Thursday, December 31, 2015
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XI..CH..P-BLOCK ELEMENTS
Elements in which the last electron enters in the any one of the three p - orbital of
their outermost shell s – p-block ele ments
•
Gen. electronic configuration of outer shell is ns
2
np
1-6
The inner core of e-config.may differ which greatly influences their physical & to
some extent chemical properties.
GROUP 13 : The boron group
Outer Electronic Configuration:-ns
2
np
1
• group members: boron (B), aluminum (Al), gallium (Ga), indium (In)&
thallium (Tl) . All, except boron, are metals.
• Boron show diagonal relationship with Silicon; both are semiconductors
metalloids & forms covalent compounds.
• Boron compounds are electron deficient, they are lack of an octet of electrons
about the B atom .
• diborane B2H6
, is simplest boron hydride
• Structure: three-center two-electron: the H atoms are simultaneously bonded to
two B atoms the B-H bridging bond lengths are greater than B-H terminal.
• - Boron oxide is acidic (it reacts readily with water to f orm boric acid)
• aluminium compounds:aluminium oxide is amphoteric
• aluminum hali des, e.g., AlCl
3
is dimer, an important catalyst in organic
chemistry have anincomplete octet, acts as Lewic acid by acc epting lone pairs
from Lewic bases, forming adduct
• aluminum hydride, e.g., LiAlH4
, a reducing agen
. Atomic and ionic radii
• The atomic and ionic radii of group 13 elements are compared to
corresponding elements of group 2. From left to right in the period, the
magnitude of nuclear charge increases but the electrons are added to, the same
shell. These electrons do not screen each other, theref ore, the electrons
experience greater nuclear charge.
• In other words, effective nuclear charge increases and thus, size decreases.
Therefore, the elements of this group have smaller size than the corresponding
elements of second group.
• On moving down the group both atomic and ionic radii are expected to
increase due to the addition of new shell s. However, the observed atomic
radius of Al (143 pm) is slightly more than that of Ga (l35 pm).
Ionization energies
The first ionization energies of group 13 elements are less than the corresponding
me mbers of the alkaline earths.
The sharp decrease in I.E. from B to Al is due to increase in size. In case of Ga, there
are ten d-electrons in its inner electronic configuration.
The very high value of 3
rd
I. E. of thallium indicates that +3 O.N. state is not stable,
rather +1 is more stable f or thallium .
Electropositive (or metallic) character
the elements of group 13 are less electropositive as compared to ele ments of group 2.
On moving down the group the electropositive (metallic) character increases because
ionization energy decreases. For e.g., Boron is a non -metal white the other elements
are typical metals.
Oxidation states
The common oxidation states of group 13 elements are +3 and + l .The stability of
the + 1 oxidation state increases in the sequence Al <Ga< In <Tl, Due to Inert pair
effect.
Hydrides
• None of the group 13 ele ments reacts directly with hydrogen. However, a no.
of hydrides of these elements have been prepared by indirect methods. The
boron hydrides are called boranes& classified in two s eries: (a) BnHn+4
called nidoboranes (b) BnHn+6
called arachnoboranes
• INUDUSTRIAL PREPERATION :-2BF
3
(g) + 6LiH(s) → B2H6
(g) + 6LiF(s)
• Laboratory method:
(i) By the reaction of iodine with sodium borohydride in a high boiling
solvent.
2NaBH4
+ I
2 → B2H6
+ 2NaI + H2
(ii) By reduction of BCl
3
with LiAlH4
4BCl
3
+ 3LiAlH4 → 2 B2H6
+ 3AlCl
3
+ 3 LiCl
Some important characteristics of boranes:
i) Lower boranes are colourless gases while higher boranes are volatile liquids
or solids.
ii) They undergo spontaneous combustion in air due to strong affinity of boron
for oxygen.
B2H6
+ 3O2 → B2O3
+ 3H2O + Heat
iii) Boranes react with alkali metal hydrides in diethyl ether to form
borohydride complexes.
B2H6
+ 2MH →2M
+
[BH4
]
-
(M= Li or Na)
Metal borohydride
• (iv) Diborane reacts with ammonia to give borazine at 450 K.
B2H6
+ 6NH3 → 3B3N3H6
+ 12H2
• Borazine has a cyclic structure similar to benzene and thus is called inorganic
benzene
• The other ele ments of this group form only a few stable hydrides. The thermal
stability decreases as we move down the group.
• AlH3
is a colourless soli d polymerized via Al - H - Al bridging units. These
hydrides are weak Lewis acids and readily form adducts with strong Lewis
base (B:) to give compounds of the type MH3
(M = Al or Ga). They also form
complex-tetrahydrido anions, [MH4]-. The most important tetrahydrido
compound is Li[AlH4
]
ether
4LiH + AlCl
3 ―――→ LiAlH4
+ 3LiCl
Dimeric structure of aluminium chloride
– Boron halides do not form dimers because the size of boron
is so small that it is unable to coordinate four large -sized
halide ions.
Anomalous properties of boron
1. Boron is a non-metal & bad conductor of electricity whereas aluminium is a metal
& good conductor. B is hard but Al is a soft metal.
2. Boron exists in two forms-crystalline and amorphous. But Al does not exist in
different f orms.
3. The melting and boiling point of boron are much higher than that of Al .
4. Boron forms only covalent compounds whereas Al forms even some ionic
compounds.
5. The hydroxides and oxides of boron are acidic in nature whereas those of
aluminium are amphoteric.
6. The trihalides of boron exist as monomers. On the other hand, aluminium halides
exist as dimers .
7. The hydrides of boron are quite stable whil e those of aluminium are unstable
Group 14 Ele ments:-The Carbon Family
Group 14 includes carbon (C), silicon (Si), germanium (Ge), tin (Sn) and lead (Pb).
General electronic configuration of carbon fa mily is ns
2
np
2
.
Covalent radius:-Covalent radius expected to increase from Cto Si,
From Si to Pb small increase is found.
Ionization Enthalpy:-The first ionization enthalpies of group 14 elements are higher
than those of the corresponding group 13 elements.
Electronegativi ty:-Group 14 ele ments are smaller in size as compared to group 13
elements that‘s why this group ele ments are slightly more electronegative than group
13
Chemical properties:-Carbon and silicon mostly show +4 oxidation state. Germanium forms stable
compounds in +4 state and only few compounds in +2 state.
Tin f orms compounds in both oxidation states. Lead compounds in +2 state are stable
and in +4 state are strong oxidizing agents.
Exception:-Pb
4
and SnF
4
are ionic in nature.
Except CCl
4
other tetrachlorides are easily hydrolysed by water.
Allotropes of Carbon:-The three types of all otropes are –
1-Diamond 2-Graphite 3-Full erence
Dia mond:-In diamond each carbon atom under goes SP
3
hybridisation. Each carbon is
tetrahedrally linked to four other carbon atoms.
Graphite:-In graphite, carbon is SP
2
-hybridized graphite has a two-dimensional sheet
like structure consisting of a number of hexagonal rings fused together.
Graphite conducts electricity along the sheet. It is very soft and Slippery
Fullerence was discovered collectively by three scientists namely R.E
Smalley,R.F Curl and H.W Kroto
1. Why is boron used in nuclear reactions?
Ans:-Because Boron can absorb neutrons.
2. By giving a balanced equation show how B(OH)
3
behaves as an acid in water.
Ans:-B(OH)
3
+2H2O [B(OH)4
]
-+H3O
+
3.Name the ele ment of group 14 which exhibits maximum tendency for
catenation?
Ans:-Carbon
4. What is the basic building unit of all silicates?
Ans:-SiO4
4-is the basic unit of all silicates.
5. What happens when NaBH4
reacts with iodine?
6. What happens when boric acid is heated
Ans:-4H3BO3
4HBO2 H2B4O7
.
7. What is producer gas?
Ans:-Producer gas is a mixture of CO and N2
in the ratio of 2:1.
8.Write the state of hybridization of ‗B‘ in BF
3
.
ANS:-Hybridisation of ‗B‘ in BF
3
is Sp
2
.
9.Mention the state of hybridization in B in BH4
-.
Ans:-Sp
3
.
10. Which oxide of carbon is regarded as anhydride of carbonic acid.
Ans:-CO2
is regarded as a hydride of carbonic acid .
What happens when
(i) Quick lime is heated with coke?
(ii) Carbon monoxide reacts with Cl
2
Ans:- (i) Cao +3C → CaC2
+CO
(iii) CO +Cl
2→ COCl
2
Give reason
(i) C and Si are always tetravalent but Ge,Sn,Pb show divalency.
(ii) Gallium has higher ionization enthalpy than Al. Explain.
Ans:-(i) Ge, Sn, Pb show divalency due to inert pair effect, Pb
2+
is more stable than
Pb
4+
.
(ii) Due to poor shielding effect of d-electrons in Ga effect ive nuclear
charge increases as compared to Al thus the I.E is higher than Al.
If B-Cl bond has a dipole moment, Explain why BCl
3 molecule has zero dipolemo ment.
Ans:- B-Cl bond has dipole mo ment because of polarity.In BCl
3
since the molecule issymmetrical thus the polarities cancel out.
What do you understand by-(a) Inert pair effect:-The pair of electron in the valence shell does not take part in
bond formation it is called inert pair effect.
(b) Allotropy:-It is the property of the element by which an element can exists in
two f orms which have same chemical properties but different physical properties due
to their structures.
Give reason for the f ollowing observations:-(a) The tendency for catenation decreases down the group in Group 14.
(b) The decreasing stability of +3 oxidations state with increasing atomic
number in group 13.
(c) PbO2
is a stronger oxidizing agent than SnO2.
(d) Molten aluminium bromide is a poor conductor of electricity.
Ans:- (i)(a) It is due to decrease in bond dissociation energy which is due to increase
in atomic size.
C-C > Si-Si >Ge-Ge>Sn-Sn>Pb-Pb.
(b) It is due to inert pair effect.
(c) PbO2
is stronger oxidizing agent than SnO2
because Pb
2+
is more
stable than Pb
4+
whereas Sn
4+
is more stable than Sn
2+
.
compound.
(d) Molten AlBr
3
is poor conductor of electricity because it is covalent.
their outermost shell s – p-block ele ments
•
Gen. electronic configuration of outer shell is ns
2
np
1-6
The inner core of e-config.may differ which greatly influences their physical & to
some extent chemical properties.
GROUP 13 : The boron group
Outer Electronic Configuration:-ns
2
np
1
• group members: boron (B), aluminum (Al), gallium (Ga), indium (In)&
thallium (Tl) . All, except boron, are metals.
