly, therefore, max. current NB
through each bulb combined in 34. (B) Let u and v be the velocity of
parallel is the electron when entering and
A
θ 1 1 when leaving the capacitor res-
C D = 2A = A pectively.
θ 2 2
θ Since component of velocity
Therefore, max. power consumed parallel to the plates remains un-
θ 1 2 1 2 changed, we have
O
θ
B
θ
M1 =
( ) 2
× 10 +
( ) 2 u cos α = v cos β
θ + θ + θ = 180° × 10 + ( 2)2 × 10 u cos β
⇒ =
⇒ θ = 60° = 5 + 5 + 20 = 30 W v cos α
= 4 : 2 : 27 = × 6 cal
10
39. (C) A = r1 + r2 = r + 0 2M 1
= . . [(R2 + r 2) = 12·6 J
⇒ r = A R2 – r 2 2
(R2 – r 2)] 12·6
i = = 3 cal
µ = 1 4·2
r = M (R2 + r 2)
when angles are small 2 48. (C)
⇒ i = µr = µA 44. (B) Drift velocity of free electrons 49. (C) The rays emerging from the
i lens are directed towards the
40. (D) On PQ, F = i B l sin 0 = 0 vd =
ne A centre of curvature of the mirror,
On QR, F = i B l sin 120° i i.e., these are normally incident
=
ne π r 2 on the mirror and retrace their
3
= iB l i path to form the image coincident
2 vd ∝ 2
r with the object
On RP, F = i B l sin 120° when i and r are both doubled
3 v L
= iB l vd = O M C
2 2
41. (B) For monoatomic gas γ 45. (C) At t = 0 the capacitor acts as
20 cm 60 cm
(= Cp/Cv ) is larger than that for a a short whereas in the steady
diatomic gas. state it acts as open circuit. (Continued on Page 1633 )
4 a2
–9 20. (A) Closing S1 and S4 will put in 4 R
or = =
3 a2 – 16 circuit two resistances of 4Ω each 3 R – 1·5
⇒ a = 5 cm connected in parallel and exclude ⇒ R = 6·0 cm
● Sodium and potassium are the seventh and eighth ● Mobility and electrical conductivity of ions in
most abundant elements respectively by weight in the aqueous solution :
earth’s crust. ■ Alkali metal ions exist as hydrated ions M+ (H2O)x
■ NaCl and KCl occur in large amounts in sea water. in the aqueous solution.
The largest source of Na is the rock salt (NaCl). ■ The degree of hydration decreases with increase in
Sea water contains nearly 3% NaCl. ionic size from Li+ to Cs+, i.e., Li+ ion is the mostly
■ Various salts including, Na2B4O7.10H2O (borax), hydrated [Li (H2O)6] +.
Na 2CO3.NaHCO3.2H2O (trona), NaNO3 (Chile salt
■ The mobility of ions and electrical conductivity of
petre) and Na2SO4.10H2O (mirabilite) are found as
ions in aqueous solution are inversely proportional
natural deposits. to the size of hydrated ions. Hence among alkali
■ Potassium occurs mainly as deposit of KCl metal ions, the lithium ion has lowest mobility and
(sylvine), a mixture of KCl and NaCl (sylvinite) and electrical conductivity. The mobility of ions and
the double salt KCl.MgCl2.6 H 2O (carnallite). electrical conductivity decrease in the order
● There is no convenient source of rubidium and only one Cs+ > Rb+ > K+ > Na+ > Li+
of caesium and hence these elements are obtained as
by-products from lithium processing. ● Reducing character—The increasing order of redu-
cing character in gaseous state depends upon ioniza-
● Francium does not occur appreciably in nature due to
its transitory existence. tion energy (IE) of atoms and hence expected order is
as :
General Characteristics of Alkali Metals Li < Na < K < Rb < Cs
(A) Atomic Properties IE (kJ mol– 1) 520 496 419 403 376
● Electronic configuration—All the elements have one ■ The reducing character of any metal in solution is
valence electron (ns 1) over the electronic configuration best expressed in terms of its Standard electrode
of inert gases. The outermost s-electron is very well potential (E°) which depends on its (I) sublimation
screened from the nuclear charge in these elements. (II) ionization and (III) hydration enthalpies.
Points to Remember
● Lithium can not be stored in kerosene oil because it is very Hence, while dilute solutions are paramagnetic, the concen-
light and hence floats over surface. Hence it is kept trated solutions become diamagnetic.
wrapped in paraffin wax. Other alkali metals can be stored ● A granular material prepared from quick-lime and NaOH solu-
in kerosene oil.
tion followed by heating to dryness, is known as sodalime. It
● Microcosmic salt, Na (NH4) HPO4.4 H2O, is some times
is used as an absorbent for CO2 and in decarboxylation
used in place of borax for performing bead test for coloured
organic reactions.
basic radicals.
● All alkali metals except Li, dissolve in mercury forming ● Following are some important compounds of alkali metals
amalgams with evolution of heat. These amalgams are which are most often known by common and commercial
used as reducing agents in organic chemistry. names :
● Polyhalide formation—Alkali metal halides react with halo- (i) Na2CO3, Soda ash
gens and interhalogens forming ionic polyhalides. (ii) K2CO3, Pearl ash
KI + I2 → KI 3 (iii) A mixture of Na O and dil. HCl, Oxone or Soda-bleach
2 2
KBr + ICl → K [BrICl] (iv) Na2CO3.NaHCO3.2 H2O, Sodium sesquicarbonate, used
KF3 + BrF3 → K [BrF 4] for wool washing
● All alkali metal sulphates form alums (except Li2SO4).Li2SO4 (v) NaCl, Rock salt
is not isomorphous with other sulphates.
(vi) Na2SO4.10 H2O, Glauber’s salt
● Sodium-lead (Na-Pb) alloy is used in the preparation of
(vii) NaNO3, Chile salt petre
antiknock compound, Pb (C2H5)4.
(viii) Na2B4O7.10 H2O, Borax
● Liquid sodium is used as a coolant in nuclear reactors.
(ix) Na3[AlF6], Cryolite
● Lithium metal is used as scavenger in the metallurgical
operations to remove oxygen and nitrogen; because Li ● Some complexes of alkali metals with crown ethers and
reacts with both O2 and N2. cryptands are known. Complexes with cryptands are known
● When the concentration of alkali metals in liquid ammonia is as cryptates. The term cryptate comes from the fact that
increased beyond 3M, the solvated electron undergoes a metal ion remains hidden in the structure.
pairing process. ● Base consisting of a soluble metal hydroxide, is known as
[2e (NH3)x]– [e2 (NH3)x]2– alkali. Alkali metals form caustic alkalies.
