The Department of School Education, Government of Andhra Pradesh
(DSEAP) will release the results of AP - DEECET 2015 on 8th September
2015. The results of DEECET / AP DIETCET 2015 can be obtained from the
official website deecetap dot cgg dot gov dot in .
The counseling schedule also will be released along with the results
of AP DEECET 2015. The counseling is likely to be held in October
first week. The detailed schedule also will be displayed on the
website.
AP - DEECET is for admission into D.Ed course in Government and
Private DIET colleges in Andhra Pradesh for the academic year 2015-16.
The duration of the course is two years.
The candidates who have completed D.Ed course will be eligible for the
posts of SGTs (Secondary Grade Teachers) in Andhra Pradesh. The SGT
posts will be filled with D.Ed passed candidates only as per the
Supreme Court guidelines.
Senior Inter Chemistry Important Topics - Alkanes, Organic Compounds and Chemistry in Everyday Life
Chemistry In Everyday Life: Expect two 2 marks questions in I.P.E.
Definitions and 2 examples of antacids, antihistamines, antiseptics,
antibiotics, analgesics (narcotic & non-narcotic), tranquilizers,
antifertility
drugs, artificial sweetening agents, food preservatives, antioxidents
in food, difference between soap & detergent, constituents of dettol.
But there is a possibility of 4 marks question structures of
Serotonin, bithionol, Saccharin and Chloramphenicol.
For objective exams: Practice and remember the structures and the main
parts of structures of drugs and other molecules, examples of all the
drugs,
artificial sweetening agents, food preservatives.
Halo Alkanes and Halo Arenes:
Be perfect with IUPAC nomenclature and other fundamentals of 1st year
Organic Chemistry in order to strengthen in 2nd year Organic
Chemistry. Named reactions, conversions, IUPAC names of the compounds
are very important. One 4 marks or two 2 marks questions will be given
in I.P.E. exam.
4 Marks: SN1 and SN2 mechanisms and application oriented questions. In
box: 11.1 and 11.2. Chapter end questions: 12, 13, 20, 21.
2 Marks: In box: 11.5 to 11.7 and 11.9. In text: 11.5 to 11.8. Chapter
end: 1 to 11, any bit from 17, 19, 26, 31, 32 and all named reactions.
For objective exams: SN1, SN2 based questions, conversions, all named
reactions.
Organic Compounds Containing C, H, O:
6 Marks (2M + 4M) or 8 Marks (4 named reactions x 2 M = 8 M) questions
are coming in I.P.E. Better to prepare own notes for preparation and
properties of alcohols, phenols, ethers, aldehydes, ketones,
carboxylic acids separately.
From alcohols, phenols, ethers: 2 Marks: In box: 12.1 to 12.7. In
text: 12.1, 12.3, 12.5 to 12.9. Chapter end: 1 to 10, 12, 13
4 Marks: Chapter end questions: 15, 16, 21, 22. . 8 Marks: All named
reactions like Reimertieman, Kolbe's, esterification, Williamson's,
Aldol condensation and crossed aldol condensation.
From aldehydes, Ketones, Carboxylic acids: 2 Marks: In box: 12.8,
12.9, 12.12. In text: 12.14, 12.15, 12.16, 12.18, 12.20. Chapter end:
1b, 3, 10, 11, 12. H.V.Z. Cannizzaro, Rosenmund.
4 Marks: 15, 22, 24. For objective exams: Comparison of b.p.s,
acidic nature, different ethers reactions with HI or RX, Iodoform,
Aldol, Cross aldol condensation reactions.
Organic Compounds Containing N:
Most of the times one 2 marks and one 4 marks questions are given in
previous I.P.E.
2 Marks: Sandmeyer's reaction, Gattermann reaction. In box: 13.2 & 13.4.
In text: 13.2, 13.3, 13.4 13.8 13.9. Chapter end: 1 to 10.
