epoxide

His epoxide skin burns at the touch of the air.

Some ways can even make only one enantiomer of the epoxide.

Because of this small ring, an epoxide is very reactive.

How will I know if heptachlor epoxide is in my drinking water?

This is the reverse of the formation reaction from an epoxide.

How will heptachlor epoxide be removed from my drinking water?

Just as long as they don't hold up the epoxide."

Low temperatures are also beneficial when epoxide migration is not desired.

How does heptachlor epoxide get into my drinking water?

I've got the first epoxide mixture curing right now, is that what you wanted?"

In the next step, O is cleaved with the formation of an epoxide.

Nucleophilic opening of the epoxide can occur by attack at either the 1 or 2 position.

Heptachlor epoxide is more likely to be found in the environment than its parent compound.

Notice that the alcohol retains the configuration of the starting epoxide.

To prevent epoxide migration, weakly basic conditions may be employed.

This epoxide is then attacked by water creating two hydroxyl groups in the center of the structure.

After opening the epoxide, an alcohol is left.

An important criterion for epoxy resins is the epoxide content.

In the second step, this mixture is treated with base to give the epoxide:

Overall, the Payne rearrangement represents a migration of the epoxide.

It is the sulfur analogue of an epoxide or aziridine.

Gormley et al. have shown that the reaction does not proceed through an epoxide.

An epoxide is a cyclic ether with three ring atoms.

Note that the epoxide and ester functional groups survive intact.

"In particular, the epoxide sample I suggested you look into on Thursday.