∆E = Ep – Er = qv
and
( )d∆E
dt
. v
= ∆Cv
= Heat of reaction at constant volume are known as Kirchhoff’s equations which show
Thus the heat of reaction at constant volume and at a variation of heat of reaction at constant pressure and
given temperature is given by the difference in the internal constant volume respectively.
energies of the products and the reactants. ● Kirchhoff’s equation shows that change in heat of
Heat of reaction at constant pressure—For the reaction at constant pressure or volume per degree
change of temperature is shown by differences in
reaction at constant pressure and temperature
heat capacities of products and reactants at constant
∆H = qp pressure or volume.
If Hp and Hr are the enthalpies of the products and ● If molar heat capacities of products and reactants are
reactants respectively, then same, then the heat of reaction is independent of
temperature.
∆H = Hp – H r
● The molar heat capacities of solids are almost equal
∆H = Hp – H r = qp to each other and hence heat of reactions involving
= Heat of reaction at constant pressure solids are almost independent of temperature.
Thus, the heat of reaction at constant pressure and at
Types of Heat of Reactions
a given temperature is given by the difference in the
enthalpies of the products and reactants. (1) Heat of formation—The quantity of heat evolved
Relation between heat of reaction at constant or absorbed when one mole of a compound is formed
∆ E) and constant pressure (∆
volume (∆ ∆ H) from its elements. It is expressed as ∆Hf ·e.g.,
∆H = ∆E + P∆V 1
H2(g) + O → H2O(l) , ∆Hf = – 68 k cal
2 2(g)
= ∆E + ∆nRT
(2) Heat of combustion—The quantity of heat
∆n = Difference in number of moles of gaseous evolved when one mole of a substance is completely
products and gaseous reactants. oxidised e.g.,
R = Gas constant, T = Temperature in kelvin.
CH4(g) + 2O2(g) → CO2(g) + 2H2O(l)
If ∆n = 0 ∆H = ∆E
∆H = – 213 k cal
If ∆n = Positive ∆H > ∆E The heat of combustion is very useful in—
If ∆n = Negative ∆H < ∆E (a) Calculating the heat of formation which is
otherwise not possible in many cases.
Variation of heat of reaction with temperature—
The variation of heat of reaction with temperature is given (b) Calculating the calorific value of fuels.
by Kirchhoff’s equation (c) Elucidating the structure of organic compounds.
∆E2 – ∆E1 = ∆Cv (T2 – T 1) (3) Heat of solution—The quantity of heat evolved
and ∆H2 – ∆H1 = ∆Cp (T2 – T 1) or absorbed when one mole of a solute is dissolved
completely in a large excess of water, so that the further
where ∆Cv is difference in heat capacities of products and dilution does not produce any heat change e.g.,
reactants at constant volume and ∆Cp is difference in heat
HCl(g) + nH2O → HCl(aq), ∆H = –39·3 k cal
capacities of products and reactants at constant pressure.
Heat of reaction depends on— (4) Heat of neutralisation—The quantity of heat
(i) Physical state and the amount of substance evolved when one equivalent (equivalent mass) of an acid
is completely neutralised by one equivalent (equivalent
(ii) Temperature
mass) of a base in dilute solution e.g.,
(iii) In the case of reactions involving gases whether
the reaction is taking place at constant volume or at HCl(aq) + NaOH(aq) → NaCl(aq) + H2O(l)
constant pressure. ∆H = –13·68 k cal
Example 1. In a certain process, 678 J of heat is Example 2. Given the following information
absorbed by a system while 290 J of work is done on
A+B → C+D, ∆ H°° = – 10·0 k cal
the system. What is the change in internal energy
for the process ? C + D → E, ∆ H°° = 15·0 k cal
Solution : q = + 678 J
Calculate ∆H°° for each of the following reactions :
Since, work is done on the system, w has a positive
value (a) C + D → A + B
w = + 290 J (b) 2C + 2D → 2A + 2B
∴ ∆E = q + w = 678 + 290 = 968 J (c) A + B → E
OBJECTIVE QUESTIONS
1. The heat change taking place 5. The enthalpies of the elements in (C) ∆H < T∆S
during the reaction at a particular their standard states are assu-
(D) ∆H = Zero
temperature which does not med to be—
involve any change of volume is (A) Zero at 298 K 10. The property which can be
represented by— (B) Unity at 298 K classified as an intensive pro-
(A) ∆G (B) ∆H (C) Zero at all temperatures perty is—
(C) ∆E (D) ∆n (D) Zero at 273 K (A) Mass
6. 2C (s) + 2O2(g) → 2CO2(g) (B) Temperature
2. Which of the following proceeds
with the positive value of ∆S ? ∆H = –188 k cal (C) Volume
1 The heat of combustion of carbon (D) Heat capacity
(A) SO2(g) + O 2(g) → SO3(g) (s) is—
2 11. If for H2(g) = 2H(g) ; ∆H = 104 k cal
(A) – 188·0 k cal
(B) HCl(g) → H(g) + Cl(g) the heat of atomisation of hydro-
(B) + 188 k cal
gen is—
(C) Freezing of ice-cream (C) – 94·0 k cal
(D) + 94·0 k cal (A) 52 k cal (B) 104 k cal
(D) None of these
(C) 208 k cal (D) None of these
3. In which of the following reac- 7. The occurrence of a reaction is
tions heat of neutralisation has impossible when— 12. 2·1 g of Fe combines with S
highest numerical value ? (A) ∆H is +ve and ∆S is +ve evolving 3·77 kJ. The heat of
formation of FeS in kJ/mole is—
(A) NH4OH and HCl (B) ∆H is –ve and ∆S is +ve
(B) CH3COOH and NaOH (A) –3·77 (B) –1·79
(C) ∆H is +ve and ∆S is –ve
(C) NH4OH and CH 3COOH (C) –100·5 (D) None of these
(D) ∆H is –ve and ∆S is –ve
(D) NaOH and HCl 13. The temperature of 5 ml of a
8. Hess’s law deals with— strong acid increases by 5°C
4. At constant T and P, which one
of the following statements is (A) Change in heat of reaction when 5 ml of a strong base are
correct for the reaction ? (B) Rate of reactions added to it. If 10 ml of each are
1 (C) Equilibrium constants mixed, temperature should in-
CO(g) + O 2(g) → CO2(g) (D) Influence of pressure on crease by—
2
(A) ∆H = ∆E volume of a gas (A) 5°
(B) ∆H < ∆E 9. For a reversible reaction at (B) 10°
(C) ∆H > ∆E equilibrium— (C) 15°
(A) ∆H = T∆S (D) Cannot be known
(D) ∆H is independent of physi-
cal state of reactants (B) ∆H > T∆S (Continued on Page 1603 )
( a
)
P + 2 V = RT
V
37. (C) The Balestein test is performed to detect halogens
in organic compound.
a
PV + = RT A copper wire is heated in the Bunsen flame till it does
V
not impart any green colour to flame. The heated end
PV a
+ = 1 is dipped in the organic compound and heated again.
