Ilovepdf Merged
Ilovepdf Merged
1. When a haloalkane is heated with KCN in aqueous ethanoic solution, the product formed is-
a) Alkyl nitrite
b) nitro alkane
c) alkane nitrile
d) carbylamine
2. Amine that cannot be prepared by Gabriel phthalimide synthesis is-
a) Aniline
b) benzyl amine
c) tertiary-butylamine
d) isobutylamine
3. Which of the following amine has highest boiling point?
a) Pentaamine
b) 2-methylbutanamine
c) 2,2-dimethylpropamine
d) 3-methylbutamine
4. The amine that reacts with NaNO2 and HCl to give yellow oily liquid is-
a) Ethylamine.
b) Diethylamine
c) Isopropyl amine
d) Secondary butylamine
5. Sandmeyer reaction of diazonium salt is a replacement of N2 by-
a) Halogen Cl or Br
b) Hydroxyl group
c) Coupling
d) Hydrogen
6. One of the following amines will not undergo Hoffmann bromamide reaction-
a) CH3CONHCH3
b) CH3CH2CONH2
c) CH3CONH2
d) C6H5CONH2
7. The correct order of the basic strength of methyl substituted amines in aqueous solution is
a) CH3NH2 > (CH3)2NH > (CH3)3N
b) (CH3)2NH > CH3NH2 > (CH3)3N
c) (CH3)3N >CH3NH2 > (CH3)2NH
d) (CH3)3N > (CH3)2NH > CH3NH2
8. The correct statement regarding the basicity of arylamine is
a) arylamines are generally more basic than alkylamines because of aryl group
b) arylamines are generally more basic than alkylamines because the nitrogen atom in
aryalamines is sp- hybridised
c) arylamines are generally less basic than alkylamines because the nitrogen lone- pair
electrons are delocalised by intraction with the aromatic ring π- electron system
d) arylamines are generally more basic than alkylamines because the nitrogen loan-pair
electrons are not delocalised by interaction with the aromatic ring π-electron system.
9. What reagent is used in Hinsberg test of amines?
a) (CH3CO)2O and pyridine
b) C6H5SO2Cl followed by aq. NaOH
c) NaNO2 in aq. H2SO4
d) CH3I(excess) followed by AgOH
10. Aniline reacts with sodium nitrite and hydrochloric acid at 273 -278 K to give:
a) Benzene
b) Benzene diazonium chloride
c) Chlorobenzene
d) o-chloroaniline
11. Propane amide on reaction with bromine in aqueous NaOH gives:
a) Propanamine
b) ethanamine
c) N-Methyl ethanamine
d) Propanenitrile
12. The gas evolved when methylamine reacts with nitrous acid is:
a) NH3
b) N2
c) H2
d) C2H6
13. Which of the following is not correct regarding aniline?
a) It is less basic than ethyl amine
b) It can be steam distillated
c) It reacts with sodium to give hydrogen
d) It is soluble in water
14. Acetamide and ethylamine can be distinguished by reacting with:
a) Aq. HCl and heat
b) Aq. NaOH and heat
c) Acidified KMnO4
d) Bromine water
15. Given below are two statements labelled assertion (A) and reason(R).
Assertion(A)- Hinsberg's reagent can be used to distinguish primary amines from secondary
amines.
Reason(R)- Benzenesulphonyl chloride is called Hinsberg's reagent.
Select the most appropriate answer from the option given below :
a. Both A and R are true and R is the correct explanation of A.
b. Both A and R are true but R is not the correct explanation of A.
c. A is true but R is false.
d. A is false but R is true.
16. Given below are two statements labelled assertion (A) and reason(R).
Assertion(A)- Solubility of amines in water decreases with increase in molar mass.
Reason(R)- Intermolecular H bonds formed by the higher amines are weaker.
Select the most appropriate answer from the option given below :
a. Both A and R are true and R is the correct explanation of A
b. Both A and R are true but R is not the correct explanation of A.
c. A is true but R is false.
d. A is false but R is true.
17. Given below are two statements labelled assertion (A) and reason(R).
Assertion(A)- Amines behave as a Lewis base.
Reason(R)- Amines have an unshared pair of electrons on nitrogen atom.
Select the most appropriate answer from the option given below :
a. Both A and R are true and R is the correct explanation of A.
b. Both A and R are true but R is not the correct explanation of A.
c. A is true but R is false.
d. A is false but R is true.
