Recall that a thermal reaction, specifically here a Diels-Alder reaction, begins with the rotation of the single bond in the diene, facilitated by the provided heat.

CO2Me heat + CO2Me CO2Me "CO2Me CO2Me CO2Me CO2Me CO2Me CO2Me CO2Me . Show transcribed image text.

CO2Me 2 heat CO2Me CO2Me CO2Me CO2Me CO2Me CO2Me o search a @ e苷 . Show transcribed image text.

Question: Which of the following is the main kinetic product of the Diels-Alder reaction OPh CO2Me OPh OPh OPh ...CO,Me CO Me "CO,Me II) III) I) O a. I O b. II O c. III The reaction of quinoline with Br2/ H2SO4 produces 5-bromoquinoline as major product.

Question: How would you carry out the following synthesis (more than one step is required)? What stereochemical relationship between the -CO2Me group attached to the cyclohexane ring and the-CHO groups would your synthesis produce, i.e. the CO2Me is on the same side or the opposite sides with the CHO groups? (1 pt). ? CHO CO2Me CO2Me CHO

CO Me 2 heat CO Me CO2Me CO2Me CO2Me CO2Me CO2Me CO2Me CO2Me Your solution’s ready to go! Our expert help has broken down your problem into an easy-to-learn solution you can count on.

Question: Q. 1.When molecules 1 and )=(CO2Me are heated together, the transient intermediates 3 and 4 are formed, with the eventual isolation of 5 and 6 as the two final products. Propose structures for 3 and 4 and a mechanism for the formation of 5 and 6.56

Question: MeO2C→∼CO2Me→heat ?Give the major product of the following reaction

Question: Provide the product for the following reaction. MeO2C= CO2Me heat

Question: 34. Reagents X and Y in the scheme below are: CO2Me CO2Me CH2OH Reagent X? Reagent Y? HO HO LiAlH(OR)3, then H20 NaBH4, CH3OH Hz with Pd/C LiAlH4, then H2O I II III IV Reagent X IV Reagent Y IV (A) (B) IV II II IV II I III I