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Sheet Boron and Carbon Family JH Sir-4220
Sheet Boron and Carbon Family JH Sir-4220
Contents
Topic Page No.
Theory 01 - 18
Exercise - 1 19 - 27
Exercise - 2 28 - 34
Exercise - 3 35 - 37
Exercise - 4 38 - 39
Answer Key 40 - 46
Syllabus
BORON & CARBON FAMILY
(group 13th to 14th)
Boron: diborane, boric acid and borax; Aluminium: alumina, aluminium chloride
and alums; Carbon: oxides and oxyacid (carbonic acid); Silicon: silicones,
silicates and silicon carbide;
INTRODUCTION :
Group 13 to 18 of the periodic table of elements constitute the p–block. The p–block contains metals,
metalloids as well as non–metals.
The p–block elements have general valence shell electronic configuration ns2 np1–6.
The first member of each group from 13–17 of the p–block elements differ in many respects from the other
members of their respective groups because of small size, high electronegativity and absence of d–orbitals.
The first member of a group also has greater ability to form p–p multiple bonds to itself (e.g. C = C, C C, N
N) and to element of second row (e.g C = O, C = N, C N, N = O) compared to the other members of the same
group.
The highest oxidation state of p–block element is equal to the group number minus 10. Moving down the
group, the oxidation state two less than the highest group oxidation state and becomes more stable in
groups 13 to 16 due to inert pair effect (reluctance of s-subshell electrons to participate in chemical bonding)
GROUP 13 ELEMENTS : THE BORON FAMILY
Boron is a typical non-metal, aluminium is a metal but shows many chemical similarities to boron, and
gallium, indium and thallium are almost exclusively metallic in character,
Electronic Configuration :
The valence shell electronic configuration of these elements is ns2 np1.
Atomic Radii :
On moving down the group, for each successive member one extra shell of electrons is added and therefore,
atomic radius is expected to increase. Atomic radius of Ga is less than that of Al. The presence of additional
10 d-electrons offer only poor screening effect for the outer electrons from the increased nuclear charge in
gallium. Consequently, the atomic radius of gallium (135 pm) is less than that of aluminium (143 pm).
Ionization Enthalpy :
The ionisation enthalpy values do not decrease smoothly down the group. The decreases from B to Al is
associated with increases in size. The observed discontinuity in the ionisation enthalpy values between Al
and Ga and between In and TI are due to the non-availability of d- and f-electrons, which have low screening
effect, to compensate the increase in nuclear charge. The sum of the first three ionisation enthalpies for each
of the elements is very high .
Electronegativity :
Down the group, electronegativity first decreases from B to Al and then increases marginally. This is because
of the discrepancies in atomic size of the elements.
Physical Properties :
Boron is non-metallic in nature . It is extremely hard and black coloured solid. It exists in many allotropic
forms. Due to very strong crystalline lattice, boron has unusually high melting point. Rest of the member are
soft metals with low melting point and high electrical conductivity. Gallium with low melting point (303 K),
could exist in liquid state during summer. Its high boiling point (2676 K) makes it a useful material for
measuring high temperatures. Density of the elements increases down the group from boron to thallium.
Atomic and physical properties :
Elem ent B Al Ga In Tl
Atom ic Num be r 5 13 31 49 81
Atom ic M ass 10.81 26.98 69.72 114.82 204.38
Ele ctronic configuration [He] 2s 2 2p 1 [Ne] 3s 2 3p 1 [Ar] 3d 10 4s 24p 1 [Kr] 4d10 5s 2 5p1 [Xe] 4f14 5d 10 6s 26p1
Atom ic Ra dius / pm 85 143 135 167 170
Ionic Ra dius M 3+ / pm 27 53.5 62 80 88.5
i H1 801 577 579 558 589
Ioniza tion e ntha lpy
i H2 2427 1816 1979 1820 1971
(kJ m ol –1)
i H3 3659 2744 2962 2704 2877
Ele ctrone ga tivity 2.0 1.5 1.6 1.7 1.8
Density/[g cm –3 ( a t 293 K)] 2.35 2.70 5.90 7.31 11.85
Me lting point / K 2453 933 303 430 576
Boiling point / K 3923 2740 2676 2353 1730
2Al(s) + 2NaOH (aq) + 6H2O () 2Na+ [Al(OH)4]– (aq) + 3H2(g)
Sodium tetrahydroxoaluminate (III)
Al(OH)3 is amphoteric and reacts principally as a base. However, Al(OH)3 shows some acidic properties
when it dissolves in NaOH forming aluminate. The Al(OH)3 is reprecipitated by the addition of CO2, showing
that the acidic properties are very weak.
CO2 + H2O H2CO3 CO32– + 2H+ ; 2Al3+ + 3CO32– + 3H2O 2Al(OH)3 + 3CO2
In concentrated solutions above 1.5 M and pH greater than 13, it exists as dimer [(OH)3Al—O—Al(OH)3]2–.
Aluminates are important constituents of portland cement.
Ga2O3 and Ga(OH)3 are both amphoteric compounds. Tl2O3 and ln2O3 are completely basic and form neither
hydrates nor hydroxides.
(iii) Reactivity towards halogens :
These elements react with halogen to form trihalides (except Tl I3 )..
2E(s) + 3X2 (g) 2EX3 (s) (X = F, Cl Br, I)
Properties :
(i) It exists in five forms, four of which are crystalline and one is amorphous. All crystalline forms are very
hard made up of clusters of B12 units. All crystalline forms are black in appearance and chemically
inert. However, it is attacked at high temperature by strong oxidising agents such as a mixture of
hot concentrated H2SO4 and HNO3 or Na2O2. But amorphous form is brown and chemically
active.
(ii) Reaction with air : Burns in air or oxygen forming B2O3.
4B + 3O2 2B2O3
Also burns in nitrogen at white heat.
High temperatur e, pressure
2B + N2 2BN ; BN + 3H2O H3BO3 + NH3
(iii) Action of alkalies and acids :
2B + 2NaOH + 2H2O 2NaBO2 + 3H2
fused
2B + 6NaOH
2Na3BO3 + 3H2
Properties :
It is a acidic oxide and is anhydride of boric acid and it reacts with alkalies or bases to form borates.
3Na2O + B2O3 2Na3BO3 (sodium orthoborate).
It reacts with water slowly to form orthoboric acid.
H2O + B2O3 2HBO2 ; HBO2 + H2O H3BO3
When heated with transition metal salts, it forms coloured compounds.
3B2O3 + Cr2(SO4)3
3SO3 + 2Cr(BO2)3(green)
2B2O3 + 2Cu(NO3)2 4NO2 + O2 + 2Cu(BO2)2 (blue)
ORTHOBORIC ACID (H3BO3) :
Preparation :
(i) It is precipitated by treating a concentrated solution of borax with sulphuric acid.
Na2B4O7 + H2SO4 + 5H2O Na2SO4 + 4H3BO3
(ii) From Colemanite: Powdered colemanite is suspended in water and excess SO2 is passed through it.
On filtering and cooling the filtrate, white crystals of H3BO3 are obtained.