• Boron show diagonal relationship with Silicon; both are semiconductors
metalloids & forms covalent compounds.
• Boron compounds are electron deficient, they are lack of an octet of electrons
about the B atom .
• diborane B2H6
, is simplest boron hydride
• Structure: three-center two-electron: the H atoms are simultaneously bonded to
two B atoms the B-H bridging bond lengths are greater than B-H terminal.
• - Boron oxide is acidic (it reacts readily with water to f orm boric acid)
• aluminium compounds:aluminium oxide is amphoteric
• aluminum hali des, e.g., AlCl
3
is dimer, an important catalyst in organic
chemistry have anincomplete octet, acts as Lewic acid by acc epting lone pairs
from Lewic bases, forming adduct
• aluminum hydride, e.g., LiAlH4
, a reducing agen
. Atomic and ionic radii
• The atomic and ionic radii of group 13 elements are compared to
corresponding elements of group 2. From left to right in the period, the
magnitude of nuclear charge increases but the electrons are added to, the same
shell. These electrons do not screen each other, theref ore, the electrons
experience greater nuclear charge.
• In other words, effective nuclear charge increases and thus, size decreases.
Therefore, the elements of this group have smaller size than the corresponding
elements of second group.
• On moving down the group both atomic and ionic radii are expected to
increase due to the addition of new shell s. However, the observed atomic
radius of Al (143 pm) is slightly more than that of Ga (l35 pm).
Ionization energies
The first ionization energies of group 13 elements are less than the corresponding
me mbers of the alkaline earths.
The sharp decrease in I.E. from B to Al is due to increase in size. In case of Ga, there
are ten d-electrons in its inner electronic configuration.
The very high value of 3
rd
I. E. of thallium indicates that +3 O.N. state is not stable,
rather +1 is more stable f or thallium .
Electropositive (or metallic) character
the elements of group 13 are less electropositive as compared to ele ments of group 2.
On moving down the group the electropositive (metallic) character increases because
ionization energy decreases. For e.g., Boron is a non -metal white the other elements
are typical metals.
Oxidation states
The common oxidation states of group 13 elements are +3 and + l .The stability of
the + 1 oxidation state increases in the sequence Al <Ga< In <Tl, Due to Inert pair
effect.
Hydrides
• None of the group 13 ele ments reacts directly with hydrogen. However, a no.
of hydrides of these elements have been prepared by indirect methods. The
boron hydrides are called boranes& classified in two s eries: (a) BnHn+4
called nidoboranes (b) BnHn+6
called arachnoboranes
• INUDUSTRIAL PREPERATION :-2BF
3
(g) + 6LiH(s) → B2H6
(g) + 6LiF(s)
• Laboratory method:
(i) By the reaction of iodine with sodium borohydride in a high boiling
solvent.
2NaBH4
+ I
2 → B2H6
+ 2NaI + H2
(ii) By reduction of BCl
3
with LiAlH4
4BCl
3
+ 3LiAlH4 → 2 B2H6
+ 3AlCl
3
+ 3 LiCl
Some important characteristics of boranes:
i) Lower boranes are colourless gases while higher boranes are volatile liquids
or solids.
ii) They undergo spontaneous combustion in air due to strong affinity of boron
for oxygen.
B2H6
+ 3O2 → B2O3
+ 3H2O + Heat
iii) Boranes react with alkali metal hydrides in diethyl ether to form
borohydride complexes.
B2H6
+ 2MH →2M
+
[BH4
]
-
(M= Li or Na)
Metal borohydride
• (iv) Diborane reacts with ammonia to give borazine at 450 K.
B2H6
+ 6NH3 → 3B3N3H6
+ 12H2
• Borazine has a cyclic structure similar to benzene and thus is called inorganic
benzene
• The other ele ments of this group form only a few stable hydrides. The thermal
stability decreases as we move down the group.
• AlH3
is a colourless soli d polymerized via Al - H - Al bridging units. These
hydrides are weak Lewis acids and readily form adducts with strong Lewis
base (B:) to give compounds of the type MH3
(M = Al or Ga). They also form
complex-tetrahydrido anions, [MH4]-. The most important tetrahydrido
compound is Li[AlH4
]
ether
4LiH + AlCl
3 ―――→ LiAlH4
+ 3LiCl
Dimeric structure of aluminium chloride
– Boron halides do not form dimers because the size of boron
is so small that it is unable to coordinate four large -sized
halide ions.
Anomalous properties of boron
1. Boron is a non-metal & bad conductor of electricity whereas aluminium is a metal
& good conductor. B is hard but Al is a soft metal.
2. Boron exists in two forms-crystalline and amorphous. But Al does not exist in
different f orms.
3. The melting and boiling point of boron are much higher than that of Al .
4. Boron forms only covalent compounds whereas Al forms even some ionic
compounds.
5. The hydroxides and oxides of boron are acidic in nature whereas those of
aluminium are amphoteric.
6. The trihalides of boron exist as monomers. On the other hand, aluminium halides
exist as dimers .
7. The hydrides of boron are quite stable whil e those of aluminium are unstable
Group 14 Ele ments:-The Carbon Family
Group 14 includes carbon (C), silicon (Si), germanium (Ge), tin (Sn) and lead (Pb).
General electronic configuration of carbon fa mily is ns
2
np
2
.
Covalent radius:-Covalent radius expected to increase from Cto Si,
From Si to Pb small increase is found.
Ionization Enthalpy:-The first ionization enthalpies of group 14 elements are higher
than those of the corresponding group 13 elements.
Electronegativi ty:-Group 14 ele ments are smaller in size as compared to group 13
elements that‘s why this group ele ments are slightly more electronegative than group
13
Chemical properties:-Carbon and silicon mostly show +4 oxidation state. Germanium forms stable
compounds in +4 state and only few compounds in +2 state.
Tin f orms compounds in both oxidation states. Lead compounds in +2 state are stable
and in +4 state are strong oxidizing agents.
Exception:-Pb
4
and SnF
4
are ionic in nature.
Except CCl
4
other tetrachlorides are easily hydrolysed by water.
Allotropes of Carbon:-The three types of all otropes are –
1-Diamond 2-Graphite 3-Full erence
Dia mond:-In diamond each carbon atom under goes SP
3
hybridisation. Each carbon is
tetrahedrally linked to four other carbon atoms.
Graphite:-In graphite, carbon is SP
2
-hybridized graphite has a two-dimensional sheet
like structure consisting of a number of hexagonal rings fused together.
Graphite conducts electricity along the sheet. It is very soft and Slippery
Fullerence was discovered collectively by three scientists namely R.E
Smalley,R.F Curl and H.W Kroto
1. Why is boron used in nuclear reactions?
Ans:-Because Boron can absorb neutrons.
2. By giving a balanced equation show how B(OH)
3
behaves as an acid in water.
Ans:-B(OH)
3
+2H2O [B(OH)4
]
-+H3O
+
3.Name the ele ment of group 14 which exhibits maximum tendency for
catenation?
Ans:-Carbon
4. What is the basic building unit of all silicates?
Ans:-SiO4
4-is the basic unit of all silicates.
5. What happens when NaBH4
reacts with iodine?
6. What happens when boric acid is heated
Ans:-4H3BO3
4HBO2 H2B4O7
.
7. What is producer gas?
Ans:-Producer gas is a mixture of CO and N2
in the ratio of 2:1.
8.Write the state of hybridization of ‗B‘ in BF
3
.
ANS:-Hybridisation of ‗B‘ in BF
3
is Sp
2
.
9.Mention the state of hybridization in B in BH4
-.
Ans:-Sp
3
.
10. Which oxide of carbon is regarded as anhydride of carbonic acid.
Ans:-CO2
is regarded as a hydride of carbonic acid .
What happens when
(i) Quick lime is heated with coke?
(ii) Carbon monoxide reacts with Cl
2
Ans:- (i) Cao +3C → CaC2
+CO
(iii) CO +Cl
2→ COCl
2
Give reason
(i) C and Si are always tetravalent but Ge,Sn,Pb show divalency.
(ii) Gallium has higher ionization enthalpy than Al. Explain.
Ans:-(i) Ge, Sn, Pb show divalency due to inert pair effect, Pb
2+
is more stable than
Pb
4+
.
(ii) Due to poor shielding effect of d-electrons in Ga effect ive nuclear
charge increases as compared to Al thus the I.E is higher than Al.
If B-Cl bond has a dipole moment, Explain why BCl
3 molecule has zero dipolemo ment.
Ans:- B-Cl bond has dipole mo ment because of polarity.In BCl
3
since the molecule issymmetrical thus the polarities cancel out.
What do you understand by-(a) Inert pair effect:-The pair of electron in the valence shell does not take part in
bond formation it is called inert pair effect.
(b) Allotropy:-It is the property of the element by which an element can exists in
two f orms which have same chemical properties but different physical properties due
to their structures.
Give reason for the f ollowing observations:-(a) The tendency for catenation decreases down the group in Group 14.
(b) The decreasing stability of +3 oxidations state with increasing atomic
number in group 13.
(c) PbO2
is a stronger oxidizing agent than SnO2.
(d) Molten aluminium bromide is a poor conductor of electricity.
Ans:- (i)(a) It is due to decrease in bond dissociation energy which is due to increase
in atomic size.
C-C > Si-Si >Ge-Ge>Sn-Sn>Pb-Pb.
(b) It is due to inert pair effect.
(c) PbO2
is stronger oxidizing agent than SnO2
because Pb
2+
is more
stable than Pb
4+
whereas Sn
4+
is more stable than Sn
2+
.
compound.
(d) Molten AlBr
3
is poor conductor of electricity because it is covalent.
Wednesday, December 30, 2015
CHEM..ORGANIC..XI
Resonance Effect : The polarity produced in the molecule by the interaction of two
pi bonds or between a pi bond and lone pair of electron present on an adjacent atom.
There are two types of resonance effect:
1) Positive resonance effect : In this effect the transfer of electr ons is away fro m
an atom or substituent group attached to the conjugated system.
The atoms or groups which shows +R effect are halogens, -OH , -OR,-NH2
2) Negative resonance effect : In this effect the transfer of electrons is towards
the atom or substituent group attached to the conjugated system.
The atoms or groups which shows -R effect are –COOH , -CHO , -CN
pi bonds or between a pi bond and lone pair of electron present on an adjacent atom.
There are two types of resonance effect:
1) Positive resonance effect : In this effect the transfer of electr ons is away fro m
an atom or substituent group attached to the conjugated system.
