Question
Lewis dot structures, in general, do notrepresent the actual shapes of the molecules.In case of polyatomic ions, the net charge ispossessed by the ion as a whole and not by aparticular atom. It is, however, feasible toassign a formal charge on each atom. Theformal charge of an atom in a polyatomicmolecule or ion may be defined as thedifference between the number of valenceelectrons of that atom in an isolated or freestate and the number of electrons assignedto that atom in the Lewis structure. It isexpressed as :Generally the lowest energystructure is the one with the smallestformal charges on the atoms. The formalcharge is a factor based on a pure covalentview of bonding in which electron pairsare shared equally by neighbouring atoms. The octet rule, though useful, is not universal.It is quite useful for understanding thestructures of most of the organic compoundsand it applies mainly to the second periodelements of the periodic table. There are threetypes of exceptions to the octet rule.
  • The incomplete octet of the central atom
  • Odd-electron molecules
  • The expanded octetFrom the Kössel and Lewis treatment of theformation of an ionic bond, it follows that theformation of ionic compounds wouldprimarily depend upon:
  • The ease of formation of the positive andnegative ions from the respective neutralatoms;
  • The arrangement of the positive andnegative ions in the solid, that is, thelattice of the crystalline compound.
The Lattice Enthalpy of an ionic solid is defined as the energy required to completely separate one mole of a solid ionic compound into gaseous constituent ions. For example, the lattice enthalpy of NaCl is 788 kJ mol–1. This means that 788 kJ of energy is required to separate one mole of solid NaCl into one mole of Na+ (g) and one mole of Cl– (g) to an infinite distance.Bond length is defined as the equilibriumdistance between the nuclei of two bondedatoms in a molecule. Bond lengths aremeasured by spectroscopic, X-ray diffractionand electron-diffraction techniques . The covalent radius is measuredapproximately as the radius of an atom’score which is in contact with the core ofan adjacent atom in a bonded situation. The vander Waals radius represents the overall sizeof the atom which includes its valence shellin a nonbonded situation. Bond Angle is defined as the angle between the orbitalscontaining bonding electron pairs around thecentral atom in a molecule/complex ion. Bondangle is expressed in degree which can beexperimentally determined by spectroscopicmethods. It gives some idea regarding thedistribution of orbitals around the centralatom in a molecule/complex ion and hence ithelps us in determining its shape. Forexample H–O–H bond angle in water can berepresented as under:

Bond Enthalpy It is defined as the amount of energy required to break one mole of bonds of a particular type between two atoms in a gaseous state. The unit of bond enthalpy is $kJ mol ^{-1}$. For example, the $H - H$ bond enthalpy in hydrogen molecule is $435.8 kJ mol ^{-1} \cdot H _2(g) \rightarrow H ( g )+ H ( g ) ; \Delta_{ a } H =435.8 kJ mol ^{-1}$. Bond Orderln the Lewis description of covalent bond, the Bond Order is given by the number ofbonds between the two atoms in amolecule. The bond order, for example in $H _2$ (with a single shared electron pair), in $O _2$ (with two shared electron pairs) and in $N _2$ (with three shared electron pairs) is 1,2,3respectively. A general correlation useful forunderstanding the stablities of moleculesis that: with increase in bond order, bondenthalpy increases and bond lengthdecreases. The concept of resonance was introducedto deal with the type of difficulty experiencedin the depiction of accurate structures ofmolecules like $O _3$. According to the conceptof resonance, whenever a single Lewis structure cannot describe a moleculeaccurately, a number of structures with similar energy, positions of nuclei, bonding and non-bonding pairs of electrons are taken as the canonical structures of the hybrid which describes the molecule accurately.

Thus for $O_3$, the two structures shown above constitute the canonical structures or resonance structures and their hybrid i.e., theIII structure represents the structure of $O_3$ more accurately. This is also called resonance hybrid. Resonance is represented by a double headed arrow. In general, it may be stated that
  • Resonance stabilizes the molecule as the energy of the resonance hybrid is lessthan the energy of any single cannonical structure; and,
  • Resonance averages the bond characteristics as a whole. Thus the energy of the$O_3$ . resonancehybrid is lower than either of the two cannonical froms I and II.
  1. Which of the following techniques used to measure bond length?
  1. Spectroscopic techniques
  2. X-ray diffraction
  3. Electron-diffraction techniques
  4. All the above
  1. The unit of bond enthalpy is …
  1. $kJ mol^{–1}$
  2. $Cal mol^{-1}$
  3. $Cal$ mol
  4. $kJ$ mol
  1. With increase in bond order, bond enthalpy… and bond length ….
  1. Decreases, decreases
  2. Increases, decreases
  3. Increases, increases
  4. Decreases, increases
  1. The …. is measured approximately as the radius of an atom’s core which is in contact with the core of an adjacent atom in a bonded situation.
  1. Ionic radius
  2. Metallic radius
  3. Covalent radius
  4. None of above
  1. … is given by the number of bonds between the two atoms in a molecule.
  1. Bond Order
  2. Bond size
  3. Bond enthalpy
  4. Bond angle

Answer

  1. (d) All the above
  2. (a) kJ $mol^{–1}$
  3. (b) Increases, decreases
  4. (c) Covalent radius
  5. (a) Bond Order

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A process or change is said to be reversible, if a change is brought out in such a way that the process could, at any moment, be reversed by an infinitesimal change. A reversible process proceeds infinitely slowly by a series of equilibrium states such that system and the surroundings are always in near equilibrium with each other. Processes other than reversible processes are known as irreversible processes.
Isothermal and free expansion of an ideal gas For isothermal (T = constant) expansion of an ideal gas into vacuum; w = 0 since pex = 0. Also, Joule determined experimentally that q = 0; therefore, $\triangle\text{U}=0, \triangle =+\text{Uqw}$ can be expressed for isothermal irreversible and reversible changes as follows:
  1. For isothermal irreversible change
$\text{q}=-\text{w}=\text{nRTIn}\frac{\text{V}_\text{f}}{\text{V}_{\text{i}}}$
$=2.303\ \text{nRT}\log\frac{\text{V}_\text{f}}{\text{V}_{\text{i}}}$
  1. For isothermal reversible change
  2. For adiabatic change, q = 0
$\triangle\text{U}=\text{w}_{\text{ad}}$
In thermodynamics, a distinction is made between extensive properties and intensive properties. An extensive property is a property whose value depends on the quantity or size of matter present in the system. For example, mass, volume, internal energy, enthalpy, heat capacity, etc. are extensive properties. Those properties which do not depend on the quantity or size of matter present are known as intensive properties. For example temperature, density, pressure etc. are intensive properties. A molar property, χm, is the value of an extensive property χ of the system for 1 mol of the substance. If n is the amount of matter, χ χ m = n is independent of the amount of matter. Other examples are molar volume .
