Why do primary alkanes/alcohols undergo E2/SN2 while secondary and tertiary undergo E1 and SN1?
steric hindrance
Can you please explain? I havent gotten through that far yet to know what steric hindrance means.
basically physical obstruction. SN2 and E2 are bimolecular meaning that in order for a reaction to take place it needs the reaction of both molecules. SN1 and E1 are unimolecular, the Carbon is able to polarize due to the near by atoms who "temporarily share" their electrons with that carbon (now a carbocation/carbonium) and render it stable
I still dont understand too much. I mean I can memorize that Sn2 is for primary and methane and Sn1 is for sec/tert, but I dont understand it with words. Is there any way you can draw a picture or something to help me understand? :/
it's easier if i just send you a link to some videos, have you heard of khan academy? http://www.khanacademy.org/science/organic-chemistry/v/comparing-e2-e1-sn2-sn1-reactions
Looking at it right now. Will they talk about steric hindrance and why it goes one way or the other? it doesnt really explain steric hindrance so far in the one you linked. It did eliminate some possible mechanisms though..
theres a video specifically on steric hindrance on the site, under organic chemistry
Join our real-time social learning platform and learn together with your friends!