4 Marks: Chapter end questions 11, 15, 23, 27, 31a, 34.
For objective exams: Comparison basic nature of the compounds,
conversions, named reactions. Prepare a flow chart of all the
conversions in Organic Chemistry. Go through previous 10 years JEE
mains question papers.
Definitions and 2 examples of antacids, antihistamines, antiseptics,
antibiotics, analgesics (narcotic & non-narcotic), tranquilizers,
antifertility
drugs, artificial sweetening agents, food preservatives, antioxidents
in food, difference between soap & detergent, constituents of dettol.
But there is a possibility of 4 marks question structures of
Serotonin, bithionol, Saccharin and Chloramphenicol.
For objective exams: Practice and remember the structures and the main
parts of structures of drugs and other molecules, examples of all the
drugs,
artificial sweetening agents, food preservatives.
Halo Alkanes and Halo Arenes:
Be perfect with IUPAC nomenclature and other fundamentals of 1st year
Organic Chemistry in order to strengthen in 2nd year Organic
Chemistry. Named reactions, conversions, IUPAC names of the compounds
are very important. One 4 marks or two 2 marks questions will be given
in I.P.E. exam.
4 Marks: SN1 and SN2 mechanisms and application oriented questions. In
box: 11.1 and 11.2. Chapter end questions: 12, 13, 20, 21.
2 Marks: In box: 11.5 to 11.7 and 11.9. In text: 11.5 to 11.8. Chapter
end: 1 to 11, any bit from 17, 19, 26, 31, 32 and all named reactions.
For objective exams: SN1, SN2 based questions, conversions, all named
reactions.
Organic Compounds Containing C, H, O:
6 Marks (2M + 4M) or 8 Marks (4 named reactions x 2 M = 8 M) questions
are coming in I.P.E. Better to prepare own notes for preparation and
properties of alcohols, phenols, ethers, aldehydes, ketones,
carboxylic acids separately.
From alcohols, phenols, ethers: 2 Marks: In box: 12.1 to 12.7. In
text: 12.1, 12.3, 12.5 to 12.9. Chapter end: 1 to 10, 12, 13
4 Marks: Chapter end questions: 15, 16, 21, 22. . 8 Marks: All named
reactions like Reimertieman, Kolbe's, esterification, Williamson's,
Aldol condensation and crossed aldol condensation.
From aldehydes, Ketones, Carboxylic acids: 2 Marks: In box: 12.8,
12.9, 12.12. In text: 12.14, 12.15, 12.16, 12.18, 12.20. Chapter end:
1b, 3, 10, 11, 12. H.V.Z. Cannizzaro, Rosenmund.
4 Marks: 15, 22, 24. For objective exams: Comparison of b.p.s,
acidic nature, different ethers reactions with HI or RX, Iodoform,
Aldol, Cross aldol condensation reactions.
Organic Compounds Containing N:
Most of the times one 2 marks and one 4 marks questions are given in
previous I.P.E.
2 Marks: Sandmeyer's reaction, Gattermann reaction. In box: 13.2 & 13.4.
In text: 13.2, 13.3, 13.4 13.8 13.9. Chapter end: 1 to 10.
4 Marks: Chapter end questions 11, 15, 23, 27, 31a, 34.
For objective exams: Comparison basic nature of the compounds,
conversions, named reactions. Prepare a flow chart of all the
conversions in Organic Chemistry. Go through previous 10 years JEE
mains question papers.
Inter 2nd Year Chemistry Study Plan - Elements, Polymers and Biomolecules
P - Block Elements: Mostly two 2 marks (Group 15 or 16 or 17), two 4
marks (group 16 or 17 or 18) are coming from this lesson. This chapter
has a weightage of 12 marks. 2 Marks: From 15th group: Chapter end
questions No: 3, 5, 6, 18, 19, 21, 28, 31, 39, 45. In box: 6.2, 6.4,
6.5, 6.7, 6.9. In text: 6.2, 6.5, 6.10.
