Question
Read the passage given below and answer the following questions from 1 to 5 .
Group 14 elements: the carbon family-Carbon, silicon, germanium, tin lead and Flerovium are the members of group 14. Carbon Is the seventeenth most abundant element by Mass in the earth's crust. It is widely Distributed in nature in free as well as in the Combined state. In elemental state it is available As coal, graphite and diamond; however, in Combined state it is present as metal Carbonates, hydrocarbons and carbon dioxide Gas ( $0.03 \%$ ) in air. One can emphatically say That carbon is the most versatile element in the World. Its combination with other elements Such as dihydrogen, dioxygen, chlorine and Sulphur provides an astonishing array of Materials ranging from living tissues to drugs And plastics.
The valence shell electronic configuration of These elements is $ns ^2 np ^2$. The inner core of the Electronic configuration of elements in this Group also differs.
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 electrons is visible here also. In general the lonisation enthalpy decreases down the group. Small decrease in $\Delta iH$ from Si to Ge to Sn and Slight increase in $\Delta i H$ from Sn to Pb is the Consequence of poor shielding effect 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 values for Elements from Si to Pb are almost the same.
Physical Properties All members of group14 are solids. Carbon and Silicon are non-metals, germanium is a 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.
(i) Reactivity towards oxygen All members when heated in oxygen form Oxides. There are mainly two types of oxides, i.e., monoxide and dioxide of formula MO and $MO _2$ respectively. SiO only exists at high Temperature. Oxides in higher oxidation states Of elements are generally more acidic than Those in lower oxidation states. The dioxides $CO _2$, SiO 2 and $GeO _2$ are acidic, whereas $SnO _2$ and $PbO _2$ are amphoteric in nature. Among monoxides, CO is neutral, GeO is Distinctly acidic whereas SnO and PbO are Amphoteric.
(ii) Reactivity towards water Carbon, silicon and germanium are not Affected by water. Tin decomposes steam to Form dioxide and dihydrogen gas.
$Sn+2 H_2 O \rightarrow SnO_2+2 H_2$
Lead is unaffected by water, probably Because of a protective oxide film formation.
(iii) Reactivity towards halogen These elements can form halides of formula $M X_2$ and $M X_4$ (where $\left.X=F, C l, B r, I\right)$. Except Carbon, all other members react directly with Halogen under suitable condition to make Halides. Most of the $MX _4$ are covalent in nature. The central metal atom in these halides Undergoes $sp ^3$ hybridisation and the molecule Is tetrahedral in shape. Exceptions are $SnF _4$ And $PbF _4$, which are ionic in nature.
Carbon atoms have the tendency to link With one another through covalent bonds to Form chains and rings. This property is called Catenation. This is because C-C bonds are Very strong. Down the group the size increases and electronegativity decreases, and, thereby, Tendency to show catenation decreases. This Can be clearly seen from bond enthalpies Values. The order of catenation is $C > Si > Ge \approx Sn$. Lead does not show catenation.
  1. Which of the following is not the member of group 14 ?
  1. boron
  2. silicon
  3. germanium
  4. tin
  1. … does not show catenation.
  1. Carbon
  2. Lead
  3. Silicon
  4. Germanium
  1. Which of following elements are affected by water ?
  1. carbon
  2. silicon
  3. germanium
  4. All the above
  1. The valence shell electronic configuration of Group 14 elements is …
  1. $ns^2np^4$
  2. $ns^2np^5$
  3. $ns^2np^2$
  4. $ns^2np^3$
  1. Half-life of $^{14}C$ is … years.
  1. 6570
  2. 4570
  3. 5770
  4. 1970

Answer

  1. (a) boron
  2. (b) Lead
  3. (d) All the above
  4. (c) $ns^2np^2$​​​​​​​
  5. (c) 5770

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Read the passage given below and answer the following questions from 1 to 5.
Alkenes are unsaturated hydrocarbons containing at least one double bond. What should be the general formula of alkenes? If there is one double bond between two carbon atoms in alkenes, they must possess two hydrogen atoms less than alkanes. Hence, general formula for alkenes is $C_nH_{2n}$. Alkenes are also known as olefins (oil forming) since the first member, ethylene or ethene $(C_2H_4)$ was found to form an oily liquid on reaction with chlorine.
