What is allylic halogenation?
It is possible to add a halogen to a compound at the allylic position rather than on the double bond when there is an alkene present.
A radical chain mechanism (initiation, propagation, termination) is applied to it.
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Allylic halogenation is a chemical reaction in which a halogen atom (such as chlorine or bromine) replaces a hydrogen atom on an allylic carbon adjacent to a double bond in an organic molecule. This reaction typically occurs in the presence of a halogenating agent, such as N-bromosuccinimide (NBS) or chlorine. It is a useful method for introducing halogen atoms into organic molecules and is commonly employed in organic synthesis.
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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.
- Which of the following hydrocarbons undergo addition reaction: #C_2H_6#, #C_3H_8#, #C_3H_6#, #C_2H_2# and #CH_4#?
- How many different alkenes can be hydrogenated to form hexane?
- How to convert CH3-CHBr-CH3 into CH3-CHOH-CH2Br ?
- What stereoisomers are obtained from hydroboration–oxidation of 1-ethylcyclohexene?
- Can anyone help name the following hydrocarbon derivatives?

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