Please show how you would synthesize a terminal ALKYNE to this fluorescein dye.
Terminal alkyne should be added to the bottom aromatic (with the COOH group)
you can use any reagent possible
We can add terminal alkyne through Friedel-Craft alkylation/acylation as shown below:
Please show how you would synthesize a terminal ALKYNE to this fluorescein dye. Terminal alkyne s...
please help! the final products woukd bw fluorescein for one and rhodamine for the other (2 different outcome but still the same method) B: 7) Mechanistically show how the following compound can be converted to the final product. (8 pts.) (Hint: It is related to one of your previous experiments this semester.) OH COOH X = OH or NET ators. They are often fluorescent and have been used corneal abrasions, as antibacterials and anticancer by a Friedel-Crafts acylation reaction. Friedel-Crafts...
Show how you would synthesize the following acid using carbonation of a Grignard reagent. Show how you would synthesize the following acid using carbonation of a Grignard reagent.
Show how you can synthesize the compound from a benzene Show how you can synthesize the compound from benerene COOH - Br NH2
Problem #3 Show how you would synthesize ethyl benzoate in good yield starting from benzene. You may use any other reagent necessary
company. Your task is to synthesize alkyne containing molecules since they are useful functional groups for further reactions. I) Propose a synthetic strategy to achieve the following transformation. You may use any inorganic or organic reagent that can help achieve your transformation. Your synthetic strategy will almost certainly require at least 3-4 steps. You do not need to include mechanistic details, but you should label your reagents and reaction conditions as clearly as possible. You may but are not required)...
4. In each reaction show how you would synthesize the product from the reactant. Show the reagents, conditions, and the structures of any important intermediates along the way. Any organic reagent may be used, and more than one step may be used as well. Include mechanism (+-) H Br
Could you help me synthesize the product using the given starting materials? They are multistep reactions. If possible, could you please include the mechanisms, it would help a lot! We were unable to transcribe this image(you can also use any three carbon reagent) (you can also use any one carbon reagent)
1)How would you synthesize the following product from the assigned reactants? a. You have to show the shortest and most effective reaction schemes using the ONLY given compounds as carbon sources to make the product. You can use proper reagent(s) for each step. b. Only two reactants allowed to build the carbon backbone are shown below. c. Explain how you would confirm each step using 1H-NMR, 13C-NMR, IR, and UV-Vis spectroscopie. (no spectrums needed) o - and to make Use
0.5 pts Question 4 (10 points) Show how you would synthesize the following aromatic compound from benzene and any other reacents necessary. Hint: Retrosynthesis. P .NO2 u h CH3 The reaction code in the box is:
6. Outline a stepwise reaction scheme to show how you would synthesize each of the compounds (A and B) below starting with ethene as starting material. [Show structure of intermediates and use appropriate reagent(s) in each stepl a. 1,1-Dibromoethane 84 b. 2-Bromotetradecane