Bromotriphenylmethane (compound 1) can be converted to 2a or 2b or 2c upon treatment with the appropriate nucleophile (U. Chem. Ed. 2009, 86, 853855): -Br के लि Ph Ph= 1 Ph Ph ROH Ph Ph -OR Ph 2 2a: R=H 2b: R=CH₂ 201RCHICH

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Bromotriphenylmethane (compound 1) can be converted to 2a or 2b or 2c upon treatment with the appropriate nucleophile (U. Chem.
Ed. 2009, 86, 853855):
-Br
के लि
Ph
Ph=
1
Ph
Ph
ROH
Ph
Ph
-OR
Ph 2
2a: R=H
2b: R=CH₂
201RCHICH
Transcribed Image Text:Bromotriphenylmethane (compound 1) can be converted to 2a or 2b or 2c upon treatment with the appropriate nucleophile (U. Chem. Ed. 2009, 86, 853855): -Br के लि Ph Ph= 1 Ph Ph ROH Ph Ph -OR Ph 2 2a: R=H 2b: R=CH₂ 201RCHICH
Incorrect. Did you follow the instructions exactly when drawing this mechanistic step. What type of mechanism step is
shown here? Is it a Loss of Leaving Group or Nucleophilic Attack or Proton Tranfer or Rearrangement?
Add curved arrow(s) to draw step 1 of the mechanism for the conversion of 1 to 2b, and modify the given product draw the
resulting intermediate formed in this step.
080-080
Edit Drawing
Hint
0.1/0.5
An Sy1 process must always exhibit two core steps: loss of a leaving group and nucleophilic attack.
Assistance Used
****
Transcribed Image Text:Incorrect. Did you follow the instructions exactly when drawing this mechanistic step. What type of mechanism step is shown here? Is it a Loss of Leaving Group or Nucleophilic Attack or Proton Tranfer or Rearrangement? Add curved arrow(s) to draw step 1 of the mechanism for the conversion of 1 to 2b, and modify the given product draw the resulting intermediate formed in this step. 080-080 Edit Drawing Hint 0.1/0.5 An Sy1 process must always exhibit two core steps: loss of a leaving group and nucleophilic attack. Assistance Used ****
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