How does an SN2 reaction affect stereochemistry?

Answer 1

In an #"S"_"N"2# reaction, the stereochemistry of the product is inverted compared to that of the substrate.

An #"S"_"N"2# reaction is a backside attack. The nucleophile attacks the electrophilic center on the side that is opposite to the leaving group.

During a backside attack, the stereochemistry at the carbon atom changes. There is inversion of configuration.

Here’s a video on #"S"_"N"2# stereochemistry.

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Answer 2

An SN2 reaction typically leads to an inversion of stereochemistry at the reaction center, resulting in the formation of the inverted product configuration.

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Answer from HIX Tutor

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.

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