Question
Read the passage given below and answer the following questions from 1 to 5.
Alkaline earth elements have two electrons in the s - orbital of the valence shell. Their general electronic configuration may be represented as [noble gas] $ns^2$. Like alkali metals, the compounds of these elements are also predominantly ionic.

The atomic and ionic radii of the alkaline earth metals are smaller than those of the corresponding alkali metals in the same periods. This is due to the increased nuclear charge in these elements. Within the group, the atomic and ionic radii increase with increase in atomic number.
The alkaline earth metals have low ionization enthalpies due to fairly large size of the atoms. Since the atomic size increases down the group, their ionization enthalpy decreases. The first ionisation enthalpies of the alkaline earth metals are higher than those of the corresponding Group 1 metals. This is due to their small size as compared to the corresponding alkali metals. It is interesting to note that the second ionisation enthalpies of the alkaline earth metals are smaller than those of the corresponding alkali metals.
Like alkali metal ions, the hydration enthalpies of alkaline earth metal ions decrease with increase in ionic size down the group. $Be^{2+}> Mg^2+ > Ca^{2+} > Sr^{2+} > Ba^{2+}$ The hydration enthalpies of alkaline earth metal ions are larger than those of alkali metal ions. Thus, compounds of alkaline earth metals are more extensively hydrated than those of alkali metals, e.g., $MgCl_2$ and $CaCl_2$ exist as $MgCl_{2.}6H_2O$ and $CaCl_2· 6H_2O$ while NaCl and KCl do not form such hydrates.
The alkaline earth metals, in general, are silvery white, lustrous and relatively soft but harder than the alkali metals. Beryllium and magnesium appear to be somewhat greyish. The melting and boiling points of these metals are higher than the corresponding alkali metals due to smaller sizes. The trend is, however, not systematic. Because of the low ionisation enthalpies, they are strongly electropositive in nature. The electropositive character increases down the group from Be to Ba. Calcium, strontium and barium impart characteristic brick red, crimson and apple green colours respectively to the flame. In flame the electrons are excited to higher energy levels and when they drop back to the ground state, energy is emitted in the form of visible light. The electrons in beryllium and magnesium are too strongly bound to get excited by flame. Hence, these elements do not impart any colour to the flame. The flame test for Ca, Sr and Ba is helpful in their detection in qualitative analysis and estimation by flame photometry. The alkaline earth metals like those of alkali metals have high electrical and thermal conductivities which are typical characteristics of metals.
Chemical Properties- The alkaline earth metals are less reactive than the alkali metals. The reactivity of these elements increases on going down the group.
i) Reactivity towards air and water: Beryllium and magnesium are kinetically inert to oxygen and water because of the formation of an oxide film on their surface. Magnesium is more electropositive and burns with dazzling brilliance in air to give $MgO$ and $Mg_3N_2$​​​​​​​. Calcium, strontium and barium are readily attacked by air to form the oxide and nitride.
ii) Reactivity towards the halogens: All the alkaline earth metals combine with halogen at elevated temperatures forming their halides.
$M+X_2\rightarrow Mx_2(x=F, Cl, Br, l)$
iii) Reactivity towards hydrogen: All the elements except beryllium combine with hydrogen upon heating to form their hydrides, $MH_2. BeH_2​​​​​​​$, however, can be prepared by the reaction of $BeCl_2$ with $LiAlH_4$​​​​​​​
2 $BeCl_2+ LiAlH_4\rightarrow 2BeH_2+ LiCl+AlCl_3$​​​​​​​
iv) Reactivity towards acids: The alkaline earth metals readily react with acids liberating dihydrogen. $M + 2HCl \rightarrow MCl_2 + H_2$​​​​​​​
v) Reducing nature: Like alkali metals, the alkaline earth metals are strong reducing agents. This is indicated by large negative values of their reduction potentials. However their reducing power is less than those of their corresponding alkali metals. Beryllium has less negative value compared to other alkaline earth metals
vi) Solutions in liquid ammonia: Like alkali metals, the alkaline earth metals dissolve in liquid ammonia to give deep blue black solutions forming ammoniated ions.
$\text{M}+(\text{x+y})\text{NH}_3\rightarrow \big[\text{M}(\text{NH}_3)\text{X}\big]^{2+}+2\big[\text{e}(\text{NH}_3)\text{y}\big]^-$
From these solutions, the ammoniates, $\big[\text{M}(\text{NH}_3)6\big]^{2+}$can be recovered.
Beryllium is used in the manufacture of alloys. Copper - beryllium alloys are used in the preparation of high strength springs. Metallic beryllium is used for making windows of X-ray tubes. Magnesium forms alloys with aluminium, zinc, manganese and tin. Magnesium-aluminium alloys being light in mass are used in air-craft construction. Magnesium (powder and ribbon) is used in flash powders and bulbs, incendiary bombs and signals. A suspension of magnesium hydroxide in water (called milk of magnesia) is used as antacid in medicine. Magnesium carbonate is an ingredient of toothpaste. Calcium is used in the extraction of metals from oxides which are difficult to reduce with carbon. Calcium and barium metals, owing to their reactivity with oxygen and nitrogen at elevated temperatures, have often been used to remove air from vacuum tubes. Radium salts are used in radiotherapy, for example, in the treatment of cancer.
  1. The atomic and ionic radii of the alkaline earth metals are … than those of the corresponding alkali metals in the same periods.
  1. smaller
  2. bigger
  3. different
  4. None of above
  1. Within the group, the atomic and ionic radii of alkaline earth metals … with … in atomic number.
  1. increase, decrease
  2. increase, increase
  3. decrease, increase
  4. decrease, decrease
  1. Alkaline earth elements have … electrons in the s -orbital of the valence shell.
  1. Zero
  2. One
  3. Two
  4. Three
  1. Ionization enthalpy …. down the group of alkaline earth metals.
  1. first increases then decreases
  2. first decreases then increases
  3. increase
  4. decreases
  1. The hydration enthalpies of alkaline earth metal ions … with … in ionic size down the group.
  1. increase, decrease
  2. increase, increase
  3. decrease, increase
  4. decrease, decrease