RT RTV
Formation of a green or bluish green flame due to for-
PV
RT
= (1–
a
RTV ) mation of volatile cupric halides indicates the pres-
ence of some halogen in organic compound.
PV 38. (B) NaNO3 Chile salt petre
= z (Compressibility factor)
RT
Na(NH4)HPO4 Microcosmic salt
∴ z = (1–
a
RTV ) NaHCO3
Na 2CO3·10H2O
Baking soda
Washing soda
31. (C) Molecular formula of sulphur molecule is S8. It has
staggered ring structure 39. (B) In benzene each carbon atom is sp 2 hybridized
and further due to resonance C—C bond lengths are
S S S
equal
S S
S
←→
S S
32. (B) k V = 19·5 × 10–5 ohm–1 cm–1
40. (B) In metallic sodium outer shell electron is loosely
C = 0·01 mole/dm3, V = 100 × 1000 cm3 mole–1 attached to the Kernel of the atom. To and fro oscil-
µV = k V × V = 19·5 × 10 –5 × 105 lation of these loose electrons cause lustre of sodium
= 19·5 ohm –1 cm2 mole–1 metal.
C(Coke) H O
µ∞ = 390 ohm–1 cm2 mole–1. 2
41. (A) CaO → CaC2 → C2H2
Acetic acid being monobasic acid its equivalent con- Calcium Acetylene
ductance is equal to molar conductance. carbide
(λV = µV and λ∞ = µV ). The degree of dissociation ∆
42. (C) 2H 2O2 → 2H 2O + O2
λV 19·5
α = = = 0·05 H2O2 + 2KI → 2KOH + I2
λ∞ 390 (Acidified) (Violet)
N
CH2 CH2
C—C is—
(A) 260 k cal/mole (B) 180 k cal/mole
N N
(C) 130 k cal/mole (D) 80 k cal/mole
16. In the process of ice melting at –15°C—
CH2
(A) ∆G < 0 (B) ∆G > 0
48. (A) 2O 3 → 3O2
(C) ∆G = 0 (D) It cannot be predicted
2 Vol. 3 Vol.
17. For an adiabatic process which of the following is
Vol. of O2 3 correct ?
= = 1·5.
Vol. of O3 2 (A) q = 0 (B) ∆E = q (C) q = +w (D) P∆V = 0
On heating ozone is decomposed to oxygen and 18. In a closed vessel 2 moles of CO and 1 mole O 2 are
volume is increased to 1·5 times. ignited to get CO2. If ∆ H and ∆E are the change in
49. (A) In DNA pairs of bases are held together with H- enthalpy and change in internal energy respectively,
bonding. then—
50. (B) For gases (A) ∆H < ∆E (B) ∆H > ∆E
5 x = 0 for monoatomic (C) ∆H = ∆E (D) Not definite
Cp = R+x x = R for diatomic
2 19. The relationship which describes variation of vapour
3
3
x = R for polyatomic gases pressure with temperature is called—
Cv =
2
R+x 2 (A) Hess’s law
For Ar (monoatomic gas) (B) Arrhenius equation
5 (C) Clausius-Clapeyron equation
Cp R (D) Kirchhoff’s equation
2
= = 1·66
Cv 3 20. Two moles of an ideal gas expand spontaneously into
R
2 a vacuum. The work done is—
For CO2 (polyatomic gas) (A) Zero (B) 2 J (C) 4 J (D) 8 J
5 3
R+ R ANSWERS
Cp 2 2 4
= = = 1·33. 1. (C) 2. (B) 3. (D) 4. (B) 5. (A) 6. (C) 7. (C)
Cv 3 3 3
R+ R
2 2 8. (A) 9. (A) 10. (B) 11. (A) 12. (C) 13. (A) 14. (C)
●●● 15. (D) 16. (B) 17. (A) 18. (A) 19. (C) 20. (A) ●●●
1. (A) Mass of 1 mole (= 6·02 × 1023 molecules) of CO2 Concentration of A is halved and B is doubled the
= 44g rate
6. (A) 58·8
w = × 48250 = 14·7 g
7. (B) Standard reduction potential of copper (E° Cu2+/Cu 2 × 96500
14. (D)
= + 0·34 V) is much higher than aluminium (E°Al3+/Al =
15. (A) Concentration of succinic acid in water layer
– 1·66 V) 1·843
Cu 2+ ions are reduced when placed its solution in Al = g/ml
100
container. Concentration of succinic acid in ether layer
8. (D) 0·127
= g/ml
9. (B) Gas law equation is PV = nRT 50
Concentration in
PV
∴ n = Distribution coefficient (K) water layer
RT between water and ether = Concentration in
Moles of gas in larger balloon ether layer
10 × 80 1·843 50
n = K = ×
RT 100 0·127
= 7·25
Moles of gas in smaller balloon
16. (A)
3 × 1·11 Mass
n′ = 17. (A) Density =
RT Volume
No. of smaller balloons filled Unit cell content (Z) in bcc = 2
10 × 80 Molar mass = M g
= = 240·24 2M
3 × 1·11 Mass of unit cell = g
N0
≈ 240
Edge length of unit cell = a
10. (A) Volume of unit cell = a 3
11. (C) The rate law equation for the reaction 2M
∴ Density =
r = k[A] [B]2 …(1) N0a 3
:
:O
:
OH
C—OH + Mg :O:
P P
| X
:O:
R
:
:O
:O
26. (D)
:
OBJECTIVE QUESTIONS
11. Protein chondrin is found in— 15. The mast cells are found in— (B) Investing bone
(A) Blood (A) Adipose tissue (C) Cartilage bone
(B) Areolar tissue (B) Yellow fibrous tissue (D) Reticular bone
(C) Bone (C) Areolar tissue 19. The bone of mammals contains
(D) Cartilage (D) White fibrous tissue longitudinal Haversian canals,
16. The camel’s hump is composed which are connected by trans-
12. Which of the following proteins,
of a tissue which provides water verse canals, called—
is not found in the connective
tissue ? when oxidized. It is— (A) Inguinal canal
(A) Collagen (B) Elastin (A) Areolar tissue (B) Bidder’s canal
(B) Adipose tissue (C) Volkmann’s canal
(C) Ossein (D) Actin
(C) Muscular tissue (D) None of these
13. Ligaments join—
(D) None of these 10. The pericardium of heart is com-
(A) Muscle to bone
17. The formation of cartilage is posed of—
(B) Bone to bone
known as— (A) Areolar tissue
(C) Skin to muscles
(A) Chondrogenesis (B) Reticular tissue
(D) Nerves to muscles
(B) Diapendesis (C) White fibrous tissue
14. Osteoclasts are associated (C) Haemopoisis (D) Yellow fibrous tissue
with— (D) Ossification
(A) Bone formation 18. A bone which is formed by the
ANSWERS
(B) Bone breakdown transformation of the connective 1. (D) 2. (D) 3. (B) 4. (B) 5. (C)
(C) Muscle formation tissue, called— 6. (B) 7. (A) 8. (B) 9. (C) 10. (C)
(D) Bone regeneration (A) Replacing bone ●●●
OBJECTIVE QUESTIONS
1. The key point in Lamarck’s view 4. Who published the book ‘Origin (C) Geographical isolation
