ORGANIC CHEMISTRY MASTERINGCHEM ACCESS
9th Edition
ISBN: 9780137249442
Author: Wade
Publisher: INTER PEAR
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Chapter 15, Problem 15.41SP
An important variation of the Diels-Alder reaction is intramolecular, in which the diene and the dienophile are connected. This type of Diels-Alder reaction makes two new rings. Draw the compound produced in each of these examples; try to predict stereochemistry (using models will help). In some cases, Lewis acid catalysts are used; that can be ignored for this problem.
Prof. H. Miyaoka, Tokyo U. Synthesis Letters, 2011, 547. (R and R2 are different alkyl groups.)
Prof. A. Kirschning, Leibnitz U. Hannover Organic Letters, 2014, 16, 568. (Ar1 and Ar2 are different aryl groups.)
Prof. H. Zhai, Lanzhou U. Organic Letters, 2014, 16, 216.
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Refute or Defend: Once cyclopentadiene is distilled, it can be stored for a long period of time (e.g., weeks) before using it in a Diels-Alder reaction
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Imagine that you used isoprene as diene – in that case you don’t have to worry about assigning endo vs exo. Draw the "endo" and "exo" products of the Diels-Alder reaction between isoprene and maleic anhydride, and explain why the distinction is irrelevant here.
Chapter 15 Solutions
ORGANIC CHEMISTRY MASTERINGCHEM ACCESS
Ch. 15.2 - Prob. 15.1PCh. 15.2 - Prob. 15.2PCh. 15.2 - Prob. 15.3PCh. 15.4 - Prob. 15.4PCh. 15.4 - Prob. 15.5PCh. 15.5 - Treatment of an alkyl halide with AgNO3 in alcohol...Ch. 15.5 - Propose a mechanism for each reaction, showing...Ch. 15.6 - When Br2 is added to buta-1,3-diene at 15 C, the...Ch. 15.7 - Prob. 15.9PCh. 15.7 - When N-bromosuccinimide is added to hex-1-ene in...
Ch. 15.7 - Prob. 15.11PCh. 15.9 - Addition of 1-bromobut-2-ene to magnesium metal in...Ch. 15.10 - Show how you might synthesize the following...Ch. 15.11 - Predict the products of the following proposed...Ch. 15.11 - Prob. 15.15PCh. 15.11A - Prob. 15.16PCh. 15.11B - Prob. 15.17PCh. 15.11B - Predict the products of the following Diels-Alder...Ch. 15.12C - Prob. 15.19PCh. 15.12C - Prob. 15.20PCh. 15.13C - Prob. 15.21PCh. 15.13D - Using the examples in Table15-2 to guide you,...Ch. 15.14 - Phenolphthalein is an acid-base indicator that is...Ch. 15 - Prob. 15.24SPCh. 15 - Prob. 15.25SPCh. 15 - Show how the reaction of an allylic halide with a...Ch. 15 - Prob. 15.27SPCh. 15 - A solution was prepared using 0.0010 g of an...Ch. 15 - Prob. 15.29SPCh. 15 - Prob. 15.30SPCh. 15 - Prob. 15.31SPCh. 15 - Prob. 15.32SPCh. 15 - Prob. 15.33SPCh. 15 - Give the structures of the products represented by...Ch. 15 - Furan and malemide undergo a Diels-Alder reaction...Ch. 15 - Prob. 15.36SPCh. 15 - Prob. 15.37SPCh. 15 - Prob. 15.38SPCh. 15 - Prob. 15.39SPCh. 15 - Determine whether each structure is likely to be...Ch. 15 - An important variation of the Diels-Alder reaction...
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- The below reaction is a retro Diels-Alder reactions. Is is the reverse process of a Diels-Alder reaction with the formation of a diene and dienophile from some cyclohexene. It can be accomplished spontaneously with heat. Determine the product of the reaction. 4 Heatarrow_forwardDraw structural formulas for the diene and dienophile that combine in a Diels-Alder reaction to form the product shown CH3CH2O. Diene + Dienophile Co,CH3 •Consider E Z stereochemistry of alkenes. •Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the sign from the drop-down menu. C. P. opy aste %3Darrow_forwardDraw structural formulas for the diene and dienophile that combine in a Diels-Alder reaction to form the product shown. lo Diene + Dienophile CAM • Consider E/Z stereochemistry of alkenes. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple products using the + sign from the drop-down menu. Ⓡ Mill ChemDoodleⓇ Y -CI Sn [F CN < 46arrow_forward
- In Section 24.5, we learned how to use resonance OCH3 hybrids to understand the regiochemistry of Diels-Alder reactions. Frontier MO theory, on the other hand, explains the regiochemistry by taking into account the extent of orbital overlap between the frontier MOs. Consider the diene and dienophile shown here having the two different approaches indicated. In both cases, the p orbital contributions are shown for the pertinent frontier MOs. The relative contributions by the p AOs to the frontier MOs are indicated by the p AO sizes. Use this information to explain which approach is favored. CH30 LOCH3arrow_forwardPlease ex plain and Please show all arrow pushing mechaarsas. Thank you!arrow_forwardFor our Diels-Alder Reaction lab, they asked to provide heat to the structures and I'm a little unsure of what the products will look like, if you can help, please?arrow_forward
- Draw structural formulas for the diene and dienophile that combine in a Diels-Alder reaction to form the product shown. • • • Diene + Dienophile H Consider E/Z stereochemistry of alkenes. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu. ChemDoodle ?arrow_forwardIs this the correct order and conditions to produce the diels-alder product on the right? Thank youarrow_forwardWhich of the following correctly describes the known mechanism of the Diels-Alder reaction? Select one: A. A strained 4-member ring intermediate is formed which rearranges to a 6- member ring. B. A di-radical, 6-member ring intermediate is formed. C. The mechanism is a one-step process with bond-making, bond breaking changes occurring simultaneously. D. A zwitterion species (molecule with full +1 and -1 charges) is rapidly formed as an intermediate. E. A resonance-stabilized carbocation intermediate is formed in a slow step.arrow_forward
- 1) In the Diels-Alder reaction there are two reaction components: a DIENE (must be a conjugated diene); and a DIENOPHILE (an ene usually with electron withdrawing substituents). a. Bicyclic diene A reacts readily with appropriate alkenes by the Diels-Alder reaction, whereas diene B is totally unreactive. Explain. b. Write the three reactions and show the product for diene A reacting with dienophiles I, II, and III. Rank I, II, and III in terms of their expected reactivity in a Diels Alder reaction. Justify your assigned ranks. A B || LOCH3 IIIarrow_forwardThe Diels-Alder Reaction THE DIELS-ALDER REACTION Pre-Laboratory Questions/Exercises Sec. No. Name 1. What problems might arise if the solvent were not anhydrous? 2. Sketch the highest occupied molecular orbital (HOMO) of butadiene, sketch the lowest unoc- cupied molecular orbital (LUMO) of ethylene, and show that these orbitals have the correct symmetry for cycloaddition. aboocne 9orollo ds To dos onRgonq blaow DoTwod worl o alilelorCIs ya 3 HOT 3. In the reaction between a 1,3-cyclopentadiene and maleic anhydride, why is the major product the more sterically hindered endo cycloadduct rather than the exo? о S O endo exo majoro minor DA O shas works h ece tarrow_forwardWhich of the following structures, A or B, has the faster rate of reaction in a Diels-Alder reaction? Give a brief explanation that includes the terms "donating group", "withdrawing group", "energy of the electrons", "HOMO". H :0: A H₂N. Barrow_forward
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