The atoms or groups which shows +R effect are halogens, -OH , -OR,-NH2
2) Negative resonance effect : In this effect the transfer of electrons is towards
the atom or substituent group attached to the conjugated system.
The atoms or groups which shows -R effect are –COOH , -CHO , -CN
Q.1. What effect does branching of an alkane
chain has on its boiling point?
Ans. As the branching increases, the surface
area of an alkane approaches that of a sphere. Since a sphere has
minimum surface area, therefore, Vander Waal forces of attraction are minimum
and hence the boiling point of the alkane decreases with branching.
Q2. Among Cis and Trans structure of Hex-2-ene which has higher
boiling point and why?
Ans:
The dipole moment of a molecule depends upon dipole-dipole interactions. Since
cis-isomer has higher dipole moment, therefore it has higher boiling point
Q3. Write IUPAC names of the following compounds )
(a) CH3CH=C(CH3)2 (b) CH3CH(CH3)CH=CH2
Ans. (a)
2-Methylbut-2-ene (b) 3-Methylbut-1-ene
Q.4. Out of benzene, m–dinitrobenzene
and toluene which will undergo nitration most easily and why?(L-II)
Ans. -CH3 group is electron donating while –NO2 group is electron withdrawing. Therefore,
maximum electron density will be in toluene, followed by benzene and at
least in m-dinitrobenzene. Therefore, the ease of nitration decreases in the
order:
Toluene> benzene> m-dinitrobenzene.
Q5. Explain why (CH3)3C+ is more stable than CH3CH2+ and +CH3. (L-I)
Ans. Greater the number of alkyl groups
attached to a positively charged carbon atom, the greater is the
hyperconjugation interaction and +I effect of methyl group greater is the
stabilisation of the cation.Thus, CH3)3C+ is more stable than CH3CH2+ and +CH3.
Q6. Explain electromeric effect, resonance effect and
hyperconjugation.
Ans: Electromeric effect is defined
as the complete-electrons totransferoneof
o
the atoms joined by a multiple bond on the demand of an attacking
reagent. It is represented by E
and the shifting of the electrons is shown by a curved arrow.
The
resonance effect is defined as ‘the
polarity produced in the molecule by the interaction of two-bndsπ or
between-bondandlone pairaof electronsπ present on an adjacent atom’. The effect
is transmitted through the chain.
Hyperconjugation involves
delocalisation of σ electrons—Hbondof an ofalkyl groupC directly
attached to an atom of unsaturated system or to an atom with an unshared p
orbital. The—H σbondelectronsofthealkylgroupenterofinto partialC conjugation
with the attached unsaturated system or with the unshared p orbital.
Hyperconjugation is a permanent effect.
Monday, December 28, 2015
CHEM..CLASS XI..ORGANIC..QUESTIONS..
Q.1. Write structures of different chain isomers of alkanes corresponding to the molecular
formula C4H10 and C5 H12. Also write their IUPAC names.
Q.2. Write IUPAC names of the following compounds :
(i) (CH3)3CCH2C(CH3) 3
(ii) (CH3) 2 C(C2H5) 2
(iii) tetra – tert-butylmethane
Q.3. Write structural formulas of the following compounds:
(i) 3-Methylhexane
(ii) 3-ethyl-2, 2–dimethylpentane
Q.4. Define conformers/rotamers.
Ans.The spatial arrangements of atoms which can be converted into one another by
rotation around a C-C single bond are called conformations or conformers or rotamers
Q.5. Write IUPAC names of the following compounds:
(i) CH3 – CH = CH2
(ii) CH3 – CH2 – CH = CH2
(iii) CH3 – CH = CH–CH3
Q.6. Out of pentane, 2-methylbutane and 2,2-dimethylpropane which has the highest
boiling point and why?
Ans. Pentane having a continuous chain of five carbon atoms has the highest boiling point
(309.1K) whereas 2,2 – dimethylpropane boils at 282.5K. With increase in number of
branched chains, the molecule attains the shape of a sphere. This results in smaller area of
contact and therefore weak intermolecular forces between spherical molecules, which are
overcome at relatively lower temperatures.
Q.7. Calculate number of sigma (σ) and pi (π) bonds in the following
(i) CH2 = C (CH2CH2CH3) 2
(ii) CH2 = CH – CH – CH3
|
CH3
(iii) CH3 – CH = CH–CH3
Q.8. Write structures and IUPAC names of different structural isomers of alkenes
corresponding to C5H10
Ans.pent-1-ene
pent-2-ene
2-methylbut-2-ene
3-methylbut-1-ene
2-methyl-but-1-ene
Q.9. Discuss about structural isomerism and stereoisomerism.
Ans. Structural Isomerism: Compounds having the same molecular formula but different
structure i.e. different arrangement of atoms within the molecule are called structural
isomers and the phenomenon is called as structural isomerism.
Types:
• Chain isomerism
• Position isomerism
• Functional isomerism
• Metamerism
• Tautomerism
Stereoisomerism: Isomers which have the same structural formula but have
different relative arrangement of atoms or groups in space are called stereoisomers and the
phenomenon is called as stereoisomerism.
Q.10. Draw cis and trans isomers of the following compounds. Also write their IUPAC names
:(i) CHCl = CHCl
(ii) C2H5CCH3 = CCH3C2H5
Q.11. Write IUPAC names of the products obtained by addition reactions of HBr to hex-1-ene
(i) in the absence of peroxide and
(ii) in the presence of peroxide.
Q.12. Define Hückel rule.
Ans. Huckel Rule gives information about the aromaticity. According to this rule, the
necessary and sufficient conditions for a molecule to be aromatic are:
Planarity
Complete decolisation of the pi electrons in the ring.
Presence of (4n+2) pi electrons in the ring where n is an integer (n= 0,1,2…)
Q.13How would you convert the following into benzene?
(i)Ethyne (ii) Ethene (iii) Hexane
Q.14. Out of benzene, m–dinitrobenzene and toluene which will undergo
nitration most easily and why?
Ans. -CH3 group is electron donating while –NO2 group is electron withdrawing. Therefore,
maximum electron density will be in toluene , followed by benzene and at least in m-dinitrobenzene. Therefore, the ease of nitration decreases in the order:
Toluene> benzene> m-dinitrobenzene
Q.15. Arrange benzene, n-hexane and ethyne in decreasing order of acidic behaviour. Also
give reason for this behaviour.
Benzene Hexane Ethyne
sp
3
sp
2
sp
Since s-electrons are close to the nucleus, therefore as the s-character of the orbital making
the C-H bond increases, the electrons of C-H bond lie closer and closer to the carbon atom.
In other words, the partial positive charge on the H-atom and hence the acidic character
increases as the s character of the orbital increases.
Thus the acidic character decreases in the order:
Ethyne> Benzene> Hexane
Q.16.Why does benzene undergo electrophilic substitution reactions easily and nucleophilic
substitutions with difficulty?
Ans. Due to the presence of an electron cloud containing 6 pi electrons above and below the
plane of the ring, benzene is a source of electrons. Consequently, it attracts the
electrophiles towards it and repels nucleophiles. As a result, benzene undergoes
electrophilic substitution reactions easily and nucleophilic substitution with difficulty.
Q.17. Draw the cis and trans structures of hex-2-ene. Which isomer will have higher b.p. and
why?
Ans. cis-Hex-2-ene & Trans-Hex-2-ene
The dipole moment of a molecule depends upon dipole-dipole interactions. Since cis-isomer
has higher dipole moment, therefore it has higher boiling point.
Q.18. Explain the extra ordinarily stability of benzene though it contains three double
bonds?
Ans. Resonance or delocalisation of electrons usually leads to stability. Since in benzene all
the six pi electrons of the three double bonds are completely delocalised to form one lowest
molecular orbital which surrounds all the carbon atoms of the ring, therefore, it is extra-ordinarily stable.
Q.19. What are the necessary conditions for any system to be aromatic?
Ans. The necessary conditions for a molecule to be aromatic are:
(i)It should have a single cyclic cloud of delocalised pi electrons above and below the plane of
the molecule.
(ii)It should be planar. This is because complete delocalisation of pi electrons is possible only if
the ring is planar to allow cyclic overlap of p-orbitals.
(iii)It should contain Huckel number of electrons, i.e. (4n+2) pi electrons where n=0,1,2,3….etc.
formula C4H10 and C5 H12. Also write their IUPAC names.
Q.2. Write IUPAC names of the following compounds :
(i) (CH3)3CCH2C(CH3) 3
(ii) (CH3) 2 C(C2H5) 2
(iii) tetra – tert-butylmethane
Q.3. Write structural formulas of the following compounds:
(i) 3-Methylhexane
(ii) 3-ethyl-2, 2–dimethylpentane
Q.4. Define conformers/rotamers.
Ans.The spatial arrangements of atoms which can be converted into one another by
rotation around a C-C single bond are called conformations or conformers or rotamers
Q.5. Write IUPAC names of the following compounds:
(i) CH3 – CH = CH2
(ii) CH3 – CH2 – CH = CH2
(iii) CH3 – CH = CH–CH3
Q.6. Out of pentane, 2-methylbutane and 2,2-dimethylpropane which has the highest
boiling point and why?
Ans. Pentane having a continuous chain of five carbon atoms has the highest boiling point
(309.1K) whereas 2,2 – dimethylpropane boils at 282.5K. With increase in number of
branched chains, the molecule attains the shape of a sphere. This results in smaller area of
contact and therefore weak intermolecular forces between spherical molecules, which are
overcome at relatively lower temperatures.
Q.7. Calculate number of sigma (σ) and pi (π) bonds in the following
(i) CH2 = C (CH2CH2CH3) 2
(ii) CH2 = CH – CH – CH3
|
CH3
(iii) CH3 – CH = CH–CH3
Q.8. Write structures and IUPAC names of different structural isomers of alkenes
corresponding to C5H10
Ans.pent-1-ene
pent-2-ene
2-methylbut-2-ene
3-methylbut-1-ene
2-methyl-but-1-ene
Q.9. Discuss about structural isomerism and stereoisomerism.
Ans. Structural Isomerism: Compounds having the same molecular formula but different
structure i.e. different arrangement of atoms within the molecule are called structural
isomers and the phenomenon is called as structural isomerism.
Types:
• Chain isomerism
• Position isomerism
• Functional isomerism
• Metamerism
• Tautomerism
Stereoisomerism: Isomers which have the same structural formula but have
different relative arrangement of atoms or groups in space are called stereoisomers and the
phenomenon is called as stereoisomerism.