of organic evolution is— of Species by Natural Selection (D) Reproductive isolation
(A) Origin of species in 1859 ? 7. The unit of natural selection is
(B) Inheritance of acquired cha- (A) Lamarck (B) Oparin the—
racters (C) Wallace (D) Darwin (A) Individual (B) Family
(C) Overpopulation 5. The ultimate source of organic (C) Population (D) Species
(D) Natural selection evolution is— 8. The Darwinian fitness of an orga-
2. Co-discoverer of Darwinism (A) Mutation nism is a measure of—
was— (B) Sexual reproduction (A) Its ability, relative to others
(A) Ruskin (B) Buffon (C) Natural selection in the population, to pass its
(C) Malthus (D) Wallace (D) Hormonal action genes to the next genera-
3. Galapagos islands are associa- 6. Phenomenon of ‘Industrial Mela- tion
ted with the name of— nism’ demonstrates— (B) The number of offspring it
(A) Wallace (B) Malthus (A) Natural selection produces
(C) Darwin (D) Lamarck (B) Induced mutation (Continued on Page 1623 )
C.S.V. / February / 2008 / 1617
Model Paper for Various Medical Entrance Examinations 17. Which of the following is liver-
produced growth-promoting an-
abolic peptides of vertebrate
Breakdown of Fatty Acids (ii) In this step, two hydrogen atoms are removed
between α- and β-carbons, as a result α-, β-
The long chain fatty acids are broken down by the unsaturated fatty acyl CoA is formed in presence
process of α-oxidation and β-oxidation. The latter pro- of FAD–containing enzyme acyl–CoA dehydro-
duces acetyl CoA (2-carbon unit). genase.
α -oxidation (iii) This step involves the addition of a water mole-
cule across the double bond to form corres-
● The long chain of fatty acid by this process is broken ponding β-hydroxyacyl–CoA in presence of
down until it is reduced to 12 C–atoms. enzyme enol hydrase.
● Fatty acids with less than 13 C–atoms are not affec- (iv) In presence of NAD—specific β-hydroxyacyl–
ted by this process. CoA dehydrogenase enzyme, β-hydroxyacyl–
α-oxidation occurs in the following sequential series— CoA is dehydrogenated. Two H–atoms are
(i) In presence of an enzyme fatty acid peroxidase removed from the β-carbon atom (β-oxidation)
and hydrogen peroxide (H2O2), the fatty acid is which now bears a carbonyl function and β -keto
oxidatively decarboxylated to form an aldehyde. fatty acyl–CoA is formed.
In this process CO2 comes from carboxylic group
(v) This is the final step which involves the thioclas-
and oxidation occurs at α-carbon atom which is
tic cleavage of β-keto fatty acyl—CoA in presence
converted into aldehyde group.
of an enzyme β-ketoacyl thiolase to form
(ii) In presence of an enzyme fatty aldehyde dehy-
an active 2C unit acetyl–CoA and a fatty acyl–
drogenase, the aldehyde is further oxidised to
CoA molecule.
form the new fatty acid containing one less car-
bon atom than in the original fatty acid. NAD+ is The fatty acyl–CoA so produced again re-enters
reduced in this reaction. the β-oxidation losing further 2 carbon unit. This
sequence continues until whole molecule is
Aldehyde dehydrogenase degraded.
Aldehyde →
NAD + H2O
New fatty acid + NADH + H + Worth Remembering
● Each turn of β-oxidation generates one FADH2 [step (ii)],
one NADH + H+ [step (iv)] and one acetyl–CoA [step (v)].
The new fatty acid will be oxidised again and again till ● In the last turn of β-oxidation spiral, two acetyl–CoA
it consists of 12 C–atoms. molecules are produced.
● Each turn of β-oxidation generates 5 ATPs. However, in
β-oxidation the first turn there is consumption of 2 ATP molecules [in
● β-oxidation is the chief method of fatty acid degrada- the step (i)] hence, in this turn there will be a net gain of
only 3 ATPs.
tion in plants.
● A huge amount of energy is generated in the form of ATP
● It takes place in mitochondria (and also in glyoxy- by mitochondrial oxidation of fatty acids through β-
somes) and involves sequential removal of 2C in the oxidation spiral and TCA cycle. For example, one mole-
form of acetyl CoA molecules from the carboxyl end cule of palmitic acid (16–C atom) on complete oxidation
will produce 129 ATP molecules.
of fatty acid.
OBJECTIVE QUESTIONS
1. Lipids or fats are a diverse group 5. Which one of the following is a (B) α-reduction
of organic compounds found in— polyunsaturated fatty acid ? (C) Both (A) and (B)
(A) Plants (A) Linoleic acid (D) Fatty acid reduction
(B) Animals (B) Oleic acid
10. Fatty acid molecules containing
(C) Micro-organisms (C) Erucic acid
one or more double bonds
(D) All of the above (D) All of the above
(—CH — —CH—) are called—
2. In which of the following organic 6. Palmitoleic fatty acid is obtained (A) Saturated fatty acids
or inorganic compounds, lipids from— (B) Unsaturated fatty acids
are soluble ? (A) Olive oil (C) Both (A) and (B)
(A) Water (B) Marine algae (D) Stearic acid
(B) Alcohol (C) Pine oil
(C) Ether (D) Both (B) and (C) ANSWERS
(D) In both (B) and (C) 7. Triolein is a simple triglyceride 1. (D) 2. (D) 3. (A) 4. (D) 5. (A)
3. Triglycerides are sometimes since it contains— 6. (D) 7. (A) 8. (B) 9. (A) 10. (B)
called— (A) One type of fatty acid ●●●
(A) Nature’s store house of (B) Two types of fatty acids
energy (C) Three types of fatty acids
(B) Enzymes (D) Four types of fatty acids
(C) Co-factors
8. How many fatty acids are found
(D) All of the above in each molecule of triglyceride ?
