One other important reaction: Gilman reagents only add once to acid chlorides to form the ketone whereas Grignards and organolithiums add twice to form the alcohol
@natepadol30675 жыл бұрын
Great video Dave!!! We love how thorough and how amazing you are are at explaining science to our class -the board of Mrs. Kelly’s 6th period class at LFC in Allen, Texas
@pjb31944 жыл бұрын
youre in 6th grade learning university level 2nd year organic chemistry?
@natepadol30674 жыл бұрын
@Pierce Bassett 6th period, not 6th grade. we are taking college level science class in high school
@NewWesternFront Жыл бұрын
@@natepadol3067 still, AP only does genchem I and a ittle II no? different program?
@vegatronld5 жыл бұрын
Good stuff Dave.
@laura18700 Жыл бұрын
I am so impressed by your knowledge. you were born to teach. love you xoxo
@emilyconte67574 жыл бұрын
Your hair looks great!!!
@samueltanner47693 жыл бұрын
Nice job
@aishubalan69824 жыл бұрын
Super Dave sir and please explain about carbenes sir
@ProfessorDaveExplains4 жыл бұрын
Already finished, coming soon!
@aishubalan69824 жыл бұрын
Thank you soo much sir waiting
@anirudhbhadri59114 жыл бұрын
What if the ring is not benzene but cyclohexane
@organicchemistry63574 жыл бұрын
What are the limitations of the Gilman reaction? Are there any functional groups that make this reaction impossible?
@illidan1248256344 жыл бұрын
It can only perform a conjugate(1,4) addition instead of a direct(1,2) addition on a alpha, beta-unsaturated carbonyl unlike say a Grignard reagent.