Q.10. Draw cis and trans isomers of the following compounds. Also write their IUPAC names
:(i) CHCl = CHCl
(ii) C2H5CCH3 = CCH3C2H5
Q.11. Write IUPAC names of the products obtained by addition reactions of HBr to hex-1-ene
(i) in the absence of peroxide and
(ii) in the presence of peroxide.
Q.12. Define Hückel rule.
Ans. Huckel Rule gives information about the aromaticity. According to this rule, the
necessary and sufficient conditions for a molecule to be aromatic are:
Planarity
Complete decolisation of the pi electrons in the ring.
Presence of (4n+2) pi electrons in the ring where n is an integer (n= 0,1,2…)
Q.13How would you convert the following into benzene?
(i)Ethyne (ii) Ethene (iii) Hexane
Q.14. Out of benzene, m–dinitrobenzene and toluene which will undergo
nitration most easily and why?
Ans. -CH3 group is electron donating while –NO2 group is electron withdrawing. Therefore,
maximum electron density will be in toluene , followed by benzene and at least in m-dinitrobenzene. Therefore, the ease of nitration decreases in the order:
Toluene> benzene> m-dinitrobenzene
Q.15. Arrange benzene, n-hexane and ethyne in decreasing order of acidic behaviour. Also
give reason for this behaviour.
Benzene Hexane Ethyne
sp
3
sp
2
sp
Since s-electrons are close to the nucleus, therefore as the s-character of the orbital making
the C-H bond increases, the electrons of C-H bond lie closer and closer to the carbon atom.
In other words, the partial positive charge on the H-atom and hence the acidic character
increases as the s character of the orbital increases.
Thus the acidic character decreases in the order:
Ethyne> Benzene> Hexane
Q.16.Why does benzene undergo electrophilic substitution reactions easily and nucleophilic
substitutions with difficulty?
Ans. Due to the presence of an electron cloud containing 6 pi electrons above and below the
plane of the ring, benzene is a source of electrons. Consequently, it attracts the
electrophiles towards it and repels nucleophiles. As a result, benzene undergoes
electrophilic substitution reactions easily and nucleophilic substitution with difficulty.
Q.17. Draw the cis and trans structures of hex-2-ene. Which isomer will have higher b.p. and
why?
Ans. cis-Hex-2-ene & Trans-Hex-2-ene
The dipole moment of a molecule depends upon dipole-dipole interactions. Since cis-isomer
has higher dipole moment, therefore it has higher boiling point.
Q.18. Explain the extra ordinarily stability of benzene though it contains three double
bonds?
Ans. Resonance or delocalisation of electrons usually leads to stability. Since in benzene all
the six pi electrons of the three double bonds are completely delocalised to form one lowest
molecular orbital which surrounds all the carbon atoms of the ring, therefore, it is extra-ordinarily stable.
Q.19. What are the necessary conditions for any system to be aromatic?
Ans. The necessary conditions for a molecule to be aromatic are:
(i)It should have a single cyclic cloud of delocalised pi electrons above and below the plane of
the molecule.
(ii)It should be planar. This is because complete delocalisation of pi electrons is possible only if
the ring is planar to allow cyclic overlap of p-orbitals.
(iii)It should contain Huckel number of electrons, i.e. (4n+2) pi electrons where n=0,1,2,3….etc.
Friday, December 25, 2015
CLASS XII CHEMISTRY
Smallest repeating unit in a space lattice is called unit cell.
Thereare4 typesofunitcells,7crystalsystemsand14bravaislattices.
. Types of unit cell No.ofatomsperunitcell
Simple cubicunitcell 8x1/8=1
FCC(Facecenteredcubic) 8x1/8+6x1/2=4
BCC(Body centeredcubic) 8x1/8+1x1=2
End centered 8x1/8+1/2 x 2 = 2 10.
Hexagonalclosepackingand cubicclosepackinghaveequal packing efficiencyi.e.74% 11. Packingefficiency= Volume occupied by the sphere*100/Volume of unit cell
Radius ratiois the ratio of radius of void to the radius of sphere .
For tetrahedral void radius ratio = 0.225
Foroctahedralvoidradiusratio = 0.414
.No.oftetrahedralvoid=2x N (N=No.ofparticles)
.No.ofoctahedral void=N
Simplecubicunitcell a=2r
. FCC a=4r/√ 2
BCC a=4r/√ 3
Point defect or Atomic defect‐>it is the deviation from ideal arrangement of constituent atom
.Point defects are two types
(a)Vacancy defect
(b)Interstitial defect
Frenkel defect
is the combination of vacancy and interstitial defects.Cations leave their actual
lattice sites and come to occupy the interstitial spaces.Density remains the same
eg.AgCl.
Thereare4 typesofunitcells,7crystalsystemsand14bravaislattices.
. Types of unit cell No.ofatomsperunitcell
Simple cubicunitcell 8x1/8=1
FCC(Facecenteredcubic) 8x1/8+6x1/2=4
BCC(Body centeredcubic) 8x1/8+1x1=2
End centered 8x1/8+1/2 x 2 = 2 10.
Hexagonalclosepackingand cubicclosepackinghaveequal packing efficiencyi.e.74% 11. Packingefficiency= Volume occupied by the sphere*100/Volume of unit cell
Radius ratiois the ratio of radius of void to the radius of sphere .
For tetrahedral void radius ratio = 0.225
Foroctahedralvoidradiusratio = 0.414
.No.oftetrahedralvoid=2x N (N=No.ofparticles)
.No.ofoctahedral void=N
Simplecubicunitcell a=2r
. FCC a=4r/√ 2
BCC a=4r/√ 3
Point defect or Atomic defect‐>it is the deviation from ideal arrangement of constituent atom
.Point defects are two types
(a)Vacancy defect
(b)Interstitial defect
Frenkel defect
is the combination of vacancy and interstitial defects.Cations leave their actual
lattice sites and come to occupy the interstitial spaces.Density remains the same
eg.AgCl.
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CLASS XI CHEM PERIODIC TABLE...SOME IMP Q&A
Q.State Mendeleev Periodic Law.
Ans: The chemical and physical properties of the elements are periodic functions of their atomic
masses.
Q State modern periodic law.
Ans-The chemical and physical properties of the elements are periodic functions of their atomic
numbers.Mosley state this law.
Q.Why are isotopes not considered in Mendeleev’s periodic table?Name the elements which are
predicted by Mendeleev as eka –silicon and eka –aluminum ?
Ans.Because Mendeleev gave priority to similarities in properties.
Germanium and gallium.
Q. What are Dobereiner’s triads? Give example of 2 triads ?
Ans: he arranged the elements in several sets of 3 elements .these sets were called triads which
resembled with each other in chemical properties and atomic mass of the middle element was
approx the mean of the atomic masses of the remaining two.
Example (i) chlorine, bromine and iodine A.T of cl =35.5 and iodine =127 .middle element bromine
has (35.5 +127)/2 =81.25
(ii) Calcium (40) ,strontium(88.5) and barium (137)
Q Write the general E.C of s, p, d and f Block elements.(L2)
Ans: (i) s block- ns
1-2
(ii) p block – ns
2
np
1-6
(iii) d block – (n-1)d
1-10
ns
1-2
(iv) f block -- (n-2) f
1-14
(n-1)d
0-1
ns
Q Assign the position of the element having outer electronic configuration
(i)ns
2
np
4
for n=3 , {L3]
(ii) (n-1) d
2
ns
2
for n=4
(iii) (n-2)f
7
(n-1)d
1
ns
2
for n=6
Ans: (i) n= principal no. which shows no of periods. N=3 so E.C =3s23p4=elements having position 3
rd
period 16
th
group.
(ii) n=4 so elements belong in 4
th
period .it is d block element .d2= 2 electron in d orbital it belongs to
4
th
group in d block.
(iii) n=6 and electron goes in fshell, so it is f block element having 6
th
period and 7
th
element of
lanthanides series.
Q. Which out of F or Cl has a more negative electron gain enthalpy?
Ans. Cl has more negative electron gain enthalpy. It is because there is more inter electronic
repulsion between valence electrons of F, due to smaller size than Cl.
Q.1 Consider the following species
N
-3
, O
-2
, F-, Na
+
, Mg
+2
and Al
+3
(a). what is common in them?
(b). arrange them in the order of increasing ionic radii.
Ans. (a). They have same number of electrons.
(b). Al
3+
<Mg
2+
<Na
+
<F
-<O
2-<N
3
Q. Explain Screening effect ?
Ans..Screening effect. The inner electrons between valence electron and nucleus shield the
valence electrons from nucleus; it is called shielding effect.
Q.2 (a). Which is largest in size- Cu
+
, Cu
+2
, Cu and why?
Ans.. Cu is largest due to less effective nuclear charge. It has 29 electrons, 29 protons, Cu
+
has 28
electrons and 29 protons, Cu
2+
has 27 electrons and 29 protons.
Q. How does electro negativity vary down the group 17 and why? How does it vary from left to
right in the period? Name an element having highest electro negativity.
Ans. Electro negativity decreases down the group due to increase in atomic size. It increases along
the period from left to right due to decrease in atomic size.
Fluorine (F) has highest electro negativity.
Q.1 Would you expect the second electron gain enthalpy of O as positive, more negative or less
negative than the first? Justify your answer.
Ans. Second electron affinity of O is largely +ve because of repulsion between negatively charged
ions and second electron to be added. Energy required to overcome repulsion is more than the
energy released in gaining electron, so net energy is absorbed.
Q.Explain why Halogens have very high negative electron gain enthalpy?
Ans.The electron gain enthalpy for halogens is highly negative because they can acquire the nearest
stable noble gas configuration by accepting an extra electron.
Q. How would you explain the fact that the first ionization of Na is lower than that of Mg but its
second ionization enthalpy is higher than that of Mg? (L-3)
Ans. The electronic configurations of Na and Mg are: Na:1s
2
2s
2
2p
6
3s
1
And Mg: 1s
2
2s
2
2p
6
3s
2
thus, the
first electron in both the cases has to be removed from the 3s orbital, but the nuclear charge of Na is
lower than that of Mg, therefore, the first ionization energy of Na is lower than that of Mg. But after
the removal of the first electron, Na acquire the nearest noble gas configuration (Ne) which makes
Na highly stable, but an electron is still left in the p orbital of Mg. Hence second ionization energy of
Na is higher than that of Mg.
Q. Explain why Electron gain enthalpy of noble gases is positive. (L-1)
Ans. Noble gases have large positive electron gain enthalpies because the extra electron has to be
placed in the next higher principal quantum energy level, thereby producing highly unstable
electronic configuration.