4. Which one of the following is a (A) Two (B) Three
saturated fatty acid ? (C) One (D) Four
(A) Lignoceric acid
9. The energy in fatty acid molecule
(B) Palmitic acid is transformed into ATP by a pro-
(C) Myristic acid cess known as—
(D) All of the above (A) β-oxidation
Dikaryon
Primary mycelium
Gills Pores
Epiba- Annulus
sidium
Stipe
Volva
Mycelium
Epibasidium
A
B
Hypobasidium
Hypobasidium
A D
C
B C Pileus
Basidiospores
Sporidia
Sterigma
G Log of wood
Epibasidium Peridiole
Volva
Brand spore
D
E E F
Fig. : (A–E). Basidiomycetes. Different types of Fig. : (A–G). Basidiomycetes. Common types of basidiocarps. (A)
basidia. (A) Stichobasidial type; (B) Chiasto- basidiocarp of Agaricus with gills on the underside of pileus;
basidial type; (C) Tuning-fork type; (D) Holo- (B) basidiocarp of Boletus with pores on the underside of
basidium; (E) Stichobasidial type with a pileus; (C) basidiocarp of Lycoperdon; (D) basidiocarp of
terminal cluster of septate, sickle-shaped Geaster; (E) fruit bodies of Cyathus; (F) mature fruit body of
sporidia. Phallus; (G) fruit bodies of Fomes.
Rusts and Smuts are Parasitic Club ● Black stem rust of wheat uses barberry leaf (bushes)
Fungi as an alternate host.
● Rusts and Smuts are club fungi that parasitize Important Smut Diseases of Cereals
cereal crops such as corn, wheat, oats and rye.
● Rusts and smuts do not form basidiocarps. They Name of Loose Smut Covered Smut
spores produce, resembling soot. Cereals
● Some smuts enter seeds and exist inside the plant,
becoming visible only near maturity. Wheat Ustilago nuda (race of Tilletia caries
● In corn smuts, the mycelium grows between the corn Ustilago tritici )
kernels and secrets substances that cause the deve- Oat Ustilago avenae Ustilago hordei (a race
lopment of tumors on the ears of corn. of Ustilago kolleri )
● The life cycle of rusts, which may be particularly com- Barley Ustilago nuda Ustilago hordei
plex, often requires two different plant host species to
complete the cycle. Corn Ustilago maydis
OBJECTIVE QUESTIONS
1. Which division of fungi is com- 6. Clamp connection is characteris- (C) Ustilago avenae
monly known as club fungi ? tic of certain group of— (D) All of the above
(A) Deuteromycetes (A) Fungi
ANSWERS
(B) Oomycota (B) Algae
(C) Basidiomycota (C) Bryophytes 1. (C) 2. (D) 3. (B) 4. (A) 5. (B)
(D) Zygomycetes (D) All of the above 6. (A) 7. (B) 8. (C) 9. (A) 10. (B)
●●●
2. Which of the following groups is/ 7. Anticancer substance calvacin is
are comprised of club fungi ? obtained from—
(Continued from Page 1577 )
(A) Truffles (A) Sac fungi For lens u = – 20 cm,
(B) Puffballs (B) Club fungi f = 15 cm,
(C) Mushrooms (C) Red algae v = ?
(D) All of the above 1 1 1
(D) Myxophycean cells – =
3. The part of mushroom that is v u f
8. In certain members of Basidio- 1 1 1
visible above the ground is a— + =
mycetes, the basidium bears four v 20 15
(A) Ascocarp
spores exogenously, each
(B) Basidiocarp ⇒ v = 60 cm
usually at the tip of a minute stalk
(C) Ascogonium known as— Radius of curvature of the mirror
(D) Zygospore (A) Conidiophore r = 60 – 10 = 50 cm
4. In which fungus is the dikaryotic (B) Basidiophore 50. (B) There is one input (A) and
stage longer lasting ? one output (Y) connected accord-
(C) Sterigmata
(A) Club fungi ing to Boolean expression
(D) Both (B) and (C) –
(B) Imperfect fungi A = Y
(C) Sac fungi 9. Puccinia graminis tritici causes—
read as ‘NOT A equals Y’ mean-
(D) Zygospore fungi (A) Black stem rust of wheat
ing that Y is negation (or inver-
5. Conidiospores are formed— (B) Loose smut of oat sion) of A.
(A) By sporangia (C) Covered smut of oat Since there are only two digits 0
(B) By sac, club and imperfect (D) Loose smut of barley and 1 in binary system, we have,
fungi 10. 'Loose smut of corn' is caused Y = 0 if A = 1 and Y = 1 if A = 0.
by— The logic symbol of NOT gate is
(C) When nutrients are in short
supply (A) Ustilago nuda A Y
(D) During sexual reproduction (B) Ustilago maydis ●●●
1. Match Column A (Types of Fruit) 7. The least number of t RNA 16. RQ is measured by—
with Column B (Common english molecules for each of the twenty (A) Auxanometer
name of fruits) then select the amino acids found in protein is— (B) Potometer
correct answer from the options (A) Four (B) Three (C) Ganong’s Respirometer
given below— (C) One (D) Two (D) Porometer
Column A Column B
8. Quantasome discovered by Park 17. Gynobasic style is chiefly found in
(a) Drupe 1. Strawberry and Biggins (1964) has— family—
(b) Pome 2. Plum (A) 100 chlorophyll molecules (A) Solanaceae
(c) Etaerio of 3. Brinjal (B) 300 chlorophyll molecules (B) Cucurbitaceae
achnes (C) 230 chlorophyll molecules
(C) Malvaceae
(d) Berry 4. Pear (D) 230 chlorophyll and about
(D) Labiatae
(a) (b) (c) (d) 50 carotenoid molecules
(A) 2 4 3 1 9. In pteridophytes, xylem consists 18. Fermentation is—
(B) 2 4 1 3 of— (A) Anaerobic respiration
(C) 2 1 4 3 (A) Tracheids (B) Aerobic respiration
(D) 2 3 4 1 (B) Xylem parenchyma (C) Incomplete oxidation of
(C) Both (A) and (B) carbohydrates
2. Ethnobotany is a branch of
(D) None of the above (D) Anaerobic complete oxida-
Botanical science which deals
10. Lock and Key theory (Template tion of carbohydrates
with—
(A) The study of plants used by theory) of enzyme action was 19. All the appendages which are
people (particularly by primi- given by— epidermal in origin are referred to
tive people) (A) Buchner (B) Fischer as—
(B) The study of plants of eco- (C) Koshland (D) Umberger (A) Trichomes
nomic value 11. The skeleton of the shoot is (B) Ground tissues
(C) The study of shrubs and formed by the—
(C) Mesophylls
trees (A) Root (B) Stem
(D) None of these (D) None of the above
(C) Leaf (D) Bud
