Starting with acetic acid or benzoic acid, and
anything else required, outline a rational synthesis for
phenylacetic acid.
Thank you for your help!
Starting with acetic acid or benzoic acid, and anything else required, outline a rational synthesis for...
Propose a reasonable mechanism for the lab synthesis of
phenylacetylene starting from benzene and acetic acid. Please
include CURVED ARROW METHOD. Thank you
III. Mechanism Based Questions (please note that application of the curved arrow method is required in this seçtion. 1) Propose a reasonable mechanism for the laboratory synthesis of phenylacetylene starting from benzene and acetic acid. (15 points)
Suggest a reasonable synthesis for the following compound using
the given starting material and anything else you need.
Question 3 (9 points) Suggest a reasonable synthesis for the following compound using the given starting material and anything else you need. (Hint: Show the intermediates, not only the conditions, for partial credit) ОН several steps
Starting with nitrobenzene and using any other reagents of your choice, outline a synthesis of para-chloroaniline Using acetic acid as your only source of carbon atoms, show how could you make N-ethylacetamide:
3) Starting from a 2 carbon molecule of your choice (only caveat is 2 carbons. It can have anything else on it) design a synthesis of the compound below (4 points)
Starting with benzene or toluene, outline a synthesis of each of the following compounds using diazonium salts as intermediates a) 3,4,5-Tribromobenzonitrile b) 2,6-Dibromobenzoic acid
Somewhere in this synthesis I’m supposed to create benzoic
acid. Is there a way to do this without doing gattermann?
Extra Credit Propose an efficient and elegant synthesis of the following compound. More than one step is required. You cannot use CHCL C?CHO, or CICOOR as reagents. CH3
Provide a step-wise synthesis of the molecule shown below using
the two starting materials provided and anything else you may
need.
5. Provide a stepwise synthesis of the molecule shown below using the two starting materials provided and anything else you may need. a. anything plus any other molecule containing 1 C plus any other reagents necessary. cl Hint: this is a highly convergent synthesis. You will need to prepare two separate molecules, then birng them together to form the...
17. Outline the reactions necessary to accomplish the synthesis of the following compound starting from benzene. Provide the necessary reagents/reactants and include the structure of intermediate organic products. Any additional organic starting materials used (excluding solvents) must not contain more than 3 carbons. You do not need to provide the mechanism of each reaction. ОН 18. Outline the reactions necessary to accomplish the synthesis of the following compound. Provide the necessary reagents/reactants and include the structure of intermediate organic products....
Experiment 12: Synthesis of Benzoic Acid pre-lab (4 pts) 1 (2 pts) Refer to the introduction on the general process of hydrolysis of nitriles to carboxylic acids. Starting with benzonitrile (shown below), show how it is converted to benzoic acid under basic conditions. N 2) (2 pts) The reaction for the synthesis of benzoic acid via benzonitrile hydrolysis is shown below: 1) NaOH, HO YOH + NaCl 2) HCI, H,0 Benzonitrile Density = 1.0 g/mL MM = 103.04 g/mol Benzoic...
Question 4 Outline the correct reaction sequence that will successfully transform the indicated starting material into the indicated product Input your answer as uninterrupted sequence of letters. Do not separate the letters by commas, spaces, dashes, or anything else. If you do then the robo-grader will not recognize it as the correct answer A CHCOOOH BH,80, C. N O /NO/H, 80, Heat D. KOHE the Mal Ho