WESTCLUSTER SCHOOL COMMON EXAMINATION2024-25
STD:XII CHEMISTRY(043)
Max. Marks:70 DATE: 20-12-24
SET: 2-KEY
SECTIONA
1 (b) 0.31 volt 1
2 (d) In covalent compounds, Fluorine can form single bond only while
oxygen forms multiple bond 1
3
(b) triamminebromochloronitroplatinum(IV) chloride 1
4 1
(a) A = C2H4, B = C2H5OH, C = C2H5NC, D = C2H5CN
5 (c) Glycine 1
6 (c) 2-methoxypropane 1
7 (b) 1
8 (a) Primary amine 1
9 (d) Carbylamine reaction 1
10 (b)289,500 C 1
11 c) Peptide bond 1
12 1
(b) Slope = - k, intercept= [R0]
13 (a)Both A and R are true and R is the correct explanation of A 1
14 (a)Both A and R are true and R is the correct explanation of A 1
15 (d)A is false but R is true 1
16 (a)Both A and R are true and R is the correct explanation of A 1
17 ΔTf=i⋅Kf⋅m ½+½
=2x1.86°Ckg/molx 0.3mol/kg
½+½
ΔTf=1.116 °C
Determine the new freezing point of the solution:
The freezing point of pure water is 0 °C. Therefore, the freezing point of
the solution will be:
Freezing point=0 °C− ΔTf =0 °C− 1.116 °C=− 1.116 °C
18 (a) [Xe} 1
(b)because they have ability to adopt multiple oxidation states they have
variable oxidation state
1
19 (A) CH3-CO-CH3 (C) CH3-CO-CH3 (D) CHI3 ½+½
½+½
(b)
20 (a) ortho-Halotoluene para-Halotolune 1
(b) (c)
+ CHI3
21 ½+½
½+½
OR
½+½
½+½
SECTION C
22 (a) ½+½
½+½
23 (a) Copper in the first transition series exhibits +1 oxidation statemost 1
frequency. This is because Cu is 3d104s1 When one electron is lost, the
configuration becomes most stable due to fully filled d10 configuration. 1
(b)
1
(c) This is due to the interconversion of dichromate (orange) to chromate ion
(Yellow)
24 (a) A-III : B-II : C-I : D-II ½+½
2
(b) chlorobenzene , carbon to which chlorine is attached is sp -hybridised
and is more electronegative than the corresponding carbon in cyclohexyl ½+½
chloride which is sp3 -hybridised chlorobenzene C -Cl bond has some
double bond character so its bond length is smaller
25 (a) Vitamin C, Fat soluble vitamins are A, D, E and K (any One) ½+½
(b) Any differences related 1+1
26 ½+½
2 −1
(a) Λm matches with (c) S cm mol
Ecell matches with (d) V
κ matches with (a) S cm−1
G∗ matches with (b) m−1 ½+½
(a) Primary batteries contain a limited amount of reactants and are discharged
when the reactants have been consumed. Secondary batteries can be 1
recharged but take a long time to recharge. Fuel cells run continuously as
long as the reactants are supplied to it and products as removed
immediately, also pollution free and more efficiency
OR
½+½
(a)
½+½
(b) A= Strong electrolyte
B= Weak electrolyte ½+½
(c) At Cathode Ag and at anode Ag+
27 (a) Acetophenone is a methyl ketone and hence responds to the Iodoform test, but 1
benzo phenome is not. In acetophenoneCOCH3 group is present. CHI3Iodoform.
Yellow ppt formation
(b) 1
Related any conversion
(c) Structure of IUPAC name
1
28 Named reactions -Each reaction -1 mark( any 3) 1+1+1
SECTION D
29 (a) ½+½
½+½
A plot between ln k and 1/T
(b) No it is not possible. Thisis explained with the help of Arrhenius equation according
to this the rate constant is equal to collision frequency and every collision among the
reacting species will lead to the products. Since this does not happen. It is not possible for 1
a chemical reaction to have activation energy equal to zero.
