E1 (vid 3 of 3) Unimolecular Beta Elimination With Hydride Shift and Zaitsev's Rule

Описание: https://leah4sci.com/SNE presents: E1 Reaction Part 3 - Unexpected Elimination Products With Hydride Shift/carbocation rearrangement following Zaitsev's rule

📺Watch Next: E2 Reaction Rate and Mechanism    • E2 Reaction Rate & Mechanism (vid 1 of 4) ...  

Are you struggling with Organic Chemistry? Download my free ebook the "10 Secrets To Acing Organic Chemistry" HERE: http://leah4sci.com/orgo-ebook/

This video is part 3 for the E1 reaction and takes you through the process of identifying the product in unimolecular beta elimination reaction when there is more than one potential product, and a few more hidden products following a hydride shift

Note: Error in audio. When the bromine leaves initially, it grabs the electrons that bound it to the carbon atom in the molecule. It does not take any hydrogens with it, when it leaves.

My complete substitution/elimination video series can be found on my website using this link:
http://leah4sci.com/nucleophilic-subs...

You can also find many more substitution and elimination problems with video explanations in my membership site
http://studyhall.leah4sci.com/join/

I also offer private online tutoring where you can work directly with me to learn the answers to your specific questions and difficulties.
Visit my website for more information
http://leah4sci.com/organic-chemistry...

Let’s connect:▸Instagram:   / leah4sci  
▸Facebook:   / leah4sci  
▸X / Twitter:   / leah4sci  
▸Pinterest:   / leah4sci