What does SN2 stand for?
In this case, the rate-determining step is bond formation. The concentration of the electrophile and nucleophile both affect the rate of reaction.
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SN2 stands for "substitution nucleophilic bimolecular."
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
- Are triflate, tosylate and mesylate the only good leaving groups?
- Why do amines act as nucleophiles?
- Why do primary alkyl halides generally undergo SN2 mechanisms?
- Why does specific rotation of plane-polarized light INCREASE with increased concentrations of the stereoisomer?
- How does doubling the concentration of nucleophile affect the rate of a reaction with an SN1 mechanism?
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