Ca2B6O11 + 4SO2 + 11H2O 2Ca(HSO3)2 + 6H3 BO3
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Properties:
It is a weak monobasic acid soluble in water and in aqueous solution the boron atom completes its octet by
accepting OH– from water molecules:
B(OH)3(aq) + 2H2O() [B(OH)4]– (aq) + H3O+(aq). pK = 9.25.
It, therefore, functions as a Lewis acid and not as a proton donor like most acids.
Since B(OH)3 only partially reacts with water to form H3O + and [B(OH)4]–, it behaves as a weak acid. Thus
H3BO3 can not be titrated satisfactorily with NaOH as a sharp end point is not obtained. If certain organic
polyhydroxy compounds such as glycerol, mannitol or sugars are added to the titration mixture, then B(OH)3
behaves as a strong monobasic acid and it can be now titrated with NaOH and the end point is detected
using phenolphthalein as indicator (pH = 8.3 - 10.0).
The added compound must be a cis-diol, to enhance the acid properties. The cis-diol forms very stable
complex with the [B(OH)4]–, thus removing it from solution. The reaction is reversible and thus removal of one
of the products shifts the equilibrium in the forward direction and thus all the B(OH)3 reacts with NaOH; in
effect it acts as a strong acid in the presence of the cis-diol.
B(OH)3 + NaOH Na[B(OH)4] + NaBO2 + 2H2O
HB(OH)4 + 2 + H+ + 4H2O
Ethanol does not form similar complex but catechol, salicylic acids, mannitol form similar complexes.
When heated it first forms metaboric acid (HBO2) and then boron trioxide.
Orthoboric acid is greasy to touch less soluble in cold water but more soluble in hot water. In the solid state,
the B(OH)3 units are hydrogen bonded together in to two dimensional sheets with almost hexagonal symmetry.
The layered are quite a large distance apart (3.18 Å) and thus the crystal breaks quite easily into very fine
particles.
Properties :
(i) Borax is a white powder, less soluble in cold water, more soluble in hot water.
(ii) Its aqueous solution is alkaline because of its hydrolysis to weak acid H3BO3 and strong alkali NaOH.
Na2B4O7 + 7H2O 4H3BO3 + 2NaOH
(iii) Action of heat.
When borax powder is heated, it first swells due to loss of water in the form of steam but at 740oC it becomes
converted into colourless transparent borax bead.
Na2B4O7.10H2O Na2B4O7 + 10 H2O
740 º C
Na2B4O7 2NaBO2 + B2O3 (borax bead)
(iv) Oxidation of boric acid or sodium metaborate with H2O2.
Na2B4O7 2NaBO2 + 2H2O2 + 6H2O Na2 [(OH)2B (O—O)2B(OH)2].6H2O
Sodium per oxoborate is used as a brightner in washing powder. In very hot water (over 80ºC) the peroxide
linkages —O—O— break down to give H2O2.
(v) It is a useful primary standard for titrating against acids. One mole of it reacts with two moles of acid. This is
because when borax is dissolved in water both B(OH)3 and [B(OH)4]– are formed, but only the [B(OH)4]–
reacts with HCl.
[B4O5(OH)4]2– + 5H2O 2B(OH)3 (weak acid) + 2[B(OH)4]– (salt)
2[B(OH)4]2– + 2H3O+ 2B(OH)3 + 4H2O
On cooling, the white flakes of boric acid are obtained
Borax is also used as a buffer since its aqueous solution contain equal amounts of week acid and its salt.
Borax-bead test :
Borax reacts with certain metal salts such as, Ni2+, Co2+, Cr3+, Cu2+, Mn2+ etc. to form coloured metaborates.
The colour of the metaborates can be used to identify the metallic ions (cations) in salts.
740 º C
Na2B4O7·10H2O
10H2O
Na2B4O7 2NaBO 2 B 2O 3 ; CuO + B2O3 Cu(BO2)2 (blue bead)
glassy mass
Uses : It is used
1. in borax bead test, 2. in purifying gold, 3. as flux during welding of metals and 4. in production of glass.
DIBORANE (B2H6) :
Binary compounds of B with H are called boron hydrides or boranes. These compounds form following two
types of series :
BnHn+4 - B2H6, B5H9, B6H10, B10H14
BnHn+6 - B4H10, B5H11, B6H12, B9H15
The chemistry of diborane has aroused considerable interest because of its usefulness in many synthetic
reactions and also because the elucidation of its structure helped to clarify the basic concepts about the
structure of electron deficient compounds.
453 K
(iv) 2BF3 + 6NaH B2H6 + 6NaF (Industrial method)
Properties :
(i) B2H6 is colourless gas and highly reactive (boiling point 183 K).
(ii) Controlled pyrolysis of diborane leads to most of the higher boranes.
It catches fire spontaneously in air and explodes with O2. Reaction with oxygen is extremely
exothermic.
B2H6 + 3O2 B2O3 + 3H2O H = – 2160 kJ mol–1
Mixtures of diborane with air or oxygen inflame spontaneously producing large amount of heat. Diborane has
a
higher heat of combustion per unit weight of fuel than most other fuels. It is therefore used as a rocket fuel.
At red-heat the boranes decomposes to boron and hydrogen.
(iii) Reaction with water is instantaneous.
B2H6 + 6H2O 2B(OH)3 + 6H2
Dibroane is also hydrolysed by weaker acids (e.g. alcohols) or aqueous alkali.
B2H6 + 6ROH 2B(OR)3 + 6H2
B2H6 + 2KOH + 2H2O 2KBO2 + 6H2
Ratio 2NH : 1 B H
3 2
6 B3N3H6 borazine.
higher temperatur e ( 200 ºC)
Borazine is much more reactive than benzene. Borazine readily undergoes addition reactions which do not
occur with benzene. Borazine also decomposes slowly and may be hydrolysed to NH3 and boric acid at
elevated temperature. If heated with water, B3N3H6 hydrolyses slowly.
B3N3H6 + 9H2O 3NH3 + 3H3BO3 + 3H2O
COMPOUNDS OF ALUMINIUM :
ALUMINIUM OXIDE (Al2O3) :
It is also called alumina. It occurs in nature in the form of bauxite and corundum. It is also found in the form
of gems. Some important aluminium oxide gems are :
(A) Oriental Topaz-yellow (Fe3+), (B) Sapphire-blue (Fe2+ / 3+ / Ti4+),
3+
(C) Ruby-red (Cr ), (D) Oriental Emerald-green (Cr3+ / V3+)
Preparation :
Pure Al2O3 is obtained by igniting Al2(SO4)3, Al(OH)3 or ammonium alum.
Al2(SO4)3 Al2O3 + 3SO3 ; 2Al(OH)3 Al2O3 + 3H2O
Properties :
It is a white amorphous powder insoluble in water but soluble in acids (forming eg., AlCl3) as well as alkalies
(forming e.g., NaAlO2), Thus amphoteric in nature. It is a polar covalent compound. Exists in two forms -
Al2O3 or corundum and -Al2O3.
Addition of Cr2O3 or Fe2O3 makes alumina coloured.