Measurement of $\triangle\text{U}$ and $\triangle{Η}$: Calorimetry We can measure energy changes associated with chemical or physical processes by an experimental technique called calorimetry. In calorimetry, the process is carried out in a vessel called calorimeter, which is immersed in a known volume of a liquid. Knowing the heat capacity of the liquid in which calorimeter is immersed and the heat capacity of calorimeter, it is possible to determine the heat evolved in the process by measuring temperature changes. Measurements are made under two different conditions: i) at constant volume, qV ii) at constant pressure, qP
Explain the determination of DeltaU of a reaction calorimetrically.
∆U Measurements For chemical reactions, heat absorbed at constant volume, is measured in a bomb calorimeter. Here, a steel vessel (the bomb) is immersed in a water bath. The whole device is called calorimeter. The steel vessel is immersed in water bath to ensure that no heat is lost to the surroundings. A combustible substance is burnt in pure dioxygen supplied in the steel bomb. Heat evolved during the reaction is transferred to the water around the bomb and its temperature is monitored. Since the bomb calorimeter is sealed, its volume does not change i.e., the energy changes associated with reactions are measured at constant volume. Under these conditions, no work is done as the reaction is carried out at constant volume in the bomb calorimeter. Even for reactions involving gases, there is no work done as $\triangle\text{v}=0$ Temperature change of the calorimeter produced by the completed reaction is then converted to qV, by using the known heat capacity of the calorimeter with the help of equation
b)$\triangle{Η}$ Measurements Measurement of heat change at constant pressure (generally under atmospheric pressure) can be done in a calorimeter shown in Figure. We know that $\triangle{Η}=\text{qp}$ (at constant p) and, therefore, heat absorbed or evolved, qP at constant pressure is also called the heat of reaction or enthalpy of reaction, $\triangle\text{rΗ}$ In an exothermic reaction, heat is evolved, and system loses heat to the surroundings. Therefore, qP will be negative and ∆rH will also be negative. Similarly in an endothermic reaction, heat is absorbed, qP is positive and $\triangle\text{rΗ}$ will be positive.
THERMODYNAMICS - NCERT Class 11 Chemistry
  1. For adiabatic change, q = 0 then …
  1. $\triangle\text{U}=\text{w}_{\text{ad}}$
  2. $\triangle\text{U}=\text{q}+\text{w}$
  3. $\triangle\text{U}=\text{w}-\text{q}$
  4. $\triangle\text{U}=\text{w}_{\text{rev}}$
  1. The technique for measure energy changes associated with chemical or physical processes by an experimental technique called …
  1. Colourimetry
  2. Calorimetry
  3. Titration
  4. Photometry
  1. A property whose value depends on the quantity or size of matter present in the system is known as …
  1. Extensive
  2. Intensive
  3. Reversible
  4. Irreversible
  1. If there is no work done …
  1. V = 0
  2. V = 1
  3. V = 2
  4. V = 3
  1. In an endothermic reaction, heat is absorbed, qP is … and $\triangle\text{rΗ}$ will be …
  1. Positive, Positive
  2. Negative, Negative
  3. Positive, Negative
  4. Negative, Positive
Read the passage given below and answer the following questions from (i) to (vi).
The atomic theory of matter was first proposed on afirm scientific basis by JohnDalton, a British schoolteacher in 1808. His theory, called Dalton’s atomictheory, regarded the atom as the ultimate particle ofmatter Dalton’s atomic theory was able to explainthe law of conservation of mass, law of constantcomposition and law of multiple proportion verysuccessfully. However, it failed to explain the results ofmany experiments.In mid 1850s many scientists mainlyFaraday began to study electrical dischargein partially evacuated tubes, known ascathode ray discharge tubes.Electrical discharge carried out in the modifiedcathode ray tube led to the discovery of canalrays carrying positively charged particles. Thecharacteristics of these positively chargedparticles are listed below.
  1. Unlike cathode rays, mass of positivelycharged particles depends upon thenature of gas present in the cathode raytube. These are simply the positivelycharged gaseous ions.
  2. The charge to mass ratio of the particlesdepends on the gas from which theseoriginate.
  3. Some of the positively charged particlescarry a multiple of the fundamental unitof electrical charge.
  4. The behaviour of these particles in themagnetic or electrical field is opposite tothat observed for electron or cathoderays.
The smallest and lightest positive ion wasobtained from hydrogen and was called
proton. This positively charged particle wascharacterised in 1919. Later, a need was feltfor the presence of electrically neutral particleas one of the constituent of atom. Theseparticles were discovered by Chadwick (1932)by bombarding a thin sheet of beryllium byα-particles. When electrically neutral particleshaving a mass slightly greater than that ofprotons were emitted. He named theseparticles as neutrons.J. J. Thomson, in 1898, proposed that an atom possesses a spherical shape (radiusapproximately 10–10 m) in which the positivecharge is uniformly distributed. The electronsare embedded into it in such a manner as togive the most stable electrostatic arrangementMany different names are given tothis model, for example, plum pudding, raisinpudding or watermelon. This model can be visualised as a pudding or watermelon ofpositive charge with plums or seeds (electrons)embedded into it. An important feature of thismodel is that the mass of the atom is assumed to be uniformly distributed over theatom.Rutherford and his students (Hans Geiger andErnest Marsden) bombarded very thin gold foilwith α–particles. Rutherford’s famous α–particle scattering experiment.The observations of Scattering experiment are as follows-:
  1. most of the α–particles passed throughthe gold foil undeflected.
  2. a small fraction of the α–particles wasdeflected by small angles.
  3. a very few α–particles (∼1 in 20,000)bounced back, that is, were deflected bynearly 180°.
On the basis of observations andconclusions from this experiment, Rutherford proposed the nuclearmodel of atom. According to this model:
  1. The positive charge and most of the massof the atom was densely concentrated inextremely small region. This very smallportion of the atom was called nucleusby Rutherford.