3. Most of the history of life con- 12. Coenzyme is— 20. Net gain of ATP in glycolysis
cerns the evolution of— (A) Always a protein from one molecule of glucose
(A) Plants and animals is—
(B) Non-protein organic mole-
(B) Prokaryotes cule (A) 8 (B) 4
(C) Eukaryotes (C) A non-protein inorganic com- (C) 2 (D) 0
(D) Photosynthesizers pound
21. The ultimate biological unit which
4. Birbal Sahni Institute of Palaeo- (D) Often a metal
controls heredity is called—
botany is situated at— 13. True bulbs are found— (A) Gene (B) Genotype
(A) Lucknow (B) Delhi (A) Only among monocotyle-
(C) Kolkata (D) Kanpur (C) Genome (D) Chromosome
dons
5. An octamer of four histones (B) Only among dicotyledons 22. When yeast ferments glucose,
complexed with DNA is called— (C) Equally both in monocotyle- the products are—
(A) Nucleosome (B) Telomere dons and in dicotyledons (A) C2H5OH + Energy
(C) Satellite (D) Karyotype (D) Largely in dicotyledons and (B) C2H5OH + CO2 + Energy
6. Protoplasm term was used by rarely in monocotyledons (C) CO2 + H2O + Energy
Purkinje (1839) and Von Mohl 14. Glycolysis is found in cytoplasm (D) CH3OH + H2O + Energy
(1846). It was called as physical of virtually all types of aerobic/
basis of life by— anerobic cells. In this process, 23. The nucleus of a bacterium is—
(A) Julian Huxley glucose is converted into a com- (A) Absent
(B) Hugo de Vries pound which is— (B) Well-defined
(C) Dujardin (A) Citric acid (B) Pyruvic acid (C) Incipient
(D) Linnaeus (C) Acetyl CoA (D) PEP (D) Found always near the pili
Paper I
Max. Marks : 100] [Time : 2 Hours
where, v x
vy
= horizontal component of velocity
rotation
= mg
l
2 ()
when the object strikes the Also, torque = Iα, where I = moment of inertia of
ground at B the rod about the axis of rotation
= ux + ax t = ux (˙.˙ ax = 0) ml 2
=
= 100 m/s 3
ux = 100 m/s If aCM be the acceleration of the centre of mass,
A aCM
then α =
(l /2)
uy = 0
∴ mg ()l
2
= Iα or
mgl ml 2 aCM
2
=
3
×
l /2
mgl 2ml 2.aCM
h = 2000m or =
2 3l
3gl 2 3g
vx ⇒ aCM = = ms– 2
B 4ml 2 4m
O
3 × 10
vy = ms– 2
v 4m
v y = vertical component of velocity at 15
∴ aCM = ms– 2
B = uy + ayt = gt 2m
(˙.˙ uy = 0, ay = + g) where m is the mass of the rod.
(b) We know that
1 1 2h
But h = uy t + a t 2 = gt 2 ⇒ t = n ∝ T
2 y 2 g
where, n = frequency and T = tension in the
2h wire.
∴ vy = g × = 2gh
g
n = KT 1/2
= 2 × 10 × 2000 = 200 ms– 1 where, K is the constant of proportionality.
∴ tan θ =
v x 100 1
= =
v y 200 2
∆T
T
= 2
∆n
n
,( )
where, ∆T is change in tension and ∆n change
∴ θ = tan – 1 () 1
2 in frequency.
∆T
(c) Clearly, % change in tension = × 100
T
[Angular momentum] = [ML2T– 1]
[Impulse]
[Energy]
=
=
[MLT– 1]
[ML2T–2]
= 2
∆n
n ( )
× 100
2×5
[Torque] = [ML2T– 2] = × 100 = 2
500
[Force] = [MLT– 2] 6. (a) Let us consider a current element d y at a
[Moment of Inertia] = [ML2] distance y from the wire carrying current I.
Hence, the dimensional formulae of energy and The magnetic field b
torque are same. acting on the current
5. (a) When the support is withdrawn, the rod will element due to infini- i
rotate about the axis passing through the hinged tely long conductor, l
dy
point. µ0
B =
l 2πy a
y
∴ Force acting on dy x
length,
d F = idy B I
Now, total force acting on the conductor of
length (l ),
l (x + l ) (x + l )
µ0I µ0Ii
l /2 F = ∫ idyB = ∫ idy =
l /2 x x 2πy 2π
mg
C.M. (x + l )
= ∫
x
()1
y
dy =
µ0Ii
2π
= [lny ]x
(x + l )
m get
or = 4 × 10 – 3 ° = E
Ecell
l cathode – Eanode
→
concentration of I2, therefore, order of reaction Tautomerises
w.r.t. I2 is 0. O
As given in the expression that Rate = ||
k[CH3COCH3][H+]. Ph—C—CH3
The total order of reaction is 2. Acetophenone
Now, substitute the values in the expression. (ii) Carbylamine reaction—When a primary
amine reacts with chloroform and alcoholic
2 × 10 – 2 = k[2·5 × 10– 2][1·5 × 10– 3]
KOH give isocyanides or carbylamines
2 × 10 – 2 mol lit– 1 s–1 which have unpleasant smell.
∴ k =
2·5 × 10– 2 × 1·5 × 10– 3 mol2 lit–2 ∆
Ar—NH2 + CHCl3 + 3KOH (alc.) →
= 0·535 × 10– 3 →
Ar—N==C + 3HCl + 3H2O
= 5·33 × 10– 4 mol– 1 lit sec– 1 Aryl carbylamine
or L mol–1 sec –1 (d) As the given alkene is buten-2 which is a
(c) Given ν = 3·3 × 1015 (
1 1
–
22 n 2 ) symmetrical alkene thus, addition of HBr to it
does not follow Markovnikoff’s rule hence the
λ = 6600A° = 6600 × 10–10 metre product formed would be same in both cases
c i.e., in presence of peroxide and in absence of
and ν = peroxide.
λ
5. (a) The formula suggests that the compound is
∴
c
λ
= 3·3 × 1015 ( )
1 1
–
22 n 2
CH3
|
3 × 108 CH3—C—OH
6·6 × 10–7
= 3·3 × 1015 ( )1 1
–
4 n2 |
CH3
1 1
⇒ 0·138 =– i.e., a tertiary alcohol, therefore, alkane from
4 n2 which it is formed must be
1 1 138 1000 – 552 448
⇒ = – = = CH3 CH3
n2 4 1000 4000 4000
| H2O/H2SO 4
|
4000 63·24
⇒ n2 = ⇒n= = 2·988 ≈ 3 CH3—CH → CH3—CH—OH
448 21·16 | |
4. (a) Caprolactum on heating with traces of water CH3 CH3
gives ε-amino caproic acid which is mono- Isobutane t-butanol
In presence of alkali (pH > 7) dissociation of On solving the value of α, we get α = 0·08625 mol/L
Zwitter ion favours formation of an anion
R ∴ [H+] = [HSO3–] = 0·08625 mol/L
+ | [SO 3– –][H+]
H3N—CH—COO– + OH– and Ka 2 =
[HSO3–]
Zwitter ion Now, substitute of the value of [H+] and [HSO 3–]
R
in above equation, we get
Base |
→ H2N—CH—COO– + H2O [SO 3– –][0·08625]
8·3 × 10– 5 =
Anion [0·08625]
Hence it will coagulate at anode (+ ve electrode) [SO 3– –] = 8·3 × 10– 5 mol/L
(d) The structures of 1-butene and 2-butene are as (b) N2O4 2NO 2
CH3—CH2—CH = CH2 CH3—CH = CH—CH3
t=0 1 0
1-butene 2-butene
teq 1 – 0·4 0·4 × 2 = 0·8
More substituted alkenes are more stable than
less substituted alkenes. The more is the Total no. of moles = 1 – 0·4 + 0·8 = 1·4
stability, the lesser is the reactivity.