Answer

  1. (a) smaller
  2. (b) increase, increase
  3. (c) Two
  4. (d) decreases
  5. (c) decrease, increase

Need a full question paper?

Generate a complete, print-ready paper with questions like this in minutes — across 16+ boards, with answer keys.

Start Generating Free

Similar questions

Read the passage given below and answer the following questions from $1$ to $5.$
Quantitative measurement of properties isreaquired for scientific investigation. Earlier, two different systems of measurement, i.e., the English System and the Metric System were being used indifferent parts of the world. The metric system, which originated in France in late eighteenth century. The SI system has seven base units. these are listed as follow.
 
Base Physical Quantities
Unit
1
Length
Metre – m
2
Mass
Kilogram – kg
3
Time
Second – s
4
Electric current
Ampere- A
5
Thermodynamic Temperature
Kelvin – K
6
Amount of substance
Mole – mol
7
Luminous intensity
Candela- cd
Here, Mass of a substance is the amount of matter present in it, while weight is the force exerted by gravity on an object. Density of a substance is its amount of mass per unit volume. The mole, symbol mol, is the SI unit of amount of substance. One mole contains exactly $6.02214076 \times 10^{23}$ elementary entities. This number is the fixed numerical value of the Avogadro constant, NA, when expressed in the unit per moland is called the Avogadro number. The amount of substance, symbol $n$, of a system is a measure of the number of specified elementary entities. An elementary entity may be an atom, a molecule, an ion, an electron, any other particle or specified group of particles.There are three common scales to measure temperature - ${ }^{\circ} C$ (degree celsius), ${ }^{\circ} F$ (degree fahrenheit) and K (kelvin). Here, K is the Slunit. Generally, the thermometer with celsius scale are calibrated from $0^{\circ}$ to $100^{\circ}$, where these two temperatures are the freezing point and the boiling point of water, respectively. The fahrenheit scale is represented between $32^{\circ}$ to $212^{\circ}$.
The temperatures on two scales are related to each other by the following relationship:
$^\circ{F} = 9 (^\circ{C}) + 32$
$5$
The kelvin scale is related to celsius scaleas follows:
$K = ^\circ{C} + 273.15$
  1. The metric system,which originated in … in late eighteenthcentury.
  1. Ukraine
  2. German
  3. Russia
  4. France
  1. The SI system has …. base units.
  1. $7$
  2. $3$
  3. $9$
  4. $1$
  1. The symbol for SI unit of thermodynamic temperature is …
  1. Kelvin
  2. $K$
  3. Degree Celsius
  4. ${}^\circ C$
  1. A prefix giga equivalents to:
  1. $10^9$
  2. $10^{10}$
  3. $10^{11}$
  4. $10^{12}$
  1. The fahrenheit scale is represented between..
  1. $0^\circ F \ to\ 100^\circ F$
  2. $32^\circ F \ to\ 212^\circ .F$
  3. $15^\circ F \ to\ 373^\circ F$
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
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.
Branched chain hydrocarbons: In a branched chain compound small chains of carbon atoms are attached at one or more carbon atoms of the parent chain. The small carbon chains (branches) are called alkyl groups. For example:

