Ochem Q

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2-bromo-3-dimethyl butane reacting with methanol, what kind of reaction is this? I think its both SN1 and E1? is that true? :xf:


Sn1 with proton transfer to secondary carbon so create tertiary carbon cation and -OH add to it. need confirm
 
hausee i think you are correct.

substitution is mostly favored over elimination.

In this case, I believe both Sn1 and E1 products will form, just Sn1 would be major.

Of course, there will be rearrangements.
 
hausee i think you are correct.

substitution is mostly favored over elimination.

In this case, I believe both Sn1 and E1 products will form, just Sn1 would be major.

Of course, there will be rearrangements.

but MeOH is so week, is E1 actually happening?
 
I've learned that E1 product always occurs with Sn1 Products, but substitution is always favored over E1.

If I am not correct, please enlighten me.

For E1, do you need a strong base?
 
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