  2. The nucleus is surrounded by electronsthat move around the nucleus with a veryhigh speed in circular paths called orbits.Thus, Rutherford’s model of atomresembles the solar system in which thenucleus plays the role of sun and theelectrons that of revolving planets.
  3. Electrons and the nucleus are held together by electrostatic forces of attraction.
  1. The atomic theory of matter was first proposed on afirm scientific basis by:
  1. John Dalton
  2. Ernest Rutherford
  3. J.Thomson
  4. Henry Moseley
  1. The cathode rays start from … and move towards the….
  1. Anode, Cathode
  2. Centre, Anode
  3. Cathod, Anode
  4. Cathod, Centre
  1. Negativelycharged particles in atoms, called…
  1. Protons
  2. Electrons
  3. Neutron
  4. Positron
  1. The smallest and lightest positive ion wasobtained from …. and was called proton.
  1. Oxygen
  2. Nitrogen
  3. Carbon
  4. Hydrogen
  1. Electrically neutral particles having a mass slightly greater than that of protons, these particles termed as:
  1. Protons
  2. Electrons
  3. Neutron
  4. Positron
  1. J.J. Thomson’s atomic model is also named as:
  1. Plum pudding
  2. Raisin pudding
  3. Watermelon
  4. All the above
Read the passage given below and answer the following questions from 1 to 5 .
Carbon exhibits many allotropic forms; both crystalline as well as amorphous. Diamond and graphite are two wellknown crystalline forms of carbon. In 1985, third form of carbon known as fullerenes was discovered by H.W.Kroto, E.Smalley and R.F.Curl. For this discovery they were awarded the Nobel Prize in 1996.
Diamond It has a crystalline lattice. In diamond each carbon atom undergoes $sp ^3$ hybridisation and linked to four other carbon atoms by using hybridised orbitals in tetrahedral fashion. The C-C bond length is 154 pm . The structure extends in space and produces a rigid three- dimensional network of carbon atoms. It is very difficult to break extended covalent bonding and, therefore, diamond is a hardest substance on the earth. It is used as an abrasive for sharpening hard tools, in making dyes and in the manufacture of tungsten filaments for electric light bulbs. Graphite Graphite has layered structure. Layers are held by van der Waals forces and distance between two layers is 340 pm . Each layer is composed of planar hexagonal rings of carbon atoms. C-C bond length within the layer is 141.5 pm . Each carbon atom in hexagonal ring undergoes $sp ^2$ hybridisation and makes three sigma bonds with three neighbouring carbon atoms. Fourth electron forms a $\pi$ bond. The electrons are delocalised over the whole sheet. Electrons are mobile and, therefore, graphite conducts electricity along the sheet. Graphite cleaves easily between the layers and, therefore, it is very soft and slippery. For this reason graphite is used as a dry lubricant in machines running at high temperature, where oil cannot be used as a lubricant.
Fullerenes Fullerenes are made by the heating of graphite in an electric arc in the presence of inert gases such as helium or argon. The sooty material formed by condensation of vapourised Cn small molecules consists of mainly C60 with smaller quantity of C70 and traces of fullerenes consisting of even number of carbon atoms up to 350 or above. Fullerenes are the only pure form of carbon because they have smooth structure without having 'dangling' bonds. Fullerenes are cage like molecules. C60 molecule has a shape like soccer ball and called Buckminsterfullerene. It contains twenty six-membered rings and twelve five-membered rings. A six membered ring is fused with six or five membered rings but a five membered ring can only fuse with six membered rings. All the carbon atoms are equal and they undergo $sp ^2$ hybridisation. Each carbon atom forms three sigma bonds with other three carbon atoms. The remaining electron at each carbon is delocalised in molecular orbitals, which in turn give aromatic character to molecule. This ball shaped molecule has 60 vertices and each one is occupied by one carbon atom and it also contains both single and double bonds with C-C distances of 143.5 pm and 138.3 pm respectively. Spherical fullerenes are also called bucky balls in short.
Uses of Carbon Graphite fibres embedded in plastic material form high strength, lightweight composites. The composites are used in products such as tennis rackets, fishing rods, aircrafts and canoes. Being good conductor, graphite is used for electrodes in batteries and industrial electrolysis. Crucibles made from graphite are inert to dilute acids and alkalies. Being highly porous, activated charcoal is used in adsorbing poisonous gases; also used in wateof filters to remove organic contaminators and in airconditioning system to control odour. Carbon black is used as black pigment in black ink and as filler in automobile tyres. Coke is used as a fuel and largely as a reducing agent in metallurgy. Diamond is a precious stone and used in jewellery. It is measured in carats (1 carat = 200 mg ). Carbon Monoxide Direct oxidation of C in limited supply of oxygen or air yields carbon monoxide. $2 C ( s ) O ( g ) \rightarrow$ $2 CO ( g )$

When air is used instead of steam, a mixture of CO and $N_2$ is produced, which is called 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. Carbon monoxide is a colourless, odourless and almost water insoluble gas. It is a powerful reducing agent and reduces almost all metal oxides other than those of the alkali and alkaline earth metals, aluminium and a few transition metals. This property of CO is used in the extraction of many metals from their oxides ores.
$\text{Fe}_2\text{O}_3(\text{s})+3\text{CO}(\text{g})\xrightarrow{\triangle}2\text{Fe}(\text{s})+3\text{CO}_2\text{(g)}$
$\text{ZnO}\text{(s)}+\text{CO}\text{(s)}\xrightarrow{\triangle}\text{Zn}(\text{s})+\text{CO}_2(\text{g})$
In CO molecule, there are one sigma and two π bonds between carbon and oxygen: C ≡ O Because of the presence of a lone pair on carbon, CO molecule acts as a donor and reacts with certain metals when heated to form metal carbonyls. The highly poisonous nature of CO arises because of its ability to form a complex with haemoglobin, which is about 300 times more stable than the oxygen-haemoglobin complex. This prevents haemoglobin in the red blood corpuscles from carrying oxygen round the body and ultimately resulting in death.
  1. In diamond each carbon atom undergoes … hybridisation.
  1. sp
  2. $sp^2$
  3. $sp^3$
  4. $sp^3d$
  1. Carbon atom in hexagonal ring undergoes … hybridisation.
  1. $sp$
  2. $sp^2$
  3. $sp^3$
  4. $sp^3d$
  1. C—C bond length within the layer in graphite is … pm.
  1. 5
  2. 5
  3. 180
  4. 90
  1. Fullerenes was discovered by …
  1. W.Kroto
  2. Smalley
  3. F.Curl
  4. All the above
  1. The C–C bond length in diamond is … pm.
  1. 5
  2. 5
  3. 180
  4. 154
Read the passage given below and answer the following questions from 1 to 5.
