Why is a Grignard reagent a nucleophile?
Because it contains a carbon centre more or less directly bound to an electropositive metal centre.
Check out this previous response. In organic chemistry, there aren't many methods for creating carbon-carbon bonds. Grignards provides the most straightforward and methodical approach.
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A Grignard reagent is a nucleophile because it has a negatively charged carbon atom that is highly electron-rich and can donate electrons to form a covalent bond with an electrophile, resulting in the formation of a new carbon-carbon bond.
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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.

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