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OpenStudy (anonymous):
|dw:1423935070138:dw|
OpenStudy (anonymous):
Should I do a Nu attack with NaOH, then dehydration and then CH3Ch2Br?
OpenStudy (anonymous):
Will that make sense?
OpenStudy (anonymous):
@Kainui that's the last one for the day
OpenStudy (anonymous):
@Kainui
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OpenStudy (abb0t):
That's not an epoxide
OpenStudy (anonymous):
sorry my bad,but the reaction that I wrote, does it make sense?
OpenStudy (anonymous):
@abb0t was I right at least?
OpenStudy (anonymous):
@Kainui ?
OpenStudy (abb0t):
If I was your professor, I would probably only give you \(\sf \frac{1}{3}\) credit (and thats being very generous), because you didn't show what you used to form your product.
But, you can do an Sn\(_2\) reaction to make an alkoxide. Proceed via williamson synthesis.
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OpenStudy (anonymous):
I agree @abb0t ,I just wanted to see if I'm right at all
OpenStudy (anonymous):
|dw:1423944258553:dw|
OpenStudy (anonymous):
|dw:1423944296481:dw|
OpenStudy (anonymous):
|dw:1423944390399:dw|
OpenStudy (anonymous):
@abb0t is that right?
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OpenStudy (anonymous):
does it suffice in your opinion?
OpenStudy (abb0t):
Yeah, you sort of took a longer route than i expected, but yes, essentially right. You could of just reacted it with something like a sodium ethoxide or something and proceeded via Sn\(_2\).