1000 º C
-Al2O3 -Al2O3
Uses :
1. It is used for the extraction of aluminium.
2. It is used for making artificial gems.
3. -Al2O3 is used in making furnace linings. It is a refractory material.
4. Corundum is extremely hard and is used as ‘Jewellers rouge’ to polish glass.
ALUMINIUM CHLORIDE (AlCl3.6H2O) :
It is a colourless crystalline solid, soluble in water. It is covalent. Anhydrous AlCl3 is a deliquescent white solid.
Preparation :
(i) By dissolving aluminium, Al2O3, or Al(OH)3 in dilute HCl :
2Al + 6HCl 2AlCl3 + 3H2 Al2O3 + 6HCl 2AlCl3 + 3H2O; Al(OH)3 + 3HCl AlCl3 + 3H2O
The solution obtained is filtered and crystallized when the crystals of AlCl3.6H2O are obtained.
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(ii) Anhydrous AlCl3 is obtained by the action of Cl2 on heated aluminium.
(iii) By heating a mixture of Al2O3 and coke and passing chlorine over it.
Al2O3 + 3C + 3Cl2 2AlCl3 (anhydrous) + 3CO
Properties :
(i) Action of heat : Hydrated salt when heated strongly is converted to Al2O3.
2AlCl3.6H2O Al2O3 + 6HCl + 3H2O
(ii) Action of moisture on anhydrous AlCl3 : When exposed to air, anhydrous AlCl3 produces white fumes of HCl
AlCl3 + 3H2O Al(OH)3 + 3HCl
(iii) Action of NH3 : Anhydrous AlCl3 absorbs NH3 since the former is a Lewis acid.
AlCl3 + 6NH3 AlCl3.6NH3 (white solid)
(iv) Action of NaOH solution : When NaOH solution is added dropwise to an aqueous AlCl3 solution, a gelatinous
precipitate of Al(OH)3 is first formed which dissolves in excess of NaOH solution to give a colourless solution
of sodium meta-aluminate.
AlCl3 + 3NaOH Al(OH)3 + 3NaCl ; Al(OH)3 + NaOH NaAlO2 + 2H2O
This reaction is important as a test to distinguish between an aluminium salt from salts of Mg, Ca, Sr, and
Ba. (When NaOH solution is added to their salt solutions, a white precipitate of hydroxide forms which does
not dissolve in excess of NaOH).
(v) Action of NH4OH solution : When NH4OH solution is added to a solution of AlCl3, a white precipitate of
Al(OH)3 is formed which does not dissolve in excess of NH4OH.
AlCl3 + 3NH4OH Al(OH)3 (white gelatinous) + 3NH4Cl
This reaction is important as a test to distinguish an Al salt from a Zn salt. (With a Zn salt a white precipitate
of Zn(OH)2 is formed which dissolves in excess of NH4OH solution).
(vi) Hydrolysis with water : When AlCl3 is dissolved in water, it undergoes hydrolysis rapidly to produce Al(OH)3
which is a weak base and HCl which is a strong acid. Hence the solution is acidic to litmus.
[Al(H2O)6]3+ [Al(H2O)5OH]+2 + H+
The complex cation has a high tendency to get dimerised.
(iii) Ferric alum K2SO4 . Fe2(SO4)3. 24H2O (iv) Ammonium alum (NH4)2SO4 . Al2(SO4)3 . 24H2O
Alums are double salts which when dissolved in water produce metal ions (or ammonium ions) and the
sulphate ions.
Preparation :
A mixture containing solutions of M2SO4 and M’2(SO4)3 in 1 : 1 molar ratio is fused & then the resulting mass
is dissolved into water. From the solution thus obtained, alums are crystallised.
Uses : It is used
1. As a mordant in dye industry. The fabric which is to be dyed is dipped in a solution of the alum and
heated with steam. Al(OH)3 obtained as hydrolysis product of [Al(H2O)6]3+ deposits into the fibres and
then the dye is absorbed on Al(OH)3.
2. as a germicide for water purification
3. As a coagulating agent for precipitating colloidal impurities from water.
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GROUP 14 ELEMENTS : THE CARBON FAMILY
Carbon (C), silicon (Si), germanium (Ge), tin (Sn) and lead (Pb) are the members of group 14. Naturally
occurring carbon contains two stable isotopes: 12C and 13C. In addition to these third isotopes, 14C is also
presents , it is a radioactive isotope with half-life 5770 years and used for radiocarbon dating. Silicon is a
very important component of ceramics, glass and cement. Germanium exists only in traces. Tin occurs
mainly as cassiterite, SnO2 and lead as galena, PbS. Ultrapure form of germanium and silicon are used to
make transistors and semiconductor devices.
Electronic Configuration
The valence shell electronic configuration of these elements is ns2 np2.
Covalent Radius
There is a considerable increase in covalent radius from C to Si, thereafter from Si to Pb a small increase in
radius is observed. This is due to the presence of completely filled d and f orbitals in heavier members.
Ionization Enthalpy
The first ionization enthalpy of group 14 members is higher than the corresponding members of group 13.
The influence of inner core electron is visible here also. In general the ionisation enthalpy decreases down
the group. Small decreases in iH from Si to Ge to Sn and slight increase in iH from Sn to Pb is the
consequence of poor shielding effects of intervening d and f–orbitals and increase in size of the atom.
Electronegativity
Due to small size, the elements of this group are slightly more electronegative than group 13 elements. The
electronegativity value for elements from Si to Pb are almost the same. Carbon has higher electronegativity
as compared to other elements of the group. As a result it can accept electrons and can form negative ions
of type C22– in acetylides and C4– in methanides.
Physical Properties
All group 14 members are solids. Carbon and silicon are non-metals, germanium is metalloid whereas tin
and lead are soft metals with low melting points. Melting points and boiling points of group 14 elements are
much higher than those of corresponding elements of group 13 due to stronger metallic bonding.
Atomic and physical properties
Element C Si Ge Sn Pb
Atomic Number 6 14 32 50 82
Electronic configuration [He] 2s 2 2p2 [Ne] 3s 2 3p2 [Ar] 3d10 4s 2 4p2 [Kr] 4d10 5s 2 5p2 [Xe] 4f14 5d10 6s 2 6p2
Ionic Radius M +4 / pm – 40 53 69 78
Ionization enthalpy
I H2 2352 1577 1537 1411 1450
(kJ mol–1)
Diamond is unaffected by concentrated acids but graphite changes to Mellitic acid also called benzene
hexa-carboxylic acid with hot concentrated HNO3 and to graphite oxide with a hot concentrated HF/HNO3.
(Mellitic acid)
Si, Ge and Sn also have a diamond type of structure. Ge liquid expands when it forms the solid. This property
is unique to Ga, Ge and Bi.
-Sn -Sn
grey tin white tin
(Diamond structure) (Metallic)
OXIDES OF CARBON :
CARBON MONOXIDE (CO) :
Preparation :
(i) It is formed together with CO2, when carbon or carbonaceous matter is oxidized by air or oxygen. It is also
produced when CO2 is reduced by red- hot carbon; this reaction is of importance in metal extractions.
