Crystal Field Theory (CFT); it accounts for d-orbital splitting, colour, and magnetic behaviour.
Methylamine > Ammonia > Aniline; +I effect of methyl increases basicity; aniline has -M effect.
Enantiomeric excess = % of major enantiomer – % of minor enantiomer = observed specific rotation/actual specific rotation ×100.
NO₂ group withdraws electrons by -I and -M, deactivating ortho/para positions via destabilizing intermediates.
E = E° – (RT/nF) ln Q, where Q = product/reactant ratio; at 298K, E = E° – (0.059/n) log Q.
Order is experimental sum of concentration exponents; molecularity is theoretical number of molecules colliding in elementary step.
Due to small energy difference between (n-1)d and ns orbitals, allowing participation of both in bonding.
It causes nearly identical radii of Zr/Hf, Nb/Ta, Mo/W, leading to similar chemical properties and difficult separation.
Type-I (lyophilic) are solvent-loving, reversible; type-II (lyophobic) are solvent-hating, irreversible, need stabilizers.
Homotopic protons are chemically equivalent; enantiotopic protons give same NMR signal but in chiral environment split.
No Description Added
Crystal Field Theory (CFT); it accounts for d-orbital splitting, colour, and magnetic behaviour.
Methylamine > Ammonia > Aniline; +I effect of methyl increases basicity; aniline has -M effect.
Enantiomeric excess = % of major enantiomer – % of minor enantiomer = observed specific rotation/actual specific rotation ×100.
NO₂ group withdraws electrons by -I and -M, deactivating ortho/para positions via destabilizing intermediates.
E = E° – (RT/nF) ln Q, where Q = product/reactant ratio; at 298K, E = E° – (0.059/n) log Q.
Order is experimental sum of concentration exponents; molecularity is theoretical number of molecules colliding in elementary step.
Due to small energy difference between (n-1)d and ns orbitals, allowing participation of both in bonding.
It causes nearly identical radii of Zr/Hf, Nb/Ta, Mo/W, leading to similar chemical properties and difficult separation.
Type-I (lyophilic) are solvent-loving, reversible; type-II (lyophobic) are solvent-hating, irreversible, need stabilizers.
Homotopic protons are chemically equivalent; enantiotopic protons give same NMR signal but in chiral environment split.