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Course Requirements


Course Description

                                                     Syllabus

🔹 Unit I – Ionic and Covalent Bonding

Hours: 8 | Marks: 8


A) Ionic Bond (आयनिक बंध)

Definition:

Electron transfer द्वारे तयार होणारा bond

Example:

NaCl


Factors affecting ionic bond formation:


1) Ionization Energy

Electron काढण्यासाठी लागणारी energy


2) Electron Affinity

Electron स्वीकारण्याची क्षमता


3) Lattice Energy

Crystal formation energy


Born–Haber Cycle

Purpose:

Lattice energy calculate करण्यासाठी


B) Covalent Bond (सहसंयुज बंध)


Directional Nature

Specific direction मध्ये bond तयार होतो


Valence Bond Theory (VBT)

Bond formation due to orbital overlap


Limitations of VBT

Cannot explain:

  • Magnetic properties


Hybridization

Definition:

Mixing of orbitals


Types with Examples:

HybridizationGeometryExample
spLinearBeCl₂
sp²Trigonal planarBF₃
sp³TetrahedralCH₄
sp³dTrigonal bipyramidalPCl₅
sp³d²OctahedralSF₆
sp³d³Pentagonal bipyramidalIF₇

🔹 Unit II – Mole Concept and Volumetric Analysis

Hours: 7 | Marks: 7


A) Mole Concept


Definition:

1 mole = 6.022 × 10²³ particles


Avogadro Law:

Equal volume contains equal molecules


Terms:


Atomic Mass


Molar Mass


Concentration Terms:


Molarity (M)

Molality (m)

Normality (N)

Mole fraction


Numericals Included


B) Volumetric Analysis


Important Terms:

Titrant

Titrate

Indicator

End point


Standard Solution


Primary Standard Substance

Example:

Na₂CO₃


🔹 Unit III – Organic Chemistry

Hours: 8 | Marks: 8


A) Alkyl Halides

Preparation and reactions

Example:

Ethyl bromide


B) Aryl Halides

Preparation from diazonium salts

Benzyne mechanism


C) Alcohols

Example:

Ethyl alcohol


D) Phenols

Important Reactions:


Reimer–Tiemann Reaction

Kolbe Reaction

Fries Rearrangement

Claisen Rearrangement


E) Ethers


Williamson Synthesis


Reaction with HI


🔹 Unit IV – Stereochemistry

Hours: 7 | Marks: 7


A) Optical Isomerism


Terms:

Chiral carbon

Enantiomers

Diastereomers

Meso compounds


Configuration:

D / L system

R / S system


B) Geometrical Isomerism

Types:

Cis – Trans

E – Z system


C) Conformational Isomerism


Projection:

Newman projection

Sawhorse projection


Conformations:

Ethane

Butane

Course Outcomes

1. Describe Born-Haber’s cycle.

2. Predict molecular geometries using hybridization

3. Define the mole in terms of mass, volume, and number of particles.

4. Solve problems on concentrations (molarity, normality, molality, mole fraction).

5. Explain the requirements for standard solutions and primary standard substances.

6. Compare the reactivity of halogenated hydrocarbons.

7. Write the mechanisms of SN reactions.

8. Design syntheses of organic molecules containing C-X, and C-O bonds.

9. Differentiate between enantiomers and diastereomers.

10. Assign configurations to the stereoisomers.

Course Curriculum

Teacher

MAYURESH SAHASTRABUDDHE SIR

5 Rating
2 Reviews
147 Students
5 Courses

"Good day, everyone! I'm Mayuresh, and I'm incredibly thrilled to be your chemistry teacher. For as long as I can remember, the intricate dance of atoms and molecules has captivated me. From the enchanting world of chemical reactions to the marvels of the periodic table, my aim is to ignite that same sense of wonder and curiosity within each of you. With a background in M.Sc Chemistry, I'm here not only to teach but also to inspire and guide you through the exciting realms of chemistry. Together, let's uncover the mysteries, perform fascinating experiments, and delve into the depths of this captivating scientific discipline."

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BSC Semester 4 Chemistry minor (NEP)

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