Actually I just read something up on how it depends on the nature of the carbon atom as in if it is a primary carbon or tertiary?
With tertiary forming a more stable carbocation
Which alkyl halide would you expect to undergo an SN2 reaction most slowly?
1-bromo-4-methylpentane
1-bromo-3-methylpentane
1-bromo-2-methylpentane
1-bromo-2,2-dimethylbutane
I am really confused with this topic and no I have been reading up on it, but I do not know how to approach such a question
1-bromohexane
1 answer