What is an alkyl halide?
Let's just take it word for word.
The alkyl group here is a propyl group; a three-carbon alkyl group. The halide portion is evidently the bromide substituent. Just as bromine is a halogen, it as a substituent is a halide.
Halogens tend to be fairly electronegative. Or, at least enough that we consider alkyl halides to be reactive at the carbon directly connected to the halide. The electron-withdrawing quality of the halide polarizes the bond towards the halide, meaning most of the electron density is found nearer the halide than near the directly-attached carbon. Evidently, that means the halide possesses a partial negative charge.
So, the aforementioned directly-attached carbon has a partial positive charge, and we call that an electrophilic center.
Because of that, it is reactive towards electron donation from a nucleophile, simply because electrons are attracted to a partial positive charge.
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An alkyl halide is a compound in which one or more hydrogen atoms in an alkane molecule have been replaced by halogen atoms (fluorine, chlorine, bromine, or iodine). These compounds are also known as haloalkanes or halogenoalkanes.
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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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