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OpenStudy (anonymous):

Hey, just for clarification about epoxides

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

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.

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?

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\(_2\).

OpenStudy (anonymous):

right!

OpenStudy (abb0t):

|dw:1423944940880:dw|

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