Dienophile is electron deficient species.
QUESTION 12 Exhibit 14-4 The following molecules may be prepared using the Diels-Alder reactions. Write the...
provide the required diene and dienophile for each of the following Diels-Alder reactions (12 pts) Provide the required diene and dienophile for each of the following Diels-Alder reactions HNO2 a) -OMe H Me NMe2 Me b) OMe Me NC Me Me Me OMe c) NC Me
4. Provide the appropriate starting materials (diene and dienophile) for the following Diels-Alder reactions: CH2CH3 CH2CH3 Heat CO2CHs "Cо-Cна сосн, сосн Heat сосн сосн
Post- Laboratory Questions: 1. Draw the product of the following Diels-Alder reactions 2. What starting materials would be used to prepare the following compound by the Diels- Alder reaction? 3. Cyclopentadiene dimerizes easily. Before using cyclopentadiene in a reaction, it is necessary to crack the diene. Draw the Diels-Alder reaction for the dimerization of cyclopentadiene. 4. What are the products of the following Diels-Alder reactions? Show the stereochemistry where applicable
1. Determine the structures of the starting materials for the Diels-Alder reactions. (12 pts) CO.CH HỌCÓ CO.CH CN 2. Determine the structures of the products for the Diels-Alder reactions. (13 pts) NCH) 4"
Forward and Retro Diels-Alder Post-Lab Questions: Someone please help me with 3 or 4! My lab is a couple of chapters ahead of the lecture for it so it is very confusing!! I ldille. Forward and Retro Diels-Alder Post-Lab Questions: 3. Provide the appropriate product(s) for each of the following Diels-Alder reactions. Your answers must be stereospecific: HEC Heat CH2CH3 Heat CHO 4. Provide the appropriate starting materials (diene and dienophile) for the following Diels-Alder reactions: CH2CH3 CH2CH3 Heat CO_CH3...
3). Provide products of the following Diels-Alder reactions (include stereochemistry) 4). What starting material would be necessary to prepare the following compound by Diels-Alder reaction?
(2) Diels-Alder reactions of a diene with a dienophile are known to undergo a concerted reaction. However, 2,3-Di- tert-1,3-butadene does not undergo Diels-Aider reactions. Explain 2,3-di-tert-1,3-butadiene (4) Propose mechanisms for the following steps 1 and 2. Slep 1 Step 2 Bry Br NaBH CH acetic acid (I) Using> as a symbol, rank the following alkyl bromides in order of decreasing reactivity. (6 pts) Br Cн,Br -Br (a) For hydrolysis by an Sy1 mechanism (b) For hydrolysis by an S,2 mechanism...
Question 1 Identify all compounds below that CANNOT be made by the electrophilic aromatic substitution reactions introduced in Sections 18.1-18.6 SOH Question 2. Match each pair of structures with the appropriate term. KEY 1 = Constitutional isomers 2 - Diastereomers 0 000 3 = Different conformations 4 = Resonance structures 5 = Bond-shift isomers Question 3. In this reaction, FeBrz is acting as a and the complex that is formed will react with benzene as a/n :Br: : Br-Br: Br-Br-Fe-Br:...
3) (D) Which one of the following molecular orbitals will have the highest energy? 4) Choose how many "occupied MOS" can occur for the conjugated t-system of B-carotene and LED compounds? NH beta-carotene (a) 22 and 6 5) The diene LED material (b) 11 and 6 (c) 22 and 12 (d) 11 and 12 is not suitable for Diels-Alder [4+2) cycloaddition? 6) Which one of bicyclic isomers is appropriate for both Diels-Alder and 1,2-/1.4-additions? 7) Both 1.2- and 1,4-additions of...
3. (12 points) Predict the products of the following Diels-Alder reactions, showing stereochemistry where appropriate: howens iste soled anoton gniwolloton b anola b) NOVA . - haloom on to 4. (16 points) Consider the nitration of Piperonal and answer the cos of following questions. sdom onge antwollo stamo s ) tavlobyrd orallo ar moi ne bodo ubota O HNO 306. CHO Chronogronivelo Piperona ONO a) Starting with 134 mg of piperonal (MW 134), calculate the percentage yield of the above...