OH-(alcoholic) +CH3(CH2)2Br- →Product+Product. The nature of OH in the above reaction is:
Correct answer: A. Nucleophile
- A. Nucleophile
- B. Lewis base
- C. Ligand
- D. All of the above
Explanation
A nucleophile is a molecule or substance that tends to donate electrons or react at electron-poor sites such as protons. As OH- has extra electrons it can attack the electrophilic carbon. So, it acts as a nucleophile.
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About Alkyl Halides
Alkyl halides are named and related to their carbon-halogen structure, polarity and reactivity. The key reactions are nucleophilic substitution by SN1 and SN2 mechanisms and elimination by E1 and E2 mechanisms, including how substrate structure, nucleophile, base, solvent and temperature influence substitution versus elimination.
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