Structure of Double Bond Carbon-carbon double bond in alkenes consists of one strong sigma $(\sigma)$ bond (bond enthalpy about $397\ kJ\ mol^{–1)}$ due to head-on overlapping of $sp^2$ hybridised orbitals and one weak pi $\pi$ bond (bond enthalpy about $284\ kJ\ mol^{–1})$ obtained by lateral or sideways overlapping of the two 2p orbitals of the two carbon atoms. The double bond is shorter in bond length (134 pm) than the C–C single bond (154 pm). You have already read that the pi $(\pi)$ bond is a weaker bond due to poor sideways overlapping between the two 2p orbitals. Thus, the presence of the pi $(\pi)$bond makes alkenes behave as sources of loosely held mobile electrons. Therefore, alkenes are easily attacked by reagents or compounds which are in search of electrons. Such reagents are called electrophilic reagents. The presence of weaker$(\pi)$-bond makes alkenes unstable molecules in comparison to alkanes and thus, alkenes can be changed into single bond compounds by combining with the electrophilic reagents. Strength of the double bond (bond enthalpy, $681\ kJ\ mol^{–1}$) is greater than that of a carbon-carbon single bond in ethane (bond enthalpy, $348\ kJ\ mol^{–1}$). Orbital diagrams of ethene molecule are shown in Figure.

Geometrical isomerism: Doubly bonded Carbon atoms have to satisfy the remaining two Valences by joining with two atoms or groups. If the two atoms or groups attached to each Carbon atom are different, they can be Represented by YX C = C XY like structure. YX C = C XY can be represented in space in the Following two ways:

In (a), the two identical atoms i.e., both the X or both the Y lie on the same side of the Double bond but in (b) the two X or two Y lie Across the double bond or on the opposite Sides of the double bond. This results in Different geometry of (a) and (b) i.e. disposition Of atoms or groups in space in the two Arrangements is different. Therefore, they are Stereoisomers. They would have the same Geometry if atoms or groups around C = C bond Can be rotated but rotation around C = C bond Is not free. It is restricted. For understanding This concept, take two pieces of strong Cardboards and join them with the help of two Nails. Hold one cardboard in your one hand And try to rotate the other. Can you really rotate The other cardboard ? The answer is no. The Rotation is restricted. This illustrates that the Restricted rotation of atoms or groups around The doubly bonded carbon atoms gives rise to Different geometries of such compounds. The Stereoisomers of this type are called Geometrical isomers. The isomer of the type (a), in which two identical atoms or groups lie On the same side of the double bond is called Cis isomer and the other isomer of the type (b), in which identical atoms or groups lie on The opposite sides of the double bond is called Trans isomer. Thus cis and trans isomers Have the same structure but have different Configuration (arrangement of atoms or groups In space). Due to different arrangement of Atoms or groups in space, these isomers differ In their properties like melting point, boiling Point, dipole moment, solubility etc. Geometrical or cis-trans isomers of but-2-ene Are represented below:

Cis form of alkene is found to be more polar Than the trans form. For example, dipole Moment of cis - but - 2-ene is 0.33 Debye, Whereas, dipole moment of the trans form Is almost zero or it can be said that trans - but - 2 -ene is non-polar. This can be understood by drawing geometries of the two forms as given below from which it is clear that in the trans - but - 2 -ene, the two methyl groups are in opposite directions, Therefore, dipole moments of $C - CH_3$ bonds cancel, thus making the trans form non-polar.

In the case of solids, it is observed that the trans isomer has higher melting point than the cis form. Geometrical or cis-trans isomerism is also shown by alkenes of the types XYC = CXZ and XYC = CZW
Preparation – From alkynes: Alkynes on partial reduction with calculated amount of dihydrogen in the presence of palladised charcoal partially deactivated with poisons like sulphur
compounds or quinoline give alkenes. Partially deactivated palladised charcoal is known as Lindlar’s catalyst. Alkenes thus obtained are having cis geometry. However, alkynes on reduction with sodium in liquid ammonia form trans alkenes.

From alkyl halides: Alkyl halides (R-X) on heating with alcoholic potash (potassium hydroxide dissolved in alcohol, say, ethanol) eliminate one molecule of halogen acid to form alkenes. This reaction is known as dehydrohalogenation i.e., removal of halogen acid. This is example of $\beta-$elimination reaction, since hydrogen atom is eliminated from the $\beta$ carbon atom (carbon atom next to the carbon to which halogen is attached).

Nature of halogen atom and the alkyl group determine rate of the reaction. It is observed that for halogens, the rate is: iodine > bromine > chlorine, while for alkyl groups it is: tert > secondary > primary.
Physical properties Alkenes as a class resemble alkanes in physical properties, except in types of isomerism and difference in polar nature. The first three members are gases, the next fourteen are liquids and the higher ones are solids. Ethene is a colourless gas with a faint sweet smell. All other alkenes are colourless and odourless, insoluble in water but fairly soluble in non- polar solvents like benzene, petroleum ether. They show a regular increase in boiling point with increase in size i.e., every $–CH_2$ group added increases boiling point by 20–30 K. Like alkanes, straight chain alkenes have higher boiling point than isomeric branched chain compounds.