Q. Explain why cations are smaller and anions are larger in size than their parent atom. (L-2)
Ans.The ionic radius of cation is always smaller than the parent atom because the loss of one or
more electrons increases the effective nuclear charge. As a result, the force of attraction of nucleus
for the electrons increases and hence, the ionic radii decreases. In contrast, the ionic radius of an
anion is always larger than its parent atom because the addition of one or more electrons decreases
the effective nuclear charge. As a result, the force of attraction of the nucleus for the electrons
decreases and hence the ionic radii increases.
Q Arrange the following order of the property indicated:
(a). F, Cl, Br and I (negative electron gain enthalpy)
(b). Mg, Al, Si and Na (ionization enthalpy)
(c). C, N, O and F (second ionization enthalpy)
Q. Arrange the following elements in increasing order of metallic character: B, Al, Mg and K.
Q. Why is fluorine (F2) more reactive than chlorine (Cl2)?
Q.Explain why
(i). Be has higher first ionization enthalpy than B?
(ii). O has lower first ionization enthalpy than N and F?
Q.3 ∆iH1 value of Mg is more as compared to that of Na while its ∆
iH2 value is less. Explain.
Ans. ∆iH1 value of Mg is more than that of Na due to greater symmetry and smaller size. But ∆iH2
value of Na is higher because Na
+
ion has the configuration of noble gas element neon while Mg
+
ion
does not have a symmetrical configuration.
Q. The increasing order of reactivity among group 1 elements is Li<Na<K<Rb<Cs whereas among
the group 17 elements, it is F>Cl>Br>I. Explain
Ans: The chemical and physical properties of the elements are periodic functions of their atomic
masses.
Q State modern periodic law.
Ans-The chemical and physical properties of the elements are periodic functions of their atomic
numbers.Mosley state this law.
Q.Why are isotopes not considered in Mendeleev’s periodic table?Name the elements which are
predicted by Mendeleev as eka –silicon and eka –aluminum ?
Ans.Because Mendeleev gave priority to similarities in properties.
Germanium and gallium.
Q. What are Dobereiner’s triads? Give example of 2 triads ?
Ans: he arranged the elements in several sets of 3 elements .these sets were called triads which
resembled with each other in chemical properties and atomic mass of the middle element was
approx the mean of the atomic masses of the remaining two.
Example (i) chlorine, bromine and iodine A.T of cl =35.5 and iodine =127 .middle element bromine
has (35.5 +127)/2 =81.25
(ii) Calcium (40) ,strontium(88.5) and barium (137)
Q Write the general E.C of s, p, d and f Block elements.(L2)
Ans: (i) s block- ns
1-2
(ii) p block – ns
2
np
1-6
(iii) d block – (n-1)d
1-10
ns
1-2
(iv) f block -- (n-2) f
1-14
(n-1)d
0-1
ns
Q Assign the position of the element having outer electronic configuration
(i)ns
2
np
4
for n=3 , {L3]
(ii) (n-1) d
2
ns
2
for n=4
(iii) (n-2)f
7
(n-1)d
1
ns
2
for n=6
Ans: (i) n= principal no. which shows no of periods. N=3 so E.C =3s23p4=elements having position 3
rd
period 16
th
group.
(ii) n=4 so elements belong in 4
th
period .it is d block element .d2= 2 electron in d orbital it belongs to
4
th
group in d block.
(iii) n=6 and electron goes in fshell, so it is f block element having 6
th
period and 7
th
element of
lanthanides series.
Q. Which out of F or Cl has a more negative electron gain enthalpy?
Ans. Cl has more negative electron gain enthalpy. It is because there is more inter electronic
repulsion between valence electrons of F, due to smaller size than Cl.
Q.1 Consider the following species
N
-3
, O
-2
, F-, Na
+
, Mg
+2
and Al
+3
(a). what is common in them?
(b). arrange them in the order of increasing ionic radii.
Ans. (a). They have same number of electrons.
(b). Al
3+
<Mg
2+
<Na
+
<F
-<O
2-<N
3
Q. Explain Screening effect ?
Ans..Screening effect. The inner electrons between valence electron and nucleus shield the
valence electrons from nucleus; it is called shielding effect.
Q.2 (a). Which is largest in size- Cu
+
, Cu
+2
, Cu and why?
Ans.. Cu is largest due to less effective nuclear charge. It has 29 electrons, 29 protons, Cu
+
has 28
electrons and 29 protons, Cu
2+
has 27 electrons and 29 protons.
Q. How does electro negativity vary down the group 17 and why? How does it vary from left to
right in the period? Name an element having highest electro negativity.
Ans. Electro negativity decreases down the group due to increase in atomic size. It increases along
the period from left to right due to decrease in atomic size.
Fluorine (F) has highest electro negativity.
Q.1 Would you expect the second electron gain enthalpy of O as positive, more negative or less
negative than the first? Justify your answer.
Ans. Second electron affinity of O is largely +ve because of repulsion between negatively charged
ions and second electron to be added. Energy required to overcome repulsion is more than the
energy released in gaining electron, so net energy is absorbed.
Q.Explain why Halogens have very high negative electron gain enthalpy?
Ans.The electron gain enthalpy for halogens is highly negative because they can acquire the nearest
stable noble gas configuration by accepting an extra electron.
Q. How would you explain the fact that the first ionization of Na is lower than that of Mg but its
second ionization enthalpy is higher than that of Mg? (L-3)
Ans. The electronic configurations of Na and Mg are: Na:1s
2
2s
2
2p
6
3s
1
And Mg: 1s
2
2s
2
2p
6
3s
2
thus, the
first electron in both the cases has to be removed from the 3s orbital, but the nuclear charge of Na is
lower than that of Mg, therefore, the first ionization energy of Na is lower than that of Mg. But after
the removal of the first electron, Na acquire the nearest noble gas configuration (Ne) which makes
Na highly stable, but an electron is still left in the p orbital of Mg. Hence second ionization energy of
Na is higher than that of Mg.
Q. Explain why Electron gain enthalpy of noble gases is positive. (L-1)
Ans. Noble gases have large positive electron gain enthalpies because the extra electron has to be
placed in the next higher principal quantum energy level, thereby producing highly unstable
electronic configuration.
Q. Explain why cations are smaller and anions are larger in size than their parent atom. (L-2)
Ans.The ionic radius of cation is always smaller than the parent atom because the loss of one or
more electrons increases the effective nuclear charge. As a result, the force of attraction of nucleus
for the electrons increases and hence, the ionic radii decreases. In contrast, the ionic radius of an
anion is always larger than its parent atom because the addition of one or more electrons decreases
the effective nuclear charge. As a result, the force of attraction of the nucleus for the electrons
decreases and hence the ionic radii increases.
Q Arrange the following order of the property indicated:
(a). F, Cl, Br and I (negative electron gain enthalpy)
(b). Mg, Al, Si and Na (ionization enthalpy)
(c). C, N, O and F (second ionization enthalpy)
Q. Arrange the following elements in increasing order of metallic character: B, Al, Mg and K.
Q. Why is fluorine (F2) more reactive than chlorine (Cl2)?
Q.Explain why
(i). Be has higher first ionization enthalpy than B?
(ii). O has lower first ionization enthalpy than N and F?
Q.3 ∆iH1 value of Mg is more as compared to that of Na while its ∆
iH2 value is less. Explain.
Ans. ∆iH1 value of Mg is more than that of Na due to greater symmetry and smaller size. But ∆iH2
value of Na is higher because Na
+
ion has the configuration of noble gas element neon while Mg
+
ion
does not have a symmetrical configuration.
Q. The increasing order of reactivity among group 1 elements is Li<Na<K<Rb<Cs whereas among
the group 17 elements, it is F>Cl>Br>I. Explain
Monday, December 21, 2015
CHEMISTRY..STRUCTURE OF ATOM..Q&A
Q1 State Heisenberg Uncertainty Principle ?
Ans. It is impossible to determine the exact position & exact momentum or velocity of microscopic particle.
Q2-Write E.C. for Oxygen ?
Q3. Which orbital has quantum no(a) n= 3 & l=1
(b) n= 2, l= 0
Ans: (a)3p orbitals. (b) 2s
Q4.Find the wave length of Yellow emission of sodium whose frequency 5.09 x 10
14
per sec ?
Ans:(hint: wave length = C/V0)
Q5. How was Neutron discovered? Write equation only?
Q6. Calculate the wave length of an electron whose KE is 3x 10
-25 J ?
Q7. An element with mass number 81 contains 31.7% more neutrons as compare to protons find out atomic symbol of element(Br)
Q8. What is threshold frequency?
Ans –The minimum frequency required to eject out electron from an atom.
Q9.Write the draw back of Rutherford Atomic Model ?
Ans (1). He was unable to explain the stability of Atom.
(2). He could not explain the line spectrum.
Q10.Give the points of Rutherford Model ?
Ans. 1. Atom is neutral.
2.Whole mass is concentrated in nucleus.
3.Electrons are revolving in orbits.
Q10-A 10 g Table Tennis Ball is moving with a speed of 90 m/s which is measured with an accuracy of 4% find out uncertainty in it speed as well as position.
Ans:
m = 10g
m = 0.01kg
∆v = 4% of 90 m/s
= 3.6 m/s
∆x = h/4π m∆v
Put the values
=1.46 x 10
-33
m
Q.11 How many electrons with l=2 are there in an atom having atomic number 54 ?
Ans. 3d
10
& 4d
10
= 20.
Q. What is electronic configuration of Cu (z=29) and Cr (z=24) by aufbau principle?
Q.Define Pauli’s exclusion principle ?
Ans. No two electrons in an atom can have same set ofall four quantum numbers. If three are same one Quantum number must have different value.
Q.Define Aufbau Principle. Give a Suitable example ?
Q. a) Where is the probability of finding an electron is zero?
b) How many maximum electrons can be found in 3d orbital with spin quantum
number -1/2?
c) Which quantum no. determines the orientation of the orbital?
Ans.a) at Node.
b) 5-electrons.
c) magnetic quantum no
Q. Why is s-orbital orbital considered non directional while p-orbital directional?
Ans. Electron density in s-orbital is equal in all direction while it dumble shaped along one axis in p-orbitals.
Q4.Which of the following can exhibit maximum Para magnetism: Ca, Fe
+2
,Cu
+2
?
Ans.Fe
2+
due to presence of 4 unpaired electrons in 3d orbitals.
Q..What will be the increasing order of energy of 2s, 3s, 3d, 4f in atom?
