Give a curly arrow or fish hook mechanism for the following reaction, indicating clearly both major...
Give the products for the following reaction, predicting the major product, and indicating by which mechanism each is formed. Reaction between 1-Bromo-1,4-dimethylcyclohexane and MeOH with heat. Explain each of the mechanism, and why other mechanisms do not work.
T ylic uelydration reaction, draw the curved arrow mechanism leading to the major alkene product and one of the minor alkene products. Draw a picture of the hyperconjugation interaction that explains the greater thermodynamic stability of the major product versus the minor product. Concisely explain why the uncatalyzed dehydration reaction would not form the carbocation intermediate Me catalytic H2SO4 -он H,0
9. Give the curved arrow mechanism for each reaction. H2SO4 b. H,o OH c. H20 H2SO d. OH H2o 10. For the following reaction, H,so, H,O он a. Give the curved arrow mechanism for the reaction, showing formation of both products b. Identify the major product and explain why it is favored. c. Draw the energy diagram for the formation of the major product. 11. Give the major organic product for the following reactions. If a racemic mixture is expected,...
11b) Draw a curved arrow mechanism for the following reaction. Your mechanism should explain BOTH products HO £ * a OPP c) The product of part B does not follow Zaitsev's Rule. Explain (1 sentence) why in this particular Tatooinian biochemical system the less crowded product could be the major product.
Compounds A and B both undergo slow reaction in water. What is the major product (or major products) of each reaction? Is there minor a product, or multiple minor products? If so, what are they? Draw the mechanism for each reaction and use those pictures to explain why each of the observed products are major or minor. H2O
6. Give the major organic product from each mixed aldol reaction. Then explain why the reaction conditions favor one product instead of generating a mixture of products. NaOH a. + Н,о "СС, NaOH b. Н.о a. LDA c. b. О H н 7. Give the curved arrow mechanism for this reaction. NaOH, H,O Н heat
6. Give the major organic product from each mixed aldol reaction. Then explain why there conditions favor one product instead of generating a mixture of products. NaOH HO H CCI, NaOH HO a. LDA ht 7. Give the curved arrow mechanism for this reaction. he NaOH, H2O heat halla Τ Η 3. Give the major organic aldol product for each reaction, along with the dehydration product possible) formed after heating. NaOH heat H2O heat NaOH H2O ix heat NaOH HO
Organic chemistry help! please help 27. (ps) For the following reaction (a) (2pts) Circle the major expected product (b) (5pts) Give the detailed mechanism for the formation of the major product. (Include all steps, intermediates, resonance structures, and electron movement arrows.) (c) pts) Explain important factors related to why one product is fowered -=- Na NHI, 1 +
please help with organic chemistry! mechanisms? 5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following products. Please provide a detailed explanation to the formation of each product. You should use structures of intermediates in your answer. (8 points). осн, CH,он OCH Br + 6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one of them does not react with CH3CH20' to give an elimination product. Provide the structure of this compound and briefly explain why it does not react...
13. Give the curved arrow mechanism for each alkylation reaction. a. LiNiPr, (LDA) a. b. CH,Br CH, a. LiNiPr, (LDA) b. CHy-CHCH, b. 14. Explain why reaction G gives good yields of the product shown, while the yields are not as good with reaction H. о a. LDA G: b. CH,I CH a. LDA H: b. CH,I CHy 15. Give the major organic product of each reaction. Cl2 a. LDA CH,CO,H b. PЬСH, a. LDA Br2 b. f. b. CH,CH,CI...