C(s) + CO2(g) 2CO(g)
(ii) In the laboratory it can be prepared by dehydrating methanoic acid with concentrated sulphuric acid .
373 K
HCOOH (liq) CO(g) + H2O
conc.H2SO 4
(iii) If oxalic acid is dehydrated in the same way, CO2 is formed as well.
conc. H SO ,
H2C2O4 2
4
CO + CO2
–H2O
(iv) On commercial scale it is prepared by the passage of steam over hot coke. The mixture of CO and H2 thus
produced is known as water gas or synthesis gas.
4731273 K
C (s) + H2O (g) CO (g) + H2(g) (water gas).
When air is used instead of steam, a mixture of CO and N2 is produced, which is called producer gas.
1273 K
2 C (s) + O2 (g) + 4 N2 (g) 2 CO (g) + 4 N2 (g) (Producer gas).
Water gas and producer gas are very important industrial fuels. Carbon monoxide in water gas or producer
gas can undergo further combustion forming carbon dioxide with the liberation of heat.
(v) K4Fe(CN)6 + 6H2SO4 (concentrated) + 6H2O 2K2SO4 + FeSO4 + 3(NH4)2SO4 + 6CO
Properties :
(i) Carbon monoxide is a colourless, odourless gas which burns in air with a blue flame, forming CO2. It is
sparingly soluble in water and is a neutral oxide. CO is toxic, because it forms a complex with haemoglobin
in the blood and this complex is more stable than oxy-haemoglobin. This prevents the haemoglobin in the red
blood corpuscles from carrying oxygen round the body. This causes oxygen deficiency, leading to
unconsciousness and then death.
Hb—O2 + CO Hb—CO + O2
Ordinary gas masks are no protection against the gas, since it is not readily adsorbed on active charcoal. In
the presence of air, a mixture of manganese (IV) oxide and copper(II) oxide catalytically oxidizes it to CO2,
and this mixed catalyst is used in the breathing apparatus worn by rescue teams in mine disasters.
(ii) Carbon monoxide is a powerful reducing agent, being employed industrially in the extraction of iron and
nickel . Fe2O3(s) + 3CO(g) 2Fe(s) + 2CO2(g) ; NiO(s) + CO(g) Ni(s) + CO2(g)
(iii) CO is readily absorbed by an ammonical solution of copper (I) chloride to give CuCl.CO.2H2O. It reduces an
ammonical solution of silver nitrate to silver (black) and, in the absence of other gaseous reducing agents,
this serves as a test for the gas. It can be estimated by reaction with iodine pentoxide, the iodine which is
produced quantitatively being titrated with standard sodium thiosulphate solution.
5CO(g) + 2O5(s) 2(s) + 5CO2(g)
H2CO3 / HCO3– buffer system helps to maintain pH of blood between 7.26 to 7.42.
A solution of carbonic acid in water will slowly turn blue litmus red and when the solution is boiled, all the
CO2 is evolved.
(iv) Carbon dioxide, which is normally present to the extent of ~ 0.03% by volume in the atmosphere, is removed
from it by the process known as photosynthesis. It is the process by which green plants convert atmospheric
CO2 into carbohydrates such as glucose. The overall chemical change can be expressed as :
hv
6 CO2 + 12 H2O C6H12O6 + 6 O2 + 6 H2O
Chlorphyll
By this process plants make food for themselves as well as for animals and human beings. But the increase
in combustion of fossil fuels and decomposition of limestone for cement manufacture in recent years seem
to increase the CO2 content of the atmosphere. This may lead to increase in green house effect and thus,
raise the temperature of the atmosphere which might have serious consequences.
(v) Gaseous CO2 is extensively used to carbonate soft drinks. Being heavy and non–supporter of combustion it
is used as fire extinguisher. A substantial amount of CO2 is used to manufacture urea.
CARBIDES :
The binary compounds of carbon with other elements (less electronegative or of similar electronegativity) are
called carbides. They are classified into following 3 categories :
(i) Ionic (ii) Covalent (iii) Interstitial (or metallic)
(i) Ionic carbides (or salt like carbides) : Generally formed by the most electropositive elements such as
alkali and alkaline earth metals and aluminium (Boron is exception). Based on the product obtained on
hydrolysis, they are further sub-classified into three types.
(a) Methanides : These give CH4 on reaction with H2O.
Al4C3 + 12H2O 4Al (OH)3 + 3CH4 ; Be2C + 4H2O 2Be (OH)2 + CH4
These carbides contain C4– ions in their constitution.
(b) Acetylides : These give C2H2 on reaction with H2O.
CaC2 + 2H2O Ca (OH)2 + C2H2 ; Al2 (C2)3 + 6H2O 2Al (OH)3 + 3C2H2
SrC2 + 2H2O Sr (OH)2 + C2H2
Such compounds contain C22– [: C C :]2 ions.
(c) Allylides : These give 1-propyne on reaction with H2O.
Mg2C3 + 4H2O 2Mg (OH)2 + CH3– C CH
..
4
Such compounds contain C34– [: C – C C :] ions.
..
It suggests that the coordination number of silicon must be 4 and from VBT point of view we can say that Si
is sp3 hybridized. Therefore silicate structures must be based upon SiO44– tetrahedral units.
(iii) SiO44– tetrahedral units may exist as discrete units or may polymerise into larger units by sharing corners.
(B) Pyrosilicate :
In these silicates two tetrahedral units are joined by sharing oxygen at
one
6–
corner thereby giving [Si2O7] units.
(–) charge will be present on the oxygen atoms which is bonded with one Si atom.
(C) Cyclic silicates :
If two oxygen atoms per tetrahedron are shared to form closed rings such that the structure with general
formula (SiO32–)n or (SiO3)n2n– is obtained, the silicates containing these anions are called cyclic silicates.
Si3O96– and Si6O1812– anions are the typical examples of cyclic silicates.
O
–
O
–
–
O O
O
–
O
–
O O
O– O–
O
–
O O O O
O O
– –
O– O
–
–
O
–
O O –
O O O O
–
O–
6–
–
O 12–
Si3O9 Si6O18
Similarly, double chain silicates can be drawn in which two simple chains are joined together by shared
oxygen. Such compounds are also known as amphiboles. The asbestos mineral is a well known example of
double chain silicates. The anions of double chain silicates have general formula (Si4O11)n6n
O– O–
O– O–
O O
O O O O O
O– O– O–
O O O
O– O
–
O
–
O O O O O O
O– O––
– –
O O
In this manner several molecules may combine to form a long chain polymer whose both the ends will be
occupied by –OH groups. Such compounds are generally represented from the following formula.
The polymer chain depicted above is terminated by incorporating a small quantity of the monochlorosilane
derivative into the hydrolysis mixture.
Silicones can be prepared from the following types of compounds only.
(i) R3SiCl (ii) R2SiCl2 (iii) RSiCl3
Silicones from the hydrolysis of (CH3)3 SiCl
H2O
(CH3)3 SiCl (CH3)3 Si (OH)
Silicones from the hydrolysis of a mixture of (CH3)3 SiCl & (CH3)2 SiCl2
The dichloro derivative will form a long chain polymer as usual. But the growth of this polymer can be blocked
at any stage by the hydrolysis product of mono-chloro derivative.
