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I was hooping someone can help me with these
1) why is this called benzaldehyde, a benzyl group should have a CH2 group outside the ring, which this one doesn't have, instead this one is a phenyl group so why isn't it called phenylaldehyde?
http://i274.photobucket.com/albums/jj243/113zami/benzaldehyde.jpg
2) In some of destroyer answers like #29 they have (+)and (-) in front of the answer what is referring to…enantiomers??
3) What does reflux in organic chemistry mean?
4) #8 destroyer does this reaction also work the same way with the other halogens or only the Cl2? I could not find this reaction in my text
5) #13destroyer is choice D meta directing?
6) Between tertiary non allylic and secondary allylic carbocation which one is more stable?
7) what's the advantage of a Soxhlet extractor? I know how it functions but don't understand what's the advantage of using it
thanks
1) why is this called benzaldehyde, a benzyl group should have a CH2 group outside the ring, which this one doesn't have, instead this one is a phenyl group so why isn't it called phenylaldehyde?
http://i274.photobucket.com/albums/jj243/113zami/benzaldehyde.jpg
2) In some of destroyer answers like #29 they have (+)and (-) in front of the answer what is referring to…enantiomers??
3) What does reflux in organic chemistry mean?
4) #8 destroyer does this reaction also work the same way with the other halogens or only the Cl2? I could not find this reaction in my text
5) #13destroyer is choice D meta directing?
6) Between tertiary non allylic and secondary allylic carbocation which one is more stable?
7) what's the advantage of a Soxhlet extractor? I know how it functions but don't understand what's the advantage of using it
thanks
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