Draw the structure of the product formed when the dienophile shown below is reacted with 1,3- cyclohexadiene.
Diels-Alder reaction:
The most well known Diels-Alder reaction is the thermal [4+2] cycloaddition reaction. The pericyclic reaction proceeds stereospecifically and in a single step.
The diene in the given Diels-Alder reaction is 1,3-cyclohexadiene and dienophile is fumaric acid. COOH groups in fumaric acid are trans to each other and they are also trans to each other in the product.
The reaction is given in the image below:
Draw the structure of the product formed when the dienophile shown below is reacted with 1,3- cyclohexadiene.
6 6) Starting from 1,3-cyclohexadiene and (E)-methyl but-2-enoate, draw a reasonable synthesis for the product shown below. (12 points) он CH3 + enantiomer 0 CO Me
Draw the structure of each of the following compounds: 1,4-Cyclohexadiene 1,3-Cyclohexadiene (Z)-1,3-Pentadiene (2Z,4E)-Hepta-2,4-diene 2,3-Dimethyl-1,3-butadiene
Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOCH3. Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOCH3. Indicate the stereochemistry of the product.
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....
draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NaOH3. Indicate the stereochemistry of the product. explanations are highly appreciated. thank you. (please show answer with dash and wedge) Draw the structure of the product that is formed when the compound shown below undergoes an elimination reaction with NAOCH3. Indicate the stereochemistry of the product Interactive 3D display mode CH3 CH3 Н.С" Br ШИ
Draw the organic product formed when the structure shown below undergoes a reaction with CH3C?CNa. Draw the organic product formed when the structure shown below undergoes a reaction with CH3C?CNa.
Draw the product formed when the structure shown below undergoes solvolysis in CH3CH2OH with heat. Interactive MarvinView Alkyl Halides: Substitution reaction with (2S,3R)-2-chloro-3-methylpentane with CH3O- Alkyl Halides: Reaction of 3-chloro-2,2-dimethylpentane and ethanol Draw the product formed when the structure shown below undergoes a substitution with NaOCH3. Interactive MarvinView Draw the product formed when the structure shown below undergoes solvolysis in CH3CH2OH with heat.
Part A Draw the structure of the product that is formed when the compound shown below is treated with the following reagents: 1) BHZ. THF: 2) H2O2. HO Interactive 3D display mode CH3 ОН Part A Draw the product formed when the compound shown below undergoes reaction with HCl in MeOH. Interactive 3D display mode CH3 H,C
is a compound that contains two double bonds. When 1,3-cyclohexadiene reacts with DBr (analogous to HBr) the following is observed. DBr O & & major product not formed a) Using words and structures, explain this distribution of products. b) Another product is formed in this reaction, shown below. Write a mechanism to explain its formation.
Draw the structure of the product that is formed when the compound shown below undergoes a reaction with H2C=O and then is treated with water.