The hydrocarbon layer along the silicon-oxygen chain makes silicones water-repellent.
Silicones find a variety of applications because of their chemical inertness, water repelling nature, heat
resistance and good electrical insulation property.
Products having the physical properties of oils, rubbers and resins can be produced using silicones. Silicone
varnishes are such excellent insulators and so heat-resistance that insulating wiring with them enabled
motors to work over-loads that would have set fire to the insulation formerly used. Silicone fluids are used as
hydraulic systems of planes as they are thermally stable and their viscosity alters very little with temperature.
Silicone rubbers are used in placed of ordinary rubber as they retain their elasticity at much lower temperature
than ordinary rubber.
COMPOUNDS OF TIN :
STANNOUS OXIDE (SnO) :
Preparation :
By heating stannous hydroxide, Sn(OH)2, in absence of air.
Sn(OH)2 SnO + H2O
Properties :
SnO is an amphoteric dark grey or black solid oxide, insoluble in water. It dissolves in acids to form
stannous salts.
SnO (basic) + 2H+ Sn2+ + H2O ;
SnO (acidic) + 4OH– + H2O [Sn(OH)6]4– or SnO22– (stannite)
Stannites are only known in aqueous solutions.
(ii) PbO2 is an oxidising agent and reduced to PbO since stability of Pb(II) > Pb(IV) based on inert pair effect.
(a) It oxidizes HCl to Cl2.
PbO2 + 4HCl PbCl2 + 2H2O + Cl2
Preparation :
It is prepared by heating PbO at 450oC for a long time.
450ºC
6PbO + O2 2Pb3O4
Properties :
(i) It is a red powder insoluble in water but when heated with concentrated HNO3 it gives a red precipitate of
PbO2.
Pb3O4 + 4HNO3 2Pb(NO3)2 + PbO2 + 6H2O
Uses : It is used as an oxidizing agent, for making metal protecting paints like red oxide paint, for making
special lead cement and for making flint glass.
Preparation:
Pb(OH)2·PbCO3 (basic lead carbonate) + 4HCl 2PbCl2 + CO2 + 3H2O
Properties :
It is a white crystalline solid, insoluble in cold water but soluble in boiling water. It dissolves in concentrated
HCl forming a complex ion.
2 HCl + PbCl2 H2PbCl4 (chloroplumbous acid)
Group 13th
1. The decrease in stability of higher oxidation state in p–block with increasing atomic number is due to :
(A) increase in bond energy as going down the group.
(B) the reluctance of s-sub shell electrons to participate in the chemical bonding.
(C) both are correct.
(D) none is correct.
2.* Which of the following facts regarding boron and silicon is true ?
(A) Boron is used to make boron steel or boron carbide control rods for nuclear reactor.
(B) Boron and silicon form halides which are not hydrolysed.
(C) Boron and silicon react with magnesium to form magnesium boride and magnesium silicide which are
decomposed by acids to give volatile borane and silane, respectively.
(D) Both boron and silicon react with alkali to form borates and silicates containing BO33– and SiO44– tetrahedral
units, respectively.
9. Borax is:
(A) Na2B4O7 (B) Na2B4O7.4H2O (C) Na2B4O7.7H2O (D) Na2B4O7.10H2O
17. The product obtained in the reaction of diborane with excess of ammonia at low temperature is :
(A) B2H6. NH3 (B) B2H6. 2NH3 (C) (BN)x (D) Borazine
21. Aluminium is more reactive than iron. But aluminium is less easily corroded than iron because:
(A) aluminium is a noble metal
(B) oxygen forms a protective oxide layer on aluminium surface
(C) iron unergoes reaction easily with water
(D) iron forms both mono and divalent ions
24. Alum is found to contain hydrated monovalent cation [M(H2O)6]+ , trivalent cation [M(H2O)6]3+ and SO42– in
the ratio of :
(A) 1 : 1 : 1 (B) 1 : 2 : 3 (C) 1 : 3 : 2 (D) 1 : 1 : 2
34. Which of the following statements about anhydrous aluminium chloride is correct ?
(A) It exists as AlCl3 molecule (B) It is not easily hydrolysed
(C) It sublimes at 100ºC under vacuum (D) It is a strong Lewis base
35. Aqueous ammonia is used as a precipitating reagent for Al3+ ions as Al(OH)3 rather than aqueous NaOH,
because :
(A) N H4 is a weak base (B) NaOH is a very strong base
(C) NaOH forms [Al(OH)4]- ions (D) NaOH forms [Al(OH)2]+ ions
37. Aluminium vessels should not be washed with materials containing washing soda because :
(A) washing soda is expensive
(B) washing soda is easily decomposed
(C) washing soda reacts with aluminium to form soluble aluminate
(D) washing soda reacts with aluminium to form insoluble aluminium oxide
Group 14th
38. Diamond and graphite are :
(A) isomers (B) isotopes (C) allotropes (D) none of the above
46.* The carbide which does/do not give propyne on hydrolysis is/are :
(A) Al4C3 (B) CaC2 (C) Fe3C (D) Mg2C3
51. CCl4 is inert towards hydrolysis but SiCl4 is readily hydrolysed because
(A) carbon cannot expand its octet but silicon can expand its octet
(B) ionisation potential of carbon is higher than silicon
(C) carbon forms double and triple bonds
(D) electronegativity of carbon is higher than that of silicon
52. A colourless gas which burns with blue flame and reduces CuO to Cu is :
(A) N2 (B) CO (C) CO2 (D) NO2
54. Which of the following compound is obtained on heating potassium ferrocyanide with concentrated H2SO4?
(A) CO2 (B) CO (C) C2H2 (D) (CN)2
60. The hydroxide of which metal ion is soluble in excess of sodium hydroxide solution :
(A) Fe3+ (B) Cr3+ (C) Sn2+ (D) Cu2+
61. Unlike PbCl4, P4 and PBr4 are not found because :
(A) bromine and iodine are more electronegative than chlorine.
(B) iodine and bromine are smaller in size.
(C) larger iodine and bromine are able to reduce Pb4+ to Pb2+ or Pb.
(D) the statement is incorrect.
62. Water transported through lead pipes becomes poisonous due to the formation of :
(A) Pb (OH)2 (B) PbO (C) PbO2 (D) Pb3O4
63. Which of the following halides is least stable and has doubtful existence? [JEE 1996, 1]
(A) C4 (B) Ge4 (C) Sn4 (D) Pb4
H O condensati on
64. Me2SiCl2 2
(A) (B).
The nature of product (B) may be
(A) only linear polymers (B) cyclic products
(C) (A) and (B) both (D) none of these
66. Which of the following anions is present in the simple single chain structure of silicate?
(A) SiO44– (B) Si2O76– (C) (Si2O52–)n (D) (SiO32–)n
68. Which silicon compound is used in machinery (with moving parts) in a manner similar to the use of an
allotrope of carbon (crystalline) which possesses properties of both a covalent network solid and a molecular
solid ?
