10.1 Free Radical Halogenation | Organic Chemistry

[@briannaheaslip7442]

I was beyond confused in lecture when my professor discussed this but now I completely understand!! Your videos are absolutely amazing and really helped get me through orgo-1. Thank you for all you do!!!

[@ChadsPrep]

Excellent, Brianna - glad the channel is helping!

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[@ChadsPrep]

Glad you find so much to enjoy on the channel - light in the darkness: you nailed it! God bless you too!

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I love your shirt in this video Mr.Chad! That was a great reminder for me right now. You are a light for us orgo students! Thank you for all you do🙂

[@ChadsPrep]

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Thank you for posting such helpful videos. Organic chemistry is oftentimes very overwhelming and these videos make it not so daunting.

[@ChadsPrep]

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[@ChadsPrep]

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[@ChadsPrep]

Thank you - twice!

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[@satwikjakhar5585]

unlucky to study these topics in 12th standard...INDIA But thankyou I was confused where to substitute chlorine on 0,1,2or 3 degree to find major product

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[@ChadsPrep]

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[@OyinademiEhikioya]

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[@ChadsPrep]

Thank you - to you as well

[@bonbonpony]

So if Br prefers the most substituted carbons, how can we make primary alkyl bromides, like 1-bromobutane, for example? :q Could radical bromination do that somehow? Or do we need to put an -OH group at the end of the carbon chain first and then substitute it with bromine? But if the latter is the case, we still need some way to put the -OH group at the end of the chain (let's suppose we don't have the alcohol yet, just an alkane). Wouldn't it involve putting another leaving group there (i.e. the halogen) in the first place? How is the usual way of doing it?

[@xolityy-8696]

thank you

[@ChadsPrep]

Welcome!