The unusual properties of water in the Condensed phase (liquid and solid states) are Due to the presence of extensive hydrogen Bonding between water molecules. This leads To high freezing point, high boiling point, high Heat of vaporisation and high heat of fusion in Comparison to $H_2S$ and $H_2Se$. In comparison To other liquids, water has a higher specific Heat, thermal conductivity, surface tension, Dipole moment and dielectric constant, etc. these properties allow water to play a key role In the biosphere. In the gas phase water is a bent molecule with a bond angle of $104.5^\circ$ , and O–H bond length Of 95.7 pm
It is a highly polar molecule. Its orbital overlap. In the liquid Phase water molecules are associated together By hydrogen bonds. The crystalline form of water is ice. At Atmospheric pressure ice crystallises in the Hexagonal form, but at very low temperatures It condenses to cubic form.
Density of ice is Less than that of water. Therefore, an ice cube Floats on water. In winter season ice formed On the surface of a lake provides thermal Insulation which ensures the survival of the Aquatic life. This fact is of great ecological Significance. Structure of Ice Ice has a highly ordered three dimensional Hydrogen bonded structure. Examination of ice crystals with X-rays shows that each oxygen atom is Surrounded tetrahedrally by four other oxygen Atoms at a distance of 276 pm.
Hydrogen bonding gives ice a rather open Type structure with wide holes. These holes can Hold some other molecules of appropriate size Interstitially.
Water reacts with a large number of Substances. Some of the important reactions Are given below.
Amphoteric Nature: It has the ability to act as an acid as well as a base i.e., it behaves As an amphoteric substance. In the Brönsted Sense it acts as an acid with $NH_3$ and a base with $H_2S.$
$\text{H}_2\text{O}(\text{l})+\text{NH}_3(\text{aq})\rightleftharpoons\text{OH}^-(\text{aq})+\text{NH}^+_4\text{aq}$
$\text{H}_2\text{O}(\text{l})+\text{H}_2\text{S}(\text{aq})\rightleftharpoons\text{H}_3\text{O}^+(\text{aq})+\text{HS}^-\text{(aq)}$
The auto protolysis (self-ionzation) of water takes palace as follow:
$\text{H}_2\text{O}(\text{l})+\text{H}_2\text{O}(\text{l})\rightleftharpoons\text{H}_3\text{O}^+(\text{aq})+\text{OH}^-(\text{aq})$
$\text{acid-1 base-2 (acid-2) base-1}$
$\text{(acid) (base) (conjugate acid) (conjugate base)}$
Redox Reactions Involving Water: Water Can be easily reduced to dihydrogen by highly Electropositive metals.
$2\text{H}_2\text{O}(\text{l})+2\text{Na}\text{(s)}\rightarrow2\text{NaOH}\text{(aq)}+\text{H}_2\text{g}$
Thus. it is a great source of dihydrogen.
water is oxidished to $O_2$ during photosynthesis.
$6\text{CO}_2\text{g}+12\text{H}_2\text{O}(\text{l})\rightarrow\text{C}_6\text{H}_{12}\text{O}_6(\text{aq})+6\text{H}_2\text{O}{\text{l}}+6\text{O}_2\text{(g)}$
With fluorine also it is oxidised to $O_2.$
$2\text{F}_2\text{g}+2\text{H}_2\text{O}(\text{l})\rightarrow4\text{H}^+(\text{aq})+4\text{F}^-(\text{aq})+\text{O}_2\text{(G)}$
Hydrolysis Reaction: Due to high Dielectric constant, it has a very strong Hydrating tendency. It dissolves many ionic Compounds. However, certain covalent and Some ionic compounds are hydrolysed in water.
$\text{P}_4\text{O}_{10}(\text{s})+6\text{H}_2\text{O}(\text{l})\rightarrow4\text{H}_3\text{PO}_4\text{(aq)}$
$\text{SiCl}_4{\text{l}}+2\text{H}_2\text{O}(\text{l})\rightarrow\text{SiO}_2\text{(s)}+4\text{HCl}\text{(aq)}$
Hydrates Formation: From aqueous Solutions many salts can be crystallised as Hydrated salts. Such an association of water Is of different types viz., Coordinated water e.g.,

Hard and Soft Water- Rain water is almost pure (may contain some Dissolved gases from the atmosphere). Being a Good solvent, when it flows on the surface of The earth, it dissolves many salts. Presence of Calcium and magnesium salts in the form of Hydrogencarbonate, chloride and sulphate in Water makes water ‘hard’. Hard water does Not give lather with soap. Water free from Soluble salts of calcium and magnesium is Called Soft water. It gives lather with soap Easily. Temporary hardness is due to the presence of Magnesium and calcium hydrogen- Carbonates. It can be removed by:
Boiling: During boiling, the soluble $Mg(HCO_3)_2$ is converted into insoluble $Mg(OH)_2$ And $Ca(HCO_3)_2$ is changed to insoluble $CaCO_3$. It is because of high solubility product of $Mg(OH)_2$ as compared to that of $MgCO_3$, that $Mg(OH)_2$ is precipitated. These precipitates can Be removed by filtration. Filtrate thus obtained
Will be soft water.
$\text{Mg}(\text{HCO}_3)_2\xrightarrow{\text{Heating}}\text{Mg}(\text{OH})_2\downarrow+2\text{CO}_2\uparrow$
$\text{Ca}(\text{HCO}_3)_2\xrightarrow{\text{Heating}}\text{CaCO}_3\downarrow+\text{H}_2\text{O}+\text{CO}_2\uparrow$
Clark’s method: In this method calculated Amount of lime is added to hard water. It Precipitates out calcium carbonate and Magnesium hydroxide which can be filtered off.
Permanent Hardness is due to the presence of soluble salts of Magnesium and calcium in the form of Chlorides and sulphates in water. Permanent Hardness is not removed by boiling.