(A) Silica gel (B) Zeolite (C) Silicone (D) Asbestos
2. Boron resembles more with ................. than its own family members.
3. Among the metals Na, Mg and Al, the metal with highest melting point is .................
4. Hydrogen gas is liberated by the action of aluminium with concentrated solution of .................
14. An alloy of copper which has beautiful golden yellow colour is called ................
Group 14th
15. Carbon exhibits the unique property of forming chains of identical atoms, called __________.
17. A mixture of __________ and CO2 is obtained when oxalic acid is heated with conc. H2SO4 .
20. Carbon monoxide is poisonous because it combines with _____ and the product becomes incapable of
absorbing ________.
22. Carbon monoxide forms a volatile coordination compound with nickel, it is __________.
27. The formula of litharge is _________ and that of red lead is _________ both are used as ________ in
paints.
28. In drinking soda __________ gas is present under high pressure in water.
29. The C–C bond length in diamond is _________ while the C–C bond length in graphite is __________.
30. Carbon monoxide is absorbed in a solution of _______ under pressure while carbon dioxide is absorbed
in a solution of ––––––––.
32. Carbon monoxide combines with chlorine in the presence of sunlight to produce __________.
38. Borax forms orthoboric acid when warmed with conc. sulphuric acid.
41. Boron compounds are covalent while aluminium compounds are electrovalent or covalent.
Group 14th
44. Silicon forms lesser number of hydrides than carbon.
48. Anhydrous tin () chlorine can be obtained by passing dry chlorine gas over heated tin.
54. White lead has high covering power when it is used as a paint.
55. Tin exists in three allotropic forms, white tin, grey tin and brittle tin.
63. Assertion : AlCl3 forms dimer Al2Cl6 but it dissolves in H2O forming [Al(H2O)6]3+ and Cl– ions.
Reason : Aqueous solution of AlCl3 is acidic due to hydrolysis.
Group 14th
64. Assertion : Si–Si bonds are much weaker then Si–O bonds.
Reason : Silicon forms double bonds with itself.
(t) Hydrolysis
Group 14th
71. Column I Column II
(a) Asbestos (i) Oxygen
(b) Silicones (ii) Allylides
(c) Red lead (iii) PbCl4
on
(D) SnCl2.2H2O
s tan ding
(s) complex crosslinked polymer
5. Water softener is :
(A) Borax (B) Zeolite (C) Both (A) and (B) (D) None of these
Group 14th
H O condensati on
9. Me2SiCl2 2
(A) (B).
The nature of product (B) may be
(A) only linear polymers (B) cyclic products
(C) (A) and (B) both (D) none of these
12. CCl4 is inert towards hydrolysis but SiCl4 is readily hydrolysed because
(A) carbon cannot expand its octet but silicon can expand its octet
(B) ionisation potential of carbon is higher than silicon
(C) carbon forms double and triple bonds
(D) electronegativity of carbon is higher than that of silicon
14. CO is absorbed by
(A) CHCl3 (B) pyrogallol
(C) CCl4 (D) ammonical solution of copper (I) chloride
20. Identify the statement that is/are correct as far as structure of diborane is concerned:
(A) There are two bridging hydrogen atoms in diborane
(B) Each boron atom forms four bonds in diborane
(C) The hydrogen atoms are not in the same plane in diborane
(D) All B-H bonds in diborane are similar
10. Which of the following statements about anhydrous aluminium chloride is/are incorrect:
(A) It exists as AlCl3 molecule (B) It is a strong Lewis base
(C) It sublims at 100oC under vacuum (D) It is not easily hydrolysed
Group 14th
11. Select the correct statement(s) .
(A) The graphite is diamagnetic and diamond is paramagnetic in nature.
(B) Graphite acts as a metallic conductor along the layers of carbon atoms and as semi-conductor
perpendicular to the layers of the carbon atoms.
(C) Graphite is less denser than diamond
(D) C60 is called as Buckminster fullerence
15. Which of the following statement(s) is/are false for soluble bicarbonates?
(A) They give pink colour with phenolphthalein
(B) They do not liberate carbondioxide with phenol.
(C) They give white precipitate with magnesium sulphate in cold.
(D) They liberate carbondioxide on reaction with dil. H2SO4
Group 13th
1. Explain why aluminium, though an electropositive metal, finds extensive use as a structural material
4. What happens when NaOH (aq) is added drop wise to a solution of GaCl3 in water ?
10. Bring out points of similarity and dissimilarity between boron and aluminium ?
Ans. Borax solution in water produces weak acid H3BO3 and its salt Na[B(OH)4] in equimolar quantity.
Na2B4O7 + 7H2O 2Na [B(OH)4] + 2H3BO3
14. Which indicator can be used to detect the end point of borax-acid titration ?
15. Under what conditions boric acid can be titrated against sodium hydroxide using phenolphthalein as indicator.
18. What will be the nature of reagent attacking the borazine molecule ?
19. Pure BBr3 and BI3 are colourless, but they become coloured on exposure to light, why ?
20. Complete the following reaction and write the structure of the product formed.
Excess NH
B 2H 6
3
High temp.
21. Complete the following reaction and identity compound (A) and (B).
NH HF B O
B(OH)3
4 2
( A ) 2
3
(B )
Fusion
27. Discuss the change in coordination number when crystalline AlCl3 is heated ?
28. Consider the compounds, BCl3 and CCl4, How will they behave with water ? Justify.
30. Explain what happens when boric acid is heated above 370 K ?
31. What do you understans by (a) inert pair effect. (b) allotropy and (c) catention ?
38. How far do you agree with the phenomenon concept of inert pair effect ? Justify your answer.
39. Why alkali metals should not be used for drying CCl4 and other chlorocarbons?
40. Why in reactions of HCl & SO2 , PbO2 shows oxidising nature? Explain.
41. Dilute HCl is preferred over dilute H2SO4 for the preparation of CO2 from lime stone. Explain.
(A) + N2 (C) + carbon
49. How carbonates and bicarbonates can be differentiated from one another ?
51. Which crystalline allotropic form of carbon has the lowest energy ?
52. Give reactions to show that CO2 is an acidic oxide and SnO2 is an amphoteric oxide.
53. Diamond and graphite both are allotropic forms of carbon, still only graphite is used as lubricant. Why ?
55. Write the chemical reactions involved in the hydrolysis of Alkyl trichlorosilane.
58. Why PbO, a base, is not completely dissolved in HCl and H2SO4 but dissolves in HNO3.
59. Which among the following oxides of lead is strong oxidising agent ?
PbO, PbO2, Pb3O4
61. What is the formula and the colour of Buckminster fullerene in toluene ?
62. What happens when Ag2C2 is allowed to react with dil. HCl ?
63. During reduction of SiO2 into Si, SiO2 is taken in excess, why ?
69. If the starting material for the manufacture of silicones is RSiCl3, write the structure of the product formed.
2. Compound (X) on reduction with LiAlH4 gives a hydride (Y) containing 21.72% hydrogen along with other
products. The compound (Y) reacts with air explosively resulting in boron trioxide. Identify (X) and (Y). Give
balanced reactions involved in the formation of (Y) and its reaction with air. Draw structure of (Y).
