Draw the curved arrow notation and predict the products when one equivalent of hydroxide in DMSO at room temperature is added to 5-bromo-1- iodopentane. 5th attempt Part 1 (3 H DMSO Draw the curved arrow notation. : -O: + Br See Periodic Table Н C F Br I HONOSEPH
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![Draw the curved arrow notation and predict the products when one equivalent of hydroxide in DMSO at room temperature is added to 5-bromo-1-
iodopentane.
5th attempt
Part 1 (3
H
DMSO
Draw the curved arrow notation.
:
-O:
+
Br
See Periodic Table
Н
C
F
Br
I
HONOSEPH](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F44924c29-c29e-4e5a-aefa-98d57c1ee1ac%2Fc2ebf5f1-66e3-46f2-b0bc-97fed676ea42%2Fsmgvf7j_processed.png&w=3840&q=75)
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- Draw the curved arrow notation and predict the products when one equivalent of methoxide in DMSO a: rcom ten:perature is sdced to S-brome-1. 1odepentane. Part 1 ht See Periodic Table O See Hint DMSO Draw the curved arrow notation. Part 2 Select the major byproduct. Chooso one: O A, I- O B. HI O C. CH:OH O D Er. O E. HerElectrostatic potential maps of anisole and thioanisole are shown. Which do you think is the stronger acid, p-methoxybenzoic acid or p-(methylthio)benzoic acid? Explain.The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?
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