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Internal 3 30thaug Slash Definite Integrals
Internal 3 30thaug Slash Definite Integrals
SUBJECT S
PHYSICS Center Of Mass And Collision, RBD
Hydrocarbons (Alkanes, Alkenes, Alkynes),
CHEMISTRY
Aromatic Compounds, Alkyl Halide
Application Of Derivative, Indefinite integration,
MATHS
Definite integration(4.0 To 6.0)
TEST DATE: 30-AUG-2023 (WEDNESDAY)
-:SYLLABUS DETAILS:-
PHYSICS
CENTER OF MASS:-
1.0 SYSTEM OF PARTICLES, 1.1 System of Particles and Mass Center, 1.2 Center of Mass Frame of
Reference or Centroidal Frame, 1.3 Application of Newton’s Laws of Motion to a System of
Particles, 2.0 IMPULSE OF A FORCE, 2.1 Impulse Momentum Principle, 2.2 Impulsive Motion, 3.0
MOMENTUM AND KINETIC ENERGY, 3.1 Internal and external Forces and System of interacting
Particles, 3.2 Principle of Conservation of linear momentum, 3.3 Application of Methods of
Impulse and Momentum to a System of Particles, 3.4 Application of Methods of Work and Energy
to a System of Particles, 4.0 IMPACT BETWEEN TWO BODIES, 4.1 Central and Eccentric Impact, 4.2
Head–on (Direct) Central Impact, 4.3 Oblique Central Impact, 4.4 Oblique Central Impact when one
or both the colliding bodies are constrained in motion, 5.0 VARIABLE MASS SYSTEM, 5.1 Rocket
propulsion
CHEMISTRY
HYDROCARBON:-
ALKANES-INTRODUCTION, GENERAL METHODS OF PREPARATIONS, PHYSICAL
PROPERTIES,CHEMICAL PROPERTIES,ALKENESINTRODUCTION, ELIMINATION REACTIONS,
PREPARATION OF ALKENES, PHYSICAL PROPERTIES OF ALKENES/ HYDROCARBONS,CHEMICAL
PROPERTIES, SUBSTITUTION REACTION,POLYMERIZATION,ISOMERISATION, DIENES
ALKYNESINTRODUCTION, PHYSICAL PROPERTIES, CHEMICAL PROPERTIES, USES OF
ACETYLENE,LABORATORY TEST FOR ALKYNS
AROMATIC COMPOUND:-
1.0 AROMATIC CHARACTER : [THE HUCKEL 4n + 2 RULE] 2.0 STRUCTURE OF BENZENE 3.0
PREPARATION OF ARENES 3.1 Benzene 3.2 Toluene 4.0 COMPARISION OF AROMATIC
COMPOUNDS WITH ALKENES 5.0 ELECTROPHILIC AROMATIC SUBSTITUTION REACTIONS IN
BENZENE RING 5.1 Halogenation 5.2 Nitration 5.3 Sulphonation 5.4 Friedel Craft reaction 5.5
Gatter Mann Koch Formylation 5.6 Gattermann formylation 6.0 ACTIVATING AND DEACTIVATING
EFFECTS 6.1 Activating Groups or Electron Releasing Groups (ERG) 6.2 Deactivating Group or
Electron Withdrawing Group (EWG) or Meta 7.0 DIRECTIVE INFLUENCE OF SUBSTITUENTS IN
BENZENE 8.0 REACTIONS OF ALKYL BENZENES
ALKYL HALIDES:-
1.0 CLASSIFICATION 1.1 Alkyl halides 1.2 Types of monohalo derivatives 1.3 Isomerism 2.0 PHYSICAL
PROPERTIES 2.1 Reactivity order 2.2 Bond energy values 2.3 Boiling point 2.4 Dipole Moments 3.0
GENERAL METHOD OF PREPARATION OF MONOHALIDES 3.1 From alkane 3.2 From alkenes and
alkynes 3.3 By Alcohols 3.4 Borodine – Hunsdicker's reaction 3.5 By halide exchange 3.6 By reaction
of alkanes with sulphuryl chloride (SO2Cl2) 4.0 CHEMICAL PROPERTIES 4.1. Type of SN 4.2 Wurtz
Reaction 4.3 Halogenation of alkyl halides 4.4 Reduction 4.5 Formation of Organometalic
compounds 4.6 Friedel - Crafts reaction 5.0 DIHALIDE 5.1 Classification 5.2 General Method of
Preparation 5.3 Physical Properties 5.4 Chemical Properties
MATHS
APPLICATIONS OF DERIVATIVES:-
(A). TANGENT AND NORMAL 1.0 TANGENT TO THE CURVE AT A POINT 2.0 MYTHS ABOUT
TANGENT 3.0 NORMAL TO THE CURVE AT A POINT 4.0 THINGS TO REMEMBER 5.0 ANGLE OF
INTERSECTION BETWEEN TWO CURVES 5.1 ORTHOGONAL CURVES 6.0 LENGTH OF TANGENT,
SUBTANGENT,NORMAL & SUBNORMAL 7.0 APPROXIMATION 8.0 RATE MEASUREMENT (B).
MONOTONOCITY 9.0 MONOTONOCITY AT A POINT 10.0 MONOTONICITY OVER AN INTERVAL 11.0
GREATEST AND LEAST VALUE OF A FUNCTION 12.0 SPECIAL POINTS 13.0 PROVING INEQUALITIES
USING MONOTONICITY 14.0 SIGNIFICANCE OF THE SIGN OF IIND ORDER DERIVATIVE 15.0
PROVING INEQUALITIES USING GRAPHS & CONCAVITY 16.0 ROLLE'S THEOREM 17.0 LAGRANGE'S
MEAN VALUE THEOREM (LMVT) 18.0 SPECIAL NOTE (C). MAXIMA - MINIMA 19.0 INTRODUCTION
20.0 DERIVATIVE TEST FOR ASCERTAINING MAXIMA/MINIMA 21.0 SUMMARY OF WORKING RULE
FOR SOLVING REAL LIFE OPTIMIZATION PROBLEM 22.0 SHORTEST DISTANCE BETWEEN TWO
CURVES 23.0 USEFUL FORMULAE OF MENSURATION TO REMEMBER 24.0 POINT OF INFLECTION