ÏHCH,CH,NH,The product of the reaction isa semicarbazone.a hydrazone.an oxime.an imine.SelectG4)Draw TemplatesMoreQ2Erase The mechanism of the reaction can be presented in several ways. Some books show the carbonyi protonated first, while othersshow nucleophilic attack occurring first. Several proton transfer steps are needed and will generate a key intermediate,the carbinolamine.Carbinolamines are not isolated and will undergo dehydration to give the product. Draw curved arrows of the protonatedcarbinolamine to show the key dehydration step.Add curved arrows to show the dehydration. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentallydelete a vital part of the structure, click the undo button in the lower left.TemplatesSelectDrawC H NOMore: OH₂+HHErase

The given question explains the reaction between aldehyde and amine to form corresponding imine as…

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Ï H CH,CH,NH, The product of the reaction is a semicarbazone. a hydrazone. an oxime. an imine. Q2Q

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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