Note : More substituted alkenes contain more Now, Kx =
x NO
2 [ ]
no. of alkyl group.
Hence, 2-butene is more stable and less
xN O
[ 2 4 ]
0·8 0·6
reactive to Br2 than 1-butene. where x NO = and x N O =
2 1·4 2 4 1·4
6. (a) In 1-butyne the terminal hydrogen is weakly 2
acidic whereas in 2-butyne, there is no such
hydrogen is available. The reason is that carbon
∴ Kx = ( ) 0·8
1·4
0·6
1·4
= 0·76
atoms of the triple bond are more electro-
As Kp = Kx (Ptotal)∆ng = 0·76 × (1) = 0·76 atm
negative due to sp hybridization. Due to greater
electronegativity, the shared pair of electron of (˙.˙ ∆ng = 2 – 1 = 1)
Note : The effective volume of the vessel The dipole moment due P—C bonds in
occupied by H2 gas is 20 – 10 = 10 litre. (C2H5)3P are in opposite direction of the dipole
8. (a) Fluorine (F 2) is more reactive than chlorine (Cl2). moment of the lone pair on P atom, while the
This is on account of lower bond dissociation dipole moments of N—C bonds in (CH3)3N are
energy (158·8 kJ/mol) of F2 molecule as in same direction as the direction of dipole
compared to Cl 2 molecule (242·6 kJ/mol). moment of lone pair on N atom. Hence, the
Lower bond dissociation energy of F2 is due to dipole moment of (CH3)3N is definitely higher
the greater interelectronic repulsion which is than that of (C2H5)3P.
consequently due to very small size of F atoms. 10. (a) P(15) = 1s22s 22p63s 23p33d 0, N(7) = 1s22s 22p 3
(b) CrO42– is more oxidising than MoO42–. CrO2–
4 ion
As P contains vacant d-orbit, thus it can exceed
has very high standard reduction potential as its octet and utilize d-orbitals for multiple bond-
compared to MoO42– and hence CrO42– is strong ing, whereas N cannot exceed its octet due to
the absence of d-orbital and hence cannot form
oxidising agent. Moreover, the most stable
NO43– ion.
oxidation state of Mo is + 6 and hence its
reduction to lower oxidation state is rather (b) The molecular orbital configuration of B 2 is
difficult. B2 KK σ (2s)2 σ* (2s)2 π(2px )1 π (2py )1.
(c) Two substances can be represented as : As it contains two unpaired e–, therefore, it is
·· ·· paramagnetic and the molecular orbital con-
SiH3—O—SiH3 and CH3—O—CH3
·· ·· figuration of C2 is C2 = KK σ (2s)2 σ* (2s)2 π
In case of (SiH3)2O, Si—O bond shows pπ-dπ (2px )2 π (2py )2.
bonding due to availability of vacant d orbitals At it does not contain any unpaired e– thus it is
on Si atom. As a result of this lone pair of diamagnetic.
electrons on O atom are engaged in π bond
(c) When ∆0 < P
formation and are not available for donation. In
case of (CH3)2O, CH3—O bond cannot form
eg eg
such π bonding as C atom does not possess
vacant d orbitals. The lone pairs of oxygen atom ∆0 ∆0
in this case are available for donation. Hence
(SiH3)2O is a weaker base than (CH 3)2O.
T2g T2g
9. (a) The empirical formula of the compound is d5 d6
··
PtCl2(NH3)2. Since chlorine is not precipitated (5 unpaired electrons) (4 unpaired electrons)
by AgNO3 and hence all Cl atoms are in
µ = (5 + 2) 5BM µ = (6 + 2) 6BM
coordination sphere. Since the product of
churning with AgNO3 are [Pt(NH3)4](NO3)2 and When ∆0 > P
Ag2[PtCl4], the compound should be a dimer of eg eg
PtCl2(NH3)2 i.e., a coordination isomer of
PtCl2(NH3)2 µ = √1(1 + 2) ∆0 ∆0 µ = √0(0 + 2)
[Pt(NH3)4] 2+ [PtCl4] 2–
→
T2g T2g
AgNO3
d5 d6
[Pt(NH3)4] (NO3)2 + Ag2[PtCl4] (Unpaired electron) (Zero unpaired electron)
1. Write the location and function of the following : (c) Which type of ovule is shown in diagram (c) ?
(a) Cytoskeleton (b) Synergid Give one reason.
(c) Phytol chain (d) Sieve tube element (d) What is the type of flower called given in
(e) Centromere diagram (d) ? Give examples of such flower.
2. Refer the following diagrams (a) to (e) : (e) Which type of aestivation is shown in (e) ? Give
examples.
3. Write down the types of placentation, inflorescence
P and fruit of the following :
(a) Pea (b) Coriander (c) Wheat (d) Sunflower
Mucilagenous (e) Mustard
(a)
sheath 4. Differentiate between the following [Give one
important difference] :
Q (a) Culm and Caudex
(b) Slime moulds and Fungi
(c) Biological magnification and eutrophication
(d) White rust and Brown rust
5. Match the Column I and Column II :
Column I Column II
(a) Jacob and Monod (i) Neurospora
Head (b) One gene one (ii) Operon
enzyme hypothesis (iii) Reverse trans-
P
(c) Griffith criptase
Sheath (d) Temin and Baltimore (iv) Okazaki fragments
(b)
(e) DNA polymerase (v) Transformation
(vi) Transduction
(vii) Conjugation
6. Fill in the blanks with suitable words given in boxes :
Marsilea Coralloid Usnea Eichhornia
Q root
Monoecious Pneumato- Geitono- Cycas
phores gamy
Chalaza Pinus Dioecious Vivipary Xenogamy Oscillatoria
Nucellus (a) Rhizophora has both……… and …………
Raphe
Integuments
(b) Aquatic plants are ………… (Pteridophyte) and
Antipodal cells
Embryo sac
…………… (Angiosperm).
(c) Secondary nucleus (c) Plant bearing both male and female flowers is
Egg cell called ………… (and the pollination between
Synergids different flowers of the same plant is called
Micropyle ………
Hilum
(d) …………… has ……………
Funicle
7. (a) Give any two conditions for seed habit.
