2-Phenylacetaldehyde with benzaldehyde in the presence of sodium hydroxide undergoes a crossed aldol reaction. H so HOT orol Step 1: Add curved arrows. Select Draw Templates More Complete the mechanism for the reaction by adding missing curved arrows, atoms, bonds, charges and nonbonding electrons. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the structure, use the undo button in the lower-left corner of the panel to reset the structure. H ||||||||||||C H 0 G 1) H H 0- H /M Q2Q Select Drew Templates More Erase 10% NaOH CH 5 °C Step 3: Complete the intermediate and add curved arrows to form the final product. Step 2: The aldehyde is added. Complete the structure and add curved arrows. Select Draw Templates More ICH H jo H H 5C Erese O Erase Q2Q Final product HO +H₂O

2-Phenylacetaldehyde with benzaldehyde in the presence of sodium hydroxide undergoes a crossed aldol reaction. H so HOT orol Step 1: Add curved arrows. Select Draw Templates More Complete the mechanism for the reaction by adding missing curved arrows, atoms, bonds, charges and nonbonding electrons. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the structure, use the undo button in the lower-left corner of the panel to reset the structure. H ||||||||||||C H 0 G 1) H H 0- H /M Q2Q Select Drew Templates More Erase 10% NaOH CH 5 °C Step 3: Complete the intermediate and add curved arrows to form the final product. Step 2: The aldehyde is added. Complete the structure and add curved arrows. Select Draw Templates More ICH H jo H H 5C Erese O Erase Q2Q Final product HO +H₂O

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...

See similar textbooks

Similar questions

5. Consider the below aldol reaction. Draw the product if all reactants are consumed and condensation, if possible, occurs. +2 H H NaOH EtOH A
e aldol condensation is complete once the aldol product above undergoes an elimination upon heating. Complete the mechanism for the reaction by adding missing bonds, and curved arrows. Do not delete any of the predrawn bonds, atoms and nonbonding electrons.
Propose a mechanism for the aldol reaction below 2 H3C H OH-, H2O se H3C H
Can someone help me with the synthesis?
Modify the given copies of the starting materials to draw the two ẞ-hydroxyaldehydes formed by mixed aldol reactions. H3C H H3C H H3C H H3C H Edit Drawing
Propose a crossed aldol reaction where the following compound would be the only product. Propose a mechanism for the reaction. OH
Part 1 - Draw the full mechanism for the cross-aldol reaction between acetone and benzaldehyde Part 2 - Draw the product that would form if we added only one mole each of acetone and benzaldehyde. Part 3 - After forming the initial product, we see the elimination of water to give the final product as a solid that we collect. What drives this product formation?
2‑Phenylacetaldehyde with benzaldehyde in the presence of sodium hydroxide undergoes a crossed aldol reaction.
Show the mechanism of the given aldol reaction.
If you react acetaldehyde and acetone in the precensce of NaOH in H2O, how many aldol condensation products will form. I need help with drawing a detailed mechanism.