19.2 Synthesis of Ketones and Aldehydes | Organic Chemistry

[@ayishaharuna7347]

The best teacher ever; may God bless you so much

[@ChadsPrep]

Kind words - thank you.

[@gerrythekay]

You could also use a Grignard reagent (derived from any alkyl halide) and an acid chloride at low temperature to form a ketone. This is the Eberle Kahle ketone synthesis.

[@peerhaseeba7673]

Oh myy thank you so much sir ❤

[@ChadsPrep]

Very welcome - Happy Studying!

[@lmthagod328]

This video has really helped a lot I wish u would the mechanisms more but it really helped me ace my finals

[@ChadsPrep]

Glad it helped!

[@nasebasumrein493]

Awesome 👏

[@ChadsPrep]

Great!

[@britany_lmp5112]

Thank you so much !! :D

[@ChadsPrep]

You're welcome!

[@mosh4491]

awesome.

[@ChadsPrep]

Glad you think so, moamer!

[@nilakennedy-young5998]

Hi! For ozonolysis, will our product always be both an aldehyde and ketone if we use zinc/ DMS?

[@billygrass8742]

complete BS just to make money from poor poor students