(c) It increases the rate constant k- Option (d)
OR
(a) Activation energy of forward reaction is E1 +E2 and product is less stable than
reactant
30 Compound B: Aniline (C6H5NH2) ½+½
Compound C: N-Phenylbenzamide (C6H5NHCOC6H5)
Compound D: Benzene diazonium chloride (C6H5N2+Cl−) ½+½
Compound E: p-Hydroxyazobenzene (C6H5N=NC6H4OH)
1
(b)
1
c) Methylamine (CH₃NH₂) Option (a)
OR
(iii) 2,4,6-Tribromoaniline
31 (a) 0.5% NaCl solution the RBC swells up by movement of water inside it. 1% NaCl
solution the RBC this solution act as hypertonic solution and the RBC Shrink by the
movement of water outside it. ½+½
(b) As the partial pressure of CO2 in the atmosphere above the drink rapidly
decreases, the solubility of CO2 in the drink also decreases. ( Due to Henry’s 1
Law)
(c) Π=iCRT ½+½
Π=3×0.2×0.0821×298 ½+½
Π=14.67 atm
½+½
(d) +ve and _-ve deviation.
OR
(a) (i) Osmatic pressure
(ii) –ve deviation.
(b) ½+½
½+½
½+½
1
(c) states that for a solution of volatile liquids, the partial vapour pressure of each
component of the solution is directly proportional to its mole fraction present
in solution.
(d) Ar<CO2<CH4<HCHO
32 1
(a) K2[Ni(CN)4]
6 0
(b) Δo>P (Strong field case, Low spin complex) t2g eg
½+½
4 2
Δo<P (High spin): t2g eg
(c) [Co(NH3)5Cl]SO4 gives white precipitate with BaCl2 solution while 1
[Co(NH3)5(SO4)][Link] not respond to this test.
[Co(NH3)5(SO4)]Clgives white precipitate with silver nitrate solution
while [Co(NH3)5Cl]SO4 does not respond to this test
1
(d) The difference in magnetic moments is mainly due to the different natures of
ligands (H2O is weak field ligand 5- unpaired electrons and CN− is strong field
ligand-1 unpaired electron) in the two complexes which makes the number of
unpaired electrons in each complex different, hence we get different values of
magnetic moments.
1
(e) The complex[Co(en)3] 3+
is more stable because en is a bidentate chelating ligand .
OR
(a) structures of optical isomers of [PtCl2(en)2] 2+ Complex 1
(b) dsp2 hybridization ; paramagnetic in nature. ½+½
(c) [Co(NH₃)₆]Cl₃ and its IUPAC name is - Hexaaminecobalt (III) chloride. 1
(d) The metal-carbon bond in metal carbonyls possess both σ and π character. The M–
C σ bond is formed by the donation of lone pair of electrons on the carbonyl
carbon into a vacant orbital of the metal. The M–C π bond is formed by the 1
donation of a pair of electrons from a filled d orbital of metal into the vacant
antibonding π* orbital of carbon monoxide. The metal to ligand bonding creates a
synergic effect which strengthens the bond between CO and the metal
(e) Any example of Homoleptic and Heteroleptic ligands ½+½
33
1
1
(b)o-Nitrophenol is steam volatile due to intramolecular hydrogen bonding
Phenol is a weak acid. Hence, it does not react with NaHCO3. However Picric
acid is having 3 strong electron with drawing groups so it reacts NaHCO3 and ½+½
evolves CO2 gas
½+½
½+½
(a) (CH3)3I + C2H5OH
½+½
(b) reagents used in the following reactions:
(i)Oxidation of a primary alcohol to aldehyde PCC/CrO3/Cu-573
(ii) Tolune to Benzoic acid KMnO4/Acid+ Heat 1
(b) any chemical distinguish
(c)
½+½
+½+½