Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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- OH H* 요 ey" (Hint: reverse cyclic aldol) Harrow_forwardQUESTION 12 Consider the following crossed aldol condensation. Which statement explains why a single cross condensation product is formed? 2,2-dimethylcyclohexanone 0 H₂C H₂C H NOCH₂CH₂ ethanol CH₂ CH₂ benzaldehyde O 2.2-Dimethylcyclohexanone has only one alpha carbon which can form an enolate. O Benzaldehyde has no hydrogens attached to the alpha carbon which eliminates the self-condenatation reaction. O 22-Dimethylcyclohexanone is sterically hindered which limits the self-condenstation reaction. All of the above.arrow_forwardSee image belowarrow_forward
- Draw the product for the following reaction.This is what my homework assignment is asking for, the question is completearrow_forwardThe enolate of an ester can be treated with a ketone to give a beta-hydroxy ester. Draw a mechanism for this aldol-like reaction. For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do not use abbreviations such as Me or Ph. EtO 1) LDA 2) ΕΙΟ OH श्र Step 1 * Incorrect. Which of the mechanistic steps is shown in this step of the mechanism? Draw step 1 of the mechanism. HC CH CH3 CH3 Edit Drawing CH3arrow_forwardDraw the intermediate and the product for the transformation below. (You should be able to upload a scanned image of hand-drawn molecules by clicking on the image tab above) 1 Ph Mg Br вк 2. H ₂0 ? A Conc. HCl H₂0 ? Barrow_forward
- Identify the side product produced in the crossed aldol condensation below. OOH CH,CH,CH,CCHCH,CHCH, NaOH H. + A OH OH CHCHCH CH,CH,CHCHCH,CH, HOCHCHCH,CH,CH, CH,CH3 B c CH,CH,arrow_forward6. For the following reaction, draw all of the synthetic intermediates that are formed in each step, including the final product. 1. H2SO4 2. mCPBA 3. MgBr-CH2CH3 4. H20 HO.arrow_forwardDraw an alkyl bromide that would produce ONLY the following alkene in an E2 elimination. Ignore any inorganic byproducts.arrow_forward
- Show structures (in blank boxes) for the reactants/products in the following reactions.arrow_forwardDraw the major product of this elimination. Consider regiochemistry and stereochemistry. Ignore byproducts. Br H₂O heat Jarrow_forward4.Which is the most thermodynamically stable product of the following aldol condensation reaction? NaOH H. Me `Me EtOH а. Е, Z b. Е, E с. Z, E d. Z,Zarrow_forward
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