[JEE 2001, (M) 5/100]
3. Write balanced equations for the reactions of the following compounds with water : [JEE 2002, (M) 5/60]
(i) Al4C3 (ii) CaNCN (iii) BF3 (iv) NCl3 (v) XeF4
4. How is boron obtained from borax. Give chemical equations with reaction conditions. Write the structure of
B2H6 and its reaction with HCl. [JEE 2002, (M) 5/60]
7. Match the reactions in Column-I with nature of the reactions in column-II. [JEE 2006, 6/184]
Column-I Column-II
(A) Bi3+ (BiO)+ (p) Heat
(B) [AIO2]– Al(OH)3 (q) Hydrolysis
(C) SiO44– Si2O 76 (r) Acidification
(D) (B4O72–) [B(OH)3] (s) Dilution by water
9. The Coordination number of Al in the crystalline state of AlCl3 is ? [JEE 2009, (P-) 4/80]
12. (Me)2 SiCl2 on hydrolysis will produce : [JEE 2003, (S) 3/84]
(A) (Me)2 Si(OH)2 (B) (Me)2 Si = O
(C) – [O(Me)2 Si O]n (D) Me2SiCl(OH)
13. Which of the following silicate is formed when three oxygen atoms of [SiO4]4– tetrahedral units are shared ?
[JEE 2005, (S) 3/84]
(A) Sheet silicate (B) Pyrosilicate
(C) Three dimensional silicate (D) linear chain silicate
14. Statement-1 : Pb+4 compounds are stronger oxidizing agents than Sn4+ compounds
Statement-2 : The higher oxidation states for the group 14 elements are more stable for the heavier mem-
bers of the group due to 'inert pair effect'. [JEE 2008, (P-) 3/82]
(A) Statement-1 is True, Statement-2 is True; Statement-2 is a correct explanation for Statement-1.
(B) Statement-1 is True, Statement-2 is True; Statement-2 is NOT a correct explanation for Statement-1
(C) Statement-1 is True, Statement-2 is False
(D) Statement-1 is False, Statement-2 is True
15. The value of n in the molecular formula BenAl2Si6O18 is : [JEE 2010, (P-) 3/84]
16.* With respect to graphite and diamond, which of the statement (s) given below is (are) correct ?
(A) Graphite is harder than diamond.
(B) Graphite has higher electrical conductivity than diamond
(C) Graphite has higher thermal conductivity than diamond.
(D) Graphite has higher C-C bond order than diamond. [JEE 2012, 4/198]
17. Concentrated nitric acid, upon long standing, turns yellow-brown due to the formation of:
[JEE Advanced 2013, P-I]
(A) NO (B) NO2 (C) N2O (D) N2O4
2. Graphite is a soft solid lubricant extremely difficult to melt. The reason for this anomalous behaviour is that
graphite. [AIEEE 2003]
(1) is a non-crystalline substance.
(2) is an allotropic form of diamond
(3) has molecules of variable molecular masses like polymers
(4) has carbon atoms arranged in large plates of rings of strongly bound carbon atoms with weak interplate
bonds.
3. Aluminium chloride exists as dimer, Al2Cl6 in solid state as well as in solution of non-polar solvents such as
benzene. When dissolved in water, it gives : [AIEEE 2004]
(1) [Al(OH)6]3– + 3HCl (2) [Al(H2O)6]3+ + 3Cl–
(3) Al3+ + 3Cl– (4) Al2O3 + 6HCl
5. Heating an aqueous solution of aluminium chloride to dryness will give : [AIEEE 2005]
(1) Al(OH)Cl2 (2) Al2O3 (3) Al2Cl6 (4) AlCl3
6. The stability of dihalides of Si, Ge, Sn and Pb increases steadily in the sequence : [AIEEE 2007, 3/120]
(1) GeX2 < SiX2 < SnX2 < PbX2 (2) SiX2 < GeX2 < PbX2 < SnX2
(3) SiX2 < GeX2 < SnX2 < PbX2 (4) PbX2 < SnX2 < GeX2 < SiX2
7. In context with the industrial preparation of hydrogen from water gas (CO + H2), which of the following is
the correct statement ? [AIEEE 2008, 3/105]
(1) CO is removed by absorption in aqueous Cu2Cl2 Solution.
(2) H2 is removed through occlusion with Pd.
(3) CO is oxidized to CO2 with steam in the presence of a catalyst followed by absorption of CO2 in alkali.
(4) CO and H2 are fractionally separated using differences in their densities.
8. Among the following substituted silanes the one which will give rise to cross linked silicone polymer on
hydrolysis is : [AIEEE 2008, 3/105]
(1) RSiCl3 (2) R2SiCl2 (3) R3SiCl2 (4) R4Si
9. Which one of the following is the correct statement ? [AIEEE 2008, 3/105]
(1) Beryllium exhibits coordination number of six.
(2) Chlorides of both beryllium and aluminium have bridged structures in vapour phase.
(3) B2H6.2NH3 is known as ‘inorganic benzene’.
(4) Boric acid is a protonic acid.
4. Consider the compounds, BCl3 and CCl4. How will they behave with water ? Justify.
7. Describe the shapes of BF3 and BH4–. Assign the hybridisation of boron in these species.
9. What are electron deficient compounds ? Are BCl3 and SiCl4 electron deficient species ? Explain.
12. Explain the difference in properties of diamond and graphite on the basis of their structures.
lajpukd svk/kkj ij ghjkrFkk xzSQ kbV d sxq.kksaesafufgr fHkUurk d ksle>kb,A
14. Suggest reasons why the B–F bond lengths in BF3 (130 pm) and BF4– (143 pm) differ.
15. If B–Cl bond has a dipole moment, explain why BCl3 molecule has zero dipole moment.
16. Aluminium trifluoride is insoluble in anhydrous HF but dissolves on addition of NaF. Aluminium trifluoride
precipitates out of the resulting solution when gaseous BF3 is bubbled through. Give reasons.
23. Explain why is there a phenomenal decrease in ionization enthalpy from carbon to silicon ?
24. How would you explain the lower atomic radius of Ga as compared to Al ?
25. What are allotropes? Sketch the structure of two allotropes of carbon namely diamond and graphite. What
is the impact of structure on physical properties of two allotropes?
27. In some of the reactions thallium resembles aluminium, whereas in others it resembles with group I metals.
Support this statement by giving some evidences.
28. When metal X is treated with sodium hydroxide, a white precipitate (A) is obtained, which is soluble in
excess of NaOH to give soluble complex (B). Compound (A) is soluble in dilute HCl to form compound (C).
The compound (A) when heated strongly gives (D), which is used to extract metal. Identify (X), (A), (B), (C)
and (D). Write suitable equations to support their identities.