In order to name such compounds, the names of alkyl groups are prefixed to the name of parent alkane. An alkyl group is derived from a saturated hydrocarbon by removing a hydrogen atom from carbon. Thus, $CH_4$becomes$ – CH_3 $and is called methyl group. An alkyl group is named by substituting ‘yl’ for ‘ane’ in the corresponding alkane. Some alkyl groups are listed in Table
Alkane Alkyl Group
Molecular formula Name of alkane Structural formula Name of alkyl group
$CH_4$ Methane $-CH_3$ Methyl
$C_2H_6$ Ethane $-CH_2CH_3​​​​​​​$ Ethyl
$C_3H_8​​​​​​​$ Propane $-CH_2CH_2CH_3$ Propyl
$C_4H_{10}​​​​​​​$ Butane $-CH_2CH_2CH_2CH_3​​​​​​​$ Butyl
$C_{10}H_{22}​​​​​​​$ Decane $-CH_2(CH_2)_8CH_3​​​​​​​$​​​​​​​ Decyl
Abbreviations are used for some alkyl groups. For example, methyl is abbreviated as Me, ethyl as Et, propyl as Pr and butyl as Bu. The alkyl groups can be branched also. Thus, propyl and butyl groups can have branched structures as shown below .
Common branched groups have specific trivial names. For example, the propyl groups can either be n-propyl group or isopropyl group. The branched butyl groups are called sec- butyl, isobutyl and tert-butyl group. We also encounter the structural unit, – $CH_2C(CH_3)_3​​​​​​​$​​​​​​​, which is called neopentyl group.
For Nomenclature of branched chain alkanes ,longest carbon chain in the molecule is identified. The numbering is done in such a way that the branched carbon atoms get the lowest possible numbers. lower number is given to the one coming first in the alphabetical listing. Carbon atom of the branch that attaches to the root alkane. in alphabetical order, the prefixes iso- and neo- are considered to be the part of the fundamental name of alkyl group. The prefixes sec- and tert- are not considered to be the part of the fundamental name.
Cyclic Compounds: A saturated monocyclic compound is named by prefixing ‘cyclo’ to the corresponding straight chain alkane. If side chains are present, then the rules given above are applied. Names of some cyclic compounds are given below.

The phenomenon of existence of two or more compounds possessing the same molecular formula but different properties is known as isomerism. Such compounds are called as isomers. The following flow chart shows different types of isomerism.
Structural Isomerism Compounds having the same molecular formula but different structures (manners in which atoms are linked) are classified as structural isomers. Some typical examples of different types of structural isomerism are given below:

(i) Chain isomerism: When two or more compounds have similar molecular formula but different carbon skeletons, these are referred to as chain isomers and the phenomenon is termed as chain isomerism. For example, $C_5H_{12}​​​​​​​$​​​​​​​ represents three compounds:
(ii) Position isomerism: When two or more compounds differ in the position of substituent atom or functional group on the carbon skeleton, they are called position isomers and this phenomenon is termed as position isomerism. For example, the molecular formula $C_3H_8O$ represents two alcohols:

