Chemistry · Alkyl Halides and Amines
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Alkyl Halides involving -C-X bond breakage and- C-Nu bond formation simultaneously.
- A
SN1
- B
SN2
- C
E1
- D
E2
In organic chemistry, the reaction involving the simultaneous breaking of a carbon-halogen bond (-C-X) and the formation of a carbon-nucleophile bond (-C-Nu) is characteristic of nucleophilic substitution reactions, particularly the S_N2 (bimolecular nucleophilic substitution) mechanism.
The reaction mechanism described, where the C-X bond breaks and the C-Nu bond forms simultaneously, follows the SN2 (bimolecular nucleophilic substitution) mechanism, not SN1.
In organic chemistry, the reaction involving the simultaneous breaking of a carbon-halogen bond (-C-X) and the formation of a carbon-nucleophile bond (-C-Nu) is characteristic of nucleophilic substitution reactions, particularly the S_N2 (bimolecular nucleophilic substitution) mechanism.
The reaction described involves simultaneous C-X bond breakage and C-Nu bond formation, which is characteristic of SN2 (substitution nucleophilic bimolecular), not E1 (elimination unimolecular).
The reaction described involves simultaneous C-X bond breakage and C-Nu bond formation, which is characteristic of SN2 (nucleophilic substitution), not E2 (elimination).
Tagged under Chemistry · Alkyl Halides and Amines · 2024