32. Give one method for industrial preparation and one for laboratory preparation of CO and CO2 each.
38. If the starting material for the manufacture of silicones is RSiCl3, write the structure of the product formed.
TRUE OR FALSE
Group 13th
33. False 34. True 35. False 36. False 37. True 38. True 39. True
40. False 41. True 42. True 43. True
Group 14th
44. T 45. F 46. T 47. T 48. T 49. F 50. F
51. T 52. F 53. T 54. T 55. T 56. T 57. F
2. (i) Al has no d-or f-electrons. Therefore, it does not exhibit inert pair effect and consequenty, it shows an
oxidation state of +3 only due to the presence of two electrons in the s-and one electron in the p-orbital of the
valence shell. As we move down the group from Ga to TI, the stability of +1 oxidation state increases while
that of =3 oxidation decreases due to inert pair effect. For (ii) and (iii) refer text.
Dry ether +
3. 4LiH + AlCl3 Li [AlH4] + 3LiCl.
–
10H O
7. (i) Na2B4O7.10H2O 2 Na2B4O7 2NaBO2 + B2O3
100
B 2H6 2NH3 B 2H6 .2NH3
tempt .
o
200 C
B 2H6 .2NH3 B 3N3H6 H2
(C) Borax from Boron (in two steps)
10. Both forms covalent compounds, e.g, BCl3 and AlCl3. Their chlorides are volatile and hygroscopic. They are
hydrolysed by water.
11. Borax solution in water produces weak acid H3BO3 and its salt Na[B(OH)4] in equimolar quantity.
Na2B4O7 + 7H2O 2Na [B(OH)4] + 2H3BO3
12. Because its melting point is very high and liquid obtained is corrosive.
14. At the end point, the pH is about 4 and thus methyl orange is used as indicator.
15. The end point in this titration is not sharp due to excessive hydrolysis of NaBO2 obtained as under.
H3BO3 + NaOH NaBO2 + 2H2O
Boric acid is complexed with a polyhydroxy compound such as glycerol or glycol. This helps in the release
of H+ as H3O+ and a sharp end point is possible.
16. Na2B4O7 + 3H2O NaBO2 + 3H3BO3
NaBO2 + 2H2O NaOH(strong alkali) + H3BO3
17. In borazine B = N bonds are polar while in benzene C = C and C – C bonds are non-polar and, therefore,
reactivity of borazine is more than benzene.
NH 4HF2 B O
21. B(OH)3 NH4BF3 2 3
BF3
laxy u
ETOOS ACADEMY Pvt. Ltd
F-106, Road No.2 Indraprastha Industrial Area, End of Evergreen Motor, BORON & CARBON FAMILY_ADVANCED # 42
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22. (i) Metaborates (ii) Orthoborates (iii) Pyroborates (iv) Perborates (v) Complex borates
Re d heat
26. (A) 2H3BO 3 B 2 O 3 3H2 O
100 º C
(C) H3BO 3 HBO 2 H2 O
160 º C
4H3BO 3 H2B 4 O 7 5H2O
Cl Cl Cl Cl
Al Al Al
27.
Cl Cl Cl Cl Cl
C.N = 4 C.N = 3
28. No reaction with CCl4 - as it does not have empty d - orbital whereas BCl3 will hydrolysed forming H3BO3.
29. No, it is weak monobasic Lewis acid according to the following reaction.
B(OH)3 (aq) + 2H2O () [B(OH)4]– (aq) + H3O+(aq)
31. (a) Reluctance of s-orbital electrons to participate in chemical bonding (more pronounced in heavier elements
of p-block).
(b) Phenomenon of existence of different forms of elements having different physical properrties.
(c) Elements (i.e. carbon) have the tendency to link with one another through covalent bonds to form chains
and rings.
675 K
SiH 4 (g) Si(s) 2H2 (g)
Pyrolysis
38. Inert pair effect is due to the ineffectively shielding of the s-electrons of the valence shell by the d-and
f-electrons of the inner shells.
39. They violently react with alkali metals according to following reactions.
IV II
40. P bO 2 4HCl P bCl2 Cl2
IV II
P bO 2 SO 2 P bSO 4
41. CaSO4 formed with H2SO4 forms a protective layer over lime stone and then reaction slowly ceases and stop.
But CaCl2 is soluble.
42. PbCl4 is less stable than SnCl4 due to more effective inert pair effect in lead. Pb–Cl bond length is more then
that of Sn–Cl.
43. Due to bigger atomic size of silicon, its reluctance for pp – pp bond does not allow to form graphite like
structure.
44. Low electronegativity and bigger size, Si does not have tendency to form p-p bonds like carbon.
COOH
P4 O10
(b) CH2 C3O2 (Carbon suboxide) + 2H2O
COOH
(c) Refer text.
47. Lead dissolves in water containing dissolved air due to the formation of lead hydroxide (a poisonous substance).
This solvent action of water is called plumbo solvency. It increases if water contains nitrates, ammonium
salts and organic acids, and decreases if water contains phosphates, sulphates, bicarbonates and carbonates.
56. (i) water proofing textiles (ii) as lubricants (iii) as anti-foaming agents.
59. PbO2
60. (i) covalent (ii), (iii) interstitial (iv) salt like (i.e. ionic)
64. (i) PbCl4 + Cl2 PbCl4 (Pb+2 to being oxidised by oxidising agent Cl2)
65. Forms carboxy haemoglobin which reduces the ability of haemoglobin to obsorb the oxygen.
66. Increase in CO2 percentage will increase the temperature of the earth.
67. (i) layered structure which can be slipped over one another as the layers are held together by weak Vander
Waal's forces.
(ii) Hard substance (formed by the three dimensional network of covalent bonds)
68. CO Neutral ; B2O3 , PbO2 and Al2O3 amphoteric ; SiO2 – acidic and Ti
Ti2O3 – basic.
3. (i) Al4C3 + H2O 4 Al(OH)3 + 3CH4 (ii) CaNCN + 3H2O CaCO3 + 2NH3
(iii) 4BF3 + 6H2O H3BO3 + 3 [BF4]– + 3H3O+ (iv) NCl3 + 3H2O NH3 + 3HOCl
(v) 6XeF4 + 12H2O 4Xe + 2XeO3 + 24HF + 3O2.
4.
Na 2B 4 O 7 .10H2 O Na 2B 4 O 7 (aq) ; Na 2B 4 O 7 2HCl 2NaCl H2B 4 O 7 (tetra boric acid)
red hot
H2B 4 O 7 5H2 O 4H3BO 3 2H3BO3 B 2 O 3 3H2O
;
Boric acid Boric anhydride
Fusion
B 2O 3 3Mg 2B 3MgO ; Reaction with HCl : B2H6 + HCl B2H5Cl + H2
Structure of B2H6 :
CH3
Cu powder |
2 H2 O
(b) Si + 2CH3Cl (CH3)2 SiCl2 (c) (CH3)2 SiCl2 HO – Si – OH
570 º C – 2HCl
|
CH3
(iii) (a) SiCl4 + 4H2O H4SiO4 or Si(OH)4 (ortho silicic acid) + 4HCl
1400 º C
(b) H4SiO4 SiO2 + 2H2O (c) SiO2 + Na2CO3 Na2SiO3 + CO2
12. (C) 13. (A) 14. (C) 15. 3 16.* (BD) 17. (B)
PART - II
1. (4) 2. (4) 3. (2) 4. (4) 5. (2) 6. (3) 7. (3)
8. (1) 9. (2) 10. (2) 11. (2)