ii-puc-chemistry-passing-package[1]
ii-puc-chemistry-passing-package[1]
ii-puc-chemistry-passing-package[1]
CONTENT
2 SOLUTIONS 4
3 ELECTROCHEMISTRY 5–6
5 SURFACE CHEMISTRY 10
GENERAL PRINCIPLES AND PROCESS OF
6 11 – 12
ISOLATION OF ELEMENTS
7 THE p-BLOCK ELEMENTS 13 – 14
9 COORDINATION COMPOUNDS 16 – 18
14 BIOMOLECULES 25 – 26
15 POLYMERS 26 – 27
3. Calculate the number of particles per unit cell of Body-Centred Cubic (BCC).
The particles are present at eight corners and at body centre.
From each corner, contribution per unit cell is 1 x8=1
8
4. Calculate the number of particles per unit cell of Face-Centred Cubic (FCC).
The particles are present at eight corners and at the centre of six faces.
From each corner, contribution per unit cell is 1 x8=1
8
6. Calculate the packing efficiency in cubic close packed (ccp) / face-centred cubic (fcc)
Let the edge length of the unit cell be ‘a’ and radius of particle be ‘r’.
From Δ ABC
AC2 = AB2 + BC2
b2 = a2 + a2 = 2a2
b = √2𝑎 But, b = 4r
Therefore, 4r = √2 𝑎
4𝑟
a= = 2√2𝑟
√2
Packing efficiency = 74 %
Packing efficiency = 68 %
Page 2
9. Sodium metal crystallises in a BCC structure. Its unit cell edge length is 420 pm.
Calculate its density. (Atomic mass of sodium = 23 𝝁, NA = 6.022x1023 mol-1)
Z X M
d=
𝑁𝐴 X 𝑎3
2 𝑋 23
=
6.022 𝑋 1023 𝑋 (420)3
46
=
6.022 𝑋 1023 (4.20)3 𝑋 10−24
d = 1.031 g 𝑐𝑚−3
Chapter–2: Solutions
2. What is the effect of temperature and pressure on the solubility of gases in liquids?
Solubility of gases in liquids,
✓ Decreases with temperature
✓ Increases with pressure.
4. Give any two differences between Ideal and Non – Ideal solutions.
Chapter–3: Electrochemistry
At Cathode :
1
H+(aq) + e- → H2(g)
2
6. Write the equations of anodic and cathodic reactions occur during rusting of iron.
At Anode :
2Fe (s) → 2Fe2+(aq) + 4e-
At Cathode :
O2(g) + 4H+(aq) + 4e- → 2H2O (l)
7. Write the equations of anodic and cathodic reactions of Hydrogen-Oxygen fuel cell.
At Anode :
2H2(g) + 4OH-(aq) → 4H2O (l) + 4e-
At Cathode:
O2(g) + 2H2O (l) + 4e- → 4OH-(aq)
Order Molecularity
It is the sum of the powers of the concentration It is the number of reacting species involved
terms in the rate law expression. in an elementary reaction.
Experimental quantity Theoretical quantity
3. Derive an integrated rate equation for the rate constant of a zero order reaction.
d[R]
− = K [R]0
dt
d[R] = − K dt (∵ [R]0 = 1)
On integration we get,
Therefore [R]0 = −K x 0 + I
Then I = [R]0
Kt = [R]o – [R]
[R]o – [R]
K =
t
4. Derive an integrated rate equation for the rate constant of a first order reaction.
Consider a first order reaction
R →−−−→ P
d[R]
− = K [R]1
dt
d[R]
= − K dt
[R]
On integration we get,
ln[R]0 = −K x 0 + I
Then I = − ln[R]0
ln [R] = - Kt + ln[R]0
Kt = ln[R]0 – ln[R]
Then, Kt = ln [𝑅]0
[R]
2.303 [𝑅]0
K= log
t [R]
5. Show that for a zero order reaction half -life period is directly proportional to initial
concentration of the reactant.
[R]o – [R]
We know that, K=
t
1
When, t = t1/2 then [R] = [R]0
2
1
[𝑅]0– [𝑅]0 1
[𝑅]0
K= 2 = 2
t1/2 t1/2
[𝑅]0
K= 2 t1/2
OR
[𝑅]0
t1/2 =
2K
6. Show that for a first order reaction half- life is independent of the initial concentration of the
reactant.
[𝑅]0
We know that, K= 2.303 log
t [R]
1
When, t = t1/2 then [R] = [R]0
2
2.303 [𝑅]0
K= 𝑡1/2
log
[𝑅]0/2
K= 2.303 log 2
𝑡1/2
0.693
t1/2 =
K
7. Explain the effect of catalyst on the activation energy of a reaction with graph.
The effect is explained by intermediate complex formation theory.
According to this theory, a catalyst combines with the reactants to form an intermediate complex which
is decomposes to products.
A positive catalyst increases the rate of reaction by providing an alternative pathway with lower activation
energy.
