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.
Give the products for the following reaction, predicting the major product, and indicating by which mechanism...
1.Predict all the products for the following reaction. Which is the major product? Why? + conc. H2SO4 heat OH 2. Give an alcohol that you could use to synthesis each of the following alkenes? din 3.Draw the mechanisms for the following two schemes (two separate mechanisms). Only show the mechanism for the most stable product for each scheme. What is the key difference in the mechanistic steps between these two reactions? ОН ОН conc H2SO4 conc H2SO4 heat heat
Application Questions 1. Predict all the products for the following reaction. Which is the major product? Why? conc. H2SO4 heat OH 2. Give an alcohol that you could use to synthesis each of the following alkenes? o in s 3. Draw the mechanisms for the following two schemes (two separate mechanisms). Only show the mechanism for the most stable product for each scheme. What is the key difference in the mechanistic steps between these two reactions? ОН conc H2SO4 heat...
Question 3. Predict the major products of the reactions below. Draw the full mechanism for the reactions, using appropriate arrows to indicate electron movement and the full structures of any intermediate(s). Use the mechanism of the reaction to provide a rationale for why the major product formed. OM (1 equivalent) ansole Bry Febr (1 culle brambenzone Fer (1 equivalent Priloromethylbenzene (9 marks) Question 4. Predict the major product from the treatment of 2,5-dibromopyridine with ammonia. Draw the full mechanism for...
Give a curly arrow or fish hook mechanism for the following reaction, indicating clearly both major and minor products expected. With reference to your mechanism and the stability of any key intermediates involved in both major and minor routes, explain why the process is regioselective.
Show the following mechanism for the reaction below. Give all the possible products that can be formed plus circle and label the major and minor products. (6 pts) H2SO4 MeOH
5. (6 pt) Will the product/products be different in this reaction? If yes, show the mechanism. CI et water + Nal rchて (8 pt) Predict the major products in each reaction. Say which mechanism predominates in case. DO NOT show the mechanisms 6. n2
5. (6 pt) Will the product/products be different in this reaction? If yes, show the mechanism. CI et water + Nal rchて (8 pt) Predict the major products in each reaction. Say which mechanism predominates in...
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
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...
Give the major products of the following reaction??
Give the major product(s) of the following reaction. HNO3 (1 mole) 3 H2S04, heat » CH
16. Give the major product that you would expect to be formed in each of the following reactions. If you think there is no reaction write NR after the arrow. In each case give the mechanism (SN1, SN2, E1 or E2) by which the product is formed. Also indicate the correct stereochemistry when applicable. Both product and the mechanism should be correct to get credit. No partial credit. Nal -BuOK Acetone t-Buo NaSH DMF Br, H NaOMe DMSO MeOH,rt t-BuOH...