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Methylbutanal undergoes an aldol reaction to form 3-hydroxy-2-isopropyl-5-methylhexanal. Additional heating in base will rm the aldol dehydration product. Step 1: add curved arrows. Select Draw Templates Mar /M C 3 Ċ Complete the mechanism for the dehydration reaction by adding missing bonds and curved arrows. Draw the aldol dehydration roduct in the læt step. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the tructure, use the undo button in the lower-left corner of the panel to reset the structure. /M TIN NH 5°C 3 OH C Step 3: complete the structure of the product. Select Draw Templates Mar ra НО 230 = @[26] ? Step 2: complete the structure and add curved arrows. Select Draw Templates More OH CM Q 20 heat

Methylbutanal undergoes an aldol reaction to form 3-hydroxy-2-isopropyl-5-methylhexanal. Additional heating in base will rm the aldol dehydration product. Step 1: add curved arrows. Select Draw Templates Mar /M C 3 Ċ Complete the mechanism for the dehydration reaction by adding missing bonds and curved arrows. Draw the aldol dehydration roduct in the læt step. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the tructure, use the undo button in the lower-left corner of the panel to reset the structure. /M TIN NH 5°C 3 OH C Step 3: complete the structure of the product. Select Draw Templates Mar ra НО 230 = @[26] ? Step 2: complete the structure and add curved arrows. Select Draw Templates More OH CM Q 20 heat

Chemistry
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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-Methylbutanal undergoes an aldol reaction to form 3-hydroxy-2-isopropyl-5-methylhexanal. Additional heating in base will form the aldol dehydration product. 10% NCH 5°C Step 1: add curved arrows. Select Draw Templates Mar |||||||||||| M Complete the mechanism for the dehydration reaction by adding missing honds and curved arrows. Draw the aldol dehydration product in the last step. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the tructure, use the undo button in the lower-left corner of the panel to reset the structure 3 Ć НО Era Q2Q Step 3: complete the structure of the product. Select Draw Templates Mar XTZ ? 10-1 Q2Q Step 2: complete the structure and add curved arrows. Select Draw Templates More ||||||| Era AND heat
Transcribed Image Text:-Methylbutanal undergoes an aldol reaction to form 3-hydroxy-2-isopropyl-5-methylhexanal. Additional heating in base will form the aldol dehydration product. 10% NCH 5°C Step 1: add curved arrows. Select Draw Templates Mar |||||||||||| M Complete the mechanism for the dehydration reaction by adding missing honds and curved arrows. Draw the aldol dehydration product in the last step. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the tructure, use the undo button in the lower-left corner of the panel to reset the structure 3 Ć НО Era Q2Q Step 3: complete the structure of the product. Select Draw Templates Mar XTZ ? 10-1 Q2Q Step 2: complete the structure and add curved arrows. Select Draw Templates More ||||||| Era AND heat
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