Why are epoxides so reactive?
Have you got a molecular model set? You should have one. Construct a 3-membered ring, and then a 6-membered ring; it will be harder to make the former.
After the oxygen site is protonated, each carbon is vulnerable to nucleophilic attack, resulting in substantial ring strain in the three-membered ring.
By signing up, you agree to our Terms of Service and Privacy Policy
Epoxides are highly reactive due to the strain in their three-membered ring structure, which causes a significant angle strain and steric hindrance.
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.

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