1-pentyne reacts with dicylohexylborane, followed by oxidation, to produce pentanal H₂C- 1-pentyne CH dicylohexylborane

Chemistry
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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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The product of the second synthetic step undergoes tautomerization in aqueous medium to form the final product. Draw the structures for both of these products.

1. Draw the product of the oxidation of the organoborane formed in Step 1. Include lone pairs and nonzero formal charges.

2. Draw the more stable tautomer that is the final product. Include lone pairs and nonzero formal charges.
 
1-pentyne reacts with dicylohexylborane, followed by oxidation, to produce pentanal.
H₂C-
1-pentyne
CH
B.
dicylohexylborane
Transcribed Image Text:1-pentyne reacts with dicylohexylborane, followed by oxidation, to produce pentanal. H₂C- 1-pentyne CH B. dicylohexylborane
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