Ans. 2s< 3s < 3d < 4f
Q.Is the energy of an electron in 2s orbital same as of that in 2p orbital? Why?
Ans. No, the energy depends upon (n+l) values in an atom. Hence 2p orbital has greater energy than
2s
Q.“In reality all the s-orbitals are spherically symmetric.” What does this represent?
Ans. The probable density of an electron in s-orbital is equally distributed at all coordinates in space.
Q.3 Give three differences between orbit and orbital.
Ans
ORBIT
1 It is a well defined circular path around the
nucleus in which electron move .
2 Maximum no. of electrons in an orbit is
2n
2
.
3. Do not have directional characteristics.
ORBITAL
1 It is a 3dimensional region around the nucleus where
the probability of finding electron is
maximum.
2 Maximum 2 electrons in an orbital.
3. Except s all have directional characteristics
QExplain the significance of Azimuthal quantum number ?
Ans. It refers as sub-energy level of an atom.
Q. How many of the following are possible: 1p, 2s, 3p, 3f, 3d. ?
Ans.2s , 3p & 3d are possible.
Q. n = 3, l = 3, m
l
= -3, ms
= +1/2. Is the given set of quantum numbers possible? If not, explain by
giving reasons.
Ans. It is not possible because 3f does not exist in an atom
Q.Explain why half-filled orbitals have extra stability ?
Ans. It has symmetrical electron density as well as greater exchange energy.
Q. Explain the significance of spin quantum number ?
Ans.The direction of spinning of an electron in an orbit as well as the net magnetic moment of an orbital.
Q.. What will be the value of n & l of the followings? (L1)
1. 4s
1
2. 5d
1
3. 4f
1
Q. What is Hund’s rule of maximum multiplicity? What is its significance?
Ans Pairing of electrons in an orbital takes place only when all orbitals of same sub-shell become singly occupied. It helps to equalize energy of a sub-shell
CHEMISTRY..SOME SIMPLE Q&A..
Q1. Define the term precision and accuracy?
Ans. The term precision refers for the closeness of set of values obtained from identical
measurement of a quantity, whereas accuracy is a related term, refers to the closeness of a single
measurement to its true value.
Q2-What do you mean by significant figure?
Ans. Total number of digits in a number including the last digit whose value is uncertain is called the
number of significant figure.
Q4. Define the law of conservation of mass ?
Ans. Matter can neither be created nor destroyed in the course of a Physical or chemical process
although it may change from one form to another.
Q5- How many significant figure are present in the following ?
(I) 0.0025 (II) 208 (III) 5005 (IV) 126000
Ans.- (I) 2 (II) 3 (III) 4 (IV) 3
Q6 Define Molarity ?
Ans. It is the number of moles of the solute dissolved per litre of the solution.
Q.7 Define Molality ?
Ans. It is the number of moles of the solute dissolved per 1000 g of the solvent.
Q8 Define mole?
Ans. The amount of substance that contains the same number of entities(atoms, molecules, ions
or other particles) as the number of atoms present in 12g of carbon-12 isotope.
Q9 How are 0.50 m Na2CO3 and 0.50 M Na2CO3 different?
Ans. 0.50 m Na2CO3 solution means that 0.5 mol (or 53g) of Na2CO3 are present in 1000 g of
solvent.
0.50 M Na2CO3 solution means that 0.5 mol (or 53g) of Na2CO3 are present in 1L of solution
Q10. a) Why Molarity varies with temperature?
b) Which concentration term is suitable when solute is present in very minute quantities or
traces?
c) What is the sum of mole fraction of all the components of a solution?
Ans. a) Because it is number of moles of solute per litre of solution, and volume varies with
temperature.
b) ppm(Parts per million)
c) 1
Q11. Calculate the mass of an atom of silver (atomic mass= 108)
Ans. Mass of 6.022x10
23
atoms of Ag = 108 g
Mass of one atom of Silver
108
6.022X10
23
= 1.79x10
-22
g
Q12. Calculate the number of moles of iodine in a sample containing 1.0x10
22
molecules?
Ans. 6.022x10
23
molecules of iodine = 1 mol of iodine
1.0x10
22
molecules of iodine =
1
6.022X10
23X1.0 X10
22
= 0.0166 mol of iodine
Q13. Calculate the volume occupied by 10 mole of CO2 at STP. ?
Ans. 1 mol of CO2 atSTP = 22.7 L
10 mole of CO2 at STP = 22.7 x 10 =227 L
Q14 A solution is prepared by dissolving 2g of the substance A in 18 g of water. Calculate the mass
percentage of solute ?
Ans. Mass of solute A = 2g
Mass of water = 18g
Mass of solution = 2+18 = 20g
Mass percentage =
Mass of A/
Mass of solution
*100g
=
2/
20
* 100
Q15 In three moles of ethane (C2H6) calculate the following:
(a) Number of moles of carbon
(b) Number of moles of hydrogen atom
(c) Number of moles of ethane
Ans. (a) 1 mole of C2H6 contain = 2 moles of carbon
3 moles of C2H6 contain = 6 moles of carbon
b) 1 mole of C2H6 contain = 6 moles of hydrogen atom
3 moles of C2H6 contain = 18 moles of hydrogen atom
c) 1 moles of C2H6 contain = 6.022 x 10
23
molecules
3 moles of C2H6 contain = 6.022 x 10
23
x 3 = 1.0807 x 10
24
molecules.
Q17 A solution is 25% H2O, 25% C2 H5 OH and 50% acetic acid by mass. Calculate mole fraction of each component.
Q18 Calculate the molarity of pure water (density of water = 1 g mL
-1
) . (L 3)
Ans. Density of water = 1 g mL
-1
Mass of 1000 mL of water = Volume x Density
1000 x 1 = 1000 g
Moles of water =
1000/18
= 55.55
Q18 Calculate the weight of carbon monoxide having same number of oxygen atoms as are
present in 88 g of carbon dioxide.
Ans. The term precision refers for the closeness of set of values obtained from identical
measurement of a quantity, whereas accuracy is a related term, refers to the closeness of a single
measurement to its true value.
Q2-What do you mean by significant figure?
Ans. Total number of digits in a number including the last digit whose value is uncertain is called the
number of significant figure.
Q4. Define the law of conservation of mass ?
Ans. Matter can neither be created nor destroyed in the course of a Physical or chemical process
although it may change from one form to another.
Q5- How many significant figure are present in the following ?
(I) 0.0025 (II) 208 (III) 5005 (IV) 126000
Ans.- (I) 2 (II) 3 (III) 4 (IV) 3
Q6 Define Molarity ?
Ans. It is the number of moles of the solute dissolved per litre of the solution.
Q.7 Define Molality ?
Ans. It is the number of moles of the solute dissolved per 1000 g of the solvent.
Q8 Define mole?
Ans. The amount of substance that contains the same number of entities(atoms, molecules, ions
or other particles) as the number of atoms present in 12g of carbon-12 isotope.
Q9 How are 0.50 m Na2CO3 and 0.50 M Na2CO3 different?
Ans. 0.50 m Na2CO3 solution means that 0.5 mol (or 53g) of Na2CO3 are present in 1000 g of
solvent.
0.50 M Na2CO3 solution means that 0.5 mol (or 53g) of Na2CO3 are present in 1L of solution
Q10. a) Why Molarity varies with temperature?
b) Which concentration term is suitable when solute is present in very minute quantities or
traces?
c) What is the sum of mole fraction of all the components of a solution?
Ans. a) Because it is number of moles of solute per litre of solution, and volume varies with
temperature.
b) ppm(Parts per million)
c) 1
Q11. Calculate the mass of an atom of silver (atomic mass= 108)
Ans. Mass of 6.022x10
23
atoms of Ag = 108 g
Mass of one atom of Silver
108
6.022X10
23
= 1.79x10
-22
g
Q12. Calculate the number of moles of iodine in a sample containing 1.0x10
22
molecules?
Ans. 6.022x10
23
molecules of iodine = 1 mol of iodine
1.0x10
22
molecules of iodine =
1
6.022X10
23X1.0 X10
22
= 0.0166 mol of iodine
Q13. Calculate the volume occupied by 10 mole of CO2 at STP. ?
Ans. 1 mol of CO2 atSTP = 22.7 L
10 mole of CO2 at STP = 22.7 x 10 =227 L
Q14 A solution is prepared by dissolving 2g of the substance A in 18 g of water. Calculate the mass
percentage of solute ?
Ans. Mass of solute A = 2g
Mass of water = 18g
Mass of solution = 2+18 = 20g
Mass percentage =
Mass of A/
Mass of solution
*100g
=
2/
20
* 100
Q15 In three moles of ethane (C2H6) calculate the following:
(a) Number of moles of carbon
(b) Number of moles of hydrogen atom
(c) Number of moles of ethane
Ans. (a) 1 mole of C2H6 contain = 2 moles of carbon
3 moles of C2H6 contain = 6 moles of carbon
b) 1 mole of C2H6 contain = 6 moles of hydrogen atom
3 moles of C2H6 contain = 18 moles of hydrogen atom
c) 1 moles of C2H6 contain = 6.022 x 10
23
molecules
3 moles of C2H6 contain = 6.022 x 10
23
x 3 = 1.0807 x 10
24
molecules.
Q17 A solution is 25% H2O, 25% C2 H5 OH and 50% acetic acid by mass. Calculate mole fraction of each component.
Q18 Calculate the molarity of pure water (density of water = 1 g mL
-1
) . (L 3)
Ans. Density of water = 1 g mL
-1
Mass of 1000 mL of water = Volume x Density
1000 x 1 = 1000 g
Moles of water =
1000/18
= 55.55
Q18 Calculate the weight of carbon monoxide having same number of oxygen atoms as are
present in 88 g of carbon dioxide.
Saturday, December 19, 2015
KINEMATICS..PHYSICS..PART 1
Rest and Motion are relative terms, nobody can exist in a state of absolute rest or of
absolute motion.
Speed:- It is rate of change of distance covered by the body with respect to time.
Speed = Distance travelled /time taken
Speed is a scalar quantity
S.I. unit is m /s
dimensional formula is[M
0
L
1
T
-1
]
*Uniform Speed:- If an object covers equal distances in equal intervals of time than the
speed of the moving object is called uniform speed.
In this type of motion, position –time
graph is always a straight line.
*Instantaneous speed:-The speed of an object at any particular instant of time is called
instantaneous speed. In this measurement, the time ∆t→0.
When a body is moving with uniform speed its instantaneous speed = Average speed =
uniform speed.