  1. The first three members of alkenes are …?
  1. Gases
  2. Liquids
  3. Solids
  4. None of above
  1. General formula for alkenes is ….?
  1. $C_nH_{2n+1}$
  2. $C_nH_{2n}$
  3. $C_nH_{2n-1}$
  4. $C_nH_{2n+2}$
  1. The colour of ethene gas is …?
  1. Red
  2. White
  3. Pale Green
  4. None of above
  1. The bond length of carbon carbon double bond is … pm ?
  1. 154
  2. 143
  3. 134
  4. 120
  1. Alkenes are also knows as …?
  1. Olefines
  2. Paraffines
  3. Oleofines
  4. Paracetofines
The ionic character of metallic halides tends toward covalent nature as per Fajan's rule. Such covalent halides behave as non-metal in their higher oxidation states. The property to hydrolyse to give oxy-acids of the element and corresponding hydro halogen acid for most non-metallic elements proceeds exceptionally in the way, keeping oxidation number of element and halide sam in oxo-acids.
Non-polar halides are immiscible in water, as they do not show hydrolysis, but halides of some elements with empty d-orbital undergo hydrolysis. Stability of halides of the higher state is governed by the inert-pair effect.

1. How does halide undergo hydrolysis to give oxy-acids of underlined element $PCl _3$ ?
2. Out of $NCl _3$ and $BCl _3$ undergoes hydrolysis to form oxy-acids? Write the chemical reaction for the correct answer.
3. Out of $PbCl _4, PbF _4, PbI _4$ and $PbBr _4$ which one doesn't exist?
OR
Non-Polar halides are immiscible in water. Why?
Read the passage given below and answer the following questions from 1 to 5 .
In p-block elements the last electron enters the outermost p orbital. As we know that the number of p orbitals is three and, therefore, the maximum number of electrons that can be accommodated in a set of p orbitals is six. Consequently there are six groups of p-block elements in the periodic table numbering from 13 to 18 . Boron, carbon, nitrogen, oxygen, fluorine and helium head the groups. Their valence shell electronic configuration is $ns ^2 np ^{1-}$ ${ }^6$ (except for He). The inner core of the electronic configuration may, however, differ. The difference in inner core of elements greatly influences their physical properties (such as atomic and ionic radii, ionisation enthalpy, etc.) as well as chemical properties. The occurrence of oxidation states two unit less than the group oxidation states are sometime attributed to the 'inert pair effect'.
Group 13 elements: the boron family This group elements show a wide variation in properties. Boron is a typical non-metal, aluminium is a metal but shows many chemical similarities to boron, and gallium, indium, thallium and nihonium are almost exclusively metallic in character. Boron is a fairly rare element, mainly occurs as orthoboric acid, $\left( H _3 BO _3\right)$, borax, $Na _2 B_4 O _7 \cdot 10 H _2 O$, and kernite, $Na _2 B_4 O _7 \cdot 4 H _2 O$. In India borax occurs in Puga Valley (Ladakh) and Sambhar Lake (Rajasthan). The abundance of boron in earth crust is less than $0.0001 \%$ by mass. There are two isotopic forms of boron $10 B(19 \%)$ and $11 B(81 \%)$. Aluminium is the most abundant metal and the third most abundant element in the earth's crust ( $8.3 \%$ by mass) after oxygen ( $45.5 \%$ ) and $Si (27.7 \%)$. Bauxite, $Al 2 O 3.2 H _2 O$ and cryolite, Na3AIF6 are the important minerals of aluminium. In India it is found as mica in Madhya Pradesh, Karnataka, Orissa and Jammu. Gallium, indium and thallium are less abundant elements in nature. Nihonium has symbol Nh, atomic number 113 , atomic mass $286 g mol ^{-1}$ and electronic configuration $[R n] 5 f^{14} 6 d^{10} 7 s^2 7 p ^2$. So far it has been prepared in small amount and half life of its most stable isotope is 20 seconds. Due to these reasons its chemistry has not been established. Nihonium is a synthetically prepared radioactive element. Here atomic, physical and chemical properties of elements of this group leaving nihonium are discussed below.
The outer electronic configuration of these elements is $n s 2 n{ }^1$. A close look at the electronic configuration suggests that while boron and aluminium have noble gas core, gallium and indium have noble gas plus 10 d electrons, and thallium has noble gas plus 14 f - electrons plus 10 d -electron cores. Thus, the electronic structures of these elements are more complex than for the first two groups of elements discussed in unit 10. This difference in electronic structures affects the other properties and consequently the chemistry of all the elements of this group. 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. However, a deviation can be seen. Atomic radius of Ga is less than that of Al. This can be understood from the variation in the inner core of the electronic configuration. The presence of additional 10 d -electrons offer only poor screening effect (Unit 2) 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 ).
