The rate of reaction increases with increasing nucleophilicity.
The number 2 denotes a second-order reaction.
Tertiary butyl substrates do not follow this mechanism.
The optical rotation of substrates always changes from (+) to (-) or from (-) to (+) in the products.
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The Correct Option isA, B, C
Approach Solution - 1
The SN2 reaction mechanism is a bimolecular nucleophilic substitution reaction characterized by:
A single step where the nucleophile attacks the electrophilic carbon and the leaving group departs simultaneously.
Statement 1:True. The reaction rate depends on the concentration of both the nucleophile and the substrate, and hence increases with increasing nucleophilicity.
Statement 2:True. The ”2” in SN2 indicates that the reaction is second-order, dependent on two reactants.
Statement 3:True. Tertiary substrates do not follow the SN2 mechanism due to steric hindrance.
Statement 4:False. Optical rotation may change, but it is not guaranteed to shift from (+) to (-) or vice versa, as this depends on the specific nucleophile and substrate.
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Approach Solution -2
Which of the following statements about the SN2 reaction mechanism is/are true?
Option 1: The rate of reaction increases with increasing nucleophilicity.
Option 2: The number 2 denotes a second-order reaction.
Option 3: Tertiary butyl substrates do not follow this mechanism.
Option 4: The optical rotation of substrates always changes from (+) to (-) or from (-) to (+) in the products.