What is halogenation of alkenes?
It's the addition of a halogen to the C=C double bond of an alkene.
An example is the addition of chlorine to ethylene.
The product has Cl atoms on adjacent carbon atoms.
By signing up, you agree to our Terms of Service and Privacy Policy
Halogenation of alkenes is a chemical reaction in which a halogen molecule, such as chlorine or bromine, adds across the carbon-carbon double bond of an alkene, forming a halogenated compound.
By signing up, you agree to our Terms of Service and Privacy Policy
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.
- What is the explanation for the relative stabilities of methyl, primary, secondary, and tertiary carbocations?
- What is the rate determining step in the nitration of benzene?
- Does acid-catalyzed alkoxylation always use alcohol as the nucleophile?
- What does anti‐Markovnikov additions indicate?
- What is acid catalyzed hydration?

- 98% accuracy study help
- Covers math, physics, chemistry, biology, and more
- Step-by-step, in-depth guides
- Readily available 24/7