Chemistry Chapter 8 Organic Chemistry Class 11 Notes FREE PDF
Introduction to Organic Chemistry
Coined by Berzelius in 1807.
Initially based on vitalism theory, suggesting living systems had a unique 'vital force'.
Discovery by Friedrich Wohler
Synthesized an organic compound from an inorganic one in 1828, debunking vitalism.
Highlights carbon's unique catenation property allowing diverse compounds.
General Organic Chemistry
Study of foundational concepts in chemical reactions.
Reaction mechanisms describe bond formation and breaking:
Sigma Bond: Stronger, overlaps along inter-nuclear axis.
Pi Bond: Weaker, overlaps perpendicularly to inter-nuclear axis.
Structural Formulas
Lewis Structures: Represent all bonding electron pairs.
Condensed Formulas: Simplified representations with central atoms.
Line-Angle Formulas
Skeletal structures showing bonds; carbon implied at intersections.
3-D representations use solid and dashed wedges for bond orientations.
Hybridization
Mixing of atomic orbitals resulting in hybrid orbitals:
Size Order: sp3 > sp2 > sp.
Electronegativity Order: sp > sp2 > sp3.
Dienes
Types of dienes:
Isolated: Double bonds separated by at least one sp3 carbon.
Stability of Dienes
Stability order: Isolated > Conjugated > Cumulated.
Forms of Carbon
Common forms include Diamond, Graphite, Carbides, Fullerenes, and Charcoal.
Fission Types
Homolytic Fission: Each atom retains one electron, forming free radicals.
Heterolytic Fission: Shared electron pair moves creating cations and anions.
Inductive Effect
Inequal electron sharing in bonds leads to inductive effects influenced by electronegativity differences.
Electron Donating and Withdrawing Groups
EDG: +I effect, increases electron density.
EWG: -I effect, decreases electron density.
Basicity of Amines
Basic strength order in gas/liquid: 3° > 2° > 1° > NH3.
Concept of Resonance
Some molecules require multiple Lewis structures to describe resonance.
Validity of Lewis Structures
Rules include octet fulfillment, maintaining atomic positions, and coplanarity.
Mesomeric Effect
Permanent polarization in conjugated systems indicating stability.