18. Given below are two statements labelled assertion (A) and reason(R).
Assertion(A)- Acylation of amines gives a mono substituted product whereas alkylation of
amines gives poly substituted product.
Reason(R)- Acyl group sterically hinders the approach of further acyl groups.
Select the most appropriate answer from the option given below :
a. Both A and R are true and R is the correct explanation of A.
b. Both A and R are true but R is not the correct explanation of A.
c. A is true but R is false.
d. A is false but R is true.
Section - B
This section contains 7 questions with internal choice in two questions. The following questions
are very short answer type and carry 2 marks each.
19. How will you distinguish between the following pairs of compounds:
i) Aniline and ethanamine.
ii) Aniline and N-methylaniline
20. Give reasons:
i) Aniline does not undergo friedal Craft reaction.
ii) (CH3)2NH is more basic than (CH3)3N in an aqueous solution.
OR
i) Although -NH2 group is o/p directing in electrophilic substitution reactions, yet aniline, on
nitration gives good yield of m-nitroaniline.
ii) pKb of methylamine is less than that of aniline.
21. Write chemical equations for the following conversion:
i) nitrobenzene to benzenoic acid
ii) aniline to benzyl alcohol
OR
i) Write the reaction involved in the following: Diazotisation
ii) Give reason:
Aromatic diazonium salts are more stable than aliphatic diazonium salts.
22. Illustrate the following with an example of reaction in each case-
i) Sandmeyer reaction
ii) coupling reaction
23. Complete the following reactions:
i) CH3CH2NH2 + CHCl3+alc.KOH------->
ii) CH3NH2+ C6H5COCl---------->
24. Ammonolysis of alkyl halides is not a good method to prepare pure primary amines. Explain.
25. State and illustrate the following:
Gabriel phthalimide synthesis.
Section- C
Section contains 5 questions with internal choice in two questions the following questions are
sort answer type and carry 3 marks each.
26. a) Write the chemical reaction of methylamine with benzyl chloride and write the
IUPAC name of the product obtained.
b) Arrange the following in the increasing order of their pkb values:
C6H5NH2 , NH3 , C2H5NH2 ,(C2H5)2 NH
27. Write the structures of main products when aniline reacts with the following reagents:
i) Br2 water.
ii) HCl
iii) (CH3CO)2O/Pyridine
28. Write the structures of A, B and C in the following:
Br2/aq. KOH NaNO2+ConcHCl/0-5 0C KI/∆
i) C6H5CONH2 ---------- ---------A ------ --------------- B ------ ---- C
KCN LiAlH4 CHCl3+alcKOH
II) CH3Cl ---- ---------- A ---- ----------- B -------------------- --- C
31. Benzene ring in aniline is highly activated. This is due to the sharing of lone pair of nitrogen
with the ring which results in increase in the electron density on the ring and hence facilitates
the electrophilic attack. The substitution mainly takes place at Ortho and para positions
because electron density is more at Ortho and para positions. On reaction with aqueous
bromine all the ortho and para position get substituted resulting in the formation of 2,4,6-
tribromoaniline. To get a monobromo compound, the amino group is acetylated before
bromination. After bromination, the bromoacetanilide is acid hydrolysed to give the desired
halogenated amine.
a) Why does -NH2 group facilitates electrophilic attack in aniline?
b) Explain why: in aniline, the substitution mainly takes place at Ortho and Para positions.
c) Show the conversion of benzene into aniline.
32. In amines the N atoms of the amino group are SP3 hybridised. Amines readily lose its
electron pair and act as a base. In aliphatic amines ,the alkyl group tends to increase the
electron density on the nitrogen atom due to the +I effect. In aromatic amines, the basic
strengths are influenced by the presence of an electron withdrawing group at the O-, m- and p-
position in the ring.
a) Lower member of aliphatic amines are soluble in water . Why?
b) Out of (CH3)3N and and (CH3)2NH which one is more basic in aqueous solution?
c) Which isomer of C3H9N which does not react with Hinsberg’s reagent.
Section- E
The following questions are long answer type and carry five marks each two questions have
internal choice.
33. An organic compound A with molecular formula C7 H7NO reacts with Br2/aq. KOH to give
compound 'B', which upon reaction with NaNO2 and HCl at 00 Celsius gives 'C'. Compound 'C'
on heating with CH3CH2OH gives hydrocarbon 'D'. compound 'B' on further reaction with Br2
water gives white precipitate of compound 'E'. Identify the compound A,B,C,D and 'E'.