(b) Among the pairs which one shows the tendency
of seed habit ?
(i) Lycopodium and Equisetum
(ii) Selaginella and Pteris
(d) Ovary (e) (iii) Dryopteris and Pteridium.
Thalamus (c) Suggest three ways to break seed dormancy.
8. Fill in the blanks :
(a) Mutation can be defined as………… variation.
(a) What is shown in diagram (a) ? What are (P) (b) Mutation leads to evolution of ………… of a
and (Q) ? gene.
(b) Tell whether the diagram (b) is T1-phage or T2- (c) Genes expressed only in homozygous state are
phage. What are (P) and (Q) ? …………
CH3
2
(b) Phytol
(Tail) H 3C
Write the functions of (1) and (2) in each diagram.
19. In photorespiration, RuBP is oxidized to form glyco- H3C
CH3
late and glycerate. Glycolate enters the PCO cycle H3C
PEROXISOME
These highly charged ions are to calcium carbonate. 4 × 3·14 × 9·1 × 10 – 28 × 10–13
adsorbed onto the surface of the Ca(OH)2(s) + CO2(g) ≈ 5 × 1012 cm/sec
negatively charged colloidal particles, → CaCO3(s) + H2O(l) The velocity of electron is greater than
thereby neutralising the surface charge the velocity of light when it is present
and allowing the colloidal particles to Although the sand in the mortar is
chemically inert, the grains are bound inside the nucleus. This condition is
come together, and the clay precipi- impossible and hence electron cannot
together by the particles of CaCO 3
tates from solution. exist in nucleus.
and the hard material results.
Q. Why does sulphur (density Q. What will be the average life
2·1 g cm 3), when carefully placed Q. What is the thyroxine ?
of radium (Ra) if its t1/2 is 1690
on top of water, float while the ☞ It is now known that the thyroid years ?
same sinks in water when a few gland produces a growth regulating
☞ The reciprocal of radioactive
drops of detergent are placed on hormone, thyroxine which contains
decay constant, k is called the
water ? iodine. Thyroxine has following struc-
average life of a radioactive subs-
☞ Surface tension of water is ture :
tance.
affected by adding detergent. The high I H 1
| | Average life (T) =
surface tension of the water keeps k
C— C
more dense sulphur float on the water 0·693
surface. When some drops of deter- HO—C C—O We know that t 1/2 =
k
gent are placed on the surface of C— —C
| | 0·693
water, the surface tension of water is 1690 years =
I H k
reduced and the sulphur sinks to the
I H 0·693
bottom of the pot containing water. | ∴ k =
| 1690
Q. Why does even painstak- C——C Hence average life,
ingly purified water conducts —C C—C H2CH(NH2) COOH. 1690
electricity to a very small extent ? C——C T =
0·693
☞ The existence of so-called | |
I H = 2433·6 years
autoionization of water was proved
many years ago by Friedrich or the value of
Most of the table salt sold in the
Kohlrauch. He found that even after 1
market contains 0·01% NaI added to = 1·44
water is painstakingly purified, it still 0·693
provide the necessary iodine in the
conducts electricity to a very small ∴ T = 1·44 × t1/2
diet.
extent, since autoionization produces
very low concentration of H3O + and Q. Cryolite is found in only = 1·44 × 1690
OH– ions even in the purest water. small amounts in nature but large = 2433·6 years
amount of cryolite is needed in
2 H2O(l) H3O+(aq) + OH– (aq) production of Al. How is demand
Q. What is the basic difference
between a sol and gel ?
Q. What biological function is met with ?
performed by mineral apatite (cal- ☞ Most of the hydrogen fluoride ☞ A colloidal solution in which
cium and phosphorus containing (HF) produced by the reaction of dispersion medium is liquid and dis-
mineral) ? fluorspar (CaF 2) and H 2SO4, is used persed phase is solid, then such a
to make cryolite. system is called sol. For example gold
☞ Hydroxy-apatite, Ca (OH)2.3 sol and sulphur sol.
Ca 3(PO4)2, is the main component of CaF2(s) + H2SO4
tooth enamel. Cavities in our teeth When the dispersion medium is
→ CaSO 4(s) + 2HF(g) solid and dispersed phase is liquid
are formed when acids decompose 6 HF(aq) + Al(OH)3(s) + 3 NaOH
the weakly basic apatite coating. This then the colloidal system is called gel.
decay can be prevented by converting → Na 3AlF6(s) + 6 H2O(l) For example, boot polish, butter,
Cryolite gellies etc.
hydroxy-apatite to much more acid-
resistant coating, fluorapatite, CaF2, Q. Why cannot an electron Q. What would be the vapour
3 Ca3 (PO 4)2, by adding a source of exist inside the nucleus of an density (VD) of PCl5 if it is 90%
fluoride ion. atom ? dissociated at 250°°C ?
UP-CPMT RESULT
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=
200 + 100
200
3
Ω
⇒ h′ = 3·96 m ∴ p.d. across the voltmeter
ANSWERS WITH HINTS 3. (D) Length of the fish = 6 cm = i × Req
1. (C) Let m be the instantaneous Real depth of the fish’s head 200
= 0·02 × = 1·33V
mass of the ascending rocket plus = 18 cm 3
fuel and v r the relative velocity of ∴ Error in voltmeter reading
aµw = 4/3 = 1·33 – 1·10 = 0·23V
the gas ejecting from the rocket.
Suppose the fuel is burnt at the ∴ Apparent depth of fish’s head 5. (D) The energy in the nth state of
rate ∆m/∆t to provide the rocket 18 a hydrogen like atom of atomic
= = 13·5 cm number Z is given by
an acceleration α. Then, 4/3
13·6
Also real depth of fish’s tail En = – Z2 2 …(i)
v r ∆m n
m – g
α = = 18 + 6 = 24 cm The first excited state, n = 2 and
∆t
∴Apparent depth of fish’s tail energy is given by
Here, v r = 250 ms –1, 13·6
24 E2 = – Z2. 2 …(ii)
m = 500 kg, = = 18 cm (2)
4/3
Since the excited atom can make
g = 10 ms –2, Hence, the length of the fish a transition to the first excited
α = 20 ms –2 = 18 – 13·5 = 4·5 cm state by successively emitting
∆m m 4. (C) (i) Let R be the resistance of two photons of energies 10·20 eV
= (α + g) the voltmeter. The voltmeter is and 17·00 eV, the energy diffe-
∆t vr
connected to 100 Ω resistance in rence between these two states
500 parallel. Hence, their equivalent will be
= (20 + 10)
250 100R En – E2 = 10·20 + 17·00
resistance is .
= 60 kg s–1 100 + R = 27·20 eV …(iii)