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Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: VITA on November 10, 2012, 10:35:20 AM

Title: How're tertiary radicals more stable than allyl radicals?
Post by: VITA on November 10, 2012, 10:35:20 AM

Hello, I'd like someone to give me a basic explanation for hyperconjugation. Simple enough for a 1st year pharmacy student to understand. I've read the doctor's notes but it wasn't detailed enough. Any kind of help would be appreciated. Thank you!

Title: Re: How're tertiary radicals more stable than allyl radicals?
Post by: Dan on November 10, 2012, 10:52:34 AM

You have already posted this question.

http://www.chemicalforums.com/index.php?topic=63443.0

Please read the Forum Rules (http://www.chemicalforums.com/index.php?topic=33740.0) before posting again.