Also justify your answer by giving relevant chemical equations.
OR
An aromatic compound 'A' on treatment with aqueous ammonia and heating forms compound
'B' which on heating with Br2 and KOH forms a compound 'C' of molecular formula C6H7N. write
the structure and IUPAC names of the compound A, B and C . Justify your answer by giving
relevant chemical equations.
34. i) Write the structure of main products when benzenediazonium chloride (C6H5N2+Cl-) reacts
with the following reagents:
a) KI b) C2H5OH
ii) write the structures of A B and C in the following reactions:
LiAlH4 HNO2 /Low temp
CH3Cl+ KCN (alc)----------------->A-- --------------------->B------------------------>C
OR
i) Write the reactions involved in the following:
a) Hoffmann’s Bromamide degradation reaction
b) Carbylamine reaction
35. i) Convert the following:
a) Phenol to N-phenylethanamide
b) Chloroethane to methanamine
c) Propanenitrile to ethanal.
ii) What happens when-
a) N-ethylethaneamine reacts with benzenesulphonyl chloride.
b) Aniline reacts with chloroform in the presence of alcoholic potassium hydroxide.
********************************
CHAPTER END TEST
CHEMISTRY THEORY (043)
TOPIC – CHEMICAL KINETICS
MM:70 Time: 3 hours
General Instructions:
Read the following instructions carefully.
a) There are 35 questions in this question paper with internal choice.
b) SECTION A consists of 18 multiple-choice questions carrying 1 mark each.
c) SECTION B consists of 7 very short answer questions carrying 2 marks each.
d) SECTION C consists of 5 short answer questions carrying 3 marks each.
e) SECTION D consists of 2 case- based questions carrying 4 marks each.
f) SECTION E consists of 3 long answer questions carrying 5 marks each.
g) All questions are compulsory.
h) Use of log tables and calculators is not allowed.
Section A
The following questions are multiple-choice questions with one correct answer. Each question
carries 1 mark. There is no internal choice in this section.
1. What kind of order of reaction decomposition of Ammonia on platinum surface is:
(a) Zero order reaction
(b) First order reaction
(c) Second order reaction
(d) Fractional order reaction
3.In the rate equation, when the concentration of reactants is unity then the rate is equal to:
(a) .specific rate constant
(b) average rate constant
(c) instantaneous rate constant
(d) None of the above
5.In the reaction 2A + B → A2B, if the concentration of A is doubled and that of B is halved, then the
rate of the reaction will
(a) increase 2 times
(b) increase 4 times
(c) decrease 2 times
(d) remain the same
6.In the Haber process for the manufacture of ammonia the following catalyst is used
(a) Platinized asbestos
(b) Iron with molybdenum as a promoter
(c) Copper oxide
(d) Alumina
8.In chemical equation H2 (g) + I2 (g) ⇌ 2HI (g) the equilibrium constant Kp depends on
(a) total pressure
(b) catalyst used
(c) amount of H2 and I2
(d) temperature
9.If the rate of a reaction is expressed by, rate = A [A]² [B], the order of reaction will be
(a) 2
(b) 3
(c) 1
(d) 0
(i) A first order reaction has a rate constant k=3.01 x 10-3 /s. How long it will take to decompose half of
the reactant?
(ii) The rate constant for a first order reaction is 7.0 x 10-4 s-1. If initial concentration of reactant is 0.080
M, what is the half-life of reaction?
(iii) The rate of a first order reaction is 0.04 mol L-1 s-1 at 10 minutes and 0.03 mol L-1 s-1 at 20 minutes
after initiation. The half life of the reaction?
(iv)The plot of t1/2 vs initial concentration [A]0 for a first order reaction .
32. Read the passage given below and answer the following questions :
A first-order reaction can be defined as a chemical reaction for which the reaction rate is entirely
dependent on the concentration of only one reactant. In such reactions, if the concentration of the first-
order reactant is doubled, then the reaction rate is also doubled.
The following reaction, A(g)⟶ΔP(g)+Q(g)+R(g)A(g)⟶ΔP(g)+Q(g)+R(g) follows first order kinetics. The
half-life period of this reaction is 69.3 s at 500°C. The gas A is enclosed in a container at 500°C and at a
pressure of 0.4 atm.
Answer the following question: -
(i) The rate constant for the reaction.
(ii) The total pressure of the system after 230 s will be.
(iii) Give an example of first order reaction.
(iv) The plot of ln[A] vs t graph is.
