The third product is not possible as the carbon of methyl group does not satisfy its valency. The rest are explained.
please show the reaction mechanism to obtain all of these products from 2-methylcyclohexanol OA као Н3РО4...
B only please 6| What products would you expect to obtain from reaction of 1-methylcyclohexanol with the following reagents? a) HBO b) Na2Cr2O7 (oxidizing agents)
help please 6) What products would you expect to obtain from reaction of T-methylcyclohexanol with the following reagents? 4) HIBI b) Na Cro oxidizing agents) How would you prepare the following ether using a Williamson synthesis?
Know the dehydration of alcohol mechanism. Dehydration of 2-methylcyclohexanol. (elimination reaction)
Propose at least three possible products with mechanism from the dehydration of 2-methylcyclohexanol.
For the dehydration of 4-methylcyclohexanol, how many products are there? Show the mechanism and label major/minor products.
1. Show, using the curved arrow notation, the mechanism of alcohol dehydration of 2- methylcyclohexanol using an acid catalyst to give the minor isomer not shown in the scheme above.
for the reaction that occurs when 4-methylcyclohexanol is heated in the presence of strong, concentrated sulfuric and phosphoric acids, give the mechanism for the reaction and list TWO test that can be performed to distinguish the product from the alcohol reactant 10B. For the reaction that occurs when 4-methylcyclohexanol is heated in the presence of strong, concentrated sulfuric and phosphoric acids, give the mechanism for the reaction and list two tests that can be performed to distinguish the product from...
5. Mechanism: (20 pts) Show the detailed reaction mechanism including all relevant arrows, intermediates, inorganic products, relevant resonance structures, and stereochemistry for the following reaction heat OH H-Br Step 1 step 2 Step 3 Step 4 Product(s) a. This is a Sx2/S1/E/Ez/ reduction / oxidation mechanism. b. What is the product if the starting alcohol is reacted with PBry? Product(s) with PBry c. Reaction with PBr; is a S2/S1/E/Ez/reduction / oxidation mechanism.
5. Mechanism: (20 pts) Show the detailed reaction mechanism including all relevant arrows, intermediates, inorganic products, relevant resonance structures, and stereochemistry for the following reaction. heat OH H-Br step 1 step 2 step 3 step 4 Product(s) a. This is a S2/Sx1/E/E2/ reduction / oxidation mechanism. b. What is the product if the starting alcohol is reacted with PBrz? Product(s) with PBrz c. Reaction with PBr3 is a S2/S1/Ej / E2 / reduction / oxidation mechanism.
Show stepwise mechanism for the formation of the 1-methylcyclohexene from 4-methylcyclohexanol. Use arrows to show the electron movements.