𝗍
↑ without catalyst
Potential with catalyst
Energy Ea Ea
Reactants
Products
→
Reaction coordinate →
2. What are Homogeneous and Heterogeneous catalysis? Give an example for each.
Homogeneous catalysis :
The process in which both reactants and the catalyst are present in the same phase.
𝐻𝐶𝑙(l)
Ex : CH3COOCH3(l) + H2O(l) →−−−−−→ CH3COOH(aq) + CH3OH(aq)
Heterogeneous catalysis :
The process in which the reactants and the catalyst are in different phases.
𝐹𝑒(𝑠)
Ex : N2(g) + 3H2(g) →−−−−−−→ 2NH3(g)
Recrystallized zone
5. Write down the reactions taking place in different zones in the Blast furnace during the
extraction of iron.
Combustion zone :
At the bottom of the furnace carbon burns with hot air gives CO2.
CO2 moves upwards meets more carbon gives carbon monoxide.
C + O2 →−−−→ CO2
C + CO2 →−−→ 2CO
Reduction zone :
At the top of the furnace CO reduces iron oxide to iron
Fe2O3 + 3CO →−−−→ 2Fe + 3CO2
Slag zone :
Limestone decomposed to CaO, which is combined with SiO2 form a slag.
CaCO3 →−−→ CaO + CO2
CaO + SiO2 →−−−→ CaSiO3
6. Draw labelled diagram of Hall – Heroult Electrolytic cell for the extraction of aluminium.
Write anode and cathode reactions.
Purified Al2O3 (bauxite) is mixed with Na3AlF6, which lowers the melting point and increases the
conductivity of the melt.
Anode :
Graphite rod
C(s) + O2-(melt) →−−→ CO (g) + 2e-
C(s) + 2O2-(melt) →−→ CO2(g) + 4e-
Cathode :
Steel vessel with carbon lining
Al3+(melt) + 3e- →−−→ Al
Overall reaction is
2Al2O3 + 3C →−−−→ 4Al + 3CO2
1. For the manufacture of Ammonia by Haber’s process, write the flow chart and chemical
equations with optimum conditions.
N2 and H2 combined in the ratio of 1:3, gives ammonia
N2(g) + 3H2(g) 2NH3(g)
According to Le Chatelier’s principle, the optimum conditions to get a good yield of ammonia are,
Optimum temperature of 700 K
High pressure of 200 atm
In presence of iron oxide as catalyst
2. Write the balanced chemical equations with conditions involved in the manufacture of
Nitric acid by Ostwald’s process.
Ammonia is oxidized by air in the presence of Pt – Rh gauze catalyst at 500 K, gives nitric oxide.
𝑃𝑡 − 𝑅ℎ 𝐶𝑎𝑡𝑎𝑙𝑦𝑠𝑡
4NH3 (g) + 5O2 (g) →−−−−−−−−−−−−−−−→ 4NO (g) + 6H2O (g)
The nitric oxide is oxidised by air, it gives nitrogen dioxide
2NO (g) + O2 (g) →−−−→ 2NO2 (g)
Nitrogen dioxide so formed, dissolves in water it gives nitric acid.
3NO2 (g) + H2O (l) →−−→ 2HNO3 (aq) + NO (g)
NO thus formed is recycled.
3. In the manufacture of sulphuric acid by contact process write reactions and optimum
conditions?
• Burning of sulphur in air gives sulphur dioxide
S + O2 →−−→ SO2
• Sulphur dioxide oxidised to sulphur trioxide with air
𝑉2 𝑂5
2SO2 + O2 →−−−→ 2SO3
According to Le Chatelier’s principle, the optimum conditions to get a good yield of SO3 are,
Optimum temperature of 720 K
High pressure of 2 bar
In presence of V2O5 as catalyst.
• Absorption of SO3 in H2SO4 gives oleum. (Fuming sulphuric acid is called oleum)
SO3 + H2SO4 →−−−→ H2S2O7
• Oleum with water gives sulphuric acid.
H2S2O7 + H2O →−−→ 2H2SO4
6. Give reason : Inter halogen compounds are more reactive than halogens (except fluorine).
This is because X – X1 bond in inter halogens is weaker than X – X bond in halogens except F – F bond.
1. Give reason : The electronic configuration of chromium is [Ar] 3d5 4s1 but not [Ar] 3d4 4s2,
similarly for copper is [Ar] 3d10 4s1 but not [Ar] 3d9 4s2.
This is because, half -filled and completely filled orbitals are more stable.
2. Transition metals and many of their compounds acts as good catalyst. Explain
Most of the transition elements and their compounds are acts as good catalysts.
The catalytic properties is due to,
✓ Variable oxidation states.
✓ Large surface area in the finely divided state.
Ex : Iron is used as a catalyst in Haber’s process.
4. Explain the manufacture of potassium dichromate (K2Cr2O7) from chromite ore (FeCr2O4)
Chromite ore is mixed with soda ash and burnt in excess of air gives sodium chromate.
4FeCr2O4 + 8Na2CO3 + 7O2 8Na2CrO4 + 2Fe2O3 + 8CO2
Sodium chromate is treated with acid gives sodium dichromate.
