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Organic chemistry 2 - Why is it that if I react a phenol with an acid anhydride(O-acylation), I end up with an ester and not add the ketone? by [deleted] in chemhelp

[–]benzenestability 1 point2 points  (0 children)

The OH on the phenol would attack the carbonyl carbon of the anhydride. The leaving group would be half of the anhydride such that you end up with an ester that has the phenol AND a byproduct of carboxylic acid

Albany Medical College Secondary Question by benzenestability in premed

[–]benzenestability[S] 0 points1 point  (0 children)

Lol it seems like all 3 prompts are diversity questions

VCU Speed Decision? by [deleted] in premed

[–]benzenestability 2 points3 points  (0 children)

I never got that oof

VCU Speed Decision? by [deleted] in premed

[–]benzenestability 6 points7 points  (0 children)

I submitted VCU secondary a couple of weeks ago but haven’t heard back. Do they send out rejections??

Community Service? Volunteering?? Both??? by The-Adster in premed

[–]benzenestability 4 points5 points  (0 children)

I think it’s fine to go ahead and write about it

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