- Joined
- Aug 6, 2007
- Messages
- 553
- Reaction score
- 5




I found this from one of the ochem websites someone on here posted.
It would form the substitution product right? E2 isn't favored through primary halides.
![]()
![]()
![]()
![]()
I found this from one of the ochem websites someone on here posted.
It would form the substitution product right? E2 isn't favored through primary halides.
![]()
![]()
![]()
![]()
I found this from one of the ochem websites someone on here posted.
It would form the substitution product right? E2 isn't favored through primary halides.
E2 is preferred when the halide is a good LG and when the substrate is unhindered (methyl, 1, or 2) and when a strong base is used( such as NaOH)
Its actually secondary so it should undergo E2 with a strong base.
I'm not seeing how it's secondary.
No, E2 is preferred in the following order of substrate. 3>2>1.
My bad... Its primary, I just took a practice test and my heat feels like its about to explode!