(iii) Functional group isomerism: Two or more compounds having the same molecular formula but different functional groups are called functional isomers and this phenomenon is termed as functional group isomerism. For example, the molecular formula $C_3H_6O$ represents an aldehyde and a ketone:

(iv) Metamerism: It arises due to different alkyl chains on either side of the functional group in the molecule. For example, $C_4H_{10}O$ represents methoxy propane $(CH_3OC_3H_7)$ and ethoxyethane $(C_2H_5OC_2H_5).$
Stereoisomerism The compounds that have the same constitution and sequence of covalent bonds but differ in relative positions of their atoms or groups in space are called stereoisomers. This special type of isomerism is called as stereoisomerism and can be classified as geometrical and optical isomerism.
Substrate and Reagent Ions are generally not formed in the reactions of organic compounds. Molecules as such participate in the reaction. It is convenient to name one reagent as substrate and other as reagent. In general, a molecule whose carbon is involved in new bond formation is called substrate and the other one is called reagent. When carbon-carbon bond is formed, the choice of naming the reactants as substrate and reagent is arbitrary and depends on molecule under observation. Example:
  1. $CH_4​​​​​​​$​​​​​​​ becomes –$ CH_3​​​​​​​$​​​​​​​, is called … group.
  1. methyl
  2. ethyl
  3. propyl
  4. butyl
  1. For the Nomenclature of branched chain alkanes …. carbon chain in the molecule is identified.
  1. shortest
  2. longest
  3. smallest
  4. none of above
  1. when two or more compounds possessing the same molecular formula but different properties is known as ….
  1. Allotrops
  2. Isotops
  3. Isomers
  4. Isobars
  1. For the Nomenclature of branched chain alkanes, the numbering is done in such a way that the branched carbon atoms get the … possible numbers.
  1. biggest
  2. Lower
  3. Highest
  4. lowest
  1. Which of the following is not an example of isomerisim?
  1. Functional
  2. Positional
  3. Chain
  4. Preconditional
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
IUPAC (International Union of Pure and Applied Chemistry) system of nomenclature. Common names are useful and in many cases indispensable, particularly when the alternative systematic names are lengthy and complicated. A systematic name of an organic compound is generally derived by identifying the parent hydrocarbon and the functional group(s) attached to it. By using prefixes and suffixes, the parent name can be modified to obtain the actual name. In a branched-chain compound, small chains of carbon atoms are attached at one or more carbon atoms of the parent chain. The small carbon chains (branches) are called alkyl groups. An alkyl group is derived from a saturated hydrocarbon by removing a hydrogen atom from carbon. Abbreviations are used for some alkyl groups. For example, methyl is abbreviated as Me, ethyl as Et, propyl as Pr and butyl as Bu.

1. Draw the structure of 3-Ethyl-4,4-dimethylheptane. (1)
2. How is the numbering in branched chain hydrocarbon done?
3. Derive the structure of 2-Chlorohexane. (2)
OR
Why $CH _4$ after becoming- $CH _3$ called a methyl group? (2)
Read the passage given below and answer the following questions from 1 to 5.
F Wohler synthesised an organic compound, urea from an inorganic compound, ammonium cyanate.
The knowledge of fundamental concepts of molecular structure helps in understanding and predicting the properties of organic compounds. You have already learnt theories of valency and molecular structure. Also, you already know that tetravalence of carbon and the formation of covalent bonds by it are explained in terms of its electronic configuration and the hybridisation of s and p orbitals. It may be recalled that formation and the shapes of molecules like methane $(CH_4)$, ethene $(C_2H_4)$, ethyne $(C_2H_2)$ are explained in terms of the use of $sp^3, sp^2$ and sp hybrid orbitals by carbon atoms in the respective molecules. Hybridisation influences the bond length and bond enthalpy (strength) in compounds. The sp hybrid orbital contains more s character and hence it is closer to its nucleus and forms shorter and stronger bonds than the sp3 hybrid orbital.The sp2 hybrid orbital is intermediate in s character between sp and sp3 and, hence, the length and enthalpy of the bonds it forms, are also intermediate between them. The change in hybridisation affects the electronegativity of carbon. The greater the s character of the hybrid orbitals, the greater is the electronegativity. Thus, a carbon atom having an sp hybrid orbital with 50% s character is more electronegative than that possessing sp2 or sp3 hybridised orbitals. This relative electronegativity is reflected in several physical and chemical properties of the molecules concerned, about which you will learn in later units.
Characteristic Features of π Bonds In a π (pi) bond formation, parallel orientation of the two p orbitals on adjacent atoms is necessary for a proper sideways overlap. Thus, in $H_2C=CH_2$ molecule all the atoms must be in the same plane. The p orbitals are mutually parallel and both the p orbitals are perpendicular to the plane of the molecule. Rotation of one $CH_2$ fragment with respect to other interferes with maximum overlap of p orbitals and, therefore, such rotation about carbon-carbon double bond (C=C) is restricted. The electron charge cloud of the π bond is located above and below the plane of bonding atoms. This results in the electrons being easily available to the attacking reagents. In general, π bonds provide the most reactive centres in the molecules containing multiple bonds.

