Enantiomeric Excess (ee)
Enantiomeric Excess (ee) When there is a chiral center in a molecule, there is a possibility of the enantiomeric mixture, […]
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Enantiomeric Excess (ee) When there is a chiral center in a molecule, there is a possibility of the enantiomeric mixture, […]
Stability Order of Carbocation , Carbanion and Free Radicals Stability order of carbocations increases as we move from primary to
Hydrocarbons Most of the organic compounds are known as hydrocarbons because they are basically made up of hydrogen and carbon
Specific Rotation Specific rotation is characteristic value for every optically active compound. Observed rotation of a compound may vary as
Wedge and Dash Projection In organic chemistry wedge and dash, projections are used to represent three-dimensional structures of compounds on
Resolution The separation of a racemic mixture or racemic modification into pure enantiomers is called resolution. Resolution is a unique
Geometric Isomerism Geometric isomerism is shown by alkenes and cyclic compounds where rotation around the bond is not possible. These
Electrophilic Substitution in Pyrrole (Reactivity and Orientation) Pyrrole, thiophene, and furan gives electrophilic aromatic substitution reaction. These compounds are more
Nucleophilic Aromatic Substitution (SNAr) Ordinarily aromatic benzene ring and their derivatives give electrophilic aromatic substitution due to the high density
Electrophile Attack Orientation in Disubstituted Benzenes Disubstituted benzenes have two substituents on the ring which makes the orientation of incoming