Section-E
33. (a) The rate of the chemical reaction doubles for an increase of 10 K in absolute temperature
from 298 K. Calculate .
(b) Explain collision frequency.
Or
During nuclear explosion, one of the products is with half-life of 28.1 years. If of was
absorbed in the bones of a newly born baby instead of calcium, how much of it will remain after 10 years
and 60 years if it is not lost metabolically.
34. The activation energy for the reaction is at 581K. Calculate the fraction of molecules
of reactants having energy equal to or greater than activation energy?
Or
In a reaction between A and B, the initial rate of reaction was measured for different initial
concentrations of A and B as given below:
The following questions are case-based questions. Each question has an internal choice and
carries 4 (1+1+2) marks each. Read the passage carefully and answer the questions that follow.
31. Molar conductivity for weak electrolytes can be obtained from molar conductivities of strong
electrolytes at infinite dilution by doing algebraic addition. For example ,molar conductivity of weak
electrolyte like CH3COOH can be obtained from molar conductivities at infinite dilution of strong
electrolytes like CH3COONa , HCl and NaCl according to Kohlrauch’s law
Λ°m CH3COOH = [Λ°mCH3COO- + Λ°mNa+]+[ Λ°mH++ Λ°mCl-]-[ Λ°m Na+ + Λ°mCl-]
(i) What is the expression of Λ°m for an electrolyte AmBn ?
(ii) Define limiting molar conductivity.
(iii) Calculate Λ°m for AgCl if Λ°m (AgNO3) = 133.4, Λ°m(KCl)=149.9, Λ°m(KNO3)=144.9
Scm2mol-1
OR
Calculate Λ°m for HAc if Λ°m (HCl) = 425.9, Λ°m(NaCl)=126.4, Λ°m(NaAc)=91.0 Scm2mol-1
32. The standard electrode potentials are very important and we can extract a lot of useful information
from them. If the standard electrode potential of an electrode is greater than Zero then it’s reduced
form is more stable compared to hydrogen gas. Similarly, if the standard electrode potential is
negative than hydrogen gas is more stable than the reduced form of the species. It can be seen that
the standard electrode potential for Fluorine is the highest indicating that F 2 gas has the maximum
tendency to get reduced to Fluoride ion F- and therefore Fluorine gas is the strongest oxidizing agent
and Fluoride ion is the weakest reducing agent.
(i) Which element can act as the strongest reducing agent?
(ii) How cell potential can be measured?
(iii) Which electrode can work as anode in galvanic cell?
(iv) Find out E°Cell for Zn/Zn2+(0.1M//Cu2+(0.10M)/Cu
[given E°Zn2+/Zn and E°Cu2+/Cu are -0.76 V and +0.34 V respectively]
OR
Write cell reaction for the above galvanic cell and mention cathode and anode.
SECTION E
The following questions are long answer type and carry 5 marks each. Two questions have an internal
choice.
33. a. Why does the cell voltage of a mercury cell remain constant during its life time ?
b. Write the reaction occurring at anode and cathode and the products of
electrolysis of aq KCl.
c. What is the pH of HCl solution when the hydrogen gas electrode shows a potential of -0.59 V at
standard temperature and pressure?
OR
a. Molar conductivity of substance “A” is 5.9×103 S/m and “B” is 1 x 10-16 S/m. Which of the two is most
likely to be copper metal and why?
b. What is the quantity of electricity in Coulombs required to produce 4.8 g of Mg from molten MgCl 2? How
much Ca will be produced if the same amount of electricity was passed through molten CaCl 2?
(Atomic mass of Mg = 24 u, atomic mass of Ca = 40 u).
c. What is the standard free energy change for the following reaction at room temperature? Is the reaction
spontaneous?
Sn(s) + 2Cu2+ (aq) ---- Sn2+ (aq) + 2Cu+ (s)
Given E°Sn2+/Sn and E°Cu2+/Cu are -0.14 V and +0.34 V respectively
34. (i) State Faraday’s Laws of electrolysis?
(ii)Three electrolytic cells A, B, C containing solutions of ZnSO4 , AgNO3 and CuSO4 respectively are
connected in series. A steady current of 1.5 amperes was passed through them until 1.45 g of silver
deposited at the cathode of cell B. How long did the current flow? What mass of copper and zinc were
deposited?
35. The molar conductivity of 0.025 mol L-1 methanoic acid is 46.1 S cm2mol- . Calculate its degree of
dissociation and dissociation constant. Given = 349.6 S cm2mol-1
and
OR
(a) Depict the galvanic cell in which the reaction takes place.
