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The Wittig Reaction is a little tricky because both E and Z alkenes can be formed by it and usually students forget this important point. It really just depends on the Ylide that is being used. If the ylide contains a group on the negatively charged carbon that can resonate and stabilize the Ylide, then you will get a E alkene product. Otherwise if the Ylide just contains a carbon chain with no resonance, all you get is a Z alkene product. ●How to Make a Phosphonium Ylide: • Phosphonium Ylide for The Wittig Reac... ●Wittig Reaction Made Easy • Wittig Reaction + Ylides Made Easy! P... ●Wittig Reaction Mechanism Made Easy: • The Wittig Reaction Mechanism Made Ea... ●Wittig Reaction Bloopers/Outtakes: Coming Soon ●Private Tutoring Information: I offer in-person private tutoring in Boston and NYC, and if you live elsewhere on this awesome planet I offer online Skype tutoring that is accompanied with a whiteboard program. For more info check here: http://orgomadeeasy.org/private-tutor... and contact me via my "Orgo Made Easy" Facebook page or email: [email protected] Make sure you share this with your friends if you found it helpful, and I would love it if you leave some comments to let me know if I'm on the right track ;). Subscribe to get updated when I make new videos! / orgomadeeasy Connect with me on Facebook/Instagram/Twitter! Facebook------------------------------- / orgomadeeasy Instagram------------------------------- / frankmwong Tweet Tweet--------------------------- / orgomadeeasy Official Website-----------------------http://OrgoMadeEasy.org/ Donations Accepted Here----------http://OrgoMadeEasy.org/donate/ Private Tutoring-----------------------http://OrgoMadeEasy.org/private-tutor...