How do Grignard reagents react?
With carbonyl species it usually reacts quantitatively.
Grignards generally do not react well with alkyl halides, though the addition of copper salts can occasionally mediate such a reaction; see here for a related question, which dealt with the action of Grignards on ketones and aldehyes.
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Grignard reagents react by donating their alkyl or aryl group to electrophiles, forming a new carbon-carbon bond. This reaction proceeds through the nucleophilic addition of the Grignard reagent to the electrophilic carbon atom of the substrate, followed by proton transfer or quenching with a suitable acidic or protic solvent.
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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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