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| DAT Discussions Discuss study tips and resources to excel on the Dental Admissions Test. | RSS: |
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#1 |
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Senior Member
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E2 reactions favors secondary and tertiary groups and wants a strong base. But what is the difference between a strong nucleophile and a strong base? I tried to find it out but I could not find a satisfying answer anywhere. I even saw someone asking the same question in this forum but I could not really understand. I know that halogens Cl-,Br-, I- are strong nucleophiles but a weak base (since they are conjugate base of strong acid(?)) and a tert-ButO- is a strong base but a weak nucleophile. but other than that how can you determine if a molecule is a strong nucleophile or strong base? Thanks guys |
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#2 |
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Senior Member
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look up polarizability
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#3 | |
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Banned
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Quote:
Unfortunately you can NOT. you have to look at the electrophile you are given, (primary, secondary, etc) , protic or aprotic solvent, and if it is a bulky base in order to determine what reaction you are doing. You can have 3 scenarios for sn1,sn2,e1,e2 1) strong nucleophile strong base 2) strong nucleophile weak base 3) weak nucleophile strong base and Yes the conjugate base of a strong acid is so weak that they don't have any basic properties. And T-butyl is bulky so it can't do backside attack. |
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#4 |
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Senior Member
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Thanks!!
I guess I was on the right track. But I thought there would be a "definition" of how to identify a strong nucleophile and a strong base. |
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