S STACM Full Member 15+ Year Member Joined Dec 24, 2006 Messages 316 Reaction score 0 Jul 6, 2008 #1 Members do not see this ad. When it comes to carbocations and radicals, will they be more stable when resonance stabilized vs. higher substitution on the cation?
Members do not see this ad. When it comes to carbocations and radicals, will they be more stable when resonance stabilized vs. higher substitution on the cation?
Mstoothlady2012 Full Member 10+ Year Member 5+ Year Member 15+ Year Member Joined Apr 7, 2007 Messages 1,714 Reaction score 4 Jul 6, 2008 #2 STACM said: When it comes to carbocations and radicals, will they be more stable when resonance stabilized vs. higher substitution on the cation? Click to expand... resonance is a way to go!! allylyic > tertiary benzyllic > tertiary Upvote 0 Downvote
STACM said: When it comes to carbocations and radicals, will they be more stable when resonance stabilized vs. higher substitution on the cation? Click to expand... resonance is a way to go!! allylyic > tertiary benzyllic > tertiary
D DentalDeac Full Member 10+ Year Member 15+ Year Member Joined May 28, 2008 Messages 228 Reaction score 0 Jul 6, 2008 #3 Mstoothlady2012 said: resonance is a way to go!! allylyic > tertiary benzyllic > tertiary Click to expand... I thought tertiary is the most stable Upvote 0 Downvote
Mstoothlady2012 said: resonance is a way to go!! allylyic > tertiary benzyllic > tertiary Click to expand... I thought tertiary is the most stable
H Hugh Mannity Full Member 10+ Year Member 15+ Year Member Joined May 15, 2008 Messages 228 Reaction score 0 Jul 6, 2008 #4 Nope, single conjugated is more stable than tertiary, and tertiary with all 3 being phenyls is the most stable of all. Upvote 0 Downvote
Nope, single conjugated is more stable than tertiary, and tertiary with all 3 being phenyls is the most stable of all.