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first1!1!! i would never be late to a doctor G video
Thank you!
IM GETTING A 100 ON THIS TEST MARK MY WORDS
Thanks for the review Dr. G! For 5E, is there any notable nucleophiles other than Gilman that will attach to the alkene beta position?
Yes. Most of the nucleophiles attack to the beta carbon but Grignard reagent always attacks to the carbonyl group.
@@orgtubeR thanks!
Thank you! For Question 1, compound A (naming) is the trans configuration assumed or should we specify that as well?
Yes. trans is missing at the begining of the name. The correct name is trans 4-boromo cyclohexane carboxylic acid. Thank you!
Thank you for clarifying! @@orgtubeR
You are very Welcome
for question 5b would it be ch2cn for the last product
No. The amide group (CONH2) convert to CN.
first1!1!! i would never be late to a doctor G video
Thank you!
IM GETTING A 100 ON THIS TEST MARK MY WORDS
Thanks for the review Dr. G! For 5E, is there any notable nucleophiles other than Gilman that will attach to the alkene beta position?
Yes. Most of the nucleophiles attack to the beta carbon but Grignard reagent always attacks to the carbonyl group.
@@orgtubeR thanks!
Thank you! For Question 1, compound A (naming) is the trans configuration assumed or should we specify that as well?
Yes. trans is missing at the begining of the name. The correct name is trans 4-boromo cyclohexane carboxylic acid. Thank you!
Thank you for clarifying! @@orgtubeR
You are very Welcome
for question 5b would it be ch2cn for the last product
No. The amide group (CONH2) convert to CN.