A allard6 Full Member 10+ Year Member Joined Dec 10, 2010 Messages 20 Reaction score 0 Points 0 Dental Student Jul 13, 2011 #1 Advertisement - Members don't see this ad (R)-2-bromobutane + Iodide ion in aprotic solvent ---> (S)-2-iodobutane I thought it would be "no reaction" since iodide is a better leaving group than bromide... What am i missing? 😕😕
Advertisement - Members don't see this ad (R)-2-bromobutane + Iodide ion in aprotic solvent ---> (S)-2-iodobutane I thought it would be "no reaction" since iodide is a better leaving group than bromide... What am i missing? 😕😕
AlbinoPolarBear Full Member 10+ Year Member Joined Jun 18, 2011 Messages 1,655 Reaction score 442 Points 5,246 Jul 13, 2011 #2 allard6 said: (R)-2-bromobutane + Iodide ion in aprotic solvent ---> (S)-2-iodobutane I thought it would be "no reaction" since iodide is a better leaving group than bromide... What am i missing? 😕😕 Click to expand... Iodine is also an awesome nucleophile for SN2 reactions. It will kick out the Bromine. Upvote 0 Downvote
allard6 said: (R)-2-bromobutane + Iodide ion in aprotic solvent ---> (S)-2-iodobutane I thought it would be "no reaction" since iodide is a better leaving group than bromide... What am i missing? 😕😕 Click to expand... Iodine is also an awesome nucleophile for SN2 reactions. It will kick out the Bromine.
G Golfguy Full Member 10+ Year Member Joined Mar 5, 2011 Messages 388 Reaction score 30 Points 4,651 Resident [Any Field] Jul 13, 2011 #3 allard6 said: (R)-2-bromobutane + Iodide ion in aprotic solvent ---> (S)-2-iodobutane I thought it would be "no reaction" since iodide is a better leaving group than bromide... What am i missing? 😕😕 Click to expand... And, in aprotic solvent Br is a better nucleophile. So I think equilibrium would lie to the left. Upvote 0 Downvote
allard6 said: (R)-2-bromobutane + Iodide ion in aprotic solvent ---> (S)-2-iodobutane I thought it would be "no reaction" since iodide is a better leaving group than bromide... What am i missing? 😕😕 Click to expand... And, in aprotic solvent Br is a better nucleophile. So I think equilibrium would lie to the left.
PooyaH Full Member 10+ Year Member 15+ Year Member Joined Apr 24, 2008 Messages 804 Reaction score 0 Points 1 Pre-Dental Jul 13, 2011 #4 Here it has nothing to do with which one is a better leaving group. Both Br and I are good leaving groups but I is better. For an SN2 reaction you need to have a strong/good leaving group and a strong nucleophile, which in this case Iodide ion is. Upvote 0 Downvote
Here it has nothing to do with which one is a better leaving group. Both Br and I are good leaving groups but I is better. For an SN2 reaction you need to have a strong/good leaving group and a strong nucleophile, which in this case Iodide ion is.
LetsGo2DSchool Membership Revoked Removed 10+ Year Member Joined Jul 11, 2009 Messages 1,191 Reaction score 5 Points 4,571 Location New York Pre-Dental Jul 13, 2011 #5 AlbinoPolarBear said: Iodine is also an awesome nucleophile for SN2 reactions. It will kick out the Bromine. Click to expand... Think of it as I(odine) will kick Bro(mine's) ass. Sometimes mnemonics help. Upvote 0 Downvote
AlbinoPolarBear said: Iodine is also an awesome nucleophile for SN2 reactions. It will kick out the Bromine. Click to expand... Think of it as I(odine) will kick Bro(mine's) ass. Sometimes mnemonics help.
A allard6 Full Member 10+ Year Member Joined Dec 10, 2010 Messages 20 Reaction score 0 Points 0 Dental Student Jul 13, 2011 #6 Thank you all!!! 🙂 Upvote 0 Downvote