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 members are soft metals with low melting point and high electrical conductivity. It is worthwhile to note that gallium with unusually 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.
  1. There are … groups of p–block elements in the periodic table.
  1. six
  2. seven
  3. eight
  4. two
  1. Boron is … in nature.
  1. metallic
  2. non-metallic
  3. metalloid
  4. All the above
  1. Boiling point of gallium is …
  1. 303K
  2. 1345K
  3. 2676 K
  4. 1854K
  1. The occurrence of oxidation states two unit less than the group oxidation states are sometime attributed to the …
  1. loan pair effect
  2. middle pair effect
  3. outer pair effect
  4. inert pair effect
  1. Density of the elements … down the group from boron to thallium.
  1. increases
  2. decreases
  3. remains constant
  4. none of above
Read the passage given below and answer the following questions from $1$ to $5$. Lithium metal is used to make useful alloys, for example with lead to make ‘white metal’ Bearings for motor engines, with aluminium to make aircraft parts, and with magnesium to make armour plates. It is used in Thermonuclear reactions. Lithium is also used to make electrochemical cells. Sodium is used To make a Na/Pb alloy needed to make $PbEt_4$​​​​​​​ and $PbMe_4​​​​​​​$​​​​​​​. These organolead compounds were Earlier used as anti-knock additives to petrol, But nowadays vehicles use lead-free petrol. Liquid sodium metal is used as a coolant in Fast breeder nuclear reactors. Potassium has a vital role in biological systems. Potassium Chloride is used as a fertilizer. Potassium Hydroxide is used in the manufacture of soft Soap. It is also used as an excellent absorbent of carbon dioxide. Caesium is used in devising Photoelectric cells. Points of Difference between Lithium and other Alkali Metals –
i) Lithium is much harder. Its m.p. and b.p. are higher than the other alkali metals.
ii) Lithium is least reactive but the strongest Reducing agent among all the alkali metals. On combustion in air it forms mainly Monoxide, $Li_2O$ and the nitride, $Li_3N$ unlike Other alkali metals.
 iii) LiCl is deliquescent and crystallises as a Hydrate, LiCl.$2H_2O$ whereas other alkali Metal chlorides do not form hydrates.
iv) Lithium hydrogencarbonate is not Obtained in the solid form while all other Elements form solid hydrogencarbonate.
v) Lithium unlike other alkali metals forms No ethynide on reaction with ethyne.
vi) Lithium nitrate when heated gives lithium Oxide, $Li_2O$, whereas other alkali metal Nitrates decompose to give the Corresponding nitrite. $4\text{LiNO}_3\rightarrow2\text{L}\text{i}_2\text{O}+4\text{NO}_2+\text{O}_2$ $2\text{NaNO}_3\rightarrow2\text{NaNO}_2+\text{O}_2$ vii) LiF and $Li_2O$ are comparatively much less Soluble in water than the corresponding Compounds of other alkali metals. Sodium carbonate is generally prepared by Solvay Process. In this process, advantage is Taken of the low solubility of sodium Hydrogencarbonate whereby it gets Precipitated in the reaction of sodium chloride with ammonium hydrogencarbonate. The Latter is prepared by passing $CO_2​​​​​​​$​​​​​​​ to a Concentrated solution of sodium chloride Saturated with ammonia, where ammonium Carbonate followed by ammonium Hydrogencarbonate are formed. The equations For the complete process may be written as $2\text{NH}_3+\text{H}_2\text{O}+\text{CO}_2\rightarrow{\text{(NH}_4)_2}\text{CO}_3$ $(\text{NH}_4)_2\text{CO}_3+\text{H}_2\text{O}+\text{CO}_2\rightarrow2\text{NH}_4\text{HCO}_3$ $\text{NH}_4\text{HCO}_3+\text{NaCl}\rightarrow\text{NH}_4\text{Cl}+\text{NaHCO}_3$ Sodium hydrogencarbonate crystal Separates. these are heated to give sodium Carbonate. The most abundant source of sodium chloride is sea water which contains $2.7$ to $2.9 \%$ by Mass of the salt. In tropical countries like India, Common salt is generally obtained by Evaporation of sea water. Approximately $50$ Lakh tons of salt are produced annually in India by solar evaporation. Crude sodium Chloride, generally obtained by crystallisation Of brine solution, contains sodium sulphate, Calcium sulphate, calcium chloride and Magnesium chloride as impurities. Calcium Chloride, $CaCl_2$​​​​​​​, and magnesium chloride, $MgCl_2$​​​​​​​ are impurities because they are Deliquescent (absorb moisture easily from the Atmosphere). To obtain pure sodium chloride, The crude salt is dissolved in minimum amount Of water and filtered to remove insoluble Impurities. The solution is then saturated with Hydrogen chloride gas. Crystals of pure Sodium chloride separate out. Calcium and Magnesium chloride, being more soluble than Sodium chloride, remain in solution. Sodium Hydroxide (Caustic Soda), NaOH is generally prepared Commercially by the electrolysis of sodium Chloride in Castner-Kellner cell. A brine Solution is electrolysed using a mercury Cathode and a carbon anode. Sodium metal Discharged at the cathode combines with Mercury to form sodium amalgam. Chlorine Gas is evolved at the anode. Cathod: $\text{Na}^++\bar{\text{e}}\xrightarrow{\text{Hg}}\text{Na}-\text{amalgam}$ Anode: $\text{Cl}^-\rightarrow\frac{1}{2}\text{Cl}_2+\text{e}^-$ The amalgam is treated with water to give Sodium hydroxxide and hydrogen gas. $2$ Na - amalgam $+ 2H_2O \rightarrow 2NaOH + 2Hg + H_2$​​​​​​​
