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Chemistry 15 Online
OpenStudy (anonymous):

Can someone help me with this chemistry question

OpenStudy (anonymous):

OpenStudy (kainui):

You've drawn it almost completely correct. But in your final product you've shown that you've only added a single oxygen atom when in fact you were adding a Methoxide anion, CH3O-.

OpenStudy (anonymous):

oh...so I should just add CH3O to both and it will be right?

OpenStudy (kainui):

I believe so. Just add a little methyl group to the oxygens and you should be fine. In this SN2 reaction that CH3O- is coming in as a nucleophile and kicking out to replace Br-

OpenStudy (anonymous):

Could I attache the methyl group to the center carbon then the O to it ?

OpenStudy (kainui):

No, the oxygen part is what's attaching. Since oxygen is more electronegative than carbon, it has electrons to donate in the reaction, so it attaches there like this: |dw:1389342227874:dw|

OpenStudy (anonymous):

for the first one it says its wrong because "The stereocenter is inverted in an SN2 reaction."

OpenStudy (sinbearciante):

Don't forget to include the correct R/S designation and the inorganic product too!

OpenStudy (anonymous):

OpenStudy (anonymous):

what does it mean by "The stereocenter is inverted in an SN2"

OpenStudy (sinbearciante):

Its referring to the configuration of the substituents around the carbon stereocenter. For example if a reactants stereocenter initially had an S configuration its Sn2 product would have an R configuration.

OpenStudy (sinbearciante):

So, looking at your latest image, you need to switch the D and H

OpenStudy (sinbearciante):

Your reactant has an R config. and so does your product

OpenStudy (anonymous):

so like this

OpenStudy (anonymous):

OpenStudy (sinbearciante):

Yup, that is what I would put

OpenStudy (sinbearciante):

and dont forget the inorganic Br- product!

OpenStudy (anonymous):

it doesn't want us to put the leaving group. It says the second product is also wrong

OpenStudy (anonymous):

OpenStudy (kainui):

I find that questions like these are what make organic chemistry harder for absolutely no reason.

OpenStudy (anonymous):

it gets harder when you have no example and your teacher didn't explain anything yet bc the tutorial is today and this is due tomorrow

OpenStudy (kainui):

@0213 Be careful. Reread the question and make sure EVERY sentence is fulfilled. For instance, your second sentence says exactly where your problem is.

OpenStudy (sinbearciante):

Well darn

OpenStudy (anonymous):

@Kainui so i have to include the leaving group?

OpenStudy (anonymous):

but what is wrong with the second product ?

OpenStudy (kainui):

No I mean, you're correct... Yes you need to include the leaving group... lol

OpenStudy (anonymous):

but it says the second product is wrong

OpenStudy (sinbearciante):

Here is a really helpful orgo link that I give to students I tutor: http://www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/intro1.htm Its better than most teachers at explaining orgo topics!

OpenStudy (kainui):

I can't see it, is there stereochemistry involved? It should be identical aside from being an isomer.

OpenStudy (anonymous):

OpenStudy (kainui):

So right now both of those are identical.

OpenStudy (anonymous):

so what do i do?........... sorry, im very tired and very sick and having 49 questions due tomorrow on orgo chem isn't a walk in a park.

OpenStudy (anonymous):

i just want to move on

OpenStudy (anonymous):

nvm

OpenStudy (sinbearciante):

At this point id take your screen shot and show the prof.!

OpenStudy (anonymous):

Its really hard to do the homework when their is no tutorial or anything and i have no idea how the online homework works....turns out i was right..except it wanted the leaving group in the second box....my prof told us never to include the leaving group bc its not a product

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