(R)-2-butanol reacts with phosphorus tribromide to give A (C4H9Br). Treatment of A with sodium cyanide in DMF gives B (C5H9)N. B is optically active. Draw the structure of B. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Show stereochemistry in a meso compound. 90-85 To th OO. [F
(R)-2-butanol reacts with phosphorus tribromide to give A (C4H9Br). Treatment of A with sodium cyanide in DMF gives B (C5H9)N. B is optically active. Draw the structure of B. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Show stereochemistry in a meso compound. 90-85 To th OO. [F
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:(R)-2-butanol reacts with phosphorus tribromide to give A (C4H9Br). Treatment of A with sodium cyanide in DMF gives B (C5H9)N. B is optically
active. Draw the structure of B.
• Use the wedge/hash bond tools to indicate stereochemistry where it exists.
Show stereochemistry in a meso compound.
Sn [F
?
ChemDoodleⓇ

Transcribed Image Text:Cyclohexene reacts with m-chloroperoxybenzoic acid to give A (C6H100). A reacts with methylmagnesium iodide in anhydrous ether to give B
(C7H₁40). Draw the structure of B.
O
• Use the wedge/hash bond tools to indicate stereochemistry where it exists.
Show stereochemistry in a meso compound.
If the reaction produces a racemic mixture, draw both stereoisomers.
●
• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
Separate multiple products using the + sign from the drop-down menu.
?
ChemDoodleⓇ
Sn [F
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