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Subject:
Organic Chemistry reaction
Category: Science > Chemistry Asked by: aesl1984-ga List Price: $8.00 |
Posted:
17 Mar 2006 11:50 PST
Expires: 27 Mar 2006 22:29 PST Question ID: 708491 |
Outline a reasonable synthesis for each of the following transitions: 1)m-iodophenol from benzene 2) ethyl acetonoate to 4-phenylbutan-2-one |
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There is no answer at this time. |
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Subject:
Re: Organic Chemistry reaction
From: stephanbird-ga on 19 Mar 2006 12:35 PST |
Define reasonable.. Why not for instance could you not take benzene, add OH- to it, and in doing so displace a H- from the ring which could combine with I2 to give HI and I-. The I- could then displace a further H- from the benzene ring to possibly give your first desired product. Looks a bit homework ish to me ;) Stephan |
Subject:
Re: Organic Chemistry reaction
From: aesl1984-ga on 23 Mar 2006 17:35 PST |
Yeah, it's an old practise test (studying for MCAT) |
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