  1. NaOH Sodium hydroxide is generally prepared Commercially by the electrolysis of … in Castner-Kellner cell.
  1. $NaCl$
  2. $Na_2CO_3$
  3. $NaHCO_3$
  4. $NaNH_2$
  1. … is used in the manufacture of soft Soap.
  1. Sodium Hydroxide
  2. Potassium Hydroxide
  3. Aluminium hydroxide
  4. Beryllium hydroxide
  1. … is used in devising Photoelectric cells.
  1. Hydrogen
  2. Lithium
  3. Caesium
  4. Helium
  1. … compounds were Earlier used as anti-knock additives to petrol.
  1. Organomagnesium
  2. Organosilicon
  3. Organochloride
  4. Organolead
  1. The sodium amalgam is treated with water to gives ….
  1. $NaOH$
  2. $Na_2CO_3$
  3. $NaHCO_3$
  4. $NaNH_2$​​​​​​​
Read the passage given below and answer the following questions from (i) to (v).
The presence of positive charge on thenucleus is due to the protons in the nucleus.As established earlier, the charge on the proton is equal but opposite to that of electron.Atomic number $(Z)=$ number of protons inthe nucleus of an atom = number of electrons in a nuetral atom. protons and neutrons present in thenucleus are collectively known as nucleons. The total number of nucleons is termed asmass number $(A)$ of the atom.
mass number $(A)=$ number of protons $(Z)+$ number of neutrons $( n )$.
Isobars are the atoms with same massnumber but different atomic number forexample, ${ }_6^4 C$ and ${ }_7^{14} N$. On the other hand, atomswith identical atomic number but differentatomic mass number are known as Isotopes. For example, considering of hydrogen atom again, $99.985 \%$ of hydrogen atoms contain only one proton.This isotope is called protium $\left(1^1 H \right)$. Rest of thepercentage of hydrogen atom contains two otherisotopes, the one containing 1 proton and 1 neutron is called deuterium ( ${ }^2{ }_1 D , 0.015 \%$ )and the other one possessing 1 proton and 2 neutrons is called tritium ( ${ }^3 T$ )..the studies of interactions of radiations with matter haveprovided immense information regarding thestructure of atoms and molecules. Neils Bohrutilised these results to improve upon themodel proposed by Rutherford. Twodevelopments played a major role in theformulation of Bohr's model of atom. Thesewere:
1. Dual character of the electromagneticradiation which means that radiations possess both wave like and particle likeproperties, and
2. Experimental results regarding atomicspectra.

James Maxwell (1870) was the first to givea comprehensive explanation about theinteraction between the charged bodies andthe behaviour of electrical and magnetic fieldson macroscopic level. He suggested that whenelectrically charged particle moves underaccelaration, alternating electrical and magnetic fields are produced and transmitted.These fields are transmitted in the forms ofwaves called electromagnetic waves orelectromagnetic radiation.radiations are characterised by theproperties, namely, frequency $(v)$ and wavelength $(\lambda)$.The SI unit for frequency $(v)$ is hertz $\left( Hz , s ^{-1}\right)$, after Heinrich Hertz. It is defined asthe number of waves that pass a given pointin one second. Wavelength should have the units of lengthand as you know that the SI units of length ismeter ( m ). Since electromagnetic radiationconsists of different kinds of waves of muchsmaller wavelengths, smaller units are used.In vaccum all types of electromagneticradiations, regardless of wavelength, travel atthe same speed, i.e., $3.0 \times 10^8 m s ^{-1}$ ( $2.997925 \times 10^8 ms^{-1}$, to be precise). This is called speedof light and is given the symbol ' c '. Thefrequency $( V )$, wavelength $(\lambda)$ and velocity of light(c) are related by the following equation.