$\text{Ca}(\text{Hco}_3)_2+\text{Ca}(\text{OH)}_2\rightarrow2\text{CaCO}_3\downarrow2\text{H}_2\text{O}$
$\text{Mg}(\text{HCO)}_3+2\text{Ca}\text{(Oh)}_2\rightarrow2\text{CaCO}_3\downarrow+\text{Mg}(\text{OH)}_2\downarrow2\text{H}_2\text{O}$
Permanent Hardness is due to the presence of soluble salts of Magnesium and calcium in the form of Chlorides and sulphates in water. Permanent Hardness is not removed by boiling.
  1. In the gas phase water is a bent molecule with a bond angle of:
  1. $104.5^\circ$
  2. $94.5^\circ$
  3. $110.5^\circ$
  4. $95.5^\circ$
  1. At Atmospheric pressure ice crystallises in the … form.
  1. Cubic
  2. Hexagonal
  3. Octagonal
  4. Pentagonal
  1. Water free from Soluble salts of calcium and magnesium is called …
  1. hard water
  2. dry water
  3. soft water
  4. None of above
  1. Water has…. Nature.
  1. acidic
  2. basic
  3. neutral
  4. amphoteric
  1. Water is…. Molecule.
  1. Polar
  2. Non- Polar
  3. Ionic
  4. All the above
Read the passage given below and answer the following questions from 1 to 5.
Chemistry is the science of molecules and theirtransformations. It is the science not so much of the one hundred elements but of the infinite variety of molecules thatmay be built from them. Chemistry plays a central role in science andis often intertwined with other branches ofscience.to understand thebasic concepts of chemistry, which begin withthe concept of matter. Let us start with thenature of matter. matter can exist in threephysical states viz. solid, liquid and gas.Particles are held very close to each otherin solids in an orderly fashion and there is notmuch freedom of movement. In liquids, theparticles are close to each other but they canmove around. However, in gases, the particlesare far apart as compared to those present insolid or liquid states and their movement iseasy and fast. different states of matter exhibitthe following characteristics:
  1. Solids have definite volume and definiteshape.
  2. Liquids have definite volume but do nothave definite shape. They take the shapeof the container in which they are placed.
  3. Gases have neither definite volume nordefinite shape. They completely occupy thespace in the container in which they are placed.
Matter can be classified as mixture or pure substance. A mixture may be homogeneous or heterogeneous. Pure substances can further be classified into elements and compounds. Particles of an element consist of only one type of atoms. These particles may exist as atoms or molecules. When two or more atoms of different elements combine together in a definite ratio, the molecule of a compound is obtained.
Every substance has unique or characteristic properties. These properties can be classified into two categories — physical properties, such as colour, odour, melting point, boiling point, density, etc., and chemical properties, like composition, combustibility, ractivity with acids and bases, etc. Physical properties can be measured or observed without changing the identity or the composition of the substance. The measurement or observation of chemical properties requires a chemical change to occur. Measurement of physical properties does not require occurance of a chemical change.
  1. Which of the following state of matter have definite volume but do not have definite shape?
  1. Solid
  2. Liquid
  3. Gas
  4. Plasma
  1. Particles are held very close to each other in … in an orderly fashion and there is not much freedom of movement.
  1. Liquid
  2. Gas
  3. Solid
  4. Plasma
  1. Particles of …. consist of only one type of atom.
  1. Compound
  2. Mixture
  3. Element
  4. All the above
  1. Water molecule comprises …hydrogen atoms and … oxygen atom.
  1. One, two
  2. Three, one
  3. One, three
  4. Two, one
  1. Which of the following is not an example of Physical Properties of substance.?
  1. Odour
  2. Melting point
  3. Density
  4. Composition
Read the passage given below and answer the following questions from (i) to (v).
Chemical properties of a substance do not change withthe change of its physical state; but rate of chemicalreactions do depend upon the physical state. Many timesin calculations while dealing with data of experiments werequire knowledge of the state of matter. Therefore, itbecomes necessary for a chemist to know the physical laws which govern the behaviour of matter indifferent states. Intermolecular forces are the forces ofattraction and repulsion between interactingparticles (atoms and molecules). This termdoes not include the electrostatic forces thatexist between the two oppositely charged ionsand the forces that hold atoms of a moleculetogether i.e., covalent bonds.Attractive intermolecular forces are knownas van der Waals forces, in honour of Dutchscientist Johannes van der Waals (1837-1923) . van der Waals forces vary considerablyin magnitude and include dispersion forcesor London forces, dipole-dipole forces, anddipole-induced dipole forces. A particularlystrong type of dipole-dipole interaction ishydrogen bonding. Only a few elements canparticipate in hydrogen bond formation, therefore it is treated as a separatecategory.
Atoms and nonpolar molecules are electricallysymmetrical and have no dipole momentbecause their electronic charge cloud issymmetrically distributed. But a dipole maydevelop momentarily even in such atoms andmolecules. The temporary dipoles of two different atomattract each other. Similarly temporary dipolesare induced in molecules also. This force ofattraction was first proposed by the Germanphysicist Fritz London, and for this reasonforce of attraction between two temporary dipoles is known as London force. dispersion force forces are always attractive and interactionenergy is inversely proportional to the sixthpower of the distance between two interactingparticles (i.e.,$1/r ^6$ where r is the distancebetween two particles). These forces areimportant only at short distances (~500 pm)and their magnitude depends on thepolarisability of the particle.
Dipole-dipole forces act between the moleculespossessing permanent dipole. Ends of thedipoles possess “partial charges” and thesecharges are shown by Greek letter delta (δ).Partial charges are always less than the unitelectronic charge $(1.6\times 10^{–19} C)$. The polarmolecules interact with neighbouringmolecules. This interactionis stronger than the London forces but isweaker than ion-ion interaction because onlypartial charges are involved. The attractiveforce decreases with the increase of distancebetween the dipoles. As in the above case herealso, the interaction energy is inverselyproportional to distance between polarmolecules. Dipole-dipole interaction energybetween stationary polar molecules is proportional to $1/r^3$ and thatbetween rotating polar molecules is proportional to $1/r ^6$​​​​​​​, where r is the distancebetween polar molecules.
Dipole–Induced Dipole Forcesare type of attractive forces operate betweenthe polar molecules having permanent dipoleand the molecules lacking permanent dipole.Permanent dipole of the polar moleculeinduces dipole on the electrically neutralmolecule by deforming its electronic cloud. Thus an induced dipole is developedin the other molecule. In this case alsointeraction energy is proportional to $1/r ^6$​​​​​​​​​​​​​​ where r is the distance between twomolecules. Induced dipole moment dependsupon the dipole moment present in thepermanent dipole and the polarisability of theelectrically neutral molecule.