2Na2CrO4 + 2H+ Na2Cr2O7 + 2Na+ + H2O
Sodium dichromate is treated with potassium chloride gives potassium dichromate.
Na2Cr2O7 + 2KCl K2Cr2O7 + 2NaCl
6. What is Lanthanide contraction? Mention one of its consequence and cause for it.
The gradual decrease in atomic and ionic radii from lanthanum to lutetium is called lanthanide contraction.
Consequence : Almost identical radii of Zr and Hf.
Cause: It is due to imperfect shielding of 4f electrons.
2. Using Valence bond theory account for the geometry and magnetic property of [CoF6]3-.
In [CoF6]3- the cobalt ion is in +3 oxidation state.
For Co3+ the electronic configuration is [Ar] 3d6 4s0
[Ar]
3d 4s 4p 4d
Fluoride is a weak ligand, hence no pairing of electrons takes place in d-orbitals.
Hybridization takes place gives six vacant sp3d2 hybridized orbitals.
Six pairs of electrons, from six fluoride ligands occupy hybrid orbitals.
[Ar]
3d sp3d2
Due to presence of unpaired electrons, the complex is paramagnetic.
It has octahedral geometry.
3. Using Valence bond theory account for the geometry and magnetic property of [Co(NH3)6]3+.
In [Co(NH3)6]3+ the cobalt ion is in +3 oxidation state.
For Co3+ the electronic configuration is [Ar] 3d6 4s0
[Ar]
3d 4s 4p
NH3 is a strong ligand, hence pairing of electrons takes place in d-orbitals.
Hybridization takes place gives six vacant d2sp3 hybridized orbitals.
Six pairs of electrons from six NH3 ligands, occupy hybrid orbitals.
[Ar]
3d d2sp3
Due to absence of unpaired electrons, the complex is diamagnetic.
It has octahedral geometry.
4. Using Valence bond theory account for the geometry and magnetic property of [NiCl4]2-.
In [NiCl4]2- the nickel ion is in +2 oxidation state.
For Ni2+ the electronic configuration is [Ar] 3d8 4s0
[Ar]
3d 4s 4p
Chloride is a weak ligand, hence no pairing of electrons takes place in d-orbitals.
Hybridization takes place gives four vacant sp3 hybridized orbitals.
Four pairs of electrons, from four chloride ligands occupy hybrid orbitals.
[Ar]
3d sp3
Due to presence of unpaired electrons, the complex is paramagnetic.
It has tetrahedral geometry.
5. Using Valence bond theory account for the geometry and magnetic property of [Ni(CN)4]2-.
In [Ni(CN)4]2- the nickel ion is in +2 oxidation state
For Ni2+ the electronic configuration is [Ar] 3d8 4s0
[Ar]
3d 4s 4p
Cyanide is a strong ligand, hence pairing of electrons takes place in d-orbitals.
Hybridization takes place gives four vacant dsp2 hybridized orbitals.
Four pairs of electrons, from four cyanide ligands occupy hybrid orbitals.
[Ar]
3d dsp2 4p
Due to absence of unpaired electrons, the complex is diamagnetic.
It has square planar geometry.
1. Explain SN1 mechanism for the conversion of tertiary butyl bromide to tertiary butyl
alcohol.
When tertiary butyl bromide is heated with aqueous potassium hydroxide, tertiary butyl alcohol is formed.
(CH3)3C-Br + KOH (CH3)3C-OH + KBr
Mechanism :
Step 1: Tertiary butyl bromide undergoes slow ionization gives carbocation.
CH3 CH3
CH3-C-Br CH3-C + + Br -
CH3 CH3
This is a slow step and hence it is a rate determining step.
Step 2: The nucleophile OH- attack carbocation and gives tertiary butyl alcohol.
CH3 CH3
CH3-C + + OH- CH3-C-OH
CH3 CH3
Rate of reaction depends only on concentration of alkyl halide, hence it is a 1st order reaction.
2. Explain SN2 mechanism for the conversion of methyl chloride to methyl alcohol.
When methyl chloride is heated with aqueous potassium hydroxide methyl alcohol is formed.
CH3 -Cl + KOH CH3 -OH + KCl
Mechanism :
The nucleophile OH- attacks the carbon atom from the side opposite to the chlorine.
The formation of C-OH and the cleavage of C-Cl bond takes place simultaneously.
Finally Cl- gets detached to give methyl alcohol.
It involves only one step hence this is the rate determining step.
Rate depends on both concentration of nucleophile and alkyl halide, hence it is a second order reaction.
When aryl halide coupling with alkyl halide in presence of sodium metal in dry ether, gives alkylarene.
This reaction is called Wurtz-Fittig reaction.
Chapter-14: Biomolecules
Glucose
Maltose
Chapter-15: Polymers
6. What are biodegradable and non-biodegradable polymers? Give an example for each.
Polymers which undergo natural break down into raw materials of nature and disappear into nature are
called biodegradable polymers.
Ex : PHBV
Polymers which cannot undergo natural break down or break down over a long period of time are called
non-biodegradable polymers.
Ex : Polythene