MS-1.
MS-1.
Pre-Board-II Examination:2024-25
SHILLONG REGION
CHEMISTRY THEORY (043)
MARKING SCHEME
SET-1
SECTION A
1 (b) 0.1 M HCl solution, conductivity is higher for strong electrolyte, conductivity decreases with dilution 1
2 (c) A= Benzaldehyde , B= Acetophenone. This is an example of crossed Aldol condensation. 1
3 (b) They are chemically reactive. 1
4 (b) atomic radii 1
5 (a) 3-Methylpent-3-en-2-one 1
6 (c ) reacts with Benzenesulphonyl chloride to form a product that is insoluble in alkali. 1
7 (d) 1 =Bromomethane, 2= 2-Bromo-2-methylpropane, 3=2- Bromobutane, 1
4= 1-Bromobutane
8 (b) reduces to one-fourth 1
9 (a) Nitrobenzene 1
10 (b) Cellulose 1
Starch contains only α glucose, sucrose contains α-D-glucose and
β-D-fructose glucose, maltose contains α-D-glucose and cellulose is a
polymer of β-D-glucose.
11 (a)Linkage isomerism 1
12 (b)Shows large negative deviation from Raoult’s law 1
∴ i = 0.3
0.18 K = i × 0.512 K kg mol-1 × 1 m
( b ) Lactose on hydrolysis with dilute acids gives an equimolar mixture of D-glucose and D-galactose.
SECTION C
22 1/2+1+1+1/2= 3
OR
23
(a) Both Ti3+ and Cu2+ have 1 unpaired electron, so the magnetic moment for both will be 1.73 BM 3
1+1+1=
(b) Mn+ has 3d54s1 configuration and configuration of Cr+ is 3d5 , therefore, ionisation enthalpy of Mn+ is
lower than Cr+
(c ) In both chromate and dichromate ion the oxidation state of Cr is +6
24 (i) As isomer A reacts with AgNO3 to give a white precipitate, Cl must be present in the ionisation sphere.
As it does not react with BaCl2, SO42− must be present in the coordination sphere. 1+1+1/2+1/2 = 3
25
(a) 1+1+1= 3
(b)
26 ( a ) When phenol is treated with bromine water, white ppt, of 2,4,6- tribromophenol is obtained.
1+1/2+1/2+1/2+1/2= 3
(b)
27 ( a ) NH2 group of aniline is acetylated first so that controlled nitration can occur at the para position. If the
NH2 group of aniline is not acetylated, then a mixture of ortho, meta and para products will form. 1+1+1= 3
(c ) C6H5NH2<C6H5CH2NH2<(CH3)3N<CH3NH2<(CH3)2NH
28 (i) Because deficiency of vitamin A and vitamin C causes night blindness and scurvy respectively. 1+1+ 1= 3
(ii) Nucleoside : A nucleoside contains only two basic components of nucleic acids i.e. a pentose sugar and a
nitrogenous base. During their formation 1-position of the pyrimidine or 9-position of the purine moitey is
linked to C1 of the sugar (ribose or deoxyribose) by a β-linkage.
Nucleotides : A nucleotide contains all the three basic components of nucleic acids, i.e. a phosphoric acid
group, a pentose sugar and a nitrogenous base. These are formed by esterification of C5‘ – OH of the sugar of
the nucleoside with phosphoric acid.
( i i i ) Maltose is a disaccharide.
SECTION D
29 (a) Solutions having equal osmotic pressure are called isotonic solutions. 1+1+2 4
(b) Cellulose acetate placed on a suitable support.
(c) RBC’s are isotonic with 0.9% NaCl solution, so they will swell and may
even burst when placed in 0.5% NaCl solution.
OR
1M KCl will have higher osmotic pressure because its dissociates to give K + and
Cl- ions while urea does not dissociate into ions in the solution.
30 Since the aromatic compound, ‘A’ does not give Tollen’s reagent test or Fehling’s test, it is not an aromatic
aldehyde. It responds to the iodoform test, indicating a methyl ketone. 1+1+1+1= 4
OR
(a) Benzene-1, 2-dicarboxylic acid
( b ) Phthalimide
(c) The conjugate base of carboxylic acid, a carboxylate ion, is stabilised by two equivalent
resonance structures in which the negative charge is at the more electronegative oxygen
atom. The conjugate base of phenol, a phenoxide ion, has non-equivalent resonance
structures in which the negative charge is at the less electronegative carbon atom.
Therefore, resonance in phenoxide ion is not as important as it is in carboxylate ion.
Further, the negative charge is delocalised over two electronegative oxygen atoms in
carboxylate ion whereas it is less effectively delocalised over one oxygen atom and less
electronegative carbon atoms in phenoxide ion.
(d) Carboxylic acids are higher boiling liquids than alcohols of comparable molecular masses.
This is due to more extensive association of carboxylic acid molecules through
intermolecular hydrogen bonding. The hydrogen bonds are not broken completely even in
the vapour phase.
Aliphatic carboxylic acids are more miscible in water due to the formation of hydrogen
bonds with water.
SECTION E
31 (a) Reaction taking place at cathode when the battery is in use: 1+1+1+2= 5
(i) Because after use it can be recharged by passing current through it in the
opposite direction.
(ii) 2H₂O(l) (dil)H₂SO₄ /Electrolysis 2H₂(g) + O 2(g)
(at cathode) (at anode)
32 (a) (i) This is because Eu²+ tends to change to Eu³+ as +3 is the common
oxidation state of lanthanoids. 1+1+1+1+1= 5
(ii)In alkaline medium, the orange colour of the solution changes to yellow due
to conversion o dichromate (Cr2O72-) ion to chromate (CrO4²-) ion.
(iii) 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.
33
(a) (i) 1+1+1+1+1= 5
(ii)
OR
( a ) (i) Reimer-Tiemann reaction : Treatment of phenol with CHCl 3 in presence of aqueous NaOH at 340K
followed by hydrolysis gives salicylaldehyde.
( b ) (i) 4-Methoxy benzoic acid < Benzoic acid < 4-Nitrobenzoic acid < 3, 4-Dinitrobenzoic acid.
The order is due to increasing -I effect.
(ii ) By Iodoform test : Acetophenone being a methyl ketone on treatment with I 2/NaOH (NaOI) undergoes
iodoform test to give yellow ppt. of iodoform but benzaldehyde does not.
(iii)