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Topic: Structure names (Read 4454 times)
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Lisa_G
Regular Member
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Structure names
«
on:
March 19, 2008, 05:33:25 PM »
could anyone please help me with this, i think only a genuis would be able to do this
http://s301.photobucket.com/albums/nn46/lisa_g10/
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azmanam
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Re: Structure names
«
Reply #1 on:
March 19, 2008, 06:18:35 PM »
Start here
http://www.cem.msu.edu/~reusch/VirtTxtJml/addene2.htm
http://www.cliffsnotes.com/WileyCDA/CliffsReviewTopic/Alkenes-Hydrohalogenation.topicArticleId-22667,articleId-22619.html
http://www.cem.msu.edu/~reusch/VirtTxtJml/addyne1.htm
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Dan
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Re: Structure names
«
Reply #2 on:
March 19, 2008, 06:21:33 PM »
These are standard reactions and are very likely all covered in the alkenes/alkynes chapter of any organic chemisry text, eg. Clayden & friends.
You should at least try doing some reading before asking on the forums.
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Lisa_G
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Re: Structure names
«
Reply #3 on:
March 21, 2008, 05:11:49 PM »
i have been looking at them sites and hav come to the conclusion:
1) 2-bromoethylbenzene
2) cis addition of D2
3) cis diol
4) phenylacetone
dont know of thats right, but can some correct me if im wrong
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Lisa_G
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Re: Structure names
«
Reply #4 on:
March 23, 2008, 08:21:37 PM »
can someone please correct me
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agrobert
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Re: Structure names
«
Reply #5 on:
March 23, 2008, 08:44:55 PM »
1. What is the purpose of ultraviolet light? Can you propose a radical mechanism for this? How is it different than addition with HBr? what about HBr with H
2
O
2
?
2. Sounds good. Why is it cis?
3. What is the purpose of NaHSO
3
? Product looks good.
4. What about mercuric oxide makes it different than other oxidants? phenyl acetone? (How many carbons do you have?
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