*Velocity:- It is defined as the displacement covered by an object per unit time.
Velocity =Displacement /Time
Velocity is a vector quantity
SI unit is m /s
Its dimensional formula is (see speed)
difference between speed & velocity :
1.Speed is scalar but velocity is vector quantity.
2.speed may be +veor zero where as velocity may be zero,+ve or -ve.
*Acceleration:- The rate of change of velocity of an object with respect to time is called
its acceleration.
Acceleration = Change in velocity /time taken
unit-m/s(2)
It may be positive ,negative or zero.
*Positive Acceleration:- If the velocity of an object increases with time , its acceleration is
positive .
*Negative Acceleration :-If the velocity of an object decreases with time , its acceleration
is negative . The negative acceleration is also called retardation or deacceleration.
absolute motion.
Speed:- It is rate of change of distance covered by the body with respect to time.
Speed = Distance travelled /time taken
Speed is a scalar quantity
S.I. unit is m /s
dimensional formula is[M
0
L
1
T
-1
]
*Uniform Speed:- If an object covers equal distances in equal intervals of time than the
speed of the moving object is called uniform speed.
In this type of motion, position –time
graph is always a straight line.
*Instantaneous speed:-The speed of an object at any particular instant of time is called
instantaneous speed. In this measurement, the time ∆t→0.
When a body is moving with uniform speed its instantaneous speed = Average speed =
uniform speed.
*Velocity:- It is defined as the displacement covered by an object per unit time.
Velocity =Displacement /Time
Velocity is a vector quantity
SI unit is m /s
Its dimensional formula is (see speed)
difference between speed & velocity :
1.Speed is scalar but velocity is vector quantity.
2.speed may be +veor zero where as velocity may be zero,+ve or -ve.
*Acceleration:- The rate of change of velocity of an object with respect to time is called
its acceleration.
Acceleration = Change in velocity /time taken
unit-m/s(2)
It may be positive ,negative or zero.
*Positive Acceleration:- If the velocity of an object increases with time , its acceleration is
positive .
*Negative Acceleration :-If the velocity of an object decreases with time , its acceleration
is negative . The negative acceleration is also called retardation or deacceleration.
PHYSICS..Unit - I Physical World And Measurement
There are four fundamental forces which govern both macroscopic and microscopic
phenomena. These are
(i) Gravitational force
(iii) Electromagnetic force
(ii) Nuclear force
(iv) Weak force
All those quantities which can be measured directly or indirectly and in terms of which
the laws of physics can be expressed are called physical quantities
The units of the fundamental quantities called fundamental units , and the units of
derived quantities called derived units.
DIMENSION & DIMENSIONAL FORMULA:
The equation which expresses a physical quantity in terms of the fundamental
units of mass, length and time, is called dimensional equation.
According to the principle of homogeneity a physical equation will be
dimensionally correct if the dimensions of all the terms in the all the terms
occurring on both sides of the equation are the same.
There are three main uses of the dimensional analysis-
1.To check the correctness of a given physical relation.
2.To derive a relationship between different physical quantities.
Significant figures: - The significant figures are normally those digits in a
measured quantity which are known reliably plus one additional digit that is
uncertain.
RULES OR FINDING SIGNIFICANT FIG.:
(i) All non- zero digits are significant figure.
(ii) All zero between two non-zero digits are significant figure.
(iii) All zeros to the right of a non-zero digit but to the left of an understood decimal
point are not significant. But such zeros are significant if they come from a
measurement.
(iv) All zeros to the right of a non-zero digit but to the left of a decimal point are
significant.
(v) All zeros to the right of a decimal point are significant.
(vi) All zeros to the right of a decimal point but to the left of a non-zero digit are not
significant. Single zero conventionally placed to the left of the decimal point is
not significant.
(vii) The number of significant figures does not depend on the system of units.
phenomena. These are
(i) Gravitational force
(iii) Electromagnetic force
(ii) Nuclear force
(iv) Weak force
All those quantities which can be measured directly or indirectly and in terms of which
the laws of physics can be expressed are called physical quantities
The units of the fundamental quantities called fundamental units , and the units of
derived quantities called derived units.
DIMENSION & DIMENSIONAL FORMULA:
The equation which expresses a physical quantity in terms of the fundamental
units of mass, length and time, is called dimensional equation.
According to the principle of homogeneity a physical equation will be
dimensionally correct if the dimensions of all the terms in the all the terms
occurring on both sides of the equation are the same.
There are three main uses of the dimensional analysis-
1.To check the correctness of a given physical relation.
2.To derive a relationship between different physical quantities.
Significant figures: - The significant figures are normally those digits in a
measured quantity which are known reliably plus one additional digit that is
uncertain.
RULES OR FINDING SIGNIFICANT FIG.:
(i) All non- zero digits are significant figure.
(ii) All zero between two non-zero digits are significant figure.
(iii) All zeros to the right of a non-zero digit but to the left of an understood decimal
point are not significant. But such zeros are significant if they come from a
measurement.
(iv) All zeros to the right of a non-zero digit but to the left of a decimal point are
significant.
(v) All zeros to the right of a decimal point are significant.
(vi) All zeros to the right of a decimal point but to the left of a non-zero digit are not
significant. Single zero conventionally placed to the left of the decimal point is
not significant.
(vii) The number of significant figures does not depend on the system of units.
PHYSICS..SOME IMPORTANT PHYSICAL CONSTANTS
Mass of an electron (Me) = 9.1x10
-31
kg.
2. Mass of a proton ( Mp) = 1.6725 x 10
-27
kg.
3. Mass of a neutron (Mn) = 1.6746 x 10
-27
kg.
4. Charge of an electron (e) =-1.6 x 10
-19
c
5. Speed of light in vacuum (c) = 3 x10
8
m/sec.
6. Planck Constant (h) = 6.6256 x 10
-34
J x sec .
7. Universal Gravitation constant (G) = 6.67 x 10
-11
Nm
2
/ kg
2.
8. Avogadro Number (NA) = 6.023 x10
23
mol
-1
.
9. Boltzmann constant (K) = 1.38 x 10
-23
J/K
10.Radius of the earth (Re) = 6400 Km. = 6.4x10
6
m
-31
kg.
2. Mass of a proton ( Mp) = 1.6725 x 10
-27
kg.
3. Mass of a neutron (Mn) = 1.6746 x 10
-27
kg.
4. Charge of an electron (e) =-1.6 x 10
-19
c
5. Speed of light in vacuum (c) = 3 x10
8
m/sec.
6. Planck Constant (h) = 6.6256 x 10
-34
J x sec .
7. Universal Gravitation constant (G) = 6.67 x 10
-11
Nm
2
/ kg
2.
8. Avogadro Number (NA) = 6.023 x10
23
mol
-1
.
9. Boltzmann constant (K) = 1.38 x 10
-23
J/K
10.Radius of the earth (Re) = 6400 Km. = 6.4x10
6
m
Friday, December 18, 2015
PHYSICS..GRAVITATION..SOME IMP Q&A
Q1.What are the factors which determine ; Why some bodies in solar system have
atmosphere and others don’t have?
Ans. The ability of a body (planet) to hold the atmosphere depends on acceleration due to gravity.
Q2.Should the speed of two artificial satellites of the earth having different masses but the same orbital radius, be the same?
Ans.Yes it is so because the orbital speed of a satellite is independent of the mass of a satellite. Therefore the speeds of the artificial satellite will be of different masses but of the same orbital radius will be the same.
Q3.Can a pendulum vibrate in an artificial satellite?
Ans. No, this is because inside the satellite, there is no gravity ,
i.e., g=0.
As t = 2π , hence, for g=0 , t = . Thus, the pendulum will not vibrate.
Q4.Why do different planets have different escape speed?
Ans. As, escape speed = , therefore its value are different for different
planets which are of different masses and different sizes.
Q5.Show that weight of all body is zero at Centre of earth?
Ans. The value of acceleration due to gravity at a depth d below the surface of earth
of radius R is given by ɠ=g(1-d/R).At the center of earth, (dept)d=R; so, ɠ =0.The
weight of a body of mass m at the centre of earth =mg’=m x 0=0.
Q6.Why does moon have no atmosphere?
Ans. Moon has no atmosphere because the value of acceleration due to gravity ‘g’
on surface of moon is small. Therefore, the value of escape speed on the surface of
moon is small. The molecules of atmospheric gases on the surface of the moon
have thermal speeds greater than the escape speed. That is why all the molecules
of gases have escaped and there is no atmosphere on moon
Q7.What are the conditions under which a rocket fired from earth, launches
an artificial satellite of earth?
Ans. Following are the basic conditions: (i) The rocket must take the satellite to
a suitable height above the surface of earth for ease of propulsion.
(ii)From the desired height, the satellite must be projected with a suitable
speed, called orbital speed.
(iii)In the orbital path of satellite, the air resistance should be negligible so that
its speed does not decrease and it does not burn due to the heat produced.
Q1.State Kepler’s laws of planetary motion. Prove second Kepler’s law using
concept of conservation of angular motion.
Q2.State universal law of gravitation. What is the significance of this law. Find the
expression for acceleration due to gravity.
Q4. Define gravitational potential energy. Derive the expression for gravitational
potential energy. What is the maximum value of gravitational potential energy?
Q5.What is escape speed? Derive the expressions for it. Calculate escape speed for
the Earth
atmosphere and others don’t have?
Ans. The ability of a body (planet) to hold the atmosphere depends on acceleration due to gravity.
Q2.Should the speed of two artificial satellites of the earth having different masses but the same orbital radius, be the same?
Ans.Yes it is so because the orbital speed of a satellite is independent of the mass of a satellite. Therefore the speeds of the artificial satellite will be of different masses but of the same orbital radius will be the same.
Q3.Can a pendulum vibrate in an artificial satellite?
Ans. No, this is because inside the satellite, there is no gravity ,
i.e., g=0.
As t = 2π , hence, for g=0 , t = . Thus, the pendulum will not vibrate.
Q4.Why do different planets have different escape speed?
Ans. As, escape speed = , therefore its value are different for different
planets which are of different masses and different sizes.
Q5.Show that weight of all body is zero at Centre of earth?
Ans. The value of acceleration due to gravity at a depth d below the surface of earth
of radius R is given by ɠ=g(1-d/R).At the center of earth, (dept)d=R; so, ɠ =0.The
weight of a body of mass m at the centre of earth =mg’=m x 0=0.
Q6.Why does moon have no atmosphere?