  1. Partial charges are always less than the unit electronic charge:
  1. $(1.6\times 10^{–19} C)$
  2. $(1.6\times 10^{–18} C)$
  3. $(1.6\times 10^{–17}C)$
  4. $(1.6\times 10^{–16} C)$
  1. Temporary dipoles are induced in molecules also. ,this force of attraction was first proposed by:
  1. Johannes van der Waals
  2. Fritz London
  3. Robert Boyle
  4. Joseph Lewis Gay Lussac
  1. Atoms and nonpolar molecules are electrically:
  1. Compositional
  2. Unsymmetrical
  3. Symmetrical
  4. All the above
  1. Partial Charges denoted by greek letter ….
  1. $\in$
  2. $\zeta$
  3. $\delta$
  4. $\eta$
  1. The attractive force … with the … of distance between the dipoles.
  1. Increase, increase
  2. Decrease, decrease
  3. Increase, decrease
  4. Decreases, increase
Read the passage given below and answer the following questions from (i) to (v).
The identity of a substance is defined not only by the types of atoms or ions it contains, but by the quantity of each type of atom or ion. The experimental approach required the introduction of a new unit for amount of substances, the mole, which remains indispensable in modern chemical science. The mole is an amount unit similar to familiar units like pair, dozen, gross, etc. It provides a specific measure of the number of atoms or molecules in a bulk sample of matter. A mole is defined as the amount of substance containing the same number of discrete entities (atoms, molecules, ions, etc.) as the number of atoms in a sample of pure 12 C weighing exactly 12 g . One Latin connotation for the word "mole" is "large mass" or "bulk," which is consistent with its use as the name for this unit. The mole provides a link between an easily measured macroscopic property, bulk mass, and an extremely important fundamental property, number of atoms, molecules and so forth. The number of entities composing a mole has been experimentally determined to be $6.02214179 \times 10^{23}$. $6.02214179 \times 10^{23}$, a fundamental constant named Avogadro's number (NA) or the Avogadro constant in honor of Italian scientist Amedeo Avogadro. This constant is properly reported with an explicit unit of "per mole," a conveniently rounded version being $6.022 \times 10^{23} / mol$. Consistent with its definition as an amount unit, 1 mole of any element contains the same number of atoms as 1 mole of any other element. The masses of 1 mole of different elements, however, are different, since the masses of the individual atoms are drastically different. The molar mass of an element (or compound) is the mass in grams of 1 mole of that substance, a property expressed in units of grams per mole ( $g / mol$ ). The following questions are multiple choice questions. Choose the most appropriate answer:
i. A sample of copper sulphate pentahydrate contains 8.64 g of oxygen. How many grams of Cu is present in the sample?
  1. A sample of copper sulphate pentahydrate contains 8.64g of oxygen. How many grams of Cu is present in the sample?
  1. 0.952g
  2. 3.816g
  3. 3.782g
  4. 8.64g
  1. A gas mixture contains 50% helium and $50\%$ methane by volume. What is the percent by \ weight of methane in the mixture?
  1. $19.97\%$
  2. $20.05\%$
  3. $50\%$
  4. $80.03\%$
  1. The mass of oxygen gas which occupies 5.6 litres at STP could be:
  1. Gram atomic mass of oxygen
  2. One fourth of the gram atomic mass of oxygen
  3. Double the gram atomic mass of oxygen
  4. Half of the gram atomic mass of oxygen
  1. What is the mass of one molecule of yellow phosphorus? (Atomic mass of phosphorus = 30)
  1. $1.993 \times 10^{-22}$ mg
  2. $1.993 \times 10^{-19}$ mg
  3. $4.983 \times 10^{-20}$ mg
  4. $4.983 \times 10^{-23}$ mg
  1. The number of moles of oxygen in 1L of air containing $21\%$ oxygen by volume, in standard conditions is:
  1. $0.186$ mol
  2. $0.21$ mol
  3. $2.10$ mol
  4. $0.0093$ mol
The s-Block Elements The elements of Group 1 (alkali metals) and Group 2 (alkaline earth metals) which have ns1and ns2 outermost electronic configuration belong to the s-Block Elements. They are all reactive metals with low ionization enthalpies. They lose the outermost electron(s) readily to form 1+ ion (in the case of alkali metals) or 2+ ion (in the case of alkaline earth metals). The metallic character and the reactivity increase as we go down the group. Because of high reactivity they are never found pure in nature. The compounds of the s-block elements, with the exception of those of lithium and beryllium are predominantly ionic. The p-Block Elements comprise those belonging to Group 13 to 18 and these together with the s-Block Elements are called the Representative Elements or Main Group Elements. The outermost electronic configuration varies from ns2np1 to ns2np6 in each period. At the end of each period is a noble gas element with a closed valence shell ns2np6 configuration. All the orbitals in the valence shell of the noble gases are completely filled by electrons and it is very difficult to alter this stable arrangement by the addition or removal of electrons. The noble gases thus exhibit very low chemical reactivity. Preceding the noble gas family are two chemically important groups of non-metals. They are the halogens (Group 17) and the chalcogens (Group 16).The non-metallic character increases as we move from left to right across a period and metallic character increases as we go down the group. These are the elements of Group 3 to 12 in the centre of the Periodic Table. These are characterised by the filling of inner d orbitals by electrons and are therefore referred to as d-Block Elements. These elements have the general outer electronic configuration (n-1)d1-10ns0-2 . They are all metals. They mostly form coloured ions, exhibit variable valence (oxidation states), paramagnetism and oftenly used as catalysts. However, Zn, Cd and Hg which have the electronic configuration, (n-1) d10ns2 do not show most of the properties of transition elements. In a way, transition metals form a bridge between the chemically active metals of s-block elements and the less active elements of Groups 13 and 14 and thus take their familiar name “Transition Elements”.The two rows of elements at the bottom of the Periodic Table, called the Lanthanoids, Ce(Z = 58) – Lu(Z = 71) and Actinoids, Th(Z = 90) – Lr (Z = 103) are characterised by the outer electronic configuration (n-2)f 1-14 (n-1)d 0–1ns2 . The last electron added to each element is filled in f- orbital. These two series of elements are hence called the Inner- Transition Elements (f-Block Elements). They are all metals. Within each series, the properties of the elements are quite similar. The chemistry of the early actinoids is more complicated than the corresponding lanthanoids, due to the large number of oxidation states possible for these actinoid elements. Actinoid elements are radioactive. Many of the actinoid elements have been made only in nanogram quantities or even less by nuclear reactions and their chemistry is not fully studied. The elements after uranium are called Transuranium Elements. The elements can be divided into Metals and Non-Metals. In contrast, non-metals are located at the top right hand side of the Periodic Table. The elements become more metallic as we go down a group; the non- metallic character increases as one goes from left to right across the Periodic Table. Periodic Table show properties that are characteristic of both metals and non- metals. These elements are called Semi-metals or Metalloids.