$c=v \lambda$
The other commonly used quantityspecially in spectroscopy, is the wavenumber.It is defined as the number of wavelengthsper unit length. Its units are reciprocal ofwavelength unit, i.e., $m^{–1}$​​​​​​​. However commonlyused unit is $cm^{–1}​​​​​​​$​​​​​​​
  1. The presence of positive charge on the nucleus is due to the …. in the nucleus.
  1. Protons
  2. Neutrons
  3. Electron
  4. Nucleons
  1. Atomic Number is denoted by:
  1. $A$
  2. $Z$
  3. $N$
  4. $M$
  1. Atomic Mass number is denoted by:
  1. $M$
  2. $Z$
  3. $N$
  4. $A$
  1. … are the atoms with same mass number but different atomic number.
  1. Isotopes
  2. Allotropes
  3. Isobars
  4. None of above
  1. Atoms with identical atomic number but different atomic mass number are known as ..
  1. Isotopes
  2. Allotropes
  3. Isobars
  4. None of above
The French physicist, de Broglie, in 1924proposed that matter, like radiation, shouldalso exhibit dual behaviour i.e., both particleand wavelike properties. This means that justas the photon has momentum as well aswavelength, electrons should also havemomentum as well as wavelength, de Broglie,from this analogy, gave the following relationbetween wavelength $(\lambda)$ and momentum (p) ofa material particle
$\lambda=\frac{\text{h}}{\text{mv}}=\frac{\text{h}}{\text{p}}$
where m is the mass of the particle, v itsvelocity and p its momentum.
Werner Heisenberg a German physicist in1927, stated uncertainty principle which is theconsequence of dual behaviour of matter andradiation. It states that it is impossible todetermine simultaneously, the exact position and exact momentum (or velocity)of an electron.Mathematically, it can be given as inequation
$\triangle\text{x}\times\triangle\text{p}_{\text{x}}\geq\frac{\text{h}}{4\pi}$
or $\triangle\text{x}\times\triangle(\text{mv}_{\text{x}})\geq\frac{\text{h}}{4\pi}$
or $\triangle\text{x}\times\triangle(\text{v}_{\text{x}})\geq\frac{\text{h}}{4\pi\text{m}}$
where $\triangle\text{x}$ is the uncertainty in position and $\triangle\text{px}(\text{or}\triangle\text{vx})$ is the uncertainty in momentum (orvelocity) of the particle.
One of the important implications of theHeisenberg Uncertainty Principle is that itrules out existence of definite paths ortrajectories of electrons and other similarparticles. The effect of Heisenberg Uncertainty Principle is significant only for motion of microscopic objects and is negligible for that of macroscopic objects. It, therefore, means that theprecise statements of the position andmomentum of electrons have to bereplaced by the statements of probability,that the electron has at a given positionand momentum. This is what happens inthe quantum mechanical model of atom. In Bohr model, anelectron is regarded as a charged particlemovingin well defined circular orbits aboutthe nucleus. The wave character of the electronis not considered in Bohr model. Further, anorbit is a clearly defined path and this pathcan completely be defined only if both theposition and the velocity of the electron areknown exactly at the same time. This is notpossible according to the Heisenberguncertainty principle. Bohr model of thehydrogen atom, therefore, not only ignoresdual behaviour of matter but also contradictsHeisenberg uncertainty principle. The structure of the atom was needed which could account for wave-particle duality of matter and be consistent with Heisenberg uncertainty Principle. This came with the advent of Quantum mechanics. This is mainly becauseof the fact thatclassical mechanics ignores theconcept of dual behaviour of matter especiallyfor sub-atomic particles and the uncertaintyprinciple. The branch of science that takes intoaccount this dual behaviour of matter is calledquantum mechanics.Quantum mechanics is a theoreticalscience that deals with the study of the motionsof the microscopic objects that have bothobservable wave like and particle likeproperties.When Schrödinger equation is solved forhydrogen atom, the solution gives the possibleenergy levels the electron can occupy and thecorresponding wave function(s) $\psi$ of theelectron associated with each energy level. A large number of orbitals are possible in anatom. Qualitatively these orbitals can bedistinguished by their size, shape andorientation. An orbital of smaller size meansthere is more chance of finding the electron nearthe nucleus. Similarly shape and orientationmean that there is more probability of findingthe electron along certain directions thanalong others. Atomic orbitals are preciselydistinguished by what are known as quantumnumbers. Each orbital is designated by threequantum numbers labelled as n, l and $m_1$.
