- Leading strand: Synthesized continuously in the 5’ to 3’ direction towards the replication fork.
- Lagging strand: Synthesized in short Okazaki fragments in the 5’ to 3’ direction away from the replication fork. These fragments are later joined by DNA ligase, ensuring the continuity of the strand.


Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.