From 16th group: Chapter end questions: 2, 7, 8, 12, 14, 15, 17, 19,
22, 27, 28, 40. In Box: 6.11, 6.12. In text: 6.15, 6.25.
From 17th group: Chapter end Questions No: 6, 5, 9, 10, 11, 17, 19,
20, 25, 31, 32. In box: 6.15, 6.16, 6.17, 6.18
4 Marks: 15th group: NH3 by Haber's process, HNO3 by Ostwald's process.
16th group: H2SO4 by contact process, O3 preparation and reactions
with Pbs, C2H4, KI, Hg and Ag.
17th group: Cl2 preparation 2 methods or reactions of Cl2 with Cold
dil. NaOH, hot conc. NaOH, Na2S2O3, excess of NH3.
18th group: Preparation, structures of XeF2, XeF4, XeF6, XeO3, XeOF4.
8 Marks: There is a possibility of asking preparation and properties
of Cl2 or O3 . For objective exams: oxyacids of S, Cl, Hydrides,
Hybridization of molecules.
d and f Block Elements and Coordination Compounds:
Expect one 2 marks question and one 4 marks question in I.P.E. from this lesson.
2 Marks: In box: 7.1, 7.8, 7.12, 7.13. In text: 7.3, 7.10, 7.11, 7.12,
7.13. Chapter end questions: 8, 30, 32, 34, 35, 47, 51, 52, 53, 55,
57, 58, 62.
4 Marks:Werner's theory with suitable examples, IUPAC names of complex
compounds are most repeated questions. Other questions to be learned
are: Lanthanide contraction and its consequences, Linkage,
Co-ordination, Ionisation, Hydrate isomerisms with examples, 4
applications of co-ordination compounds, 4 characteristic properties
of transition
elements, examples. In box: 7.12, 7.13. In text: 7.11, 7.12, 7.13, 7.16, 7.18.
For objective exams: Werner's theory applications, no. of electrons in
the ions (It is must to learn atomic numbers from 21 to 30, their
names, oxidation states, their electronic configuration), Magnetic
moment, interstitial compounds, standard reduction potential linked
questions, ionic size, oxidation states of f-block elements, bonding
types (V.B.T.), hybridization, isomerism, IUPAC nomenclature and
crystal field theory.
Polymers:
Everytime two 2 marks questions are coming in I.P.E. from this lesson.
It is advisable to prepare for I.P.E. and entrance exams at a time.
For this purpose prepare a chart for name of polymer, type of
classification based on mode of polymerisation, names of the monomers
(& their structures) present in the polymers, functional group in the
polymer, examples, uses.
2 Marks: PHBV definition and uses, PDI, Vulcanization, Names of the
monomers present in Teflon, Bakelite, Nylon-2-Nylon-6, Nylon 66, Nylon
6, Dacron, Neoprene, PVC, Buna-N, Buna-S, definitions with 2 examples
of fibres, elastomers, copolymers, polymerisation, condensation &
addition polymerisation, Thermoplastic and thermosetting polymers.
Biomolecules:
One can expect one 4 marks question or two 2 marks questions from this
lesson for I.P.E.
2 Marks: Anomers, invert sugar, essential and non essential amino
acids, Zwitter ion, Monosaccharides, glycosidic linkage, peptide bond,
nucleic acids, nucleoside, nucleotide definitions with 2 examples,
enzymes, denaturation.
4 Marks: A, D, E, K vitamins (Sources and deficiency diseases),
Hormones (types, examples & functions), structure of glucose.
For objective exams: Hydrolysis productions of disaccharides, types of
vitamins (sources, deficiency diseases), structural aspects of
disaccharides, DNA, RNA, functions of hormones.
marks (group 16 or 17 or 18) are coming from this lesson. This chapter
has a weightage of 12 marks. 2 Marks: From 15th group: Chapter end
questions No: 3, 5, 6, 18, 19, 21, 28, 31, 39, 45. In box: 6.2, 6.4,
6.5, 6.7, 6.9. In text: 6.2, 6.5, 6.10.