The principal quantum number ‘n’ isa positive integer with value of n = 1,2,3…….The principal quantum number determines thesize and to large extent the energy of theorbital. Azimuthal quantum number. ‘l’ is alsoknown as orbital angular momentum orsubsidiary quantum number. It defines thethree-dimensional shape of the orbital.. For agiven value of n, l can have n values rangingfrom 0 to n – 1, that is, for a given value of n,the possible value of l are : l = 0, 1, 2, ……….(n–1)
Magnetic orbital quantum number. ‘mlgives information about the spatialorientation of the orbital with respect tostandard set of co-ordinate axis. For anysub-shell (defined by ‘l’ value) 2l+1 valuesof ml are possible and these values are givenbuy :ml = – l, – (l –1), – (l–2)… 0,1… (l –2), (l–1)..
In 1925, George Uhlenbeck and SamuelGoudsmit proposed the presence of the fourthquantum number known as the electronspin quantum number (ms). electron has, besides charge and mass,intrinsic spin angular quantum number. Spinangular momentum of the electron — a vectorquantity, can have two orientations relative tothe chosen axis. These two orientations aredistinguished by the spin quantum numbersms which can take the values of $+½ or –½$.These are called the two spin states of theelectron and are normally represented by twoarrows, ↑ (spin up) and ↓ (spin down).the four quantum numbersprovide the following information :
  1. n defines the shell, determines the size ofthe orbital and also to a large extent theenergy of the orbital.
  2. There are n subshells in the n the shell. Lidentifies the subshell and determines the shape of the orbital (see section 2.6.2).There are (2l+1) orbitals of each type in asubshell, that is, one s orbital (l = 0), threep orbitals (l = 1) and five d orbitals (l = 2)per subshell. To some extent l alsodetermines the energy of the orbital in amulti-electron atom.
  3. ml designates the orientation of the orbital.For a given value of l, mlhas (2l+1) values,the same as the number of orbitals persubshell. It means that the number oforbitals is equal to the number of ways inwhich they are oriented.
  4. ms refers to orientation of the spin of the electron.
  1. Uncertainty principle was given by:
  1. Werner Heisenberg
  2. George Uhlenbeck
  3. Samuel Goudsmit
  4. De Broglie
  1. Quantum mechanics is a theoretical science that deals with the study of the motions of the ….. objects.
  1. Macroscopic
  2. Microscopic
  3. Laparoscopic
  4. All the above
  1. The principal quantum number …
  1. l
  2. m
  3. n
  4. p
  1. …is also known as orbital angular momentum or subsidiary quantum number.
  1. Principal quantum number
  2. Electron spin quantum number
  3. Magnetic orbital quantum number.
  4. Azimuthal quantum number
  1. George Uhlenbeck and Samuel Goudsmit proposed the presence of the fourth quantum number known as the …
  1. Principal quantum number
  2. Electron spin quantum number
  3. Magnetic orbital quantum number.
  4. Azimuthal quantum number
The ionic character of metallic halides tends toward covalent nature as per Fajan's rule. Such covalent halides behave as non-metal in their higher oxidation states. The property to hydrolyse to give oxy-acids of the element and corresponding hydro halogen acid for most non-metallic elements proceeds exceptionally in the way, keeping oxidation number of element and halide sam in oxo-acids.
Non-polar halides are immiscible in water, as they do not show hydrolysis, but halides of some elements with empty d-orbital undergo hydrolysis. Stability of halides of the higher state is governed by the inert-pair effect.

1. How does halide undergo hydrolysis to give oxy-acids of underlined element $PCl _3$ ? (1)
2. Out of $NCl _3$ and $BCl _3$ undergoes hydrolysis to form oxy-acids? Write the chemical reaction for the correct answer. (1)
3. Out of $PbCl _4, PbF _4, PbI _4$ and $PbBr _4$ which one doesn't exist? (2)
OR
Non-Polar halides are immiscible in water. Why? (2)
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).
First complete data on pressure-volume-Temperature relations of a substance in bothGaseous and liquid state was obtained byThomas Andrews on Carbon dioxide. He plottedlsotherms of carbon dioxide at variousTemperatures.
Later on it was found That real gases behave in the same manner asCarbon dioxide. Andrews noticed that at highTemperatures isotherms look like that of anldeal gas and the gas cannot be liquified even atVery high pressure. As the temperature isLowered, shape of the curve changes and dataShow considerable deviation from idealBehaviour. At $30.98^{\circ} C$ carbon dioxide remainsGas upto 73 atmospheric pressure. At 73 atmospheric pressure, liquidCarbon dioxide appears for the first time. TheTemperature $30.98^{\circ} C$ is called criticalTemperature (TC) of carbon dioxide. This is theHighest temperature at which liquid carbonDioxide is observed. Above this temperature itls gas. Volume of one mole of the gas at criticalTemperature is called critical volume $\left( V _{ c }\right)$ andPressure at this temperature is called criticalPressure (pc). The critical temperature, pressureand volume are called critical constants. A gasBelow the critical temperature can be liquifiedBy applying pressure, and is called vapour ofThe substance. Carbon dioxide gas below itsCritical temperature is called carbon dioxideVapour.
