12. What is the product of this cyclization reaction?
13. Which reaction condition best accomplishes this conversion?
14. Which diene would be an appropriate choice to synthesize the following compound by Diels-Alder reaction?
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12. What is the product of this cyclization reaction? 13. Which reaction condition best accomplishes this...
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
PLEASE ANSWER ALL QUESTIONS
Uraw the organic products expected from this reaction, label them as thermodynamic or kinetic and tell which predominates at -80°C. H(cat.) носно 5) Show how the reaction of an allylic halide with a Grignard reagent might be used to synthesize the following: 6) Which substrate would react most rapidly in an SN 2 reaction? A) CH3CH2CH=CHCH2Br B) BrCH2CH2CH=CHCH3 C) CH3CHBECH-CH2CH3 D) CH3CH2CH2CH=CHB 7) Which of the following terms best describes a Diels-Alder reaction? A) a [4+2]...
Critical Thinking Questions 1. Draw the structure for the product from the reaction of 1,3-cyclohexadiene and maleic acid (cis-2-butenedioic acid). 2. What is the product expected from the reaction of 1,3-butadiene and 3-sulfolene? Why is this not a major concern as a by-product? Part B, the dimer dicyclopentadiene is a possible contaminant of cyclopentadi- ene. It is also a diene. Can dicyclopentadiene undergo reaction with cyclopentadi- ene? Can dicyclopentadiene act as a diene and undergo reaction with the anhydride 3....
29. Predict the product for the following reaction. CH,CH SNa 30. Predict the major product for the following reaction O+ HCI 31. Predict the major product for the following reaction. HBr 32. Which diene and dienophile would react to give the following Diels-Alder product? 33. Provide the structure of the major products) for the following reaction Br2
29. Predict the product for the following reaction. CH,CH SNa 30. Predict the major product for the following reaction O+ HCI 31. Predict...
Question 7 Which reag ent would be the best choice to perform the following reaction? H2SO4 Diels-Alder H20 03
18, 22, 23
16) What diene and dienophile would react to give the product below? diere 17) Which of the following compounds is the most reactive dienophile in a Diels-Alder reaction with 1,3-butadiene? A) CH-CHOCH B) CH2-CHCHO C) CH3CHCHCH3 D) (CH3CH2 5) C .CH 18) Using resonance structures, explain the regiochemistry observed in this reaction OCH H.CO heat 19) Provide the major organic product of the following reaction H.CO ÇOCH H.COM 20) Provide the major organic product of the following...
for the reaction what's the compound names ? also need the
answers to 2,3,and 4
Draw the reaction scheme for this experiment in Chem Deode Provide the compounds' names. (1 pt) 1. heat + 2. Provide a name for the molecule below and indicate whether it is the "diene" or "dienophile" (1 pt) Name Role: Diene/ Dienophile (circle one) Why is butadiene sulfone used in this reaction as opposed to 1,3-butadiene? (1 pt) 3. 4. Which of the following would...
6 and 7
6/ Consider the ring opening of 1.3-cyclohexadiene to give 1,3,5-hexatriene. Draw the appropriate frontier orbitals and show under either disrotatory or conrotatory mode the reaction would be allowed. 7/ The following compound was produced in a Diels-Alder reaction. -CF3 CF3 Draw the diene and dienophile which react together to give this product.
Which diene and dienophile would react to give the following Diels-Alder product? a. Give the IUPAC name of the diene. b. Give the IUPAC name of the dienophile.
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...