Structures of organic compounds are represented in several ways. The Lewis structure or dot structure, dash structure, condensed structure and bond line structural formulas are some of the specific types. The Lewis structures, however, can be simplified by representing the two-electron covalent bond by a dash (–). Such a structural formula focuses on the electrons involved in bond formation. A single dash represents a single bond, double dash is used for double bond and a triple dash represents triple bond. Lone- pairs of electrons on heteroatoms (e.g., oxygen, nitrogen, sulphur, halogens etc.) may or may not be shown. Thus, ethane $(C_2H_6)$, ethene $(C_2H_4)$, ethyne $(C_2H_2)$ and methanol $(CH_3OH)$ can be represented by the following structural formulas. Such structural representations are called complete structural formulas.
These structural formulas can be further abbreviated by omitting some or all of the dashes representing covalent bonds and by indicating the number of identical groups attached to an atom by a subscript. The resulting expression of the compound is called a condensed structural formula. Thus, ethane, ethene, ethyne and methanol can be written as:

Similarly, $CH_3CH_2CH_2CH_2CH_2CH_2CH_2CH_3$ can be further condensed to $CH_3(CH_2)_6CH_3$. For further simplification, organic chemists use another way of representing the structures, in which only lines are used. In this bond-line structural representation of organic compounds, carbon and hydrogen atoms are not shown and the lines representing carbon-carbon bonds are drawn in a zig-zag fashion. The only atoms specifically written are oxygen, chlorine, nitrogen etc. The terminals denote methyl $(–CH_3)$ groups (unless indicated otherwise by a functional group), while the line junctions denote carbon atoms bonded to appropriate number of hydrogens required to satisfy the valency of the carbon atoms. Some of the examples are represented as follows: (i) 3-Methyloctane can be represented in various forms as:
  1. … synthesised an organic compound, urea from an inorganic compound, ammonium cyanate.
  1. Wohler
  2. Adams
  3. Roger
  4. William Evans
  1. Dot structure is also known as …
  1. Zig zag structure
  2. Lewis structure
  3. Line structure
  4. Bond line structure
  1. Terminals in zigzig structure denotes … Group.
  1. Bromyl
  2. Propyl
  3. Methyl
  4. Pentyl
  1. Triple dash represents …
  1. Single bond
  2. Double bond
  3. Triple bond
  4. Equivalent bond
  1. Lewis structures representing the two-electron covalent bond by …
  1. .
  2. :
  3. ?
The existing large number of organic compounds and their ever-increasing numbers has made it necessary to classify them on the basis of their structures. Organic compounds are broadly classified as open-chain compounds which are also called aliphatic compounds. Aliphatic compounds further classified as homocyclic and heterocyclic compounds. Aromatic compounds are special types of compounds. Alicyclic compounds, aromatic compounds may also have heteroatom in the ring. Such compounds are called heterocyclic aromatic compounds. Organic compounds can also be classified on the basis of functional groups, into families or homologous series. The members of a homologous series can be represented by general molecular formula and the successive members differ from each other in a molecular formula by a $- CH _2$ unit.