  1. Alkali metal and alkaline earth metal belongs to ..
  1. S – block
  2. P – block
  3. D – block
  4. F – block
  1. The metallic character and the reactivity … as we go down the group.
  1. Decreases
  2. Increases
  3. Remains Constant
  4. None of Above
  1. Group … Elements known as chalcogens.
  1. 12
  2. 14
  3. 16
  4. 18
  1. Elements Ce(Z = 58) to Lu(Z = 71) are known as:
  1. Halogens
  2. Chalcogens
  3. Actinoids
  4. Lanthenoids
  1. The elements after uranium are called … Elements.
  1. Halogens
  2. Chalcogens
  3. Actinoids
  4. Transuranium
Read the passage given below and answer the following questions from 1 to 5.
Hydrogen Peroxide $(H_2O_2)$ Hydrogen peroxide is an important chemical used in pollution control treatment of domestic and industrial effluents.It can be prepared by the following methods.
i) Acidifying barium peroxide and removing excess water by evaporation under reduced pressure gives hydrogen.
$\text{BaO}_2.8\text{H}_2\text{O}(\text{s})+\text{H}_2\text{SO}_4\text{(aq)}\rightarrow\text{BaSO}_4\text{(s)}+\text{H}_2\text{O}_2\text{(aq)}+8\text{H}_2\text{O}\text{l}$
ii) Peroxodisulphate, obtained by electrolytic oxidation of acidified sulphate solutions at high current density, on hydrolysis yields hydrogen.
$2\text{HSO}_\bar{4}(\text{aq})\xrightarrow{\text{Electrolysis}}\text{HO}_3\text{SOOSO}_3\text{H}(\text{aq})\xrightarrow{\text{Hydrolysis}}2\text{HSO}_\bar{4}\text{(aq)}+2\text{H}^+\text{(aq)}+\text{H}_2\text{O}_2\text{aq}$
This method is now used for the laboratory preparation of $D_2O_{2.}$
_{$\text{K}_2\text{S}_2\text{O}_8(\text{s})+2\text{D}_2\text{O}\text{(l)}\rightarrow2\text{KDSO}_4(\text{aq})+\text{D}_2\text{O}_2\text{(l)}$}
iii) Industrially it is prepared by the auto- oxidation of 2-alklylanthraquinols. 2 ethylanthraquinol H O oxidised product.

In this case 1% $H_2O_2$ is formed. It is extracted with water and concentrated to $\sim30\%$ (by mass) by distillation under reduced pressure. It can be further concentrated to $\sim85\%$ by careful distillation under low pressure. The remaining water can be frozen out to obtain pure $H_2O_2$. Physical Properties of the pure state $H_2O_2$ is an almost colourless (very pale blue) liquid. Its important physical properties. $H_2O_2$ is miscible with water in all proportions and forms a hydrate $H_2O_2.$ $H_2O$ (mp 221K). A 30% solution of $H_2O_2$ is marketed as ‘100 volume’ hydrogen peroxide. It means that one millilitre of 30% $H_2O_2$ solution will give 100 mL of oxygen at STP. Commercially marketed sample is 10 V, which means that the sample contains 3% $H_2O_2$ . Structure Hydrogen peroxide has a non-planar structure.
$H_2O_2$ decomposes slowly on exposure to light.
$2\text{H}_2\text{O}_2\text{(l)}\rightarrow2\text{H}_2\text{O}(\text{l})+\text{O}_2\text{(g)}$
In the presence of metal surfaces or traces of alkali (present in glass containers), the above reaction is catalysed. It is, therefore, stored in wax-lined glass or plastic vessels in dark. Urea can be added as a stabiliser. It is kept away from dust because dust can induce explosive decomposition of the compound.
Its wide scale use has led to tremendous increase in the industrial production of $H_2O_2$. Some of the uses are listed below:
i) In daily life it is used as a hair bleach and as a mild disinfectant. As an antiseptic it is sold in the market as
ii) It is used to manufacture chemicals like sodium perborate and per – carbonate, which are used in high quality detergents.
iii) It is used in the synthesis of hydroquinone, tartaric acid and certain food products and pharmaceuticals (cephalosporin)
iv) It is employed in the industries as a bleaching agent for textiles, paper pulp, leather, oils, fats,
v) Nowadays it is also used in Environmental (Green) Chemistry. For example, in pollution control treatment of domestic and industrial effluents, oxidation of cyanides, restoration of aerobic conditions to sewage wastes,
Heavy water, $D_2O$ It is extensively used as a moderator in nuclear reactors and in exchange reactions for the study of reaction mechanisms. It can be prepared by exhaustive electrolysis of water or as a by-product in some fertilizer industries. It is used for the preparation of other deuterium compounds, for example:
Dihydrogen can be used as a fuel .Dihydrogen releases large quantities of heat on combustion. The data on energy released by combustion of fuels like dihydrogen, methane, LPG etc. are compared in terms of the same amounts in mole, mass and volume Hydrogen Economy is an alternative. The basic principle of hydrogen economy is the transportation and storage of energy in the form of liquid or gaseous dihydrogen. Advantage of hydrogen economy is that energy is transmitted in the form of dihydrogen and not as electric power. It is for the first time in the history of India that a pilot project using dihydrogen as fuel was launched in October 2005 for running automobiles. Initially 5% dihydrogen has been mixed in CNG for use in four-wheeler vehicles. The percentage of dihydrogen would be gradually increased to reach the optimum level. Nowadays, it is also used in fuel cells for generation of electric power. It is expected that economically viable and safe sources of dihydrogen will be identified in the years to come, for its usage as a common source of energy.