Intermolecular forces are stronger in liquidState than in gaseous state. Molecules in liquidsAre so close that there is very little empty space between them and under normal conditionsLiquids are denser than gases.Molecules of liquids are held together byAttractive intermolecular forces. Liquids haveDefinite volume because molecules do notSeparate from each other. However, moleculesOf liquids can move past one another freely, Therefore, liquids can flow, can be poured andCan assume the shape of the container in whichThese are stored. If an evacuated container is partially filled withA liquid, a portion of liquid evaporates to fillthe remaining volume of the container withVapour. Initially the liquid evaporates andPressure exerted by vapours on the walls of The container (vapour pressure) increases. AfterSome time it becomes constant, an equilibriumls established between liquid phase andVapour phase. Vapour pressure at this stagels known as equilibrium vapour pressure orSaturated vapour pressure.. Since process ofVapourisation is temperature dependent; the Temperature must be mentioned whilereporting the vapour pressure of a liquid.
When a liquid is heated in an open vessel,The liquid vapourises from the surface. At theTemperature at which vapour pressure of theLiquid becomes equal to the external pressure,Vapourisation can occur throughout the bulkOf the liquid and vapours expand freely intoThe surroundings. The condition of freeVapourisation throughout the liquid is calledBoiling. The temperature at which vapourPressure of liquid is equal to the externalPressure is called boiling temperature at thatPressure. At 1 atm pressure boilingTemperature is called normal boiling point.If pressure is 1 bar then the boiling point isCalled standard boiling point of the liquid. Standard boiling point of the liquid is slightlyLower than the normal boiling point because 1 bar pressure is slightly less than 1 atmPressure . The normal boiling point of water is $100^{\circ} C (373 K)$, its standard boiling point is $99.6^{\circ} C (372.6 K)$.At high altitudes atmospheric pressure isLow. Therefore liquids at high altitudes boil atLower temperatures in comparison to that atSea level. Since water boils at low temperatureOn hills, the pressure cooker is used forCooking food. In hospitals surgical instrumentsAre sterilized in autoclaves in which boilingPoint of water is increased by increasing thePressure above the atmospheric pressure byUsing a weight covering the vent.Boiling does not occur when liquid isHeated in a closed vessel. On heatingContinuously vapour pressure increases.
AtFirst a clear boundary is visible between liquidAnd vapour phase because liquid is more denseThan vapour. As the temperature increases more and more molecules go to vapour phaseAnd density of vapours rises. At the same timeLiquid becomes less dense. It expands becauseMolecules move apart. When density of liquidAnd vapours becomes the same; the clearBoundary between liquid and vapoursDisappears. This temperature is called critical Temperature.
  1. First complete data on Pressure-Volume-Temperature relations of a substance in both Gaseous and liquid state was obtained by:
  1. Thomas Andrews
  2. Fritz London
  3. Robert Boyle
  4. Joseph Lewis Gay Lussac
  1. Critical Temperature (TC) of carbon dioxide is.....
  1. $24^\circ C$
  2. $30.8^\circ C$
  3. $56^\circ C$
  4. $29^\circ C$
  1. The condition of free Vapourisation throughout the liquid is called …
  1. Evaporation
  2. Melting
  3. Boiling
  4. None of above
  1. Standard boiling point of Water is....
  1. $100^\circ C$
  2. $3^\circ C$
  3. $105^\circ C$
  4. $99.6^\circ C$
  1. Boundary between liquid and vapours Disappears,This temperature is called
  1. Critical temperature
  2. Absolute temperature
  3. Normal temperature
  4. Boiling temperature
The ionic character of metallic halides tends toward covalent nature as per Fajan's rule. Such covalent halides behave as non-metal in their higher oxidation states. The property to hydrolyse to give oxy-acids of the element and corresponding hydro halogen acid for most non-metallic elements proceeds exceptionally in the way, keeping oxidation number of element and halide sam in oxo-acids.
Non-polar halides are immiscible in water, as they do not show hydrolysis, but halides of some elements with empty d-orbital undergo hydrolysis. Stability of halides of the higher state is governed by the inert-pair effect.

1. How does halide undergo hydrolysis to give oxy-acids of underlined element $PCl _3$ ? (1)
2. Out of $NCl _3$ and $BCl _3$ undergoes hydrolysis to form oxy-acids? Write the chemical reaction for the correct answer. (1)
3. Out of $PbCl _4, PbF _4, PbI _4$ and $PbBr _4$ which one doesn't exist? (2)
OR
Non-Polar halides are immiscible in water. Why? (2)