5.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS
5.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 9. (15 pts.) A)...
help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 8. (18 pts.) Complete two of the three multistep syntheses below. You will not recieve extra credit for doing all three. You do not need to provide an arrow pushing mechanism. Be as specific as possible and draw a star next the two you would like me to grade. e =
2.Help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 6. (21 pts.) Fill in the missing reagents and conditions or products to complete the synthesis below: 1. DA, THE GO! N H 3.H30, heat Br MeO-B OME
3.Help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
4.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
whoever can help, it would be amazing! 353 organic chemistry upper level. 10. (3 pts.) Which statement best describes the value of using an enamine vs. an enolate in synthesis? a) An enamine is acidic b) Enamines are more volatile and can be removed from solution more easily c) Enamine formation does not require a very strong base d) Enamines can be formed from tertiary amines 11. (6 pts.) Circle the major product for the reactions below: NH2 NH2 NH2...
Organic chemistry mechanisms i need help with systheses questions 6,7,8,9 2-hydroxybenzoic (3 pts) 5. Provide an appropriate structure for: 3,3-dimethylcyclobutanecarbonitrile. (4 pts each, unless otherwise noted, 12 pts total) 6-8. Syntheses: draw / provide the likely organic product(s) generated in each of the reactions (or reaction sequences) below. As appropriate, pay attention to regiospecificity (new bond formation and location in the product formed) and stereochemistry (direction in space of new bond(s) formed). Indicate ALL likely products: where one product does...