1. The successive members of a homologous series differ by which mass of amu?
OR
Is tetrahydrofuran is aromatic compounds?
2. Does Pyridine, pyrrole, thiophene are all heteroaromatic compounds
3. Difference between heterocyclic and homocyclic compound.
Read the passage given below and answer the following questions from 1 to 5 .
After having some idea about the terms atomsand molecules, it is appropriate here tounderstand what do we mean by atomic andmolecular masses. One atomicmass unit is defined as a mass exactly equal to one-twelfth of the mass of one carbon -12 atom.Molecular mass is the sum of atomic masses of the elements present in a molecule. It is obtained by multiplying the atomic mass of each element by the number of its atoms and adding them together. Some substances, such as sodium chloride, do not contain discrete molecules as their constituent units. In such compounds, positive (sodium ion) and negative (chloride ion) entities are arranged in a three dimensional structure. The mole, symbol mol, is the SI unit of amount of substance. One mole contains exactly $6.02214076 \times 10^{23}$ elementary entities. This number is the fixed numerical value of the Avogadro constant, $N _{ A }$, when expressed in the unit mol-1 and is called the Avogadro number. The amount of substance, symbol $n$, of a system is a measure of the number of specified elementary entities. An elementary entity may be an atom, a molecule, an ion, an electron, any other particle or specified group of particles. It may be emphasised that the mole of a substance always contains the same number of entities, no matter what the substance may be. In order to determine this number precisely, the mass of a carbon-12 atom was determined by a mass spectrometer and found to be equal to $1.992648 \times 10^{-23} g$. Knowing that one mole of carbon weighs 12 g , the number of atoms in it is equal to: $12 g / mol C -12$.
$1.992648 \times 10^{23} g / C -12$ atom. $=6.0221367 \times 10^{23}$ atoms $/ mol$.
The mass of one mole of a substance in grams is called its molar mass. the molar mass in grams is numerically equal to atomic molecular/formula mass in u.An empirical formula represents the simplestwhole number ratio of various atoms present ina compound, whereas, the molecular formulashows the exact number of different types ofatoms present in a molecule of a compound. If the mass per cent of variouselements present in a compound is known, its empiricalformula can be determined. Molecular formulacan further be obtained if the molar mass isknown.Many a time, reactions are carried out with the Amounts of reactants that are different than The amounts as required by a balanced chemical reaction. In such situations, one Reactant is in more amount than the amount required by balanced chemical reaction. The reactant which is present in the least amount Many a time, reactions are carried out with the amounts of reactants that are different than the amounts as required by a balanced chemical reaction. In such situations, one reactant is in more amount than the amount required by balanced chemical reaction. The reactant which is present in the least amount gets consumed after sometime and after that further reaction does not take place whatever be the amount of the other reactant. Hence, the reactant, which gets consumed first, limits the amount of product formed and is, therefore, called the limiting reagent.
i. One atomic mass unit (amu) is defined as a mass exactly equal to one-twelfth of the mass of one ...atom.
  1. One atomic mass unit (amu) is defined as a mass exactly equal to one-twelfth of the mass of one …atom.
  1. Hydrogen $– 1$
  2. Carbon $– 12$
  3. Oxygen $-12$
  4. Chlorine $– 35$
  1. The mass of one mole of a substance in grams is called its..
  1. Atomic mass
  2. Molecular Weight
  3. Molecular mass
  4. Molar mass.
  1. … is the sum of atomic massesof the elements present in a molecule.
  1. Atomic mass
  2. Molecular Weight
  3. Molecular mass
  4. Molar mass.
  1. One mole contains exactly …elementary entities.
  1. $02214076 \times 10^{21}$
  2. $02214076 \times 10^{22}$
  3. $6.02214076 \times 10^{23}$
  4. $02214076 \times 10^{24}$
  1. For which of the following compound , formula mass is preferred instead of molecular mass?
  1. $NaCl$
  2. $C2H6$
  3. $N2$
  4. $H2O​$
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