Ans. Moon has no atmosphere because the value of acceleration due to gravity ‘g’
on surface of moon is small. Therefore, the value of escape speed on the surface of
moon is small. The molecules of atmospheric gases on the surface of the moon
have thermal speeds greater than the escape speed. That is why all the molecules
of gases have escaped and there is no atmosphere on moon
Q7.What are the conditions under which a rocket fired from earth, launches
an artificial satellite of earth?
Ans. Following are the basic conditions: (i) The rocket must take the satellite to
a suitable height above the surface of earth for ease of propulsion.
(ii)From the desired height, the satellite must be projected with a suitable
speed, called orbital speed.
(iii)In the orbital path of satellite, the air resistance should be negligible so that
its speed does not decrease and it does not burn due to the heat produced.
Q1.State Kepler’s laws of planetary motion. Prove second Kepler’s law using
concept of conservation of angular motion.
Q2.State universal law of gravitation. What is the significance of this law. Find the
expression for acceleration due to gravity.
Q4. Define gravitational potential energy. Derive the expression for gravitational
potential energy. What is the maximum value of gravitational potential energy?
Q5.What is escape speed? Derive the expressions for it. Calculate escape speed for
the Earth
Wednesday, December 16, 2015
ORGANIC CHEM...
Organic compounds are the hydrocarbons and their derivatives and organic
chemistry is that branch of chemistry that deals with the study of these
compounds
Tetravalency of carbon
The atomic number of Carbon is 6 and its electronic configuration is 2,4 i.e. it has 4
valence electrons. Thus carbon is always tetracovalent, i.e. it forms 4 covalent
bonds with other atoms
C
Due to tetravalency of carbon it has a tetrahedron shape.
Catenation- The self linking property of carbon is known as catenation. This is the
main reason of existence of such large number of compounds
Classification of organic compounds
Organic compounds
Acyclic Cyclic
(SEE TEXT TABLE)
Functional groups:A functional group may be defined as an atom or a group of
atoms present in a molecule which largely determines the chemical properties.
CLASS OF ORGANIC NAME OF FUNCTIONAL STRUCTURE
COMPOUNDS GROUP
Alkenes double bond -C=C
Alkynes
triple bond - C Ξ C -
Halogens halogen - X ( F,Cl,Br,I )
Alcohols hydroxyl -OH
Aldehydes aldehydic(formyl) -CHO
Carboxylic acids carboxyl -COOH
Acid amides
Primary amines
amides
amino
-CONH2
- NH2
HOMOLOGOUS SERIES
Homologous series is defined as a family or group of structurally similar organic
compounds all members of which contain the same functional group, show a
gradation in physical and similarity in chemical properties and any two adjacent
members of which differ by -CH2 group. The individual members of this group are
called homologues and the phenomenon is called homology.
NOMENCLATURE OF ORGANIC COMPOUNDS
Straight chain alkanes:
The names of such compounds is based on their chain structure,and end with suffix
‗-ane‘ and carry a prefix indicating the number of carbon atoms present in the chain.
Branched chain hydrocarbons:
1.) The longest carbon chain in the molecule is identified.
2.) The numbering is done in such a way that the branched carbon atoms get the
lowest possible value.
3.) The names of the alkyl groups attached as a branch are then prefixed to the
name of the parent alkane and its position is indicated by numbers.
4.) The lower number is given to the first in alphabetical order.
5.) The carbon atom of the branch that attaches to the root alkane is numbered
1.
Organic compounds having Functional Groups:
The longest chain of carbon atoms containing the functional groups is numbered in
such a way that the functional group attached to the carbon atom gets the lowest
possible number in the chain.
When there are more functional groups then a priority order is followed as:
-COOH, -SO3H, -COOR, COCl, -CONH2, -CN, -HC=O, =C=O, -OH, -NH2, =C=C=,
-CΞ C-.
ISOMERISM
Two or more compounds having the same molecular formula but different physical
and chemical properties are called isomers and this phenomenon is called isomerism.
Chain isomerism: When two or more compounds having same molecular formula
but different carbon skeletons are referred to as chain isomers.
pentane,isopentane,neopentane(SEE STRUCTURE FROM TEXT)
Position Isomerism :
Compounds which have the same structure of carbon chain but
differ in position of double or triple bonds or functional group are called position
isomers and this phenomenon is called Position Isomerism. e g
CH3-CH2-CH=CH2 CH3-CH = CH – CH3
Functional Isomerism
Compounds which have the same molecular formula but
different functional group are called functional isomers and this phenomenon is
called functional Isomerism. e g
CH3 – CH2 – OH CH3 – O – CH3
Metamerism:
It is due to the presence of different alkyl groups on either side of
functional group in the molecule. Ex. C4H10O represents C2H5OC2H5 and
CH3OC3H7.
FISSION OF COVALENT BOND
Heterolytic cleavage: In this cleavage the bond breaks in such a way that the shared
pair of electron remains with one of the fragments.
H3C – Br
+CH3 + Br
-
Homolytic Cleavage: In this cleavage the shared pair of electron goes with each of
the bonded atom.
R – X R
. + X
.
Alkyl free radical
Nucleophiles : A reagent that brings an electron pair is called nucleophile ie nucleus
seeking e g -OH , -CN
Electrophiles: A reagent that takes away electron pair is called electrophile I e
electron seeking e g > C= O , R3C– X
Inductive Effect: The displacement of the electron along the chain of the carbon
atoms due to presence of an atom or group at the end of the chain
ɗ+++ ɗ ++ ɗ+
CH3- C H2 CH2 Cl
Resonance Effect :
The polarity produced in the molecule by the interaction of two
pi bonds or between a pi bond and lone pair of electron present on an adjacent atom.
There are two types of resonance effect:
1) Positive resonance effect : In this effect the transfer of electrons is away from
an atom or substituent group attached to the conjugated system.
The atoms or groups which shows +R effect are halogens,-OH , -OR,-
NH2
2) Negative resonance effect : In this effect the transfer of electrons is towards
the atom or substituent group attached to the conjugated system.
The atoms or groups which shows -R effect are –COOH , -CHO , -CN
Sublimation : This method is used to separate the sublimable compounds from non
sublimable compounds.
Crystallisation: This method is based on the difference in the solubilities of
compound and impurities in a suitable solvent. The impure compound is dissolved in
solvent and heated at higher temp .On cooling, from the hot and conc solution pure
compounds crystallizes out.
Distillation: This method is used to separate volatile liquids from non volatile liquids
and liquids having sufficient difference in their boiling points.
Fractional distillation: If the boiling points of two liquids is not much , they are
separated by this method.
Distillation under reduced pressure : This method is used to purify liquids having
high boiling points and decomposes at or below their boiling points.
S
team distillation : This method is used to separate substances which are steam
volatile and are immiscible with water.
Differential Extraction: When an organic compound is present in an aqueous
medium it is separated by shaking it with organic solvent in which it is more soluble
than in water. The aqueous solution is mixed with organic solvent in a separating
funnel and shaken for sometimes and then allowed to stand for some time .when
organic solvent and water form two separate layers the lower layer is run out by
opening the tap of funnel and organic layer is separated. the process is repeated
several times and pure organic compound is separated.
Chromatography :This technique is used to separate mixtures in to their
components ,purify the compounds and test the purity of compounds.It is classified
Adsorption Chromatography : It is based on the fact that different compounds are
adsorbed on an adsorbent to different degrees. Silica jel or alumina is used as
adsorbents.
Partition Chromatography : It is based on the continuous differential portioning of
components of a mixture between stationary and mobile phase.
QUANTITIVE ANALYSIS(Carbon and Hydrogen)
Let the mass of organic compound be m g. Mass of water and carbon dioxide
produced be m1 and m2 g respectively;
% of carbon = 12 x m2 x 100 /44 x m
% of hydrogen = 2 x m1 x 100 /18 x m
Nitrogen
DUMAS METHOD: A known mass of organic compound is heated with excess of
CuO in an atmosphere of CO2, when nitrogen of the organic compound is converted
into N2 gas.
The volume of N2 thus obtained is converted into STP and the
percentage of nitrogen determined by applying the equation:
Volume of Nitrogen at STP = P1V1 x 273 /760 x T1
%N = 28 x vol of N2 at STP x 100 /22400 x mass of the substance taken
Physics Notes Class.... GRAVITATION
Every object in the universe attracts every
other object with a force which is called the force of gravitation
Newton’s Law of
Gravitation
Gravitational
force is a attractive force between two masses m1
and m2 separated by a distance
r.
The
gravitational force acting between two point objects is proportional to the
product of their masses and inversely proportional to the square of the
distance between them.
Gravitational
force.
where
G is universal gravitational constant.
Dimensional formula of Gis [M-1L3T-2].
The value of G
is 6.67 X 10-11 Nm2 kg-2 and is same
throughout the universe.
The
value of G is independent of the nature and size of the bodies well as the
nature of the medium between them.
(i)
Gravitational force is a central as well
as conservative force.
(ii)
It is the weakest force in nature.
(iii)
It
is 1036 times
smaller than elect
(iv)
The law of gravitational is applicable
for all bodies, irrespective of their size, shape and
position.
(v)
Gravitational force acting between sun
and planet provide it centripetal force for orbital motion.
(vi)
Gravitational pull of the earth is
called gravity.
(vii)
Newton’s third law of motionmeansthe
holds gravitation forces between two bodies are action-reaction pairs.
Following three
points are important regarding the gravitational force
(i)
Unlike the electrostatic force, it is
independent of the medium between the particles.
(ii)
It is conservative in nature.
(i)
It expresses the force between two point
masses (of negligible volume). However, for external points of spherical bodies
the whole mass can be assumed to be concentrated at its centre of mass.
Acceleration
Due to Gravity
The
uniform acceleration produced in a freely falling object due to the
gravitational pull of the earth is known as acceleration due to gravity.
It
is denoted by g and its unit is m/s2.
It is a vector quantity and its direction is towards the centre of the earth.
The
value of g is independent of the mass of the object which is falling freely
under gravity.
The
value of g changes slightly from place to place. The value of g is taken to be
9.8 m/s2 for all practical
purposes.
The
value of acceleration due to gravity on the moon is about. one sixth of that On
the earth and on the sun is about 27 times of that on the earth.
Among
the planets, the acceleration due to gravity is minimum on the mercury.
Relation between g and a is given by
g = Gm / R2
where
M = mass of the earth = 6.0 * 1024
kg and R = radius of the earth = 6.38 * 106
m. Acceleration due to gravity at a height h above the surface of the earth is
given by
gh = Gm / (R+h)2 = g (1 –2h / R)
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