From 16th group: Chapter end questions: 2, 7, 8, 12, 14, 15, 17, 19,
22, 27, 28, 40. In Box: 6.11, 6.12. In text: 6.15, 6.25.
From 17th group: Chapter end Questions No: 6, 5, 9, 10, 11, 17, 19,
20, 25, 31, 32. In box: 6.15, 6.16, 6.17, 6.18
4 Marks: 15th group: NH3 by Haber's process, HNO3 by Ostwald's process.
16th group: H2SO4 by contact process, O3 preparation and reactions
with Pbs, C2H4, KI, Hg and Ag.
17th group: Cl2 preparation 2 methods or reactions of Cl2 with Cold
dil. NaOH, hot conc. NaOH, Na2S2O3, excess of NH3.
18th group: Preparation, structures of XeF2, XeF4, XeF6, XeO3, XeOF4.
8 Marks: There is a possibility of asking preparation and properties
of Cl2 or O3 . For objective exams: oxyacids of S, Cl, Hydrides,
Hybridization of molecules.
d and f Block Elements and Coordination Compounds:
Expect one 2 marks question and one 4 marks question in I.P.E. from this lesson.
2 Marks: In box: 7.1, 7.8, 7.12, 7.13. In text: 7.3, 7.10, 7.11, 7.12,
7.13. Chapter end questions: 8, 30, 32, 34, 35, 47, 51, 52, 53, 55,
57, 58, 62.
4 Marks:Werner's theory with suitable examples, IUPAC names of complex
compounds are most repeated questions. Other questions to be learned
are: Lanthanide contraction and its consequences, Linkage,
Co-ordination, Ionisation, Hydrate isomerisms with examples, 4
applications of co-ordination compounds, 4 characteristic properties
of transition
elements, examples. In box: 7.12, 7.13. In text: 7.11, 7.12, 7.13, 7.16, 7.18.
For objective exams: Werner's theory applications, no. of electrons in
the ions (It is must to learn atomic numbers from 21 to 30, their
names, oxidation states, their electronic configuration), Magnetic
moment, interstitial compounds, standard reduction potential linked
questions, ionic size, oxidation states of f-block elements, bonding
types (V.B.T.), hybridization, isomerism, IUPAC nomenclature and
crystal field theory.
Polymers:
Everytime two 2 marks questions are coming in I.P.E. from this lesson.
It is advisable to prepare for I.P.E. and entrance exams at a time.
For this purpose prepare a chart for name of polymer, type of
classification based on mode of polymerisation, names of the monomers
(& their structures) present in the polymers, functional group in the
polymer, examples, uses.
2 Marks: PHBV definition and uses, PDI, Vulcanization, Names of the
monomers present in Teflon, Bakelite, Nylon-2-Nylon-6, Nylon 66, Nylon
6, Dacron, Neoprene, PVC, Buna-N, Buna-S, definitions with 2 examples
of fibres, elastomers, copolymers, polymerisation, condensation &
addition polymerisation, Thermoplastic and thermosetting polymers.
Biomolecules:
One can expect one 4 marks question or two 2 marks questions from this
lesson for I.P.E.
2 Marks: Anomers, invert sugar, essential and non essential amino
acids, Zwitter ion, Monosaccharides, glycosidic linkage, peptide bond,
nucleic acids, nucleoside, nucleotide definitions with 2 examples,
enzymes, denaturation.
4 Marks: A, D, E, K vitamins (Sources and deficiency diseases),
Hormones (types, examples & functions), structure of glucose.
For objective exams: Hydrolysis productions of disaccharides, types of
vitamins (sources, deficiency diseases), structural aspects of
disaccharides, DNA, RNA, functions of hormones.
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