  1. In India, a pilot project using dihydrogen as fuel was launched in… for running automobiles.
  1. October 2005
  2. May 2004
  3. August 2014
  4. February 2010
  1. Structure Hydrogen peroxide has a … structure.
  1. Bilateral
  2. Non-planar
  3. Planar
  4. Cubic
  1. One millilitre of 30% $H_2O_2$ solution will give … mL of oxygen at STP.
  1. 30
  2. 10
  3. 100
  4. 300
  1. …. is extensively used as a moderator in nuclear reactors and in exchange reactions for the study of reaction mechanisms.
  1. $H_2O_2$
  2. $T_2O$
  3. $H_2O$
  4. $D_2O$
  1. Colour of pure state $H_2O_2$ is ..
  1. Very Pale red
  2. Very Pale yellow
  3. Very Pale green
  4. Very Pale blue
Read the passage given below and answer the following questions from 1 to 5. Uses of Dihydrogen:
  • The largest single use of dihydrogen is in the synthesis of ammonia which is used in the manufacture of nitric acid and nitrogenous
  • Dihydrogen is used in the manufacture of vanaspati fat by the hydrogenation of polyunsaturated vegetable oils like soyabean, cotton seeds
  • It is used in the manufacture of bulk organic chemicals, particularly
  • It is widely used for the manufacture of metal
  • It is used for the preparation of hydrogen chloride, a highly useful
  • In metallurgical processes, it is used to reduce heavy metal oxides to
  • Atomic hydrogen and oxy-hydrogen torches find use for cutting and welding purposes. Atomic hydrogen atoms (produced by dissociation of dihydrogen with the help of an electric arc) are allowed to recombine on the surface to be welded to generate the temperature of 4000
  • It is used as a rocket fuel in space
  • Dihydrogen is used in fuel cells for generating electrical energy. It has many advantages over the conventional fossil fuels and electric It does not produce any pollution and releases greater energy per unit mass of fuel in comparison to gasoline and other fuels.
Dihydrogen, under certain reaction conditions, combines with almost all elements, except noble gases, to form binary compounds, called hydrides. If ‘E’ is the symbol of an element then hydride can be expressed as EHx $($e.g., Mg $H_2)$ or EmHn $($e.g.,$B_2H_6)$. The hydrides are classified into three categories:
  • Ionic or saline or saltlike hydrides
  • Covalent or molecular hydrides
  • Metallic or non-stoichiometric hydrides
Ionic or Saline Hydrides are stoichiometric compounds of dihydrogen formed with most of the s-block elements which are highly electropositive in character. However, significant covalent character is found in the lighter metal hydrides such as LiH, $BeH_2$ and $MgH_2$. In fact Be $H_2$ and Mg $H_2$ are polymeric in structure. The ionic hydrides are crystalline, non-volatile and non- conducting in solid state. However, their melts conduct electricity and on electrolysis liberate dihydrogen gas at anode, which confirms the existence of $H^{–} ion$. Covalent or Molecular Hydride Dihydrogen forms molecular compounds with most of the p-block elements. Most familiar examples are $CH_4, NH_3, H_2O$ and $HF.$ For convenience hydrogen compounds of non- metals have also been considered as hydrides. Being covalent, they are volatile compounds. Molecular hydrides are further classified according to the relative numbers of electrons and bonds in their Lewis structure into:
  • electron-deficient,
  • electron-precise, and
  • electron-rich
An electron-deficient hydride, as the name suggests, has too few electrons for writing its conventional Lewis structure. Diborane $(B_2H_6)$ is an example. In fact all elements of group 13 will form electron-deficient compounds. They act as Lewis acids i.e., electron acceptors. Electron-precise compounds have the required number of electrons to write their conventional Lewis structures. All elements of group 14 form such compounds (e.g., $CH_4$) which are tetrahedral in geometry. Electron-rich hydrides have excess electrons which are present as lone pairs. Elements of group 15-17 form such compounds. (NH3 has 1 - lone pair, $H_2O – 2$ and $HF –3$ lone pairs). What do you expect from the behaviour of such compounds ? They will behave as Lewis bases i.e., electron donors. The presence of lone pairs on highly electronegative atoms like N, O and F in hydrides results in hydrogen bond formation between the molecules. This leads to the association of molecules. Metallic or Non-stoichiometric (or Interstitial ) Hydrides are formed by many d- block and f-block elements. However, the metals of group 7, 8 and 9 do not form hydride. Even from group 6, only chromium forms CrH. These hydrides conduct heat and electricity though not as efficiently as their parent metals do. Unlike saline hydrides, they are almost always non- stoichiometric, being deficient in hydrogen. For example, $La H_{2.87}, Yb H_{2.55}, TiH1_{.5–1.8}, ZrH_{1.3–1.75}$, etc. In such hydrides, the law of constant composition does not hold good. Earlier it was thought that in these hydrides, hydrogen occupies interstices in the metal lattice producing distortion without any change in its type. Consequently, they were termed as interstitial hydrides. However, recent studies have shown that except for hydrides of Ni, Pd, Ce and Ac, other hydrides of this class have lattice different from that of the parent metal. The property of absorption of hydrogen on transition metals is widely used in catalytic reduction / hydrogenation reactions for the preparation of large number of compounds. Some of the metals (e.g., Pd, Pt) can accommodate a very large volume of hydrogen and, therefore, can be used as its storage media. This property has high potential for hydrogen storage and as a source of energy. A major part of all living organisms is made up of water. Human body has about 65% and some plants have as much as 95% water. It is a crucial compound for the survival of all life forms. It is a solvent of great importance. The distribution of water over the earth’s surface is not uniform.​​​​​​​
  1. Dihydrogen, under certain reaction conditions, combines with almost all elements, except …
  1. Noble gases
  2. Halogens
  3. Alkali metals
  4. Alkaline earth metal
  1. Covalent or Molecular Hydride Dihydrogen forms molecular compounds with most of the p-block elements. Most familiar example is:
  1. $CH_4$
  2. $NH_3$
  3. $H_2O$
  4. All the above
  1. All elements of group 14 form such compounds have … geometry.
  1. pyramidal
  2. tetrahedral
  3. bilateral
  4. spherical
  1. From group 6, only … forms hydride.
  1. molybdenum
  2. tungsten
  3. chromium
  4. seaborgium
  1. Which of the following hydride is/ are deficient in hydrogen.
  1. $La H_2._{87}$
  2. $Yb H_2._{55}$
  3. TiH5–1.8
  4. All of above