Zn(s) + 2Ag+(aq) →Zn2+(aq) + 2Ag Further show:
(i) Which of the electrode is negatively charged?
(ii) The carriers of the current in the cell.
(iii) Individual reaction at each electrode.
(b) A solution of Ni (NO3)2 is electrolysed between platinum electrodes using a current of 5 amperes
for 20 minutes. What mass of Ni is deposited at the cathode?
Chapter: 5 - Coordination Compounds
2. 1 each
1|Page
3. Identify the denticity of the ligands given below: 1 each
carbonyl CO monodentate
nitrosyl NO monodentate
2|Page
5. Show the: 2 each
3|Page
7. Compare the two complexes based on CFT: 1 each
8. 1 each
9. 1 each
10. 1 each
12. What are the factors affecting the stability of the complexes? 1 each
Factors affecting the stability of a complex ion
(i) Nature of metal ion: The greater the charge and the smaller the ion's size, the
higher its charge density, and the greater the complex's stability.
4|Page
(ii) Nature of ligand: The more the basicity of the ligand, the more its tendency to
donate electron pair and therefore, more the stability of the complex.
13. When a coordination compound CoCl3.6NH3 is mixed with AgNO3, 3 moles of 1 each
AgCl are precipitated per mole of the compound.
Write
(i) Structural formula of the complex
(ii) IUPAC name of the complex .
14. Using IUPAC norms write the formulae for the following: 1 each
(a) Potassium trioxalatoaluminate (III)
(b) Dichloridobis(ethane-l, 2-diamine) cobalt (III) ion
(a) K3[Al(C2O4)3]
(b) [Co(Cl)2(en)2]+
15. For the complex [Fe(en)2Cl2], Cl, (en = ethylene diamine), identify 1 each
(i) the oxidation number of iron,
(ii) the hybrid orbitals and the shape of the complex,
(ii) The complex has two bidentate ligands and two monodentate ligands. Therefore,
the coordination number is 6 and hybridization will be d2sp3 and shape will be
octahedral.
(i) Ambidentate ligand: The monodentate ligands with more than one coordinating
atoms is known as ambidentate ligand. Monodentate ligands have only one atom
capable of binding to a central metal atom or ion. For example, the nitrate ion NO2– can
bind to the central metal atom/ion at either the nitrogen atom or one of the oxygen
atoms.
Example :
— SCN thiocyanato - S, — NCS thiocyanato-N
5|Page
(ii) Denticity of a ligand: The number of donor atoms in a ligand that forms a
coordinate bond with the central metal atom is called denticity of a ligand.
Example: If the donor atom is one then it is called a Monodentate ligand, if it is two,
then it is called Bidentate, and so on.
(iii) Crystal field splitting: It is the splitting of the degenerate energy levels due to the
presence of ligands. When a ligand approaches a transition metal ion, the degenerate d-
orbitals split into two sets, one with lower energy and the other with higher energy.
This is known as crystal field splitting and the difference between the lower energy set
and the higher energy set is known as crystal field splitting energy (CFSE)
(i) Because in the presence of strong ligands, the crystal field splitting energy is more
than the energy required to oxidise Co2+.
(ii) This is due to the formation of π – bond by back donation of electrons from metal
to carbon of CO or due to synergic bonding.
19. Compare the CFT of tetrahedral complexes and octahedral complexes. any 2
points
-2
In tetrahedral coordination entity formation, the d orbital splitting is inverted marks
and is smaller than the octahedral field splitting.
6|Page
For the same metal, the same ligands, and metal-ligand distances, it can be
shown that:
Consequently, the orbital splitting energies are not sufficiently large for forcing
pairing; therefore, low spin configurations are rarely observed.
The ‘g’ subscript is used for the octahedral and square planar complexes
which have the center of symmetry. Since tetrahedral complexes lack
symmetry, the ‘g’ subscript is not used with energy levels.
1
20.
1
22
7|Page
1
23
(i) Assertion and reason both are true; reason is the correct explanation of
assertion.
(ii) Assertion and reason both are true but reason is not the correct explanation
of assertion.
(iii) Assertion is true, reason is false.
(iv) Assertion is false, reason is true.
8|Page
a.
1 each
b.
c.
d.
e.
Ans.
a. i
b. ii
c. i
d. ii
e. iv
5
27
Ans.
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